The availability of high-temperature dielectrics is key to develop advanced electronics and power systems that operate under extreme environmental conditions. In the past few years, many improvements have been made and many exciting developments have taken place. However, currently available candidate materials and methods still do not meet the applicable standards. Polyimide (PI) was found to be the preferred choice for high-temperature dielectric films development due to its thermal stability, dielectric properties, and flexibility. However, it has disadvantages such as a relatively low dielectric permittivity. This chapter presents an overview of recent progress on PI dielectric materials for high-temperature capacitive energy storage applications. In this way, a new molecular design of the skeleton structure of PI should be performed to balance size and thermal stability and to optimize energy storage property for high-temperature application. The improved performance can be generated via incorporation of inorganic units into polymers to form organic-inorganic hybrid and composite structures.
- thermal property
- dielectric property
- energy storage
With the rapid development of the global economy and a rising population, the search for efficient and clean energy and energy storage technologies has become a priority worldwide. Because of its exceptionally fast energy conversion rate, long life, and environmental friendliness, dielectric energy storage technology has been used in applications for the electronics and power industries such as wearable electronic devices, hybrid vehicles, and weapon systems . As the trend toward high-performance miniaturized electronic devices continues, the demand for dielectric materials with high energy storage density (
Commonly known high-energy storage dielectric materials are mainly biaxially oriented polypropylene (BOPP), polyester, polycarbonate (PC), polyphenylene disulfide, polyurea, polyurethane, and polyvinylidene fluoride . Among many polymers, polyimide (PI) is a type of polymer containing an imide ring on the main chain . PI is widely used in packaging materials, insulation layers, circuit boards, and interlayer dielectrics due to its high tensile strength, excellent mechanical properties, high glass transition temperature (
The chemical groups of a dielectric medium contribute to its molar polarization; as the molar polarization increases, the
Ma et al.  used high-throughput density functional theory (DFT) to rationally design high
2. Commercial PI
Kapton PI is an aromatic PI film that has been commercially available since the mid-1960s. Due to its continuous operating temperature of 300–350°C, it is widely used as a high-temperature wire and cable insulation material. At 25°C and 1 kHz, Kapton’s
3. Structure modification of PI
The relationship between the dielectric properties of PI and molecular structure can be studied by changing the structure of the aromatic tetracarboxylic dianhydride and diamine monomers used to prepare PI. However, the preparation of the aromatic tetracarboxylic dianhydride is often complex and the yield is low while the synthetic method for phenyl-substituted aromatic diamine is relatively simple, diverse, and high yield. Consequently, modifying the structure of the aromatic diamine monomers has become the primary choice to improve the properties of PIs .
3.1 Introduction of bispyridine groups in PI chains
Peng et al.  used 5,5′-bis[(4-amino)phenoxy]-2,2′-bipyridine (BPBPA) diamine monomer (as shown in Figure 2) and different dianhydrides [BPDA, PMDA, 3,3′,4,4′-Benzophenonetetracarboxylic dianhydride (BTDA), 4,4′-Oxydiphthalic anhydride (OPDA)] to give a series of bispyridyl-containing PIs using a two-step synthesis. The bipyridyl unit enhanced the electronic polarization and coupling: The polarized PI had a εr of ≤7.2, the dielectric loss was ≥0.04, and the energy density was ≤2.77 J cm−3. At the same time, it demonstrated good thermal and mechanical properties.
3.2 Introduction of sulfonyl group in PI backbone
Tong et al.  studied the relationship between molecular structure and properties using a range of modified PIs. In this study, the εr was increased by introducing sulfonyl groups, the loss factor was reduced by introducing flexible bonds, and the Tg was increased by retaining the aromatic structure. The resulting sulfonyl-containing PI with different flexible connections gave high εr (4.50–5.98), low loss coefficients (0.00298–0.00426), high breakdown strength (mostly at 500 MV m−1 or more) and high heat resistance (Tg: 244–304°C) (Figure 3).
For the anhydride 3,3′,4,4′-diphenylsulfonetetracarboxylic dianhydride (DSDA-mDS, each repeat unit contains two -SO2-, which has the highest dipole density), the εr was not as high as expected but it can be seen that the two -SO2- units improved the stiffness of the overall chain, hindering the rotation of the dipole. Therefore, in addition to the dipole moment and dipole density, the “effective” dipole is another important factor affecting the value of the εr. Compared to ortho-symmetric OPDA-mDS, para-symmetric PI (OPDA-pDS) was more effective for PI with sulfonyl group (OPDA-pDS) in the diamine moiety (para-para bond). The symmetric structure and low free rotation energy barrier facilitate the alignment of the excimer: The εr increased to 5.98; the dielectric properties were stable at 150°C; the discharge energy density and charge and discharge efficiency increased to 7.04 J cm−3 and 91.3% at 500 MV m−1 respectively .
3.3 Introducing nitrile groups in the PI backbone
Due to the high polarity of nitrile groups, special classes of PIs containing nitrile units for piezoelectric and other dielectric applications have previously been studied . Kakimoto et al.  reported that attaching a polar -CN side group to a PI could increase its εr. Treufeld et al.  found that adding a CN dipole to the PI main chain had two main effects: Firstly, because the -CN group is directly connected to the main chain in a 90° configuration, the motion is hindered and generates significant friction with randomly stacked adjacent chains, so dipole motion (such as wobble) is introduced into the PI sample; secondly, by adding the -CN group, the PI becomes more polar, easily contaminated by impurity ions, thereby improving ion mobility. Furthermore, it has been shown that the presence of three nitrile groups on the diamine unit is more effective in improving the εr than one nitrile group. Wang et al.  studied and synthesized a series of PIs from a diamine synthesized with three nitrile groups (as shown in Figure 4) and four commercial dianhydride starting materials. All PIs showed a high Tg, thermal stability and excellent mechanical properties; the PI had a εr of 4.7 resulting from the introduction of three highly polar nitrile groups.
3.4 PI grafted with phthalocyanine oligomer at amino terminal
Unlike ordinary composite materials, graft polymers, with good properties, were synthesized by Chen et al. . The copper phthalocyanine oligomer (o-CuPc, shown in Figure 5) is a semiconductor material with unique electrical properties (εr > 103) and good thermal stability, used widely in organic optoelectronics, the dye industry, catalysis, electrochromism, and electroluminescence display and other fields. The design and synthesis resulted in a high-εr all-organic polymer material, that is, a CuPc-PI homogeneous block copolymer was prepared (see Figure 6). The CuPc-PI also showed low dielectric loss, high breakdown strength, high Ue, high thermal stability, and good mechanical properties; its overall performance was higher than the direct use of o-CuPc/PI composites obtained using CuPc as the conductive filler .
4. Polyimide-based composite dielectric materials
4.1 Simple compound
Modification of the molecular structure of the polymer can improve its dielectric properties although the effect can be small. Using a simple compounding method with a high εr filler (e.g., ceramic filler, conductive filler), a polymer with a high breakdown field strength can be obtained. This procedure has gained acceptance due to its simple preparation method.
The conductive filler polymer-based composite material can attain a high εr for relatively small additions of filler, and the large increase in εr can be explained by the percolation theory. Adding filler at the percolation threshold will greatly increase the electrical conductivity and εr of the composite material, thereby improving the transition layer between the filler and the matrix. Carbon materials such as carbon nanofibers (CNFs), carbon black, carbon nanotubes (CNTs), graphene, and graphite flakes are most commonly used in recent research. Among these conductive fillers, CNTs are a good choice due to their high electrical and thermal conductivity and high aspect ratios. Wu et al.  functionalized multi-walled carbon nanotubes (MWCNTs) with carboxyl groups prior to dispersing into PI nanofibers using electrospinning technology. Hot pressing was then performed to produce high-performance PI/MWCNT composites with a high εr, good mechanical flexibility, and excellent thermal stability. When the concentration of MWCNT was close to the percolation threshold of 12–14 vol%, the material showed a high εr, low breakdown strength, and maximum
Adding conductive particles as a filler to the polymer matrix can improve the εr of the polymer composite. When the added amount is close to the percolation threshold, the εr can be significantly increased. However, as the amount of addition increases, a conductive network is formed, and their dielectric loss will increase sharply. In general, nanostructured BT fillers and BT-based nanocrystals are the more promising materials due to their excellent dielectric and ferroelectric properties .
Fan et al.  studied the relationship between the εr and the temperature for thermosetting PI matrix nanocomposite films containing BT nanoparticles at 103 Hz. Two temperature changes were reported, namely heating from 50 to 150°C and cooling from 150 to 50°C to investigate the effects of the transition of the BT crystal phase and the free volume change in PI on the εr for BT/PI nanocomposite membranes. Theoretical models were also used to predict the εr of composite materials to study the role of the diameter and shape of the nanoparticles. Rajib et al.  prepared BT/PI nanocomposites and increased their energy density at high temperatures using different volume fractions to analyze their effect on the dielectric properties. All samples were tested at high temperatures to evaluate their energy storage capacity. The highest Ue was found when the volume fraction of BT was 20% reaching 9.63 J cm−3 at 20°C and 6.79 J cm−3 at 120°C. As a dielectric material, it is expected to maintain a high energy density value at a temperature of 120°C. A pure PI film prepared by Sun et al.  showed high breakdown strength (451 kV mm−1) and high energy density (5.2 J cm−3). The introduction of BT nanoparticles increased the εr of the nanocomposite to 6.8, while the dielectric loss was still relatively low (0.012 at 104 Hz). However, a small amount of (3 vol%) BT nanoparticles also caused a significant decrease in the breakdown field strength (275 kV mm−1), which greatly reduced the energy density (1.7 J cm−3) of the BT/PI nanocomposite.
Therefore, for BT/PI nanocomposites, future research may concern improvements in the thermal conductivity of nanocomposites and the formation of interpenetrating networks throughout the polymer matrix. Improvements in this area will make nanocomposites less susceptible to breakdown . Wang et al.  successfully prepared BT nanowire/PI (BT-NW/PI) and BT nanoparticle/PI (BT-NP/PI) composites with low volume fractions. Due to strong interfacial polarization, the εr of BT-NW filled composites was greater than that of BT-NP/PI. The εr of the composite containing 5 vol% BT-NW was 6.6 at 100 Hz, which was 94% higher than pure PI (εr = 3.4 at 100 Hz) and 22% higher than that of composite containing 10 vol% BT-NP (εr = 5.4 at 100 Hz). In addition, BT-NW also significantly improved the
Furthermore, the calcination temperature of BT has a significant influence on the εr of the PI/BT-nanocomposite film as shown in Figure 8. The εr of the PI composite film calcined at 1000°C was higher than the PI composite films calcined at 600 and 800°C; when the BT-NF content was 30 vol%, the εr of the BT-NF/PI composite film increased to 26.6 . Beier et al.  added Ba0.7Sr0.3TiO3 (BST) nanocrystals to the PMDA-1,3-bis(4-aminophenoxy)benzene (BAPB) PI system to generate nanocomposites. Compared with the εr (2.8) of pure PMDA-BAPB PI, the εr of composites containing 18 vol% BST increased to 6.2; below 1 MHz, the dielectric loss of composite materials with different contents of BST was less than 0.04. At an addition level of 10 vol% BST, the breakdown strength of PMDA-BAPB/BST nanocomposites increased, to reach a maximum value 296 V μm−1, while the energy density of the composite was twice that of pure PMDA-BAPB PI. The observed relative increases in εr and breakdown strength together with the reduction in dielectric loss for the nanocomposite with 10 vol% BST are desirable characteristics for practical applications . Wang et al.  prepared PI-based composites with good dielectric properties using CaCu3Ti4O12 (CCTO) and Zr-modified CaCu3Ti3.95Zr0.05O12 (CCTZO) particles as fillers. The results showed that at a filling content of 40 vol%, the εr of the CCTZO/PI composite film could reach a value of 70 at 10 Hz, and this was higher than that of the CCTO/PI composite film under the same conditions; at 150°C, the εr of the CCTZO/PI composite material reached ≈260 .
By changing the design of the inorganic filler, interface problems between the filler and the polymer can be improved, such as poor flake/fiber morphology. The nanosheets can increase the breakdown strength of composites because they provide a uniform insulating center and a curved path for the electrons. Boron nitride nanosheets (BNNSs) have a layered structure like graphene and are wide band gap (6 eV) insulators. Unlike traditional dielectric materials (high-εr ceramics and conductive fillers), polymer/BNNS nanocomposites may provide higher breakdown field strengths. Wan et al.  prepared three-phase composites of BNN, BT-fibers, and PI (BNNS@BT-fiber/PI) using in situ polymerization. The combination of BNNS and BT fibers can facilitate the dispersion of BNNS nanosheets in BT fibers, thereby improving energy storage performance. When the content of BNNS@BT-fiber was 20% by weight, the εr of the composite material was 47.57 at room temperature and 43.03 at 200°C at 100 kHz, demonstrating a reasonable thermal stability. At a BNNS@BT-fiber content of 1 wt%, the maximum Ue of the composite at 3438 kV cm−1 was 7.1 J cm−3, that is, about three times that of pure PI .
In order to achieve better dispersion and alignment of the filler in the PI matrix, Gu et al.  prepared micron boron nitride (mBN)/PI composites by in situ polymerization and electrostatic spinning technology. At 30 wt% mBN, the mBN/PI composite material exhibited a high εr (3.77) and low dielectric loss (0.007); the material also showed good thermal stability (λ = 0.696 W m−1 K−1), a high temperature index (279°C), and Tg was 240°C . Cheng et al.  considered that molybdenum disulfide (MoS2) had an appreciable band gap and excellent heat resistance, and prepared MoS2/PI nanocomposite films. Compared with the pure PI film, the εr of the composite film was significantly increased, while the dielectric loss remained relatively low. At a filler content of 1 vol%, the breakdown field strength reached 395 MV m−1, while
4.2 Surface modification
Because of its simple method, the compounding of fillers and polymers to produce composite materials has become accepted. However, preparation methods, external conditions, and other complications can give rise to many structural defects and electric field concentrations between the two phases of the filler and the polymer matrix. Therefore, surface treatment of the filler using a coupling agent, or decorative insulating, or conductive particles has become a key area of research [27, 28].
Halloysite (Al2Si2O5(OH)4·2H2O) is an aluminosilicate clay, which has a unique tubular structure. It has a high εr (6–8), but extremely low dielectric loss (10−3). Because there are moderate hydroxyl groups on the surface that can be chemically modified, and suitable surface modification can be performed, halloysite nanotubes (HNTs) may be an ideal filler for the preparation of dielectric polymer-based composites with high εr and low dielectric loss characteristics. Zhu et al.  used KH550 (3-aminopropyltriethoxysilane) and polyaniline (PANI) to modify the surface of HNT, and prepared HNT/PI, KH550 modified HNT/PI and PANI-HNT/PI nanocomposite membranes. Among these, at 100 Hz, the PANI-HNT/PI films attained a maximum εr of 17.3, while the dielectric loss was only 0.2. Notably, the prepared composite has high breakdown strength (>110.4 kV mm−1), and a maximum discharge energy density of 0.93 J cm−3; these properties could still be maintained at temperatures ≤300°C . Wang et al.  prepared a nanocomposite with high thermal conductivity by introducing amide-functionalized MWCNT [MWCNT@p-phenylenediamine (PPD)] into a PEI matrix, as shown in Figure 9. Compared with unmodified MWCNT, MWCNT@PPD could participate in the in situ polymerization of PEI to form covalent bonds in the matrix, thereby improving the dispersibility of the filler. This method solved the disadvantages of the traditional CNT acid treatment that can destroy their conjugate structure and greatly affect the aspect ratio. The results showed that the thermal conductivity of nanocomposites containing 4.0 wt% MWCNT@ PPD ≤0.43 W m−1 K−1 .
Yang et al.  investigated the dielectric properties of PI incorporating CCTO/Ag nanoparticles (CCTO@Ag). The use of Ag coating to modify the surface of CCTO nanoparticles increased the conductivity of the intermediate layer, thereby enhancing the space charge polarization and Maxwell-Wagner-Sillars effect, improving the electric field distortion. The results showed that when the content of CCTO@Ag was 3 vol%, the εr of PI/CCTO@Ag composites was significantly increased to 103, which was about 30 times the εr of pure PI. At the same time, the dielectric loss was very low at 0.018 . Wang et al.  used 2-phosphonobutane-1,2,4-tricarboxylic acid (PBTCA) and TH-615 acrylic-acrylate-amide copolymers to modify BT nanoparticles, and then prepared a BT/PI composite film by in situ polymerization. The results showed that this surface modification method could improve the dispersion uniformity of filler particles in the matrix and improve the interfacial compatibility between the two phases. At 103 Hz, a BT/PI film modified with 8% PBTCA had a εr of 23.5, a dielectric loss of 0.00942, a breakdown strength of 80 MV m−1, and a
However, the covalent functionalization method adopted by Fang et al.  reduced the conductivity of graphene by destroying the π-π conjugate structure of graphene. In order to overcome this shortcoming, Feng et al. decorated the surface of rGO with a solid π-π stack by insulating reduced polyaniline (R-PANI) to introduce a space effect and effectively prevent the irreversible agglomeration of rGO. At 1 kHz, the highest εr (25.84) was observed in nanocomposite films containing 20 wt% rGO@R-PANI, and the dielectric loss was 0.11. The εr and dielectric loss of rGO/PI nanocomposite films were 8.23 and 56.4, respectively. Furthermore, the 5 wt% weight loss temperature for 20 wt% rGO@ R-PANI/PI nanocomposite film was 480°C, indicating that the nanocomposite film has great potential in the field of high-temperature dielectric materials . Yue et al.  introduced reduced barium titanate (rBT), sintered in a reducing atmosphere (95N2/5H2), to PI without using any modifier or surfactant ingredients in the matrix. Surface defects of rBT and interface interactions between two phases caused by the reducing atmosphere lead to an increase in εr and Ue. Compared with pure PI, the rBT/PI composite with 30 wt% rBT exhibited the following characteristics: The εr at 1000 kHz was ≤31.6 (pure PI = 4.1), the material maintained a low dielectric loss (0.031), the Ue of 9.7 J cm−3 at 2628 kV cm−1 represented an increase of >400% (for pure PI Ue = 1.9 J cm−3 at 3251 kV cm−1) .
4.3 Core-shell structure
Recently, much work has focused on introducing an intermediate layer or an insulating shell on the surface of the filler to prevent them from directly connecting to each other. Fillers in composite materials can increase electrical conductivity and cause excessive polarization interfaces. Researchers are also attempting to introduce intermediate layers or oxide shells between fillers to reduce dielectric loss. Studies have also shown that the core-shell structure can achieve a high εr, low dielectric loss, and high energy density [28, 33].
Liu et al.  synthesized a sandwich-shaped core-shell SiO2@GO hybrid to prepare a novel SiO2@GO/PI flexible composite film using in situ polymerization. The dense SiO2 layer grafted onto the GO surface can effectively suppress leakage current. The results showed that at 40 Hz, the εr of the composite material containing 20 wt% SiO2@GO was as high as 73, which was 21 times that of pure PI (3.0), and the dielectric loss was only 0.39. In order to improve interfacial compatibility, two coupling agents, 3-aminopropyl triethoxysilane and 3-glycidoxypropyltrimethoxysilane (GPTS), were used to modify the surface of SiO2@GO: At 40 Hz, the εr of the GPTS-SiO2@GO/PI composite increased to 79 and the loss decreased to 0.25. This significant improvement in the dielectric properties was due to the improved dispersibility of the filler following GPTS modification. Wang et al.  prepared a core-shell structure of BT@SiO2 nanofibers by electrospinning, and successfully prepared a nanocomposite membrane composed of core-shell BT@SiO2 nanofibers and PI. Because SiO2 has very low dielectric loss (0.00002) and moderate εr, using a thin layer of SiO2 to isolate PI from BT nanofibers can alleviate the local field concentration. The latter is caused by the large difference in εr between the concentrations of the two phases, thereby enhancing the breakdown strength of the PI nanocomposite film. Compared with pure PI, the composite film filled with 3 vol% BT@SiO2 nanofibers had a maximum Ue of 2.31 J cm−3 at 346 kV mm−1 (pure PI
Weng et al.  synthesized a novel core-shell of Ag@Al2O3 nanoparticles as conductive fillers and doped them into PI to prepare Ag@Al2O3/PI composite films. The composite film containing 10% by weight of Ag@Al2O3 had a εr of 21, which was seven times higher than that of pure PI (3.1). This increase in εr may be due to the high electrical conductivity of the Ag@Al2O3 filler, which caused interfacial polarization inside the composite in the applied electric field. Hence, when the mass fraction of Ag@Al2O3 was increased to 30%, the maximum value of εr was 124 .
4.4 Multilayer structure
Most polymer nanocomposites are expected to achieve high energy density by combining the high breakdown strength of the polymer matrix with the high εr of the filler. In fact, when the filler is introduced into the polymer matrix, the breakdown strength often decreases, especially when the volume fraction of the composite filler is high, which does not improve the energy density of the nanocomposite. Therefore, there is a need to expand nanocomposites into multilayer structures to compensate for the reduced breakdown strength .
Chen et al.  designed a three-layer PI composite membrane by combining KTa0.5Nb0.5O3 (KTN) nanoparticles with PI. Pure PI (with high breakdown field strength) was used as the middle layer with KTN/PI nanocomposite as the two outer layers to improve the energy storage performance of the entire composite film. The results showed that the maximum discharge energy density of the triple-layer composite film (t-KPI) was 3.0 J cm−3 at 300 kV mm−1, which was much larger than the maximum discharge energy density of the equivalent single-layer composite film (1.5 J cm−3, at 210 kV mm−1); at a high electric field of 300 kV mm−1, the t-KPI composite film could still maintain 88% charge and discharge efficiency . Amin Azizi et al.  prepared large-scale high-quality hexagonal boron nitride (h-BN) films using vapor deposition technology (CVD) and transferred them to PEI films to synthesize h-BN/PEI/h-BN composite film. As shown in Figure 11, this composite film exhibits excellent charge-discharge efficiency and dielectric stability at high temperatures. At 100°C, the discharge energy density of h-BN-coated PEI reached 2.93 J cm−3, and its charge-discharge efficiency was >90%. As the operating temperature increased, its advantages become more obvious. At 200°C, the energy density of h-BN-coated PEI film was 1.19 J cm−3. Rapid cyclic discharge experiments were performed at 150°C and 200 MV m−1 to test the stability of h-BN/PEI/h-BN composite films under electric fields and high temperature. The results demonstrated that the h-BN/PEI/h-BN film coated with 19 layers of h-BN did not show any reduction in discharge energy density and charge-discharge efficiency over 55,000 charge-discharge cycles .
Chen et al.  prepared an amino-modified CNT/PI (NH2-MWCNT/PI) flexible composite film with a three-layer structure in which a high-dielectric NH2-MWCNT was inserted between pure PI layers (serving as the bottom and top layers) of the complex. Since the conductive paths of the insulating layer could be effectively isolated, the three-layer composite film showed high εr and low dielectric loss. It is worth noting that at 1 kHz, when the NH2-MWCNT content of the intermediate layer was 10 wt%, the multilayer composite film (P-10-P) gave the highest εr of 31.3, while the dielectric loss was 0.0016. In addition, the maximum energy density of the composite membrane containing 5 wt% NH2-MWCNT in the intermediate layer (P-5-P) was as high as 1.95 J cm−3, which is more than 50% higher than that of pure PI (1.41 J cm−3). The maximum energy density of the composite film P-10-P also remained at 1.31 J cm−3 . Among the various films, h-BN/PI composite film filled with 5 vol% h-BN as the outer layer could improve the heat dissipation ability of the three-layer composite material, thereby maintaining the dielectric strength and suppressing leakage current at high temperatures. Hence, this sandwich structure composite material had excellent energy storage properties and high temperature stability. At 25 and 150°C, the maximum field strengths of the composite film with a Zr and Ca modified BT (BZT-BCT) content of 1 vol% in the intermediate layer were 360 and 350 kV mm−1 respectively, while the storage densities were 2.3 and 1.83 J cm−3, respectively . Zhou et al.  proposed a method for preparing high-performance polymer dielectrics at high temperatures (designed roll-to-roll plasma enhanced CVD), which was easily adapted to large-scale production of various surface-functionalized polymer films. In this experiment, they uniformly deposited wide-band gap SiO2 on the dielectric polymer film at ambient temperature and atmospheric pressure, and their productivity was comparable to that of melt extrusion. The results showed that the introduced SiO2 layer increased the potential barrier at the electrode/dielectric interface, resulting in a significant decrease in conductivity. Therefore, compared with the pure polymer (see Figure 12), the SiO2-coated film exhibited good high-temperature capacitance performance and had a higher energy storage efficiency (η) value. For example, at 150°C, when η > 90%, the maximum Ue values of PEI-SiO2, PEN-SiO2, PI-SiO2, PC-SiO2, and FPE-SiO2 composite films were 2.12, 1.75, 1.24, 1.79, and 2.06 J cm−3, which were respectively 236, 672, 510, 1279, and 644% greater than the corresponding pure films. At 100°C, when η > 90%, Ue for PEI-SiO2 was 3.0 J cm−3 .
In conclusion, the high-temperature polyimide dielectric materials used in energy storage application have been summarized, including pure PI, structure modification of PI, PI-based nanocomposites, etc. Many methods for micro molecule dimension and macrostructure design have been analyzed. The reviewed research studies encompassed commercial products progress, material design, and specification, the fundamental theory such as dielectric properties, energy density, and thermal properties. However, the current research for available high-temperature dielectric materials still falls short of industrial application, especially operating under extreme environment conditions, due to the relatively low dielectric permittivity and higher dielectric loss, which severely limit the energy storage density. Moreover, the thermal conductivity is also a limiting factor for high-temperature polymer dielectric materials. Therefore, more fundamental research on developing high-performance intrinsic polymer and high-temperature dielectric phenomena should be focused for future application.
This work was financially supported by National Nature Science Foundation of China (No. 51977114).
Conflict of interest
The authors declare no conflict of interest.