Polyetherimide Matrix Research Articles

Roll-to-Roll Manufactured Polyetherimide Nanocomposite With Different Diameters of SiO2 Nanoparticles Exhibiting Improved High-Temperature Dielectric Energy Storage Performance.

To enhance the high-temperature energy storage performance of the polymer-based dielectric film, inorganic nanofillers with large band gaps are much more effective and have been widely adopted. However, the impact of nanoparticle diameters on the dielectric properties of polymer nanocomposites has been less studied. Herein, silicon dioxide nanoparticles (SiO2-NPs)with varying diameters (20, 60, 120, 200nm) prepared by the sol-gel method are incorporated in the PEI matrix to form PEI/SiO2 nanocomposites. The characterization results reveal a distinct correlation between the dielectric properties of polyetherimide (PEI) composites and the diameters of SiO2-NPs. Leakage current density analysis and breakdown strength simulations indicate that SiO2-NPs with smaller diameters generate more deep traps that impede the transport of charge carriers, especially under high temperatures. Notably, PEI/20nm-SiO2 exhibits a high discharged energy density of 4.4 J cm-3 with an efficiency of 90% at 150°C. Furthermore, PEI/SiO2 films with 10µm in thickness are manufactured by a large-scale solution casting process. The continuously prepared PEI/20nm-SiO2 film exhibits a discharged energy density of 3.2 J cm-3 with an efficiency of 90% at 150°C. This study not only provides a strategy for the design of high-performance dielectric polymer composites but also offers a large-scale high-temperature dielectric film for practical use.

Structure and tribological behavior of a polyetherimide/polytetrafluoroethylene matrix filled with negative thermal expansion zirconium tungstate particles

Thermal expansion mismatch stresses may be a reason for premature failure of sealing and bearing components made of polymer composites that are rubbed against metallic surfaces at elevated temperatures. It is of particular importance for polymer matrix composites loaded with anti-friction inclusions of polytetrafluoroethylene (PTFE) that possesses high coefficient of thermal expansion. In this regard, a study was undertaken to elucidate the effect of the thermal mismatch on wear and friction of amorphous polyetherimide (PEI) matrix loaded with either polytetrafluoroethylene (PTFE) particles (i) or PTFE particles covered with negative thermal expansion zirconium tungstate (ZT) α-ZrW2O8 (ii) at temperatures 23 °C, 120 °C and 180 °C. The ball-on-disk testing scheme was used according to standard with AISI 52100 steel balls rubbed against a polymer composite disks at normal force P = 5 N and sliding velocity V = 0.3 m/s. The PEI/PTFE/ZT composite demonstrated a tendency for wear rate (WR) reduction in sliding at 120 °C and 180 °C as compared to corresponding WR enhancement on the PEI/PTFE. The rationale is provided that the ZT additive effectively reduced thermal expansion of the PTFE in the PEI matrix and thus improved wear resistance of the composite. New thermal expansion-controlled wear and friction instability mechanism has been proposed and discussed.

Stretch-steering of highly aligned discontinuous fiber tape with automated fiber placement

Highly aligned discontinuous fiber (ADF) composites have been developed with mechanical properties comparable to continuous fiber composites. These materials can be stretched in the fiber direction during processing enabling the production of complex geometries. This study utilizes 57% fiber volume fraction ADF tape comprised of a thermoplastic Polyetherimide (PEI) matrix with 3 mm long IM7 carbon fibers. The Laser-Assisted Automated Fiber Placement (LA-AFP) process is used to study the limits of stretch-steering of ADF tape at small radii. An experimental technique based on photogrammetry was developed to quantify the effect of stretch parameters on the tape strain fields and path placement accuracy. The measurements captured the local in-plane strain tensor (longitudinal, transverse, and shear) across the width and along the length of steered tapes. The results demonstrate that placement path accuracy can be achieved when the tool center point (center of rotation) of the AFP head is located at the nip-point versus the roller centerline, which is typically used for steering continuous fiber tapes at large steering radii. Accuracy of the in-situ tape stretching was demonstrated up to 60% applied stretch strain. The measurements also confirm that when stretch-steering ADF tape, the resulting strain across the tape width is on average the superposition of the in-situ applied tensile strain and in-plane bending computed from the tape width and steering radius. A statistical-based methodology is presented to select the average tensile stretch levels to minimize the probability of defects forming during steering on the inner radius of the tape. The experiments show that a 12.5 mm wide tape can be accurately placed on a 50 mm radius of curvature without defects. This represents a two order of magnitude improvement in steerability over continuous fiber tapes of the same tape width found in peer-reviewed literature.

Polyimide-coated MgO nanoparticles improves high-temperature energy storage performance in polyetherimide-based nanocomposite films

Enhancing the energy storage capacity of dielectric polymers can be achieved by the introduction of inorganic nanoparticles. However, the difference in surface energy often influences the interfacial compatibility of nanoparticles with polymers, consequently limiting their comprehensive dielectric properties. Here, the magnesium oxide (MgO) nanoparticles were coated with polyimide (PI) shells via in-situ polymerization, which is beneficial to improve the scattered particles in the polyether imide (PEI) matrix. The PI buffer shell is tightly bound to the PEI matrix through automatic electrostatic interaction making the defects decrease, together with the increased dielectric permittivity (εr) attributed to MgO, significantly enhancing the discharged energy density (Udis) and storage efficiency (η) of the PI@MgO/PEI nanocomposite films in harsh conditions. Thus, the maximal Udis of the PI@MgO/PEI nanocomposites is 4.33 J/cm3 at 150 °C, twice that of the pristine PEI. Even if an η exceeds 90 %, the Udis of 3.83 J/cm3 of 1 vol%-PI@MgO/PEI at 500 MV/m and 150 °C is better than that of the most advanced dielectric polymers.

Interface engineering of polymer composite films for high-temperature capacitive energy storage

Polymer film capacitors encounter challenges in harsh conditions of high temperatures and electric fields because of large conduction loss and degraded breakdown strength (Eb). Herein, an interface engineering strategy is proposed to fluorinate the interfaces between the polyetherimide (PEI) matrix and wide bandgap boron nitride nanosheets (BNNSs) fillers. The composite films exhibit high-performance capacitive energy storage with a remarkable energy density of 5.73 J/cm3 and an ultrahigh efficiency of 91.22 % in conditions of 575 kV/mm and 150 °C. By adopting interfacial fluorination, the band structure of BNNSs is tailored to achieve a type II band alignment with PEI, promoting the dual trapping for both electrons and holes. It highly suppresses leakage current and reduces conduction loss. Typically, introducing fillers can compromise the properties of interfacial layers, creating weak points that trigger breakdown. Conversely, fluorinated interfaces exhibit an increased Young’s modulus and a reduced dielectric constant. According to the electromechanical breakdown theory, the interfacial Eb is increased. The breakdown phase propagation along the interfaces is thereby impeded, ultimately resulting in a further increase in overall Eb, reaching up to 589 kV/mm at 150 °C. Fluorinated interface engineering addresses interfacial challenges posed by fillers, enabling high-temperature energy storage capability in PEI-based capacitors.

Influences of cryo-thermal cycling on the tensile properties of short carbon fiber/polyetherimide composites

The reliability of short fiber reinforced polymer composites is crucial for their successful applications in aerospace engineering with cryo-thermal cycling (CTC). This study investigates the influences of CTC on the tensile properties of short carbon fiber (SCF)/polyetherimide (PEI) composites at room temperature (25 °C) and elevated temperature (170 °C). First, SCF surfaces were coated by carbon nanotube-polydomaine (CNT-PDA) hybrid sizing, and then SCF/PEI composites were prepared via the facile injection molding technique. Impressively and unexpectedly, the tensile strength at 25 °C and 170 °C of SCF/PEI composites is all enhanced by the CTC exposure, attributing to the enhanced mechanical properties of PEI matrix and fiber/PEI interface bonding. In addition, CNT-PDA sizing and CTC exposure have a combined effect on improving the tensile properties of SCF/PEI composites at 25 °C and 170 °C. Overall, the SCF/PEI composites exhibit excellent mechanical properties under extreme service conditions, and are thus promising to serve in aerospace components.

Polyethyleneimine NH2-UiO-66 nanofiller-based mixed matrix membranes for natural gas purification

Effective separation of CO2 from CH4 is crucial for the purification of natural gas, which requires membrane materials with high permeability, selectivity, and stability of under high pressures. In this work, a high CO2-affinity MOF-based nanofiller (Pin@NH2-UiO-66) was prepared and integrated in polyetherimide (PEI) to prepare mixed matrix membranes (MMMs) for enhanced CO2/CH4 separation capabilities. The Pin@NH2-UiO-66 nanofiller comprised an in situ-formed polyethyleneimine-NH2-UiO-66 composite prepared via a one-pot synthesis. The polyethyleneimine was covalently attached to the H2BDC-NH2 ligand allowing for a stronger integration within the PEI matrix. The polyethyleneimine affects the nucleation of MOF, leading to miniaturization of the MOF particles. The smaller-sized filler is beneficial for improved interaction at the filler-matrix interface. The numerous amino functionalities grafted onto the NH2-UiO-66 increased the CO2 adsorption sites, thereby enhancing the affinity for CO2. Owing to the improved interaction, the elevated CO2 attraction, and the inherent properties of the porous NH2-UiO-66, the fabricated MMMs preformed superior in separating CO2/CH4. The 30-Pin@NH2-UiO-66-PEI membrane (containing 30 wt% nanofiller) exhibited a CO2/CH4 selectivity of 27.7 and a CO2 permeability of 2498.9 Barrer. The CO2 permeability was 21 times greater than that of the pristine PEI membrane, and 4 times higher compared to P@NH2-UiO-66 MMM with polyethyleneimine modified MOF filler prepared by a traditional wet impregnation method. Additionally, the novel MMM demonstrates excellent separation stability under conditions that mimic industrial settings, demonstrating its potential application for natural gas purification.

Polyetherimide nanocomposite with enhanced mechanical, thermal and dielectric properties by incorporating synergistically exfoliated‐chemical functionalization induced hexagonal boron nitride nanosheets

AbstractThe present study aims to improve the mechanical, thermal and dielectric properties of polyetherimide (PEI) nanocomposite via simplified method, involving the creation of a nanocomposite using PEI incorporated with exfoliated‐chemical functionalization induced hexagonal boron nitride nanosheets (BNNS). XRD, FTIR and Raman elucidated the chemical structure of functionalized BNNS and indicated the success preparation of functionalized BNNS. Functionalization effectively improved the compatibility of nanocomposites and contributed to the property improvements. Morphological analysis unveiled a compact and dense microstructure within the nanocomposites in correlation with functionalized BNNS. Broad band dielectric spectroscopy revealed excellent dielectric properties of produced PEI nanocomposite. DMA testing verified a noteworthy enhancement in both Tg and storage modulus upon incorporating of BNNS. In summary, this comprehensive investigation highlights the impact of functionalized BNNS on mechanical, thermal and dielectric properties of developed PEI dielectric nanocomposite and is expected to expand the application of PEI in the field of high‐temperature energy storage.Highlights Polyetherimide (PEI) was used as polymer matrix and boron nitride derivatives as dielectric fillers to prepare PEI dielectric nanocomposite. Due to the influences of dielectric properties by interface polarization effect and the local distribution of electric field of the fillers in PEI matrix, the dielectric constant, breakdown strength and energy storage density of PEI nanocomposites were obviously improved compared with pure PEI. The effects of interfacial interactions between PBNNS and PEI contributes to the uniform dispersion and comprehensive property improvements of PEI dielectric nanocomposites. This work presents a systematic investigation into the fabrication of PEI/BNNS nanocomposite using a one‐step solution blending method, inspiring the research and development of PEI in the energy storage applications areas in the future.

Interfacial Engineering Using Covalent Organic Frameworks in Polymer Composites for High‐Temperature Electrostatic Energy Storage

AbstractThe use of inorganic nanofillers has been an effective method to improve high‐temperature capacitive performance of dielectric polymers, though there are unmet challenges such as undesirable organic–inorganic compatibility, and low efficiencies and energy densities. Herein, a surface functionalization strategy using covalent organic frameworks (COFs) is employed to address such challenges in realizing high‐performing polymer composites. Specifically, core–shell structured nanoparticles, where ZrO2 nanoparticles act as the core and a COF material forms the shell, are constructed and composited with the polyetherimide (PEI) matrix. The design leverages the high electron affinity (EA) of the outer COF shell to create energy traps, thereby capturing free charges and limiting electrical conduction. Concurrently, the low EA and wide bandgap of the ZrO2 core introduce energy barriers to impede charge injection and migration. This orchestrated “energy level cascade” results in a marked reduction of leakage current and energy loss. The resulting polymer composite showcases an impressive discharged energy density of 6.21 J cm−3 at an efficiency above 90%, with a maximum discharged energy density reaching 7.43 J cm−3 at 150 °C. These performance metrics position the PEI/ZrO2@COF polymer composite to surpass or be on par with state‐of‐the‐art high‐temperature PEI composites and other advanced polymer dielectrics.

Improved capacitive energy storage performance in hybrid films with ultralow aminated molybdenum trioxide integration for high-temperature applications.

Dielectric capacitors play a pivotal role in advanced high-power electrical and electronic applications, acting as essential components for electrical energy storage. The current trend towards miniaturization in electronic devices and power systems highlights the increasing demand for scalable, high-performance ultra-thin dielectric films with a high-temperature stability. While significant progress has been made in enhancing the discharged energy density (Ue) of dielectric polymers at elevated temperatures, such advancements have faced certain challenges. Herein, an innovative molecular engineering approach for the bonding of amine-functionalized molybdenum trioxide (A-MoO3) with the dianhydride monomer of polyetherimide (PEI) is presented, leading to a reduction in conduction loss and the substantial enhancement in storage energy density under high-temperature and high-field conditions. It is revealed that charge redistribution at the bonding sites induces a subtle variation in the potential energy, creating an in-built electric field between the PEI matrix and A-MoO3 based on density functional theory (DFT) analyses. The observed phenomenon leads to an increase in the electron barrier, effectively inhibiting the release of trapped electrons. Notably, at conditions of 200 °C and 100 Hz, the PEI/A-MoO3 hybrid film demonstrates a notable Ue at η > 90%, reaching up to 5.53 J cm-3, surpassing the performance of many current dielectric polymers and composites. Furthermore, the hybrid film's exceptional cycling durability, coupled with its ability to be fabricated into large-area, uniform-quality films, underscores its potential in the development of dielectric energy storage devices tailored for extreme environments.

Microwave-assisted ZnO-decorated carbon urchin resembling 'shish-kebab' morphology with self-healing and enhanced electromagnetic shielding properties.

Herein, inspired by Acacia auriculiformis fruit, the shish-kebab-like growth of ZnO on carbon urchin (ZnO@CU) was designed using microwave radiation, thus leading to a hierarchal 3D structure that can promote multiple internal reflections through polarization centers. This hierarchal structure was then dispersed in a designer polyetherimide (PEI) matrix containing dynamic covalent bonds that can undergo metathesis, triggered by temperature, to harness self-healing properties in the composite. Such key attributes are required for their potential use in EMI shielding applications where frequent repairs are indispensable. Morphological investigation revealed that the ZnO flower was periodically nucleated like 'shish-kebab' structures on CU surfaces. CU was designed from short carbon fibers using a facile modified method. The EMI shielding performance of the resulting composites was investigated in the X-band, illustrating a shielding effectiveness of -40.6 dB for 2 wt% of ZnO@CU loading, and the composite can be preserved after the self-healing procedure. The ZnO 'kebabs' on 'CU shish' facilitated multiple scattering and numerous polarization centers to improve the EMI shielding performances at extremely low filler contents. In addition, the mechanical and thermal properties of the composite showed improved structural integrity and superior resistance to extreme temperatures, respectively. Overall, the proposed ZnO@CU/PEI composite has great potential to fulfill the increasing demands for lightweight EMI shielding materials in many fields.

Improved Capacitive Energy Storage at High Temperature via Constructing Physical Cross‐Link and Electron–Hole Pairs Based on P‐Type Semiconductive Polymer Filler

AbstractIn this work, p‐type polymer semiconductor poly(2‐((3,6,7,10,11‐pentakis (hexyloxy) triphenylene‐2‐yl)oxy)ethyl methacrylate) (PMHT) is added into polyetherimide (PEI). Benefiting from the electrostatic interaction between strong electrophilic charged phenyls of the PEI matrix and strong electronegative benzophenanthrene unit of the PMHT filler, the physical cross‐linked networks are formed in polymer blends. Meanwhile, the lowest unoccupied molecular orbital level of PEI is close to the highest occupied molecular orbital level of PMHT, which is easy to establish electron–hole pair by Coulomb force. Thus, the carrier trap is constructed in the heterojunction region between PMHT filler and PEI matrix. Both physically cross‐linked networks and electron–hole pairs can promote breakdown strength (Eb) of PEI and decrease energy loss. Importantly, PMHT filler can improve the dielectric constant of PEI. As a result, 0.75 wt% PMHT/PEI delivers an ultrahigh discharge energy density (Ud) of 10.7 J cm−3 at an Eb of 680 MV m−1 and at room temperature, and maintains a charge and discharge efficiency of above 90%. In addition, a superior Ud of 5.1 and 3.3 J cm−3 is achieved at 150 and 200 °C, respectively. This paper creates a new perspective for preparing high‐properties polymer dielectrics by combining the advantages of cross‐linking and electron–hole pairs.

Fe3O4 microplate filled PEI matrix composite with remarkable nonlinear conductive characteristics, dielectric property, and low percolation threshold

As the presence of a percolating network formed by filler is indispensable for field grading composite, particulate fillers often result in high filler content that can be unfavorable in some aspects. The utilization of fillers with high aspect ratio is an effective way of reducing percolation threshold. In this work, Fe3O4 microplate (FMP) was prepared by a PVP-assisted hydrothermal method and it was adopted to fabricate composite films with different filler content by using polyetherimide (PEI) as the matrix. The composite film exhibited a percolation threshold of approximately 8 phr. The nonlinear coefficient measured 6.28 at a filler content of 10 phr. The nonlinearity in the conductive behavior of the composites was attributed to tunneling effect and Schottky emission. The filling of the FMP into PEI resulted in increase in dielectric constant and the dielectric loss maintained low. This study suggests that the FMP is a promising filler of low-filler-content field grading composite.

High CO2 adsorption of ultra-small Zr-MOF nanocrystals synthesized by modulation method boosts the CO2/CH4 separation performance of mixed-matrix membranes

The separation performance of mixed matrix membranes (MMMs) is greatly impacted by both the inherent structure of porous fillers and the interfacial compatibility between the filler and matrix. Here, ultra-small Zr-MOFs (UiO-66-mod and NH2-UiO-66-mod) with more defect sites were synthesized through a simple sodium formate modulation strategy. Then, these modulated Zr-MOFs were used as porous fillers in combination with polyetherimide (PEI) to construct a high-quality mixed matrix membrane for efficient CO2 separation. The modulated Zr-MOF not only exposed more defect sites, which significantly enhanced the CO2 adsorption capacity but also exhibited high dispersion in the PEI matrix due to strong interfacial forces, avoiding non-selective voids. The 10-UiO-66-mod-PEI and 10-NH2-UiO-66-mod-PEI membranes developed here showed admirable CO2/CH4 separation performance (CO2 permeability of around 400 and 440 Barrer, CO2/CH4 selectivity of ∼33 and ∼47, respectively) much higher than that of non-modulated UiO-66-PEI membranes, surpassing the 2008 upper bound of MMMs. This work demonstrated that the proposed UiO-66-mod-PEI and NH2-UiO-66-mod-PEI MMMs could be potential candidates for an efficient CO2 capture process.

Electromagnetic interference shielding behavior of polypyrrole-impregnated poly(ether imide)/sulfonated poly(ether ether ketone) composites

Electromagnetic interference (EMI) shielding materials are of major interest for modern society due to proliferation of electronic instruments and it reports the designing of electromagnetic radiations shielding material against electromagnetic pollution. Here, we prepared a series of composites comprising polyetherimide (PEI) with sulfonated poly(ether ether ketone) (SPEEK) by solvent casting method, having SPEEK loading ranging from 10 to 50 wt%. All the composites and PEI films were impregnated with pyrrole via in situ polymerization method to enhance their electrical conductivity. The morphology of composites was studied by SEM (scanning electron microscopy) and XRD (X-ray diffraction) analysis. Structural and thermal properties were investigated by Fourier-transform infrared spectroscopy (FT-IR), TGA and DSC, respectively. Electrical conductivity was analyzed by two probe method. Maximum conductivity of 2.24*10−4 S/cm was achieved at 50 wt% loading of SPEEK, due to the presence of conductive network between polypyrrole (PPy) and SPEEK throughout PEI matrix. These composites exhibited an average electromagnetic interference SET values up to −21 dB which makes them capable for shielding in the frequency range of 8.2–12.0 GHz (X-band). This study provides an avenue for fabrication of absorption dominating EMI shielding composites, which is promising material for commercial applications in next generation electronic instruments.

Enhanced Interfacial and Dielectric Performance for Polyetherimide Nanocomposites through Tailoring Shell Polarities

Polyimide (PI) and its derivative polyetherimide (PEI) have been widely investigated as promising candidates for dielectric energy storage due to their excellent intrinsic features. However, most of the current research for PI- or PEI-based dielectric nanocomposites only focuses on a certain polar group contained in a dianhydride monomer, while there are very few studies on exploring the effect of a series of polar groups derived from various dianhydride monomers on the dielectric properties of nanocomposites. To fill this gap, we herein fabricated and investigated a series of novel hyperbranched polyimides grafted on barium titanate nanoparticles (HBPI@BT) using different dianhydride monomers and their nanocomposites with the PEI matrix. The results showed that sophisticated hyperbranched structures effectively alleviated the incompatibility between fillers and the matrix, thus significantly improving the bonding energy of nanocomposites, especially for HBPI-S@BT/PEI (797.7 kJ/mol). The Ud of HBPI-S@BT/PEI reached 8.38 J/cm3, which is 3.3 times higher than that of pure PEI. The HBPI-F@BT/PEI nanocomposites achieved high breakdown strength (∼500 MV/m) and low dielectric loss (0.008) simultaneously. The dielectric constants of HBPI@BT/PEI nanocomposites remained at a stable level from 25 to 150 °C. This work provides us promising hyperbranched structured materials for potentially advanced dielectric applications such as field effect transistors.

Enhancing High‐Temperature Energy Density through Al2O3 Nanoplates with Charge Barrier Effect in Polyetherimide‐Based Composites

AbstractPolymer‐based dielectric composites have a wide range of applications in modern electronics and power systems owing to their incomparable reliability, but remain a challenge to energy density at high temperatures. In this work, polyetherimide (PEI)‐based nanocomposites with a small amount of aluminium oxide (Al2O3) nanoplates are prepared and obtain excellent energy density at elevated temperatures. The high‐temperature energy density of the nanocomposites is significantly improved and reaches to 5.2 J cm−3 at 550 kV mm−1 and 150 °C after adding 0.6 wt% Al2O3 nanoplates. The enhanced energy density is attributed to the wide band gap and flaky morphology of Al2O3 nanoplates that can induce charge barrier effect and thus reduce the leakage current density within the nanocomposites. Furthermore, finite element simulations further reveal the mechanism of Al2O3 nanoplates acting as charge barrier to capture the charges transmitted from PEI matrix at the interface. This work offers a promising pathway to high‐energy density polymer dielectrics capable of operating under high temperatures.

Significant enhancement of thermal conductivity and EMI shielding performance in PEI composites via constructing 3D microscopic continuous filler network

Polymer-based composites with effective heat dissipation and ideal electromagnetic interference shielding performance have gradually become an essential research focus in modern electronic industry. Herein, a method is reported by constructing 3D microscope continuous filler network into polyetherimide (PEI) matrix via incorporating function graphite nanoplatelets (GNP) with PEI microspheres, and then fillers are distributed beyond the domain area of polymer and leaded to continuous filler framework. The fabricated composites exhibit effective thermal conductivity (4.77 W m−1K−1), great EMI effectiveness (42.7 dB), ideal electrical conductivity and profound thermal property. Different scale of polymer microspheres will also change the micro-architecture from “filler-wrapped polymer” structure to “polymer-wrapped filler” structure, resulting in various thermal performance and electrical property. Finite element simulation is further employed to explore the relationship between microsphere scale and heat transfer behavior. In a word, great comprehensive performance endows PEI composites broaden prospect on the potential applications in the fields of electronic equipment.

Hydrogen Bonding of Aramid Boosts High-Temperature Capacitive Properties of Polyetherimide Blends

Polyetherimide (PEI) is the state-of-the-art commercial high-temperature polymer dielectric with excellent thermal and chemical stability and relatively high high-temperature capacitive energy storage properties. The rotation of the dipoles in the PEI chains brings the β-relaxation which seriously increases the leakage current and decreases the charge-discharge efficiency. In this work, hydrogen bonds have been introduced to limit the dipole rotation of PEI by blending aramids [1,4-poly(ether fluoromethyl naphthalene amide), PNFA] into the PEI matrix. By introducing 10 wt % PNFA, the β-relaxation of the blend has been significantly reduced which could be observed from the dielectric spectrum. To explore the mechanism of limited β-relaxation, we analyze the hydrogen bonds in the blend films by infrared spectroscopy and found that the maximum content of hydrogen-bonded carbonyl formed between PNFA and PEI chains was 14.3% when the content of PNFA was 30 wt %. The content of hydrogen bonds formed between PNFA and PEI was positively correlated with the energy storage performance of the blends. The maximum discharged energy density with an efficiency above 90% of the blend film with 30 wt % PNFA reaches 4.1 J cm-3 at 150 °C, which is about 350% higher than that of pristine PEI. This work shows that composing hydrogen bonds by the blending method could be a viable strategy for enhancing the high-temperature energy storage performance of polymer dielectrics, which could be achieved by large-scale preparation and has feasible industrial production prospects.

Functionalized superhydrophobic MWCNT/PEI nanocomposite film with anti-icing and photo-/electrothermal deicing properties

Ice accumulation often threatens the safety of human life and property. How to effectively solve the problem of solid surface icing has been the research work of many researchers. However, how to prepare superhydrophobic and anti-icing film with multi-strategy collaborative deicing is still facing great challenges. In this paper, a design strategy of photothermal and electrothermal superhydrophobic nanocomposite film based on polyetherimide (PEI) was proposed. Multi-walled carbon nanotubes (MWCNT) were dispersed in PEI matrix by solution blending method, and a lotus leaf like rectangular micropillar array was constructed on the surface of the film by laser etching technology. Then, the surface was fluorinated to further reduce the surface energy. Finally, a kind of MWCNT/PEI nanocomposite film with passive anti-icing and active deicing with photothermal and electrothermal collaboration was successfully prepared. The freezing time of droplets on MWCNT/PEI nanocomposite film is about 6.7 times longer than that of pure PEI film. This film exhibits excellent superhydrophobicity (CA = 156.6°), while also having excellent photothermal and electrothermal conversion properties. In addition, we also conducted various tests on MWCNT/PEI nanocomposite film to verify its reliability in the actual application environment. The MWCNT/PEI nanocomposite film with the function of anti-icing and photothermal and electrothermal active deicing is expected to solve the problem of solid surface icing in daily life, and also provides a new idea for the development of a new generation of anti-icing/deicing film.