Organic molecules are assembled together by weak non-covalent intermolecular interactions in solid state. Multiple crystalline packing states (crystal polymorphism) have commonly existed in the active layer for organic field-effect transistors (OFETs). Different polymorphs, even with the slightest changes in their molecular packing, can differ the charge transport mobility by orders of magnitude. Therefore, accessing new polymorphs can serve as a novel design strategy for attaining high device performance. Here, we review the state of the art in this emerging field of crystal polymorph control. We firstly introduce the role of polymorphism and the methods of polymorph control in organic semiconductors. Then we review the latest studies on the performance of polymorphs in OFET devices. Finally, we discuss the advantages and challenges for polymorphism as a platform for the study of the relationship between molecular packing and charge transport.
- organic field-effect transistors
- organic semiconductors
- structure-property relationship
- carrier mobility
An organic field-effect transistor (OFET) is a transistor using an organic semiconducting thin film as the active layer in its channel [1, 2]. Charge carriers are transported in the OFET active layer under the electric field. Through the design of new materials and the improvement of fabrication processes, many impressive developments in the field of OFETs have been achieved [3, 4, 5, 6]. It has long been realized that the morphology of the active layer has a crucial impact on its charge transport properties. Tremendous efforts have been devoted to fabricate highly ordered crystalline films to achieve high device performance, including introduction of self-assembled monolayers [7, 8, 9], annealing [10, 11], off-center spin coating [4, 12, 13], and solution shearing [14, 15]. However, the lack of knowledge on the intrinsic properties of organic semiconductors remains the barrier for high-performance materials being efficiently developed.
Polymorphism of organic semiconductors has recently received much attention in the field of OFETs [16, 17, 18]. Different polymorphic crystals have the same molecular structure but a different molecular arrangement, which can be used as an ideal platform to correlate charge transport with respect to molecular arrangement. Through investigating OFETs with different polymorphs, the relationship between molecular packing and charge transport can be obtained. Recently, some ultra-high-mobility OFETs have been obtained by controlling the polymorphic structures of organic semiconductors, revealing that the crystal polymorph control has become an efficient strategy for the manufacture of high-performance OFETs [4, 17].
1.1 What is polymorphism?
Polymorphism refers to the ability for the same compound to adopt multiple crystalline packing states. Organic molecules assemble into crystals by weak intermolecular interactions, typically via van der Waals and electrostatic interactions. Many thermodynamic and kinetics factors (such as temperature, solvent mixtures, speed of crystallization, seeding, and pH) can have significant impacts on crystal growth, leading to polymorphism prevalent among organic materials. For instance, a continuous investigation on polymorphism has indicated that approximately one-third of organic substances show polymorphism under normal pressure conditions [19, 20]. Different polymorphs often have distinct physical properties such as solubility, melting point, and electrical, optical, and mechanical properties . The interest in polymorphism has increased significantly in recent years, particularly in the pharmaceutical and material science fields [17, 22].
1.2 The role of polymorphism in OFET
The charge transport property of organic semiconductors is sensitive to the molecular packing, where a slight change in molecular packing may result in huge difference in charge carrier mobility . The side-chain engineering, which is efficient in tailoring the molecular packing, has been extensively applied to develop high-performance organic semiconductors [24, 25, 26, 27]. However, the introduction of side chains alters the molecular structure, which makes the investigation on relationship between molecular packing and charge transport very complex.
Polymorphism offers an opportunity to tailor the molecular packing of a material, without affecting its chemical components. For example, rubrene can crystallize into three crystalline polymorphs, including an orthorhombic, a triclinic, and a monoclinic phase (Figure 1a) [28, 29, 30]. Taking advantage of polymorphism, it is possible to fabricate OFETs from the same organic semiconductor but with different polymorphs, hence, with different properties (Figure 1b). Importantly, by measuring charge transport performance in OFETs from different polymorphs, a direct relationship between molecular packing and charge transport can be established. Thus, many investigations on charge transport in different polymorphs have been performed in thin-film transistors, including some benchmark organic semiconductors like pentacene derivatives [15, 31, 32], rubrene [28, 29, 30], sexithiophene (6T) [33, 34, 35, 36], and benzothieno[3,2-b]benzothiophene (BTBT) derivatives [10, 37, 38]. However, the different factors affecting the device performance, including crystallinity, grain size, and grain boundaries, are difficult to be eliminated in thin-film transistors. Thus, tremendous efforts have been paid to manufacture OFETs from highly crystalline films even single crystals [39, 40, 41, 42, 43, 44]. Especially, single-crystal OFETs from different polymorphs have attracted increasing attentions . Compared to polycrystalline films, single crystals have the advantages of high molecular ordering and minimal grain boundaries, and its structure is much easier to determine.
There is no doubt that high-performance OFETs can be obtained by tailoring molecular packing motifs in the active layer. Among the investigations on polymorphism of organic semiconductors, several high-mobility OFETs have been manufactured by polymorph control, such as the TIPS-pentacene , C8-BTBT , C6-DBTDT , and TiOPC . Tailoring polymorphs has become an emerging design strategy for high-performance organic electronics.
2. Methods of polymorph control in organic semiconductors
Though polymorphism is observed on many organic semiconductors, the fabrication of each polymorph with high purity is very difficult. For instance, even for the extensively studied organic semiconductors like pentacene and BTBT derivatives, only part of their polymorphs have been useful to establish the correlation between the material molecular packing and its charge transport properties . The difficulties for the investigations on polymorphism include the fabrication of pure polymorphs and the determination of their crystal structures, where the polymorph control is fundamental. Some of the polymorph control methods most commonly applied to organic semiconductors are discussed below.
2.1 Solvent control
Solution process is important for the fabrication of organic semiconductor devices, which has the advantages of low-cost and large-area fabrication. In solution processes, solvent-induced polymorphism has been frequently observed in organic semiconductors such as DB-TTF , DT-TTF , TIPS-pentacene , and so on. Consequently, the solvent of choice for solution-processed organic semiconductors has become a commonly practiced method for high-throughput polymorph screening. For example, the triethylsilylethynyl anthradithiophene (TES-ADT) films can crystallize into two polymorphs from different solvents [52, 53, 54]. The polymorph selectivity for solution processes mostly relates to the polarity of solvents, while the concentration can also induce polymorphism [47, 55]. For instance, the C6-DBTDT molecules can crystallize into the α-phase and β-phase crystals from high concentration and dilute chlorobenzene solutions, respectively . At the molecular level, the specific interactions between semiconductor and solvent molecules in the solution can induce the nuclei formation in a particular polymorph and therefore result in polymorph selectivity as a function of the solvent or the concentration .
2.2 Temperature control
The thermodynamic polymorphic selection is usually observed from deposition of organic semiconductors by physical vapor transport (PVT) processes . In a study by Stevens et al., TMS-DBC crystals were synthesized in a crystallization tube by PVT method, where two polymorphs grew at different temperature regions . The red low-temperature (LT) polymorph was obtained in regions with tube temperature about 25–65°C, while the yellow high-temperature (HT) polymorph grew in regions with temperature around 130–170°C. The two polymorphs were found extremely stable, which did not interconvert to the other crystal structure with subsequent solvent or thermal treatments. Temperature-induced polymorphism was also observed from TiOPC crystals fabricated by PVT technology . Sheetlike
2.3 Crystallization through kinetics control
Crystallization through kinetics control is a powerful method for accessing metastable polymorphs, especially in thin-film geometry where kinetic trapping and thin-film confinement work in synergy. In a study by Wedl et al. , thin films of dihexylterthiophene (DH3T) were fabricated by spin coating, dip coating, drop casting, and physical vapor deposition, i.e., with very different crystallization speed. Three polymorphs of DH3T were discovered from the experiment, which was noted as the α-phase, β-phase, and the metastable thin-film phase. The crystallization speed was found to be a key parameter to control the respective polymorphs present in the films. The metastable thin-film phase was obtained from deposition techniques with fast crystallization speeds, such as physical vapor deposition, spin coating, drop casting with fast solvent evaporation, and dip coating with high withdrawal velocity. In contrast, a mixture of two stable polymorphs was observed in films fabricated by both drop casting and dip coating with slow evaporation of solvent. Crystallization kinetics control was also applied in a study by Giri et al. , wherein the solution shearing method with a function of shearing speed was utilized to fabricate thin films of TIPS-pentacene. Through fast solvent evaporation and quick crystallization, metastable states were kinetically trapped, which were relaxed to more stable states with toluene vapor annealing.
2.4 Templating via heterogeneous nucleation
Organic molecules are assembled by weak intermolecular interactions into their crystalline form, which can be affected by the molecule-surface interaction and the molecule-molecule interaction from additives. In other words, substrates and additives can act as templates to alter the crystal structure of organic semiconductors.
The substrate can promote heterogeneous nucleation of a particular polymorph due to specific interface interactions. On the substrate-thin-film interface, substrate-induced polymorphs (SIPs) are usually observed in the first few molecular layers, whose molecular packing are different from that in the bulk of the film. For example, two SIPs were firstly observed in thin films of pentacene, including a thin-film phase with d-spacing of 15.4 Å and a single-layer phase with d-spacing of 16.1 Å [32, 60, 61]. In contrast, the single-crystal phase of pentacene exhibits the d-spacing of 14.1 Å [62, 63, 64]. SIPs were also observed in films of the 2,7-dioctyloxy-BTBT (C8O-BTBT-OC8) derivative . The C8O-BTBT-OC8 molecules adopt a slipped π-π stacking in bulk crystal while exhibiting a herringbone packing motif in the thin-film phase. However, the SIP of C8O-BTBT-OC8 is a metastable form induced by the substrate, which is converted to the bulk form in 6 months or by chloroform vapor annealing. Although SIPs are commonly observed in thin films of organic semiconductors, studies on the formation of SIPs are limited .
Polymer additives have been demonstrated effective for polymorph control. In a study on polymorphism of TIPS-pentacene, conjugated polymer additives including poly(3-hexylthiophene) (P3HT) and region random TIPS-pentacene-bithiophene polymer (PnBT-RRa) were used to template the formation of a polymorph . Two new polymorphs of TIPS-pentacene were obtained, including the phase II and phase III that were synthesized form TIPS-pentacene/PnBT-RRa blend and TIPS-pentacene/P3HT blend, respectively. Compared to the phase I obtained from pure TIPS-pentacene, the phase II exhibits very small changes in crystal structure, which is attributed to the structural similarity between TIPS-pentacene and PnBT-RRa as well as their strong intermolecular interactions. In contrast, the crystal structure of phase III exhibits a large difference compared to the phase I, due to the lack of structural similarity between TIPS-pentacene and P3HT. These results demonstrate the possibility of using polymer additives as templates for accessing various polymorph phases.
2.5 Postdeposition control
Postdeposition processing is a commonly used method to investigate phase transition, from which various polymorphs can be accessed. Solvent and thermal annealing is widely used for postdeposition treatments to increase crystallinity, to enlarge grain size, and in some cases to alter the molecular packing in films of organic semiconductors [67, 68, 69]. In a study by Hiszpanski et al. , three polymorphs of contorted hexabenzocoronene (c-HBC) have been obtained by the application of both thermal and solvent vapor annealing. The P21/c polymorph of c-HBC is obtained from the amorphous film by thermal annealing. In contrast, polymorph II is accessed from either the amorphous film or the P21/c polymorph by tetrahydrofuran vapor annealing. Subsequently, thermal annealing of polymorph II always yields polymorph II. From an investigation by Campione et al., α-tetrathiophene (α-4T)/LT single crystals were obtained by the floating-drop technique, and a crystal to crystal phase transition was observed at 191°C from α-4T/LT to α-4T/HT, obtaining large and thick α-4T/HT single crystals .
2.6 Other methods
In addition to the major methods summarized above, a variety of novel approaches have been developed to control polymorphs. A direct strategy to change the crystal phase is to apply pressure on crystals. For instance, pressure-induced phase transition was observed from rubrene and fullerene derivatives [72, 73, 74, 75, 76]. Ito et al. and Segara et al. reported mechanically induced phase transitions [77, 78]. The nucleation of a polymorph is often affected by many processing parameters. For example, Lee et al. successfully fabricated a metastable polymorph of quaterrylene diimide by flow-assisted crystallization . He et al. synthesized a new polymorph of Cl2-NDI by vapor sublimation in air . Even light can have effects on polymorph formation. As investigated by Pithan et al., two polymorphs of sexithiophene were obtained in dark and illumination environments .
3. Charge transport in OFETs with different polymorphs
Polymorphism is an important platform to study the charge transport mechanism in organic semiconductors because in polymorphs the crystal structure is the only variable, while the chemical structure remains identical . By studying a polymorphic organic semiconductor, changes in charge transport can be directly associated with the differences in molecular packing. Many studies have attempted without success to reveal the relationship between charge transport and molecular packing, including experimental studies and quantum chemical calculations on different polymorphs.
3.1 Theoretical studies
Charge transport in inorganic semiconductors is well described by the band-like charge transport model. In contrast, to describe charge transport in organic semiconductors is much complex, where both electron–electron and electron–phonon interactions must be taken into account [81, 82]. A phonon is described as a particle-like quantized mode of vibrational energy, which arises from oscillating atoms within a crystal. In organic crystals, the molecule packing can be significantly disrupted by thermal functions due to the weak intermolecular interactions. Therefore, the charge transport behavior of organic semiconductors is temperature dependent . It turns out that a charge-hopping model is commonly observed at near and above room temperatures , while a band-like transport model is typically observed in single crystals at lower temperatures .
Taking advantages of the quantum chemical calculations, the relationship between molecular packing and charge transport can be examined. For instance, Bredas et al. simulated the sexithiophene dimers to understand the effect of the molecular overlap on the transfer integral between adjacent molecules . First, the HOMO and LUMO energy splittings were examined with a variation in the intermolecular distance between the conjugated planes. Next, by keeping the bottom molecule and the intermolecular distance between the sexithiophene (6T) dimers (4 Å) fixed, the effects of lateral molecular displacement along the conjugated plane on the energy splittings were examined by moving the top 6T molecule. The energy splitting is directly proportional to the charge transfer integral (
3.2 Thin-film transistors with different polymorphs
Organic thin-film transistors are easy to fabricate in large area by solution processing and therefore have been widely used in various electronic devices like electronic paper  and medical sensors [90, 91]. However, the semiconductor processing method and conditions can greatly affect the molecular packing motif and consequently can dramatically affect the device performance (see Section 2). To date, the knowledge on how the charge transport in semiconductor films depends on molecular packing motif is still very limited. In this section, the relationship between molecular packing and charge transport will be discussed, giving some recent investigations as examples.
Pentacene is a benchmark organic semiconductor synthesized in 1912 , which exhibits excellent charge transport performance in thin-film transistor . To date, there are five different polymorphs known for pentacene [9, 31, 32, 94]. As shown in Figure 2, the five polymorphs of pentacene are classified by their molecular layer thickness (d-spacing), where four thin-film forms exhibit d-spacing of 14.1, 14.4, 15.0, and 15.4 Å , and a monolayer form shows d-spacing of 16.1 Å . However, among the five polymorphs, complete structural data have only been determined for the 14.1 and 14.4 Å polymorphs, where the 14.1 Å polymorph shares a similar packing as the single crystals. The single crystal of pentacene was reported with mobility around 5–40 cm2 V−1 s−1 [43, 95]. A recent study by Ji et al. reported that the polymorph with d-spacing of 16.2 Å has a mobility of up to 30.6 cm2 V−1 s−1 . As for the other polymorphs, to stabilize and isolate a pure polymorph for transistor fabrication has been challenging. Thus, more investigation on the relationship between molecular packing and charge transport for pentacene remains a serious topic of research.
In 2001, Anthony et al. introduced triisopropylsilylethynyl (TIPS) group to the pentacene core, obtaining a very soluble pentacene derivative, i.e. TIPS-pentacene . Different from the herringbone-stacked pentacene molecules, the TIPS-pentacene molecules adopt a brick-wall stacking in solid state. Several recent investigations have revealed that TIPS-pentacene exhibits polymorphism. For instance, Diao et al. fabricated five different polymorphs of TIPS-pentacene by using the solution shearing technology . The five polymorphs have been categorized into three families: I and Ib, II and IIb, and III. Within each family, there is only a slight change in one or two unit cell parameters between the polymorphs. Among different family (polymorphs I, II, and III), the main structural differences are changes in the π-π stacking distance and the extent of overlap between adjacent molecules (Figure 3). Form I has larger π-π stacking distance than that of forms II and III, where pair I in form III exhibits a record low-stacking distance of less than 3 Å. As a result, form I exhibits ambipolar charge transport property, with hole and electron mobility of 3.8 and 6.81 cm2 V−1 s−1, respectively. Form II shows the highest mobility up to 11 cm2 V−1 s−1. In sharp contrast, form III possesses the lowest mobility around 0.09 cm2 V−1 s−1. The quantum chemical calculations indicate a much smaller hole transfer integral for form III compared to form I and form II. Form II with moderate π-π stacking distance has the largest hole transfer integral and therefore exhibits the highest mobility. This result shows that small π-π stacking distance does not always help to improve charge transport properties.
2,7-Dioctylbenzothieno[3,2-b]benzothiophene (C8-BTBT) is an extensive studied air-stable organic semiconductor, which often shows very high hole mobility in OFET devices [4, 96, 97]. In a recent study by Yuan et al., ultra-high mobility up to 43 cm2 V−1 s−1 was obtained from thin-film transistors based on a metastable polymorph of C8-BTBT film . The metastable polymorph was fabricated by introducing polystyrene additive and using an off-center spin-coating method. After thermal annealing, the metastable polymorph was relaxed to the equilibrium polymorph, along with a sharp decrease of carrier mobility. However, the correlation between molecular packing and charge transport for the C8-BTBT films is difficult to establish. The authors stated that the beam damage during grazing incidence X-ray diffraction (GIXD) measurements made it impossible to obtain the precise crystal packing structure for the metastable polymorph. Moreover, the crystal alignment was also disrupted after thermal annealing, making it difficult to attribute the mobility drop entirely to crystal structure change.
5,11-Bis(triethylsilylethynyl)anthradithiophene (TES-ADT) is a high-performance organic semiconductor with good solubility . In a study by Yu and colleagues, four polymorphs of TES-ADT was obtained in thin films, including three thin-film forms (
3.3 Single-crystal transistors with different polymorphs
Single-crystal transistors are preferred for fundamental studies on structure-charge transport relationships owning to their high molecular ordering and no grain boundaries. However, structure-property investigations have been successfully performed for only a small number of organic semiconductors by means of single-crystal transistors. Compared to thin-film transistors, the manufacture of single-crystal OFETs is more complicated, which generally requires the use of high-precision deposition or micromanipulation techniques. Moreover, the preparation of single crystals with different polymorphs is very difficult. In this section, some examples of single-crystal OFETs are introduced.
Rubrene is an excellent organic semiconductor with single-crystal mobility up to 20 cm2 V−1 s−1 . Four polymorphs of rubrene, including a monoclinic, a triclinic, and two orthorhombic forms, have been known for a long time , but the structure-charge transport relationship has only been discussed recently. In an investigation by Matsukawa et al., an orthorhombic single crystal exhibited high carrier mobility up to 1.6 cm2 V−1 s−1, while that of the triclinic form was only 0.1 cm2 V−1 s−1 [29, 100].
The two polymorphs share similar π-π stacking distances, while the density of the π-stacking column in the (001) plane of orthorhombic crystal structure (Figure 4a) is much higher than that of the (0−11) plane of the triclinic crystal structure (Figure 4b). In other words, the π-π overlap along the carrier conduction direction in orthorhombic crystal is significantly larger than that in the triclinic crystal. Consequently, the orthorhombic crystal exhibits higher carrier mobility than the triclinic crystal.
Two polymorphs of tetrathiafulvalene (TTF), including a monoclinic orange crystal and a triclinic yellow crystals, were found many years ago . The single-crystal transistors of the two polymorphs were fabricated by Jiang and colleagues recently . Based on single-crystal transistors, the charge transport performance associated with molecular packing was discussed. The monoclinic
Brillante et al. investigated the polymorphism of dibenzotetrathiafulvalene (DB-TTF), and four polymorphs were found . The pure
Dithiophene-tetrathiafulvalene (DT-TTF) is a promising high-performance organic semiconductor, whose single-crystal OFETs were reported with high hole mobility up to 3.6 cm2 V−1 s−1 . Long plated crystals of DT-TTF can be easily prepared from a variety of solutions [104, 105, 106], which were named as the
Stevens et al. found two polymorphs of 7,14-bis((trimethylsilyl)ethynyl)-dibenzo[b,def]-chrysene (TMS-DBC) using the physical vapor transport technology . The first polymorph was obtained as red needles at low temperature, which was named as LT-phase (Figure 7a). The second polymorph was formed at high temperature as yellow plates and named HT-phase (Figure 7b). Further investigations found that the LT-phase can also be fabricated from solution and could not be converted into HT-phase by thermal annealing. Single-crystal OFETs of the two polymorphs were fabricated. The results revealed that the hole mobility of the HT-phase is up to 2.1 cm2 V−1 s−1, while that of the LT-phase is only 0.028 cm2 V−1 s−1.
As shown in Figure 7, the LT-phase adopts one-dimensional (1D) slipped stacking, while the HT-phase exhibits two-dimensional (2D) brick-wall stacking. Quantum chemical calculations revealed that the LT-phase possesses 1D charge transport channel along the π-stacking direction with a transfer integral of −86.8 × 10−3 eV (Figure 7b). In contrast, the HT-phase possesses exhibits 2D charge transfer channels with transfer integrals of −77.3 × 10−3 and − 41 × 10−3 eV along the t1 and t2 directions, respectively (Figure 7e). Though the HT-phase exhibits slightly smaller transfer integral (absolute value) than that of the LT-phase, its 2D charge transport channels benefit charge transfer, which allows charge carriers to take alternative pathways around defects or trap states. As a result, the HT-phase facilitates higher mobility than the LT-phase.
3.3.6 N,N′-bis-(heptafluorobutyl)-2,6-dichloro-1,4,5,8-naphthalene tetracarboxylic diimide
Würthner et al. manufactured single-crystal transistors based on
3.3.7 Dihexyl-dibenzo[d, d’]thieno[3, 2-b; 4,5-b’]dithiophene
In an investigation by He et al., dihexyl-dibenzo[d, d’]thieno[3, 2-b; 4,5-b’]dithiophene (C6-DBTDT) was synthesized efficiently ; two polymorphs of C6-DBTDT were obtained by drop casting of solutions with different concentration in chlorobenzene or toluene. The platelet-like
It is generally believed that only the HOMO level contributes to hole charge carrier transport from one molecule to another adjacent molecule. The electronic couplings of adjacent molecules in the
3.3.8 2,8-Bis(butyl(methyl)amino)-indeno[1,2-b]fluorene-6,12-dione (BMA-IFD)
In a recent investigation by Fan et al., a new molecule, indeno[1,2-b]fluorene-6,12-dione derivative, i.e., BMA-IFD, was designed and synthesized . Two polymorphs of BMA-IFD were easily obtained by crystallization from solution. The ribbon-shaped
The α-phase and the
3.3.9 Titanyl phthalocyanine
Titanyl phthalocyanine (TiOPC) is a well-known organic semiconductor and photoconductor; however, it exhibits poor solubility in common solvents. In a recent study by Zhang et al., TiOPC crystals were synthesized by physical vapor transport (PVT) technique through a two-zone horizontal tube furnace . Some sheet crystals were obtained at the temperature zone of about 210°C, while some ribbon crystals were grown at the temperature zone of about 180°C. The sheet and ribbon crystals belong to the
The crystal structures of the two polymorphs were determined, where the
4. Conclusion and outlook
Herein, the polymorphism in organic semiconductors is introduced, including the common strategies for polymorph control and investigations on OFETs from different polymorphs. Polymorphism is proved to be an excellent platform to directly correlate the molecular packing with charge transport for organic semiconductors; such investigations are very limited so far. A main challenge is to precisely tailor thermodynamic and kinetic factors of crystal nucleation and growth for large-area thin films or high-quality single crystals. Among the investigations on polymorphism, several polymorphs with outstanding charge transport performance have been obtained, demonstrating that altering the crystal polymorph structure of organic semiconductors is an efficient strategy to access high-performance OFETs. However, the majority of the high-mobility polymorphs are metastable. Consequently, getting insight into the relationship between molecular structure and crystal polymorph remains an important issue, which is essential for the rational design of molecular structures to further develop the desired crystal polymorphs with outstanding electrical characteristics.
This work is supported by the National Key R&D Program of China (2017YFA0204903), National Natural Science Foundation of China (NSFC. 51733004, 51525303, 221702085, 21673106, 21602093, 21572086, 1522203), 111 Project, and the Fundamental Research Funds for the Central Universities. The authors thank beam line BL14B1 (Shanghai Synchrotron Radiation Facility) for providing the beam time.
Conflict of interest
The authors declare no conflict of interest.