Course units: Theoretical content.
\r\n\tEqually important are the consequences deriving from the extraordinary nature of the present times. The COVID-19 pandemic and the restrictive measures to contain the infection (lockdown and "physical distancing" in primis) have revolutionized the lives, and a distortion/modification of habits, rhythms, arrangements will continue to be necessary.
\r\n\tGovernments have implemented a series of actions to mitigate the spread of infections and alleviate the consequent pressure on the hospital system. On the other hand, the Covid-19 pandemic has caused a series of other cascading effects that will probably be much more difficult to mitigate and which expose to complex consequences. The past two years have brought many challenges, particularly for healthcare professionals, students, family members of COVID-19 patients, people with mental disorders, the frail, the elderly, and more generally those in disadvantaged socio-economic conditions, and workers whose livelihoods have been threatened. Indeed, the substantial economic impact of the pandemic may hinder progress towards economic growth as well as progress towards social inclusion and mental well-being.
\r\n\t
\r\n\tAlthough in all countries the knowledge on the impact of the pandemic on mental health is still limited and mostly derived from experiences only partially comparable to the current epidemic, such as those referring to the SARS or Ebola epidemics, it is likely that the demand for intervention it will increase significantly in the coming months and years. The extraordinary growth of scientific research in the field of neuroscience now offers the possibility of a new perspective on the relationship between mind and brain and generates new scenarios in understanding the long wave of the pandemic and in the prospects for treatment. Moreover, the pandemic also has led to opportunities to implement remote monitoring and management interventions.
\r\n\t
\r\n\tOverall this volume will address the complex relationship existing between COVID-19, mental health, acquired knowledge, and possible interventions taking a highly multidisciplinary approach; from physiological and psychobiological mechanisms, and neuromodulation through medical treatment, psychosocial interventions, and self-management.
The skill gap for careers in a changing industrial sector has been identified by numerous authors [1], which has prompted educators to quickly adapt their courses, in order to prepare future engineers to excel in this new environment.
Typically, the following basic skills are in general required for engineers to succeed:
ability to design, operate and troubleshoot processes and equipment, following best recommended practices, to maximize efficiency and productivity.
teamwork, discipline and time management.
More formally, a document defining the skills and competencies needed in the automation field was proposed by The Automation Federation and International Society of Automation (ISA) [2]. It is made up of following tiers: personal effectiveness, academic, workplace, industry-wide technical, automation technical, occupation-specific knowledge, occupation-specific technical, occupation-specific requirements, and management (see Figure 1).
Automation competency model [
In this model, it is possible to observe that competencies related to Communication, Integration, Software and Cybersecurity are placed in tier 5. Therefore, this is the natural place for the training program that will be described in next sections.
The Internet of Things (IoT) can be defined as a global dynamic network where physical and virtual objects interact to enable a set of services. In this context, the Industrial Internet of Things (IIoT) is the extension of this network to industrial sectors like logistics, transportation, manufacturing, utilities, oil and gas, etc. This extension enables to gather real-time data, necessary to make better decisions across all business functions: procurement, production, shipping, maintenance, etc.
To prepare for this chapter, several reports of teaching experiences related to IIoT have been consulted. In [1], the author describes his personal experience, working with educators and practitioners. It is stated that the path toward creating the Industry 5.0 workforce should begin in elementary school, and a specific curriculum is proposed for each level.
In [3] an on-line learning infrastructure is proposed, that allows to engage in a range of programming of real-world sensing applications, using a board based on the Arduino microcontroller, with several onboard I/O devices, including a slider, a pushbutton switch, a bank of six LEDs, and analog inputs for additional sensors. In [4] a syllabus is proposed, which offers guidelines for the quality assurance and safeguarding of IoT solutions, suitable for advanced studies at postgraduate level.
This chapter describes a hands-on educational approach to teach IIoT. In Section 2, we discuss common educational challenges in this domain and how to overcome them. In Section 3, we elaborate on the experience gained from teaching an elective course to undergraduate engineering students, in terms of learning outcomes, methodology, assessment and feedback. Wherever possible, we provide the link to possible solutions of proposed problems, that we have developed in order to make it available for interested readers to test and adapt them for their own projects. Finally, we conclude this chapter.
To the best of our knowledge, there is no official document specifically describing desired competencies in the field of IIoT. Therefore, we have extracted from [2], the following main technical IIoT-related desired competencies:
Design, document, install, and support the integration of automation systems with other systems, including Enterprise Resource Planning (ERP) and Manufacturing Operations Management (MOM)
Design and operate databases for automation systems. Perform data historian duties: curation, archiving, retrieval
Determine and implement the appropriate tools and methods for cybersecurity
The required technical knowledge includes:
Network configuration, diagnostics and management
Industrial digital field protocols (including but not limited to): AS-I, Ethernet/IP, DeviceNet, Foundation fieldbus, HART, INTERBUS, Modbus, PROFIBUS
Industrial communication protocols (including but not limited to) XML, JSON, ASN.1, BACnet, ControlNet, Ethernet-TCP/IP, LonWorks, OPC UA, PROFINET
Data contextualization (online/offline), modeling (UML, Entity Relation), storage and retrieval
Therefore, it is possible to observe that there is a broad range of topics to be addressed, which is the first pedagogical challenge that instructors will encounter when trying to design an IIoT course. Here, we propose to select only a basic sub-set of skills and content, which is equivalent to focus on the expected quality and depth of learning, rather than on the number of tools or protocols included in the syllabus (see Table 1, Section 3).
Unit | Topic | Content |
---|---|---|
1 | IIoT Fundamentals 3 weeks | Industrial communication: principles, protocols and technologies. IIoT definition, architectures and use cases. Convergence of IT and OT. Design methodology. |
2 | Interfacing sensors and actuators 3 weeks | Proximity sensors, temperature sensors, vibration sensor, color sensors. Controlling DC/AC motors. |
3 | Programming with Node Red 3 weeks | Injecting nodes, debugging, managing palettes, designing dashboard. |
4 | Cloud services 3 weeks | Basic concepts. Device management. Applications: predictive maintenance, quality monitoring, personalized dashboards. |
Course units: Theoretical content.
The second challenge is the complexity of real world IIoT applications, which may impede their study, keeping in mind time and resource constraints [5]. Here, we propose to break down problems into simpler sub-problems, which can be solved within the allocated time, using available tools.
For example, the typical integration problem of a given control system to a remote dashboard can be divided into the following 5 sub-problems:
Design and implementation of a local dashboard, considering only devices able to communicate through Modbus RTU
Assuming the previous system is working, integration of devices able to communicate through Modbus TCP/IP
Integration of devices able to communicate through OPC UA
Setting up communication to remote broker through MQTT protocol
Implementation of more complex applications like computer vision, anomaly detection, etc.
These problems will be further explained in next section, in the framework of a case study centered in our experience teaching an elective course to undergraduate engineering students.
The course Industrial Internet of Things (IIoT) aims at creating the fundamentals skills required to design, implement, and maintain industrial IoT systems. It is taught as elective course to undergraduate engineering students in their prefinal year. A previous exposure to embedded system programming, instrumentation and control systems is recommended. On successful completion of this course students are able to:
Explain the key components that make up an Industrial IoT system.
Discuss protocols and standards employed at each layer of the IIoT stack.
Design, deploy and test a basic Industrial IoT system, including data analysis functionalities.
Apply best practices to meet desired requirements for IIoT applications.
Analyze the environmental effects and incorporate robustness in design of IIoT system.
Choose technology for constrained nodes and network while maintaining real time data collection.
Explain the importance of cybersecurity for IIoT networks.
The course delivery is planned in online mode and three sessions per week are conducted for 18 weeks. These sessions include concept discussions, hands-on activities, projects, and assessments. The course description document containing the syllabus (see Table 1), learning outcomes, assessment rubric and references for learning materials is shared with students at the beginning of course. All the software is open source and sessions to install Node-Red, VNC viewer, Raspbian Busters operating systems, etc. are held at the beginning of the course. It is recommended for students to have a Desktop/Laptop able to run Windows 10.
The hands-on, problem-based learning or experiential learning approach means students are given a set of problems, and while trying to solve them they learn theoretical concepts. Figure 2 summarizes the concept map for the learnings in this course, showing the topics discussed and demonstrated during hands-on sessions.
Concept map for the domain knowledge imparted in IIoT course.
Next, we describe the set of problems that were proposed to students. Note that, as discussed in previous section, they correspond to the breaking down of a more complex control system integration problem.
Consider the input/output variables shown in Table 2. We assume they correspond to a set of sensors and actuators connected to a device, e.g., PLC, Raspberry Pi, Arduino board, etc., able to act as a Modbus RTU slave, at address 01. It is required to design and implement a dashboard to supervise and control this process, which will also run at edge level, in a second device able to run Node Red [6], e.g., Desktop PC, Laptop or Raspberry Pi. This second device will act as Modbus RTU master.
Data address | Type | Internal tag | ISA S5.1Tag | Range |
---|---|---|---|---|
0 | Analog input register – read only | AI0 | TC01.PV | 0–100°C |
1 | Analog input register – read only | AI1 | FC02.PV | 0–150 lt/min |
2 | Analog input register – read only | AI2 | PC03.PV | 0–200 psi |
3 | Analog input register – read only | AI3 | SC04.PV | 0–1000 RPM |
4 | Analog input register – read only | AI4 | VC05.PV | 0–10 mm/s |
5 | Analog output register – read/write | AW0 | TC01.SP | 0–100°C |
6 | Analog output register – read/write | AW1 | FC02.SP | 0–150 lt/min |
7 | Analog output register – read/write | AW2 | PC03.SP | 0–200 psi |
8 | Analog output register – read/write | AW3 | SC04.SP | 0–1000 RPM |
9 | Analog output register – read/write | AW4 | VC05.SP | 0–10 mm/s |
10 | Discrete input coil – read only | DI0 | YC06.PV | 0/1 |
11 | Discrete input coil – read only | DI1 | YC07.PV | 0/1 |
12 | Discrete input coil – read only | DI2 | YC08.PV | 0/1 |
13 | Discrete input coil – read only | DI3 | YC09.PV | 0/1 |
14 | Discrete input coil – read only | DI4 | YC10.PV | 0/1 |
15 | Discrete output coil – read/write | DW0 | YC06.SP | 0/1 |
16 | Discrete output coil – read/write | DW1 | YC07.SP | 0/1 |
17 | Discrete output coil – read/write | DW2 | YC08.SP | 0/1 |
18 | Discrete output coil – read/write | DW3 | YC09.SP | 0/1 |
19 | Discrete output coil – read/write | DW4 | YC10.SP | 0/1 |
Input/output variables for Problem 1.
A low-cost solution for this problem is to set up an Arduino/Genuino Uno as MODBUS slave, which is a microcontroller board based on the ATmega328P microprocessor. It has 14 digital input/output pins, of which 6 can be used as PWM outputs, 6 analog inputs, and runs with a 16 MHz quartz crystal (see Figure 3). Note that, in this problem, no real sensors/actuators will be connected to this board, because we are only interested in testing communication features. This means that the board will always be sending “dummy” data to the master. This also means that students do not need to have any sensor or actuator at home during on-line classes, to work on this problem.
Example of required set-up for Problem 1.
We propose to use the library SimpleModbusSlave [7] which allows the Arduino board to communicate using Modbus RTU protocol. Note however that it does not fully comply with Modbus specifications, as only functions 3, 6 and 16 are implemented. Similarly, the check for inter character time-out and frame time-out are combined by checking a maximum time allowable when reading from the message stream. This library implements an unsigned int. return value on a call to modbus_update(), which is the total error count since the slave started. Once this function is called, the input/output register defined during setup with function modbus_configure() will be updated. Note that we have also successfully tested this library with Arduino Nano.
In addition to communication setup, it is possible to add other features in this Arduino program, to make it dynamic when visualizing the dashboard, as follows:
For variable TC01.PV it is required to program a counter that increments from 0 to 100 and then is reset to 0.
Between variables VC05.PV and VC05.SP it is required to implement a first order transfer function, to simulate a real process.
Status of discrete output variable YC06.SP must be updated to YC06. PV and Arduino built-in LED.
An example of code complying with these specifications is available in this link: https://bit.ly/3eqHmxB. It is possible to test this code, previously to developing user dashboard, with QModbus, which implements a master application through a graphical user interface, allowing communication with slaves over serial line interface [8]. Students are able to analyze Modbus frames, from master and slave.
The previous explanation corresponds to the edge layer. Now considering the gateway layer, Node Red is able to run in different devices. We have used a laptop for convenience. The following palettes must be installed:
node-red-contrib-modbus, version 5.13.3
node-red-dashboard, version 2.28.1
An example of Node-Red code is available in this link https://bit.ly/2RnA9q0, as shown in Figure 4. The corresponding dashboard is shown in Figure 5.
Example of Node-Red code for Problem 1.
Example of Node-Red dashboard for Problem 1.
For the same process described in problem 1, include the input/output variables shown in Table 3, connected through Modbus TCP/IP at address 02.
Data address | Type | ISA S5.1Tag | Range |
---|---|---|---|
0 | Analog input register – read only | TC11.PV | 0–100°C |
1 | Analog output register – read/write | FC12.SP | 0–150 lt/min |
2 | Discrete input coil – read only | YC13.PV | 0/1 |
3 | Discrete output coil – read/write | YC14.SP | 0/1 |
Input/output variables for Problem 2.
An example of Node-Red code for Problem 2 is available in this link https://bit.ly/3tpnv7x. It is possible to test this code with ModbusSlave, which enables simulation of slave devices [9]. The limitation is that this software runs only in Windows operating system. The dashboard integrating measurements from both sources Modbus RTU and TCP is shown in Figure 6.
Example of Node-Red dashboard for Problem 2.
Design a dashboard to display the OPC UA tags shown in following Table 4, which will be randomly generated by Integration Objects’ Server Simulator, which is a free to use tool [10].
Tag | Address | Type |
---|---|---|
Tag11 | ns = 2; s = Tag11 | Int16 |
Tag12 | ns = 2; s = Tag12 | Int32 |
Tag13 | ns = 2; s = Tag13 | Int64 |
Tag14 | ns = 2; s = Tag14 | UInt16 |
Tag15 | ns = 2; s = Tag15 | UInt32 |
Tag16 | ns = 2; s = Tag16 | UInt64 |
Tag17 | ns = 2; s = Tag17 | Double |
Tag18 | ns = 2; s = Tag18 | String |
Tag19 | ns = 2; s = Tag19 | Byte |
Tag20 | ns = 2; s = Tag20 | Boolean |
OPC UA tags for Problem 3.
An example of Node-Red code to solve this problem is available in this link https://bit.ly/3er1QqZ. The following palette must be previously installed: node-red-contrib-opcua. The dashboard displaying required OPC UA tags is shown in Figure 7.
Dashboard displaying required OPC UA tags.
It is required to design and implement a remote dashboard, which will run in Cloud, using Message Queueing Telemetry Transport (MQTT) protocol.
It is recommended to have at least some hardware setup (sensors, micro-controllers, power supply, etc.) available with the instructor. In case students do not have any hardware at home, they write the code and send it to the instructor for testing purpose. A schematic diagram showing the architecture for interfacing sensors and uploading the data to Cloud is shown in Figure 8. The data from the analog pin is sent to serial port of Arduino. The data from the controller board serial port is sent to the Internet gateway. Node-Red flow is run on the gateway and enable the data to be sent to Cloud.
Architecture for interfacing and uploading data to Cloud.
A snapshot of flow where a SW-420 vibration sensor has been interfaced to an Arduino Nano, which sends the values to dashboard and display them in form of chart, is shown in Figure 9.
Displaying SW-420 vibration sensor data in form of chart.
The sensors may be interfaced to the microcontrollers using various protocols. An example of this is the Zigbee protocol where sensors communicate with an end point device, which in turn sends the sensor data through routers to the Zigbee coordinator. The advantage of this type of connection is that multiple sensors can be connected to endpoint devices, and many such endpoint devices may be connected in star topologies to the controller through routers.
The Zigbee protocol is known to be secure and low power consuming as the endpoints which are inactive may sleep for the inactive duration. A typical application could be connecting crop monitoring sensors to end points and sending the data from endpoints to coordinator, which in turn may send the data to an MQTT server using the node-red-contrib-zigbee pallete (see Figure 10).
Example of Zigbee architecture for agriculture application.
Various other wireless protocols like the Sigfox and LoRa WAN may be used for interfacing the sensors to the master coordinator/controller. The advantage of some of these emerging protocols are low power consumption and high data rates [11, 12]. The IoT Gateway is used to convert the data format received from any of these protocols to internet protocols like the HTTP, MQTT, XMPP or any other light weight protocol. The Gateway also implements security for the Endpoint and Coordinator devices and may do some edge computing or data analytics before sending the data to the Cloud storage.
Students were able to interface the Raspberry Pi camera to upload images to Cloud, trying to optimize bandwidth usage. MQTT protocol and associated libraries for image transmission using Python programming are used in some of these projects for uploading data to Cloud. The Node-Red palletes required for implementing the flows were identified and installed.
Machine Learning services available on Cloud like IBM Watson were used by students, where algorithms for image recognition and classification, text recognition and other resources of AI/ML deployed. Knowledge of Raspberry Pi boards and Python programming as well as running Node-Red using Docker container was introduced. Node-Red flow was used to upload camera images and to classify objects using pretrained models from Tensorflow.js (Common Objects in Context dataset), available from pallete node-red-contribtensorflow [13, 14]. A simple flow for interfacing the camera and sending images to Cloud is shown in Figure 11. The flow consists of an inject node followed by execute node which contains the command to run the python program and a message payload node to debug the messages.
Simple flow for interfacing the camera and sending images to Cloud.
Once students have completed all the previous hands-on activities, they were requested to work on a project, so they can apply the methods they have learned. First, they must submit a project charter, describing the project goals, responsibilities of team members, resources/bill of materials, references to literature and timing charts. Students should be made conscious of the professional ethics while working on this project. We consider the following facts as academic dishonesty offenses:
Cheating: using unauthorized information. Receiving or giving unauthorized assistance.
Fabrication: invention or falsification of any information.
Plagiarism: deliberately representing the ideas, results, reports, drawings, notes, computational code, or any other product prepared by another person as one’s own.
Some of the project ideas identified by the students for this course are:
monitoring safety in personnel in industry by monitoring camera images for helmet usage,
facemask detection for crowd at public places using live video transmission.
home automation using Zigbee and MQTT protocol and Node-Red flow(s),
language translation: speech to text and vice versa for real time audio signal,
surveillance using infrared camera and live video transmission to remote control station.
Quizzes are recommended to be conducted periodically for assessing the learning outcomes. The aim of these evaluations should be to determine the understanding of concepts for implementation. As a sample a quiz may comprise following questions (with marks break) as follows:
Q1. Write Node-Red and Arduino code to solve the following problem:
Communication between Arduino and Node-Red can be implemented using any protocol (4 marks)
Two values A in [0, 100] and B in [0, 100] will be generated through Node-Red dashboard and written to Arduino board (3 marks)
Average M of these A and B will be calculated by Arduino board (3 marks)
Average M needs to be displayed back in Node-Red dashboard (3 marks)
If M is greater than 80 during 5 seconds, an alarm H will be displayed in the Node Red dashboard and Arduino built-in LED, until a RESET button (also in dashboard) is pressed (3 marks)
All values A, B, M and H will be published to Mosquitto MQTT broker, to following topics: IIoTQuiz1/Name/A, IIoTQuiz1/Name/B, IIoTQuiz1/Name/M, IIoTQuiz1/Name/H, where Name is student’s name. (4 marks)
Feedback is recommended fortnightly to understand the learning process. A sample questionnaire and the responses are shown in Figure 12 here for the course conducted by the authors for the first time for undergraduate students. The bar charts are self-explanatory and the feedback will be considered for further improvements.
(a–f) Feedback questionnaire and responses by students for the first time launch of the course.
In this chapter, a hands-on educational approach to teach Industrial Internet of Things (IIoT) was proposed. Because the set of required skills is large, we propose to focus on a basic sub-set of skills and content, trying to achieve the best possible quality and depth of learning. To overcome the complexity of real world IIoT projects, we propose to identify simpler sub-problems, which can be solved within the allocated time, using available tools. To illustrate our approach, specific examples, in terms of learning outcomes, methodology, assessment and feedback were presented. Wherever possible, link to solutions was provided for interested readers to test and adapt them for their own projects. The feedback received from students and their final performance is encouraging, as they seem to appreciate the proposed approach. We believe the same can be extended to teach similar courses like Digital Computer Networks, SCADA systems, Programmable Logic Controllers, etc. Currently, authors are planning to scale up this course, as an international MOOC, to reach a broader audience.
We are grateful to the Atal Incubation Center at JK Lakshmipat University for funding the projects for this course. We also acknowledge the support and motivation from the management in helping us to launch this course for students pursuing Bachelor in Technology degree in Electrical and Electronics Engineering.
A clean environment and sustained energy resources are essential for future generations. With growing concerns for both dwindling traditional fossil fuels and global warming, there is an urgent need to develop renewable and environmentally benign alternatives to address these issues of mankind [1, 2, 3]. Currently, humans are mainly dependent on fossil fuels and thus extract carbon from the geosphere and put it into the atmosphere where it causes global warming. There are two methods that can be helpful in preventing and reducing carbon emissions. The first and convenient way to stop carbon emissions is to move towards zero carbon-emitting resources. In view of this, hydrogen (H2) produced by photo/electrocatalytic water splitting has shown great potential to become the fuel of the future. The merits have been attributed to its high energy density and it produces only one by-product of water upon combustion [4]. Thus H2, which is a zero carbon-emitting fuel, can be a promising solution to the mitigation of climate change. The second method is to capture carbon from the atmosphere and then store it back into the geosphere. However, the geosphere sequestration of CO2 has no financial benefits. In contrast, chemical transformation of excess accumulated CO2 from air into valuable industrial products, such as fuels (methanol, ethanol), hydrocarbon (methane, ethylene) and chemicals (formic acid, acetic acid), is an effective way to solve both global warming and energy crises [5, 6]. Furthermore, it has economic significance from an industrial point of view. However, carbon-di-oxide reduction (CO2R) is a highly cumbersome and non-specific process. So far, several approaches, such as biochemical, chemical, thermal, photochemical and electrochemical catalysts have been explored to achieve aspirated activity and selectivity in this region [7, 8, 9]. Nonetheless, unlike other catalytic system electrocatalysts have gained tremendous attention due to its easy operation at ambient temperature and pressure. In addition, the selectivity of the product can be obtained by just adjusting reaction conditions, such as redox potential, electrode, and electrolyte, pH temperature and so on. The main advantage of using electrocatalysts is that they can be powered by renewable energy sources that emit zero carbon. For all these reasons, many research activities have shifted to the areas of EH2ER and ECO2RR (Figure 1) [10].
Electrochemical CO2 conversion into fuel and H2 production by using colloidal nanocrystal-based electrocatalysts.
Over the years of time metal, metal oxide, metal sulphide have shown great promise in ECO2RR and EH2ER using electrocatalysis phenomenon. These electrocatalysts are being considered as a promising system that would be able to operate on a real scale without polluting environment. Whereas, there are still many limitations that are associated with electrocatalysts, such as high cost, poor product selectivity, high overpotential and low stability [11]. Colloidal Nanocrystal (C-NC) based electrocatalysts have become indispensable to overcome these limitations to certain extent owing to their larger surface to volume ratio, precise shape, long-term durability, and the plethora of configurations [12, 13]. These factors are important in influencing their efficiency, selectivity, and durability for EH2ER and ECO2RR. For example, variation in the size and/or shape causes alteration in reactivity at different locations (edges/corners/faces) of the C-NC due to changes in a specific atomic-arrangement of active centers and crystal surface energy. The impact of these features will be discussed in detail as this chapter unfolds.
The purpose of this chapter is to elaborate on recent research developments and challenges in the field of heterogeneous C-NCs-based electrocatalysts for ECO2RR and EH2ER. In the first part of this chapter, colloidal synthesis of nanocrystals will be discussed. The second part of this chapter will address the structural aspects, such as size, shape, and composition, are important in tuning the catalytic efficiency, selectivity, and durability of NC-based catalysts for ECO2RR. Here a brief introduction of effect of ligand functionalization and effect of MOF/NCs hybrid system on ECO2RR activity will be also discussed. In the third part of this chapter, the role of C-NCs-based catalysts on EH2ER, its activity and stability is given. Moreover, the detailed mechanism of EH2ER is also discussed in this part. Finally, Authors have given extractive commentary that sheds light on the future perspective of ECO2RR and EH2ER in conclusion.
The C-NC is an inorganic material with a size of 1–100 nm and surface covering of protecting capping agents like polymer and surfactants molecules. Generally, the inorganic part exhibits characteristic features, such as optical, electrical, magnetic, and catalytic, that can be tuned by changing their physicochemical parameters, while surface capping guarantees the stabilization of these structures and paves the way for synthesizing more complex structures [14, 15]. The physical parameters like morphology and chemical composition of C-NCs can be easily adapted by varying their reaction parameters like monomer concentration forming inorganic core of NCs and judicious choice of capping substances for surface covering. Over the last two-three decades, researchers have gained good control over synthesis of high-quality and cost-effective NCs with uniform morphology and chemical constituents using colloidal synthesis [16, 17, 18, 19]. The C-NCS approach has not only enhanced efficiency, selectivity of NCs, but also improved their service life. So far, researchers have found many commercial applications of C-NCs in various fields ranging from life sciences to the material world. One of the striking applications of C-NCs is in the field of biological imaging of cells, where quantum dots are used owing to their excellent fluorescent properties and also they do not photo-chemically bleach out like organic dyes [20]. Recently, quantum dots are being used commercially in LED displays also known as
In general, C-NCs can be synthesized in both water and organic solvents. However, synthesizing a broad spectrum of NCs requires different reaction conditions that are much more feasible to achieve in organic solvents compared to water that is mainly used in the synthesis of noble metal C-NCs [14]. Therefore, in this section, authors will focus on organic phase C-NCs synthesis. Generally, C-NCs synthesis requires three major elements: 1) precursor molecules or building blocks forming inorganic core of NCs, 2) capping agents, and 3) organic solvents. Capping agents sometime act as solvent. The process of nanocrystal formation starts with transformation of precursor molecules into unstable and reactive species or monomers that usually occurs at quite high temperature. Thereafter, these monomers lead to formation of C-NCs whose growth is mainly influenced by capping agents. The crystallization of C-NCs can be best understood using widely accepted LaMer mechanism as depicted in Figure 2 [22, 23, 24, 25]. Based on this mechanism, NCs development considered to have three major steps. In the first phase, the precursor molecules are converted to the reactive species, or monomer, and then eventually reach to a supersaturated phase (I), where no particle or second phase is still visible. In the next step, reactive species concentrate to the critical limit of supersaturation (phase II), at which a thermodynamically feasible state (
The LaMer mechanism based formation of active monomers, burst nucleation, and subsequent slow growth of colloidal nanocrystals. Adapted from [
Secondly, capping agents are required to bind in such a way that it can desorb and adsorb on the surface of growing NCs during growth process, making growing NCs surface accessible for reactive monomers, yet surface covering of capping agents, overall, stabilize NCs [14, 26].
During NC synthesis, control over size uniformity is a prominent feature of contemporary synthetic methods. The LaMer mechanism discussed earlier not only explains the formation of NCs, but is also an approach to synthesize C-NCs with narrow size distributions. The essential element of LaMer approach to synthesize uniform-sized C-NCs is to divide crystallization into two disparate events; nucleation and growth. As discussed previously, the nucleation occurs for short periods of time, also known as burst nucleation, triggering a different growth phase where all nuclei then grow at the same rate without generating extra nuclei. The formation of extra nuclei during the growth phase can cause differences in the size of C-NCs because the newly formed nuclei will lag behind the previously growing NCs in growth kinetics. The several methods utilize LaMer mechanism to grow uniform size C-NCs [24, 27]. The first example is seed-mediated growth method where reaction medium is introduced pre-developed nuclei at low monomer concentration to inhibit secondary nucleation. Therefore, these pre-developed nuclei further grow up to the desired size of C-NCs without creating extra nuclei. However, in order to obtain narrow size distribution of NCs, it is still required to control growth phase as well. The second example is hot injection method where the reaction medium at high temperature is rapidly supplemented with the precursor or reducing reagents to create a state of supersaturation that triggers subsequent burst nucleation. The next example is the heating up method where reaction medium pre-treated with precursor, and capping agents is heated at high temperature to induce the LaMer crystallization. Due to the simplicity of this method it is often used to synthesize C-NCs at large scale [28, 29, 30].
Unlike the bulk materials, the physiochemical properties of C-NCs are also strongly dependent on their shape. In this chapter, authors will further discuss how the shape of C-NCs can be adapted to improve the service life, selectivity and efficiency of electrocatalysts. Generally, C-NCs shapes can be tuned by means of both thermodynamic and kinetic controls. In C-NCs synthesis, capping agents are used, primarily, to obtain the desired shape using their specific binding nature on the surface of the growing NCs [31]. If the surface adsorption of capping agents causes the decrement in surface energy of any specific facet, then the obtain shape will be favored by thermodynamically. Whereas, if capping agents serves an obstruction between growing NCs and diffusing monomers then the resulting shape of C-NCs will be governed by kinetic factors [32, 33]. Thermodynamically, the growing NCs attain it most likely shape by reducing its total surface free energy. For example, during the formation of fcc NC, the capping agents first selectively adheres to the (100) plans, which in turn, decreases their surface free energy [32]. These selective adsorptions onto the (100) plans causes transformation of cuboctahedron into cubic structure due the subsequent growth of higher energy facets. Whereas, in the kinetic regime, capping agents selectively adhere to some specific facets to lower their growth rate compare to others, resulting in various NCs shapes. Simultaneously, capping agents inhibit the diffusion of pre-deposited atoms over the NCs surface. In the real situation, however, the final shape of C-NCs is governed by the comparable kinetics of diffusion and deposition of monomers to growing NCs [32].
Thermodynamically, CO2 is a quite stable molecule (bond dissociation enthalpy of C=O is ~750 KJ mol−1), so high energy is required for its activation. Moreover, the highest oxidation state of CO2, causes problems for its selective reduction [34]. A catalyst in this regard is an alternative that offers reactive sites for its selective and rapid transformations. In this chapter, the authors are focusing specially on NC-based electrocatalyst for ECO2RR. Generally, ECO2RR involves several proton/electron transfers processes that take place at the cathode (catalyst). This process is considered to have three major stages. First, CO2 is absorbed on the catalytic surface and its binding strength depends on the structure and composition of the NC as well as the nature of the electrolyte. Once it is absorbed, an electron is transferred to the CO2 molecule that produces surface bound CO2−. Intermediate as depicted in Figure 3. This step is known as a rate-limiting step because it requires large reconstitution energy to convert linear CO2 into twisted form, that is, CO2.−. For this reason, it requires extra potential (overpotential of −1.91 V) for electrochemical CO2 conversion, even if it is thermodynamically feasible. After the formation of CO2.
Reaction pathways leading to the formation of formate, CO, and C–H products are highlighted. Adapted from [
Furthermore, it was realized that surface properties of electrocatalyst, such as, surface area, roughness, composition, and morphological design have profound influence on efficiency, selectivity and durability of electrodes in electrochemical reactions [37, 38]. It is a general understanding that the higher surface area provides good economy of the active center on the surface relative to the bulk, and thus, accelerates CO2 reduction. Similarly, Cu shows optimal coordination with CO, however, changes in surface structure, such as roughness, may deviate from their normal behavior. For example, Jiang et al. showed that the high population of under-coordinated sites on the rough surface of the Cu leads to the formation of oxygen-containing compounds and hydrocarbons compared to CO due to enhanced interaction with CO* intermediates [38]. However, it is still challenging to adjust the optimal binding energy for intermediates to increase selectivity/reactivity towards ECO2RR, because of the large number of intermediates and many possible intricate pathways involved. Until now, many bulk metal-based electrodes have been investigated from both a material and structural point of view; however, they are still facing many hurdles, such as: 1) high overpotential of the existing electrodes, 2) obtaining a mixture of products due to poor product selection of the catalyst, 3) deactivation of metal-based electrodes in short periods, 4) high cost of metal-based electrodes such as Ag, Au, Pt etc. discourages their use economically, 5) slow kinetics, or low activity. Beside there is always a competitive reaction EH2ER to the ECO2RR based on the thermodynamics. Rapid electron transfer in first step of electrochemical CO2 reduction may be an effective strategy to suppress EH2ER, which, in turn, accelerates ECO2RR. In Table 1, the authors have summarized electrochemical Eqs. (1–16) of CO2R in some valuable products such as CH4, CH3OH, HCOOH, etc., with their respective equilibrium potentials in aqueous medium (pH 6.8) at 1 atm. and 25°C with respect to standard hydrogen electrode (SHE) [39, 40]. The equilibrium potential of the ECO2RR, as provided, corresponds to the equilibrium potential of the EH2ER.
Products | Thermodynamic half-cell equations | E(V) |
---|---|---|
Methane | CO2 + 8H+ + 8e− | 0.17 |
Carbon-mono oxide | CO2 + 2H+ + 2e− | −0.10 |
Methanol | CO2 + 6H+ + 6e− | 0.03 |
Formic acid | CO2 + 2H+ + 2e− | −0.02 |
Acetaldehyde | 2CO2 + 10H+ + 10e− | 0.05 |
Acetate | 2CO2 + 8H+ + 8e− | −0.26 |
Ethanol | 2CO2 + 12H+ + 12e− | 0.09 |
Ethylene Ethylene glycol | 2CO2 + 12H+ + 12e− 2CO2 + 10H+ + 10e− | 0.08 0.20 |
Glyoxal | 2CO2 + 6H+ + 6e− | −0.16 |
Glycoaldehyde | 2CO2 + 8H+ + 8e− | −0.03 |
Acetone | 3CO2 + 16H+ + 16e− | −0.14 |
Allyl alcohol | 3CO2 + 16H+ + 16e− | 0.11 |
Propionaldehyde | 3CO2 + 16H+ + 16e− | 0.14 |
1-Propanol | 3CO2 + 18H+ + 18e− | 0.21 |
Hydroxyacetone | 3CO2 + 14H+ + 14e− | 0.46 |
Recent studies have shown that nanometer-sized (1–100 nm) electrocatalyst is not only capable of reducing overpotential, but also shows an improvement in current density for CO2 conversion. Regardless of the metal, the electronic structure of the catalysts at nanoscale is a key player in determining their efficiency, selectivity and durability for ECO2RR. Several electronic factors have been determined, such as finite size effects, and the location of the d band center that can tune the binding strength of intermediates, such as CO*, CHO*, etc., on the nanoparticle (NP) surface and thus, alter the reactivity of NP-based electrocatalysts [41, 42, 43]. In addition, the geometric effect is an important factor that is crucial in stabilizing the specific intermediate during the reduction process, which leads to an increase in selectivity [44, 45]. When using C-NC-based electrocatalysts, electronic and geometric factors can be adapted to increase selectivity, stability and activity using several approaches, such as size adjustment, shape modification, compositional control, surface functionalization and reaction conditions. As discussed earlier, the nucleation and growth process can be optimized by changing the reaction conditions (thermodynamic and kinetic of the reaction) to achieve the desired C-NCs with well-defined composition, and morphology. Therefore, C-NCs-based catalytic systems have been found to be highly promising to lead the catalytic field that can achieve higher selectivity and efficiency than existing systems. Here, our focus will be mainly on to understand how properties like size, shape, morphology, composition and surface functionalization of nanocrystal affect efficiency and durability of C-NCs-based electrocatalysts for ECO2RR.
The size is an important factor for C-NC-based electrocatalysis because different size of C-NCs show different activity/selectivity towards ECO2RR. Several studies have shown that alteration in size at nanoscale can affect both atomic distributions at various reaction sites (plans, edges, corners) and electronic structure of NCs, changing their catalytic characteristics. Therefore, the search for the optimal size C-NC showing the best efficiency, selectivity and durability requires contemporary research in this area. So far, to explore the effect of size towards ECO2RR, different sizes of electrocatalysts have been evaluated, however, our focus here is towards C-NC-based electrocatalysts. Colloidal synthesis of NCs is an excellent approach to study different sizes of NCs while keeping other factors such as shape and composition stable. Loiudice et al. synthesized spherical and cubical Cu C-NCs in the size range of 7.5–27 nm and 24–63 nm respectively for ECO2RR [46]. Their study has revealed unprecedented correlation between size of NCs and their electrochemical activity as well as selectivity for ECO2RR. The activity of Cu C-NCs increases as size of NCs within same morphology decreases, however, this does not hold while comparing cubical NCs with spherical. For example, the 44 nm cube has higher current density than 27 nm sphere. To understand this phenomenon, the propensity of Cu (100) facet towards ethylene production can provide a better understanding. Based on previous findings, it is widely accepted that the Cu (100) plane is selective for the electrochemical reduction of CO2 in ethylene. Additionally, edges in ethylene production are thought to be responsible for the absorption and stabilization of an important intermediate (i.e., COOH *) as well as inhibiting EH2ER. In this study, the X-ray diffraction pattern has shown a higher contribution of the Cu (100) plane in the nanocube than in the nanosphere and Cu foil. Interestingly, among all Cu C-NCs, a size of 44 nm exhibited highest selectivity with 50% FE for ethylene and overall 80% for ECO2RR over EH2ER. This can be ascribed to changes in atomic configuration at different sites of C-NC due to differences in size. As nanocube move from smaller to larger sizes, the number of atoms at the edges and corners decreases, however, the number of atoms at the plane site increases. As a result, it came close to the morphology of a single crystal, where all the atoms of the surface are populated on the (100) plane. And, as previously stated edges also play an important role in electrochemical reduction of CO2 into C2 products. Therefore, an optimal balance between ratio of edge to plane site in 44 nm Cu C-NC, suggesting not only its unique selectivity for C2H4, but also an overall activity towards ECO2RR.
Similarly, Zhu et al. investigated the non-monotonic size-dependent selectivity of Au C-NCs for CO2 reduction into CO [47]. Among Au C-NCs of size 4, 6, 8, 10 nm synthesized, the 8 nm exhibited a highest selectivity for CO production with FE of ~90% at −0.67 V vs. RHE as shown in Figure 4(c). Based on the DFT calculations, the group concludes that dominance of edge sites at 8 nm C-NC facilitates selective CO2 reduction in hydrocarbons, whereas depletion of corner sites inhibits EH2ER. They have further reported the unique selectivity of Au13 C-NC towards EH2ER. Although Au13 facilitates the formation of COOH* intermediate as compared to Au (211) and Au (111) facet, a stronger binding with CO* intermediate would lead to its lower tendency to produce CO2 reduction products.
TEM images of (a) the 8 nm Au NPs and (b) the C-Au NCs. (c) Potential-dependent FEs of the C-Au on electrocatalytic reduction of CO2 to CO. (d) Current densities for CO formation (mass activities) on the C-Au at various potentials. Free energy diagrams for electrochemical reduction of (e) CO2 to CO and (f) protons to hydrogen on Au(111) (yellow symbols), Au(211) (orange symbols), or a 13-atom Au cluster (red symbols) at −0.11 V. reprinted with the permission from [
Additionally, as shown in Figure 4(f), the free energy of formation (ΔG
The shape of the C-NC plays an important role in determining the selectivity/activity of the electrocatalysts. Several findings have shown that the shape-dependent C-NC activity/selectivity towards ECO2RR is typically associated with the presence of specific crystal plane. For example, Suen et al. have revealed that cubic Cu C-NC (C-Cu) with mainly (100) facet shows enhanced selectivity towards C2 products while octahedron Cu C-NC (O-Cu) with predominantly (111) facets shows selectivity for C1 products in ECO2RR [48].
Besides, Zhou et al. have illustrated the correlation between different shapes of C-NCs and their corresponding crystal planes using a stereographic triangle as depicted in Figure 5(a) [49]. The lower index surfaces, namely, the (100) (110) and (111) facets that lie on the three vertices of triangle, are present on the nanocrystal cube, octahedral, and rhombic dodecahedral, respectively. These low index surfaces are said to be less energetic, that is, catalytically less active. However, the plains lying on three sidelines of triangle and one which is residing inside the triangle are known as high index surfaces, that is, catalytically more active and stable. The high index planes (310), (311), (331), and (321) are correlated with tetrahedron, trapezohedron, trisoctahedron, and hexoctahedron, respectively, as illustrated in Figure 5(b). The high energy of these polyhedron is attributed to predominance of atomic steps, islands and kinks on their surface. For example, a concave rhombic dodecahedron Au C-NC enclosed with multiple high index planes showed excellent activity and selectivity towards CO formation [50]. In addition, this particular structure of Au C-NC was found durable for longer period of time. Summing up, low coordinating high index planes with CN less than 7 exhibits high catalytic activity, selectivity, stability whereas low index planes with higher CN greater than 6 exhibits lower catalytic activity and stability.
(a) Unit stereographic triangle of fcc single-crystal and models of surface atomic arrangement. (b) Unit stereographic triangle of polyhedral nanocrystals bounded by different crystal planes. Reproduced form [
Lattice strain has evolved as another factor that have a significant influence on electrocatalytic properties of C-NCs towards ECO2RR. It was studied that strain generates a distortion in lattice, which, in turn, alters d-band center of metallic C-NCs. The altered d-band center either facilitates or lowers the adsorption of intermediates, as a result of that changing catalytic properties. Typically, upshifting of the d-band center facilitates adsorption of reaction intermediates on the surface of C-NCs. This is because, as the d band center approaches the Fermi level, which is the highest occupied state, the antibonding orbitals move over it, causing them to empty. This, as a result, strengthens the binding strength of the reaction intermediate on the catalytic surface and, therefore, enhances the reaction kinetics [51]
In general, lattice strain in C-NCs can be induced by shaping C-NC in various morphologies, which leads to the inward displacement of atoms at high-energy locations, such as corners and edges, while the outward displacement of atoms on planes to gain overall crystal stability. These compression and expansion in the atomic arrangement in the NCS induce aeolotropic strain gradients that may improve the catalytic efficiency/selectivity of C-NCs [45]. Octahedral and Icosahedron C-NC of Pd with similar sizes were examined by huang et al. to investigate the effect of strain on ECO2RR. They observed that icosahedral/C C-NC shows higher FE (91% with −0.81 V vs. RHE) for CO production than octahedral/C C-NC in ECO2RR. The molecular simulations and DFT calculations showed that surface strain in icosahedral C-NC enhanced catalytic selectivity due to shifting in d-band center, which, in turn, facilitates absorption of a key intermediate (COOH*) in ECO2RR. Thus, surface strain in icosahedral C-NC boots catalytic efficiency and selectivity for CO2R [52].
The variation in composition of metal C-NCs is another intriguing factor that plays an important role in tuning electrocatalytic efficiency/selectivity towards ECO2RR. Among other effects of composition, the synergistic effect where the mutual synergy between both electronic and geometric effects determines the activity/selectivity of C-NCs towards ECO2RR is well known. The electronic effect can be understood by the concept of shifting in d-band center due to alteration in composition. In addition to the electronic effect, the geometrical effect also makes a significant contribution, where the particular atomic arrangement in the active center can modify the binding strength of the reaction intermediate, thereby improving the electrocatalytic efficiency/selectivity towards ECO2RR [44]. Therefore, to understand the synergistic chemistry between geometric and electronic effects in this section, the electrocatalytic efficiency, selectivity and durability of bimetallic C-NCs and doped C-NCs electrocatalysts towards ECO2RR will be discussed.
Until now, several bimetallic NCs have been investigated for ECO2RR. For example, Kortlever et al. have found an optimal composition of a novel Pd70Pt30/C electrocatalyst highly active and selective towards HCOOH production. Moreover, this has a remarkably lower onset potential close to 0 V vs. RHE, making it best catalyst till the date [53]. However, usage of noble high-cost metals discourages its application on economical scale. Incorporation of non-noble metals such as Cu, Ni, Fe, etc., in bimetallic system could serve a better alternative to address high cost and stability of electrocatalyst. Kim et al. synthesized different composition of NCs including Au, AuCu, AuCu3, Au3Cu, and Cu, which were assembled in a monolayer on glassy carbon while keeping precise control over morphology (Size, Shape etc.) [44]. When considering electronic effect solely, pristine Au NC should have shown higher activity due to its optimal binding with COOH and CO intermediates. Interestingly, they have observed higher activity for Au3Cu bimetallic C-NC than expected one. Therefore, electronic effect mere does not explain volcanic acti vity correlation for C-NCs. The geometric effect that works synergistically along with electronic effect ensure further stabilization of intermediates, thus, explaining optimal activity of Au3Cu bimetallic C-NC towards electrochemical CO2 reduction, among others. Previous studies have shown excellent properties of In based metal catalysts for selective CO2 conversion into HCOOH. However, these metal catalysts suffer from limited current density and poor stability.
Kown et al. synthesized In2O3-ZnO C-NCs that showed excellent selectivity towards formation of HCOOH [54]. The XRD pattern showed that pre reduction of these C-NCs during electrolysis leads to the formation of In-Zn bimetallic C-NCs. Among all Zn1-xInx NCs, In0.05Zn0.95 offered remarkable selectivity for HCOOH production at FE of 95% (−1.2 V vs. RHE) as well as with higher current density. The higher catalytic activity was seen in both Zn1-xInxO and Zn1-xInx with decreasing value of x. The XPS data has revealed predominance of O vacancies in bimetallic systems at lower x, which, in turn, decreases thickness of oxide layers in Zn1-xInx. Consequently, conductivity of Zn1-xInx C-NCs increases at lower x, therefore, facilitates rapid electron transfer processes in ECO2RR. Thus, highest catalytic activity of Zn0.95In0.05 C-NC is attributed to its remarkable conductivity. DFT calculations revealed that tight binding of OCHO* on pristine In, which impedes HCOOH production, has weakened by introduction of Zn in bimetallic C-NC. Therefore, mutual synergies of In with Zn in bimetallic system enhanced its catalytic selectivity in CDRR as compared to In [54]. Guo et al. have shown compositional effect in Cu3Pt C-NCs is responsible for improved activity and selectivity for CH4 [55]. It was observed that increasing Cu contents in bimetallic NC leads to desorption of more CO* intermediates that subsequently gets protonated into CH4. Moreover, Pt which shows higher affinity for H+ has significantly accelerated protonation of CO*. However, higher Cu content beyond ratio of Cu and Pt (3:1) raised CO* poisoning, and thus, declining in CH4 production [55].
In doped C-NCs, extrinsic or intrinsic introduction of impurities can cause a change in the electronic structure in a way that can enhance catalytic efficiency/selectivity and durability. For example, the incorporation of impurities can provide additional electrons (n-type) or additional vacancies (p-type), thereby, increasing the conductivity of the catalyst that would otherwise be poor in conductivity. Therefore, the increased conductivity may accelerate the electron transfer process in the ECO2RR. Although many advances have been made in the field of doped C-NCs, some studies conducted in ECO2RR. Recently, a group led by Kim et al. reported an unprecedented selectivity of vanadium (23V) doped In2O3 C-NCs towards CH3OH formation in addition to HCOOH and CO, previously not known with pristine In and In2O3 [56]. This can be understood using the commonly suggested scheme for producing CH3OH shown in the Figure 3. The CO* intermediate needs to be stabilized on the surface to proceed towards CH3OH formation otherwise it may release as CO gas and terminate the reaction. The introduction of V3+ into In2O3 strengthens the binding of CO* intermediate with NCs possibly due to the π-back donation from dopant to intermediate CO*, and thus, reaction proceeds towards CH3OH (FE of 15.8% at −0.83 V vs. RHS) [56].
In the past years, molecular organic frameworks (MOFs) have received significant attention in the field of catalysis, including ECO2RR, where they have been used primarily to provide solid support for molecular catalysts [57, 58]. The combination of MOF with C-NCs creates a class of hybrid materials that have demonstrated great potential to become future class of electrocatalysts with improved efficiency/selectivity and durability. Concerning this, a deep understanding of the material design and working principle of these novel hybrid systems is indispensable prior to implementing them practically. Recently, Guntern et al. investigated catalytic selectivity and durability of Ag C-NCs/Al PMOF hybrid system for electrochemical CO2 reduction [59]. Based on UV visible and XPS data, it was concluded that electron transfer from MOF to Ag C-NC in this hybrid system increases electron density at Ag C-NC, thereby, facilitates electron transfer to CO2.− intermediate. As in result, selectivity of Ag C-NCs/Al PMOF towards CO increases than pristine Ag C-NCs while decreases for H2ER. Additionally, a small contribution of transport events due to diffusion of reactants and products within pores of MOF adds in the selectivity of NC/MOF hybrid towards CO. Besides, NC/MOF hybrid system showed better stability compared to bare Ag C-NCs at lower potential [59].
Capping agents such as, organic ligands, surfactants or polymers are engendering factors of surface anchoring molecules that are crucial in synthesis of C-NCs based catalysts with well-defined shape, uniform size distribution and different composition. After synthesis, these capping agents can significantly alter C-NCs catalytic efficiency in both positive and negative way by staying absorbed on their surface. For example, Wang et al. reported that catalytic activity of Ag NCs modified with capping agents increased by 53-fold compared to pristine Ag NCs towards ECO2RR [60]. In Several studies it has been shown that presence of surface molecule can affect active site of NC in numerous ways: 1) by perturbing electronic structure of active sites 2) by introducing steric hindrance that impedes diffusion of absorbates reaching at active center 3) by blocking selective facets of C-NCs, which, in turn, could enhance selectivity and activity. Moreover, chiral ligands can be used to produce stereoselective products. Therefore, surface functionalized NCs has opened a new window in the field of electrocatalytic reactions where unprecedented control over efficiency/selectivity can be achieved by ligand design [61, 62]. However, researchers still have a limited understanding of how these anchoring ligands affect the local electronic environment of NC and how the backbone of anchoring ligands regulates reactivity between NC and surrounding reactants, or reaction intermediates.
Pankhurst et al. have tuned ECO2RR selectivity of Ag C-NCs using different imidazolium ligands [63]. Here they were able to introduce different organic component by varying tail and anchoring groups on imidazole motif. When performed ECO2RR, the ligand bearing NO2 anchoring group with octyl tail-found highly selective towards CO with FE of 92%. It was concluded that interaction between cationic imidazolium group with CO2 increases population of this reactant over the catalytic surface. Furthermore, an optimal chain length of ligand tail-group increased hydrophobicity of surface, and thus, increases selectivity and efficiency for ECO2RR by inhibiting EH2ER. However, electronic changes induced by ligand anchoring-group did not improve significantly properties of electrocatalyst. The next example of ligand surface functionalization for ECO2RR discusses N-heterocyclic-carbine functionalized Au C-NCs (Au C-NC-Cb) from group led by Cho et al. The significant downfield shifting in 13C NMR peaks of NHC reveals strong electron donation from ligand to metal, making Au C-NCs surface electron-rich. As in result, it facilitates the electron transfer process to CO2, and thus, enhances efficiency of Au C-NC-Cb relative to bare Au C-NCs [64].
The concept of using electric current to control various chemical reactions achieved much attention, since the time when humankind invented first power resources. Splitting of water to produce hydrogen and oxygen gas started much earlier, but now it has started at large scale in industrial process and seems to play a crucial role in combating the future energy crisis. The increasing demand for energy day by day and the shortage of fossil fuels have encouraged scientists to develop a renewable and clean source of energy.
Hydrogen is considered a clean source of energy because by-product of H2 combustion is H2O and the starting material to obtain H2 is water, therefore, an efficient and clean source to supplant the depleting fossil fuels [65, 66, 67]. Moreover, H2 produces highest energy on combustion of per unit mass relative to any other fuels, thus, leading to become a fuel of future. The H2 can be produced by electrochemical water splitting reaction which is an endothermic process with a potential of ΔE° = 1.23 V and ΔG° = 237.2 kJ mol−1. Water splitting generates both hydrogen and oxygen. For the process of electrochemical water splitting the reactions that occur at anode are called as oxygen evolution reaction (O2ER) and the reactions which occurs at cathode are called as H2 evolution reaction (H2ER) [68]. Electrocatalysis is actually an attempt to elucidate and predict observable phenomena like overall activity of the reactions that occur on the surface of electrode by the interactions of electrode/electrolyte interface. Development of an efficient electrocatalyst is important to minimize the energy losses during the electrocatalytic splitting of water to produce hydrogen and oxygen gas. Figure 6 shows a diagrammatic representation of evolution of hydrogen (Depicted to the left-side of Figure 6) and oxygen (depicted to the right side of Figure 6) gas on the surface of glassy carbon electrode (GCE) after deposition of catalyst on its surface.
Diagrammatic representation of formation of hydrogen during hydrogen evolution reaction and formation of oxygen during oxygen evolution reaction on the surface of glassy carbon electrode. Abbreviation: LSV - linear sweep voltammetry, WE - working electrode, RE - reference electrode, CE - counter electrode.
The reactions which are central to hydrogen energy are two types. These are hydrogen evolution (2H+ + 2e− → H2) and hydrogen oxidation (H2 → 2H+ + 2e−) reactions. The research of oxidizing and evolving hydrogen was started in 1960 but it gained importance in 1970 and 1990 when the shortage of oil was realized [69]. The most success in this regard was achieved when precious metals like platinum (Pt) were used. Metal NPs on the surface of carbon also showed great success in H2ER and hydrogen oxidation reaction (H2OR).
In the world of EH2ER electrochemistry, recent merge of computational quantum chemistry and nanotechnology have shown great progress in explaining fundamentals and basics of EH2ER with much emphasize on its utility and storage [51, 70, 71]. Metallic Pt is considered as ‘state of the art catalyst’ and exhibits small Tafel slope values and extremely high exchange current density (j0) [72, 73, 74]. However, because of high cost and less availability of Pt, a sustainable, cost effective, and stable catalyst needs to be developed. So, there have been efforts to synthesize the EH2ER active catalysts from the transition metals that are abundant in nature.
EH2ER kinetics has a long history and have been explained in detail [69]. EH2ER (2H+ +2e- → H2) is a process involving a series of electrochemical steps which takes place on the electrode surface and results in the evolution of hydrogen. There are two mechanisms in acidic and basic conditions accepted universally as shown in Figure 7 [75]. These steps are:
Mechanism of hydrogen evolution reaction on surface of glassy carbon electrode (GCE). Abbreviation: GCE - glassy carbon electrode.
Electrochemical hydrogen adsorption (Volmer reaction) (Eq. (1), (2))
This step is followed by.
Electrochemical desorption (Heyrovsky reaction) (Eq. (3), (4))
Or,
Chemical desorption or combination reaction (Tafel reaction) (Eq. (5))
In the above reactions, H* indicates an adsorbed hydrogen atom that has been adsorbed chemically on the surface of electrode (M) at the active site. These reaction pathways are highly dependent on electronic and chemical properties of the electrode surface [76]. Tilak et al., explained that rate controlling steps (1, 2 and 3) is predicted by deducing Tafel slope values from EH2ER polarization curves [72]. The mechanism and rate determining step is studied by the Tafel slope. Tafel slope is an inherent and interesting property because it gives information about the potential difference required to increase or decrease the current density by 10-fold. Tafel slope is also useful to determine the effectiveness of a catalyst. In order to calculate the Tafel slope the linear portion of the Tafel plots is to be fitted in the Tafel equation (η = b log (j) + a, where η = overpotential, b = Tafel slope, and j = current density) [77, 78]. Theoretical facts about Tafel slope have been derived from Butler-Volmer equation and it is proved for three limited cases. First, if the discharge reaction proceeds very quickly and H2 is evolved by the rate determining combination reaction (Tafel step). The slope value is 29 mV dec-1 at 25°C (2.3RT/2F). Second, if the discharge reaction proceeds very quickly and H2 is evolved by the rate determining desorption reaction (Heyrovsky step). The slope value for this step is 40 mV dec-1 at 25°C (4.6RT/3F). Third, if the discharge reaction proceeds very slowly and then the rate determining step will be Volmer step irrespective of the fact whether H2 is evolved by the combination reaction or the desorption reaction. The Tafel slope is 116 mV dec-1 at 25°C (4.6RT/F). The detailed mechanism is shown in Figure 7. It is evident that reaction (1) represents chemical adsorption, whereas, reaction (2) and (3) exhibits H atoms desorption from the electrode surface, which are competing with each other. Sabatier and co-workers came with an idea (Sabatier principle) that a better catalyst should not only form a strong bond with absorbed H* and facilitates the proton electron transfer process, but also it should be weak enough in facial bond breaking to assure quick release of H2 gas [79]. It is difficult to establish a quantitative relationship between energies of H* intermediate and rate of electrochemical reaction owing to absence of directly measured surface-intermediate bonding energy values [80]. However from the perspective of physical chemistry, both for H* adsorption and H2 evolution on the catalyst surface can be determined from the change in free energy of H* adsorption (∆GH*) using EH2ER free energy diagram [81]. According to Sabatier principle, under the condition ∆GH* = 0 will have maximum overall reaction rate (expressed in terms of EH2ER exchange current density, j0).
An important correlation between ∆GH* and j0 have been proposed in the form of “volcano curve” for a wide variety of electrode surfaces as illustrated in Figure 8 [81, 82]. Pt group of metals are the most efficient in the process and that’s why are found at the top of the volcano curve, because they have small Tafel slope and quasi zero onset potential.
Volcano plot for log I0 values for HER as a function of M-H bond energy. Adapted from [
However, due to high cost of Pt, various research groups have been working on modifying Pt group metals such as engineering the NCs. Crystal plane (110) of Pt NCs has been proved good surface for EH2ER. Like Pt, Palladium (Pd) NCs have been showing great promise as it is in the same group and has almost same size and its lattice matches about 0.77% to Pt, good thing about Pd is that it is comparatively cheaper than Pt. Pd has one advantage that it can adsorb hydrogen from both electrolytes and the gas phase. Pd can be loaded on various supports to increase its activity as it alters surface area and electronic conductivity of the nanocrystals [84]. Huang et al. observed that Pd C-NCs deposited on carbon paper substrate has activity higher than Pt black electrode and it required very less catalyst loading that is 0.0106 mg cm−2 [85]. One thing to be noted about Pd is that it has higher activity in acidic medium than alkaline medium because of lower Pd-H binding energy and lower activation energy, acid (32.3 ± 0.7 kJ/mol) and base (38.9 ± 3.0 kJ/mol). Ruthenium (Ru) NCs are also being explored for EH2ER. As the Sabatier principle suggest that catalyst should not have much stronger binding to the hydrogen and should possess moderate binding capacity so desorption is easy, Ru-H follows this trend as it has ~65 kcal/mol energy for Ru-H bond and thus less activation barrier for desorption process [86]. Ru C-NCs are usually used with some support as they have durability problems because of aggregation. One such example where Joshi et al. used Ru C-NCs supported with Tungsten (W). DFT calculations suggest that Ru (0001) has high H2 binding to surface energy but using W support, it could reduce the H2 adsorption energy and changes the electronic environment thus making it similar to Pt (111) and increases its activity for EH2ER process [86]. Baek et al. revealed that Ru when deposited on graphene nanoplatelets (GnP) to form Ru@GnP, its activity usually surpasses that of Pt/C in both acidic and alkaline medium. This happens because it is more stable, possess low Tafel slope (30 mV dec−1 in 0.5 M aq. H2SO4; and 28 mV dec−1 in 1.0 M aq. KOH) and also has comparatively low overpotential at 10 mA cm−2 (13 mV in 0.5 M aq. H2SO4; 22 mV in 1.0 M aq. KOH) [87]. Not only Pt, Pd, Ru, metals like Iridium (Ir) are also explored for the EH2ER process and also earth abundant metals are used but they are prone to corrosion in the presence of alkaline and acidic medium. Thus, the other way is using non-noble metals for the process.
Non-Noble metals follow this trend for the catalytic activity Nickel (Ni) > Molybdenum (Mo) > Cobalt (Co) > W > Iron (Fe) > Copper (Cu) which is calculated using the voltammetric techniques [88]. Ni shows a very good catalytic activity when using in the hybrid form of Ni/NiO/CoSe2 because this composite helps in less resistance to charge transfer. But this hybrid has poor stability as Ni does not work well in acidic medium [89]. Recent studies by Qiu et al. found that when Ni is used with graphene it forms Ni-C bonds which increases the stability as well as the activity of the catalyst and is the best one proved for the process using Ni [90]. Co when embedded with Nitrogen rich CNTs forms a very good catalyst that catalyzed at all pH ranges. The reason for this good activity at all pH ranges is the N-doped content and the structural defect caused by the caused by pyrolysis of the Co-NRCNTs at higher temperatures [91]. These Nitrogen rich Co based catalyst can also be dispersed over the nanofibers for improving the catalytic activity. These particular catalysts also showed good stability for various potential cycles of process [92]. Along with Co and Ni Other Non-Noble metals are also used for the EH2ER process including Fe, W, Mo but these all face the problem of their stability and there is still a lot to discover in this field.
To avoid using precious noble metals there have been a plethora of reports using non-noble metal-based C-NCs for EH2ER process. Some of them are transition Metal Oxides (TMOs), transition metal nitrides (TMNs), transition metal carbides (TMCs), transition metal borides (TMBs), transition metal phosphides (TMPs), transition metal dichalcogenides (TMDs). In this section the authors will discuss about the advancement in these types of NCs their advantage and disadvantages all. Although there are huge number of reports on transition metal-based compounds, but Mo and W display very good catalytic activity out of all of them. TMOs are easily available, stable, not harmful to the environment and obviously not precious like noble metals and thus is a good class of EH2ER catalysts. Out of all the TMOs, Mo (MoO2) and W (WO2) based EH2ER catalysts are best as they have high electrical conductivity as compared to other TMOs the credit goes to their monoclinic and distorted rutile crystal structure [93]. Compact MoO2 faces have a problem of aggregation and thus various research groups tried to bring changes in the catalyst by decreasing the size of structure, forming hybrid composites, doping the MoO2 or even introducing surface defects. One such example where Yu et al. encapsulated MoO2 with phosphorous-doped porous carbon embedded on rGO to form MoO2@PC-rGO which has a small tafel slope (41 mV dec-1) and less over potential (ƞ10 = 64 mV). Here electronic coupling between MoO2 and rGO along with the porous carbon layer helps in getting rid of the problem of aggregation and improves its efficiency as a EH2ER catalyst [94]. The other important metal oxide for EH2ER is WO2. Reports have revealed when WO2 have vacancies of oxygen, it provides large number of active sites and thus augmented the EH2ER process as compared to the compact WO2 counterpart. One such example where Shen et al. encapsulated WOx with Carbon on a Carbon support to form WOx@C/C which has EH2ER activity comparable to Pt metal with ultra-low overpotential (ƞ60 = 36 mV) and very small tafel slope (19 mV dec−1) which is because of the thick carbon shell helping in increase of charge transfer and also changes the Gibbs free energy values of H* for different adsorption sites [95].
TMNs are also other class of noble metal-compound based NCs for EH2ER. The importance lies in the fact that they possess more contraction of the d bands and density of state near Fermi level because of interaction of negatively charged N atom which expands the lattice and increases it efficiency as a catalyst to make it comparable to noble metals like Pt, Pd [96]. As discussed earlier, whenever NCs are encapsulated with carbon material they tend to avoid aggregation and improve the efficiency as a catalyst. One such example where Shao et al. developed MoN encapsulated with N-doped carbon material to form MoN@NC which exhibited very low overpotential (ƞ10 = 62 mV dec−1) and small tafel slope (54 mV) as depicted in Figure 9
(a) Procedure for the synthesis of MoN-NC nano-octahedrons derived from Mo-based MOFs (b) polarization curves (iR compensated) in 0.5 M H2SO4 at a scan rate of 5 mV s−1 and (c) the corresponding Tafel plots of the MoN-NC nano-octahedrons, intermediate MoO2-C, bulk MoN, and 20% Pt/C catalysts. Reprinted with the permission from [
Whenever there is introduction of another element in the lattice of the metal synergistic effect comes into effect (intercalation of crystal planes, change in the metal–metal length to have strain and also formation of heteroatom bond to give ligand effect). This result in the change of electronic properties and morphology and hence in the electrocatalytic activity of the catalyst. To reduce loading of noble metals they are doped either with other comparatively cheap noble metal or sometimes with transition metal. The authors will discuss examples of both these types. Pt can be doped with Pd to form 1-D single crystalline material (thickness 3 nm) which increases the Pt utilization efficiency this was done by Liu et al. using solution phase method directed by surfactant [99]. Pt can also be doped with non-noble metals one such example is the use of Pt-Co alloy encapsulated on carbon material, thus possessing high activity as displayed by the small tafel slope of 20 mV dec−1. This catalyst requires very less loading of Pt (ca. 5 wt %) and has activity comparable to Pt/C catalyst [100]. Using the same strategy Pd and Ru can also be doped with either noble metal or transition metals, some examples are Pd-Au catalyst, Pd-Co catalyst, Ru-Co and Ru-Ni [101, 102, 103, 104].
Transition metal can be alloyed with transition metal itself and thus it can be a very good alternative for noble metal electrocatalysts because of the cost-effective nature of them. These alloys could either be binary alloys or ternary alloys, the authors will discuss examples from both binary and ternary alloys. Ni can form alloy with various other transition metal, but Ni-Mo binary alloy is considered best for the EH2ER. Zhang et al. worked on the synthesis of MoNi4 supported over the MoO2 cuboids over the Ni foam. This catalyst has the activity similar to Pt/C with zero onset potential and ƞ10 = 15 mV and very low tafel slope of 30 mV dec−1 [105]. Ni binary alloys face the problem of corrosion which can be overcome by using the carbon support along with the Ni based alloy. Co also form binary alloys with Fe using N-doped carbon-based support. Also, Co can be alloyed with Mo forming good electrochemical catalyst for EH2ER such as Co3Mo having an overpotential of ƞ10 = 68 mV and tafel slope of 61 mV dec−1 [106]. Ternary alloys in the recent times have gained popularity for EH2ER electrochemical catalysts as electronic and morphological features of catalyst can be tuned by variation in compositions of various metals and thus it can act as the good promising substitute for the noble-metal-based EH2ER catalyst. One such example is the use of small amount of Pt (4.6%) to the Fe-Co binary alloy to form the PtCoFe@CN electrocatalyst which demonstrated activity similar to that of commercial 20% Pt/C having an overpotential of ƞ10 = 45 mV as depicted in Figure 10(b) [107]. Research is still going on to prepare the ternary alloys without using the noble metals in it and that will really be the landmark in this field as it will be a catalyst with cost-effective nature.
(a) Polarization curves (b) Tafel plots of samples (c) polarization curves of PtCoFe@CN 1st and 10000th cycles (d) Amperometric i-t curves of PtCoFe@CN. Reprinted with the permission from [
This chapter discuses a thorough study of recent acheivements by C-NCs-based elelctroctalysts for ECO2RR and EH2ER. In this chapter, the authors have tried to summarize role of C-NCs in ECO2RR and EH2ER and the scope of these two important electrocatalytic reaction in combating the energy crises for human kind in introduction part. The examples that are discussed in this chapter were taken from recent reports in literature. The first part of this chapter sheds light on colloidal synthesis of nanocystals. The second part of this chapter emphasizes on effect of shape, size and composition in determining the catalytic activity, selectivity and stability of C-NCs for ECO2RR. Here the effect of ligand functionalization and MOF/NCs hybrid system on ECO2RR activity is also illustrated. The third part of this chapter addreses the role of C-NCs-based electrocatalysts on EH2ER, its activity and stability. In this part, indepth study about mechanism of EH2ER is also discussed. Although a lot has been done in ECO2RR but ECO2RR still face a big challenge in selectivity, similarly in EH2ER a lot of research has been dedicated to find a substitute of state-of-art Pt/C catalyst which is very much expensive. However, researchers have been sucessful in discovering the costeffective electrocatalysts which are as good as Pt/C but they are still facing the stability issues.
RN, AP (Abhay Prasad), AP*(Ashish Parihar) designed the study, reviewed the literature, wrote and edited the manuscript. MSA and RS provided the inputs while editing the manuscript. The complete review article was edited and finalized by RN, AP, and AP*.
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