Conductive Polymer Research Articles

Preparation of high thermal conductivity vat photopolymerization used UV-curable resin synergistically enhanced by silicon nitride and boron nitride

Additive manufacturing (3D printing) technologies, especially vat photopolymerization (VPP), provide a cost-effective and efficient approach for the fabrication of heat dissipation devices with complex geometric designs. The incorporation of inorganic thermal conductive fillers into resin matrix is widely recognized as an effective way to enhance thermal conductivity. Notably, the synergistic effect of hybrid fillers can further enhance thermal conductivity. However, the consequent drastic increase in viscosity of the UV-curable resin may decrease the success rate and accuracy of printing on commercial VPP 3D printers. In this work, hexagonal boron nitride (h-BN) platelets and spherical h-BN together with β-Si3N4 are introduced into the UV-curable resin system. Corresponding results proved that h-BN together with β-Si3N4 provide a synergistic effect on the thermal conductivity enhancement compared to the filler in single morphology only. Moreover, owing to the spherical structure, low-viscosity UV-curable resin with high solid content can be prepared. In specific, a thermal conductive polymer composite material with a solid content of 60 wt% is prepared, which exhibits high thermal conductivity (1.42 W/mK), representing an enhancement of up to 610 % compared to neat resin. In subsequent application demonstrations, 3D printed heat dissipation devices with as-prepared resin composite material have been shown to effectively enhance the heat dissipation rate for the heating device.

Feasibility of Using the Coil-Shaped Conductive Polymer Composite to Measure Thickness

Feasibility of Using the Coil-Shaped Conductive Polymer Composite to Measure Thickness

Effects of conductive phase content on magnetic sensitivity of spiral conductive polymer composite

Flexible magnetic field sensors are essential for small dimensions, excellent precision, and flexibility in narrow gap or pipe environments. A spiral conductive polymer composite has been proposed for magnetic field detection. To investigate how conductive phase content impacts its magnetic sensitivity, the relationship between magnetic flux density and voltage difference/magnetic sensitivity was examined with different carbon nanotube contents (1 wt%∼20 wt%). From the perspectives of the equivalent network and magnetic susceptibility, the voltage difference /magnetic sensitivity of the composite was analysed by varying its carbon nanotube content. The addition of carbon nanotubes creates a contradiction in the magnetic sensitivity caused by internal equivalent impedance or induced current. The experiments demonstrate that the interpolar voltage difference /magnetic sensitivity first increases and then sharply decreases with increasing carbon nanotube content within composites. The optimum carbon nanotube content is about 8 wt%, which can be an optimal sensitive material choice for a flexible magnetic sensor.

Preparation and electromagnetic waves absorption performance of hibiscus-like CuS/SiC NWs@PANI in the GHz band

With the increasing demand for electromagnetic (EM) waves absorbing materials in communication, military, and electronic devices, the exploration of lightweight, wideband, and highly absorptive materials in the GHz frequency range has become urgent. This article presents a successful synthesis of hibiscus-like copper sulfide (CuS)/silicon carbide nanowires (SiC NWs) @polyaniline (PANI) composite material using a combination of hydrothermal and in-situ polymerization techniques. With a filling amount of only 25 wt% of CuS/SiC NWs@PANI in the paraffin transmissive matrix, the material exhibits a minimum reflection loss (RLmin) of −31.6 dB at a thickness of 2.1 mm, while providing an effective absorption bandwidth (EAB) of 4.5 GHz. As the filling amount increases to 35 wt%, the RLmin drastically reduces to −41.38 dB at a thickness of 2.3 mm. The CuS particles exhibit a unique multi-layered asymmetric hibiscus-like structure, which greatly enhances the reflection of EM waves. The conductive polymer PANI, forming a coating layer at the interface with CuS and SiC NWs, effectively enhances the conductive loss. The collaborative interactions among the components in the ternary composite material significantly boost the EM waves absorption performance. This article offers valuable insights into the preparation and real-world application of absorbent materials with distinctive microstructures, thus opening up new avenues for the design of composite absorbing materials.

Elaborate structural design of polypyrrole-based microwave absorbers: Synthesis, enhanced dielectric characteristics, and superior absorption capability

Intrinsically conductive polymers are expected as an advanced microwave absorption material due to their adjustable dielectric characteristics and low density. In this investigation, polypyrrole (PPy) with spherical aggregation and nanofiber structures were successfully synthesized by chemical oxidation polymerization strategy. The impact of reaction conditions on the structure, morphology, size, and chemical constituents has been investigated. The results indicate that the strong interfacial interaction between dopamine and pyrrole monomer leads to the formation of nanofibers. Because of the synergistic effect of favorable impedance matching, improved dielectric loss, and conductive loss, the PPy aggregations with nanosized particles exhibit outstanding absorption capability. At 6.32 GHz, the minimum reflection loss even reaches -46.73 dB. The effective absorption bandwidth (EAB) covers a broad frequency range of 6.51 GHz. Our work provides a versatile strategy for PPy-based materials with elaborately structural design to achieve excellent and modulated microwave absorption capability.

Chlorpromazine-Polypyrrole Drug Delivery System Tailored for Neurological Application.

Nowadays, drug delivery systems (DDSs) are gaining more and more attention. Conducting polymers (CPs) are efficiently used for DDS construction as such systems can be used in therapy. In this research, a well-known CP, polypyrrole (PPy), was synthesized in the presence of the polysaccharide heparin (HEP) and chlorpromazine (CPZ) using sodium dodecyl sulfate (SDS) as electrolyte on a steel substrate. The obtained results demonstrate the successful incorporation of CPZ and HEP into the polymer matrix, with the deposited films maintaining stable electrochemical parameters across multiple doping/dedoping cycles. Surface roughness, estimated via AFM analysis, revealed a correlation with layer thickness-decreasing for thinner layers and increasing for thicker ones. Moreover, SEM images revealed a change in the morphology of PPy films when PPy is electropolymerized in the presence of CPZ and HEP, while FTIR confirmed the presence of CPZ and HEP within PPy. Due to its lower molecular mass compared to HEP, CPZ was readily integrated into the thin polymer matrix during deposition, with diffusion being unimpeded, as opposed to films with greater thickness. Finally, the resulting system exhibited the ability to release CPZ, enabling a dosing range of 10 mg to 20 mg per day, effectively covering the therapeutic concentration range.

Synthesis of 3D rice-like BiOCl battery-type electrode material and evaluation of their electrochemical performance in a symmetrical supercapacitor device configuration

3D porous rice-like BiOCl nanostructure was prepared via solvothermal technique with sodium chlorate as a surfactant which serves as electrode material for the supercapacitor applications. The prepared nanoparticles supported on nickel foam textile exhibit high battery-type charge storage ability in a 3 M KOH aqueous electrolyte solution. The dominance of the battery-type charge storage mechanism of the BiOCl electrode was confirmed through the CV study. Furthermore, the GCD study revealed a good specific capacity of 501 C/g at 0.5 A/g current density and cycle stability of 80% over 2500 cycles. In the presence of a 3 M KOH electrolyte, a symmetric supercapacitor device was constructed with two identical 3D rice-like BiOCl electrodes. This configuration unveiled an impressive energy density of 21.8 Wh/kg at 772.5 W/kg power density. To illustrate its practical viability, two BiOCl/BiOCl symmetric devices were connected in series, successfully powering a red LED for approximately 50 s with high light intensity. This underscores the practical potential of the 3D rice-like BiOCl electrode in energy storage systems. In order to maximize the potential of BiOCl material in the future, the focus could be shifted towards mitigating the challenge of potential drop. This hurdle could be tackled by fabricating nanocomposites of BiOCl incorporated with conductive polymers and graphene oxide, thus elevating its overall performance.

Light‐induced Delivery of Charged Species using Ion‐selective Core–Shell Nanoparticles

AbstractControlled release systems have gained considerable attention owing to their potential to deliver molecules, including ions and drugs, in a customized manner. We present a light‐induced ion‐transfer platform consisting of a dispersion of nanoparticles (NPs, ~300 nm) with the conductive polymer poly(3‐octylthiophene‐2,5‐diyl) (POT) in the core and a potassium (K+)‐selective membrane in the shell. Owing to the photoactive nature of POT, POT NPs can be used for a dual purpose: as a host for positively charged species and as an actuator to trigger the subsequent release. POT0 and doped POT+ coexist in the core, allowing K+ encapsulation in the shell. As POT0 is photo‐oxidized to POT+, K+ is released to the (aqueous) dispersion phase to preserve the neutrality of the NPs. This process is reversible and can be simultaneously assessed using the native fluorescence of POT0 and via potentiometric measurements. The NP structure and its mechanism of action were thoroughly studied with a series of control experiments and complementary techniques. Understanding the NP and its surrounding interactions will pave the way for other nanostructured systems, facilitating sophisticated applications. The delivery of ionic drugs and interference/pollutant catching for advanced sensing/restoration will be considered in future research.

Anchoring of Fe-MIL-101-NH2 to the Polymer Membrane Matrix through the Hinsberg Reaction to Promote Conductivity of SPEEK Membranes.

SCPEEK@MOF proton exchange membranes, where SCPEEK is sulfinyl chloride polyether ether ketone and MOF is a metal-organic framework, were prepared by doping Fe-MIL-101-NH2 into polymers. The amino group in the MOF and the -SOCl2 group in thionyl chloride polyether ether ketone cross-link to form a covalent bond through the Hinsberg reaction, and the prepared composite membrane has stronger stability than other electrostatic interactions and simple physical doping composite membranes. The formation of covalent bonds improves the water absorption of the composite membrane, which makes it easy for water molecules to form hydrogen bonds. Moreover, SPEEK as a proton conductive polymer and the synergy of MOFs improve the proton conductivity of composite membranes. The composite membranes were characterized by Fourier transform infrared spectroscopy, powder X-ray diffraction, scanning electron microscopy, and atomic force microscopy. The swelling rate, water absorption, mechanical stability, ion exchange capacity, and proton conductivity of the pure sulfonated polyether ether ketone (SPEEK) membrane were compared with those of the mechanically doped SPEEK/MOF membrane and the composite membrane SCPEEK@MOF doped with different ratios of Fe-MIL-101-NH2, and all of the SCPEEK@MOF showed superior performance. When the Fe-MIL-101-NH2 loading rate of the composite membrane is 2%, the proton conductivity of the composite membrane can reach 0.202 S cm-1 at 363 K and a 98% relative humidity, which is much higher than that of the SPEEK/MOF membrane obtained by simple physical doping under the same conditions.

Light-induced Delivery of Charged Species using Ion-selective Core-Shell Nanoparticles.

Controlled release systems have gained considerable attention owing to their potential to deliver molecules, including ions and drugs, in a customized manner. We present a light-induced ion-transfer platform consisting of a dispersion of nanoparticles (NPs, ~300 nm) with the conductive polymer poly(3-octylthiophene-2,5-diyl) (POT) in the core and a potassium (K+)-selective membrane in the shell. Owing to the photoactive nature of POT, POT NPs can be used for a dual purpose: as a host for positively charged species and as an actuator to trigger the subsequent release. POT0 and doped POT+ coexist in the core, allowing K+ encapsulation in the shell. As POT0 is photo-oxidized to POT+, K+ is released to the (aqueous) dispersion phase to preserve the neutrality of the NPs. This process is reversible and can be simultaneously assessed using the native fluorescence of POT0 and via potentiometric measurements. The NP structure and its mechanism of action were thoroughly studied with a series of control experiments and complementary techniques. Understanding the NP and its surrounding interactions will pave the way for other nanostructured systems, facilitating sophisticated applications. The delivery of ionic drugs and interference/pollutant catching for advanced sensing/restoration will be considered in future research.

Aqueous Conductive Polymer Composites with Good Printability and Conductivity for Flexible Electronics

Aqueous Conductive Polymer Composites with Good Printability and Conductivity for Flexible Electronics

Advancements in nanohybrids: From coordination materials to flexible solar cells

This comprehensive review explores the forefront of nanohybrid materials, focusing on the integration of coordination materials in various applications, with a spotlight on their role in the development of flexible solar cells. coordination material-based nanohybrids, characterized by their unique properties and multifunctionality, have garnered significant attention in fields ranging from catalysis and sensing to drug delivery and energy storage. the discussion investigates the synthesis methods, properties, and potential applications of these nanohybrids, underscoring their versatility in materials science. Additionally, the review investigates the integration of coordination nanohybrids in perovskite solar cells (PSCs), showcasing their ability to enhance the performance and stability of next-generation photovoltaic devices. the narrative further expands to encompass the synthesis of luminescent nanohybrids for bioimaging purposes and the development of layered two-dimensional (2D) material-based nanostructured hybrids for energy storage and conversion. the exploration culminates in an examination of the synthesis of conductive polymer nanostructures, elucidating their potential in drug delivery systems. lastly, the article discusses the cutting-edge realm of flexible solar cells, emphasizing their adaptability and lightweight design. Through a systematic examination of these diverse nanohybrid materials, this review sheds light on the current state of the art, challenges, and prospects, providing valuable insights for researchers and practitioners in the fields of materials science, nanotechnology, and renewable energy.

Montmorillonite/Poly(Pyrrole) for Low-Cost Supercapacitor Electrode Hybrid Materials.

Conductive polymers such as polypyrrole have been widely used as pseudo-capacitive electrodes for supercapacitors. This work demonstrates a simple method to improve the performance of conductive polymer electrodes by adding montmorillonite in order to perform capacitive behavior. Conductive composite polymers (CCPs) based on montmorillonite/polypyrrole (MMT/PPy(Cl)) have been synthesized by polymerization using FeCl3 as an oxidizing agent. During the preparation of CCP, the effect of MMT/pyrrole mass ratio and the influence of the amount of added H+ and temperature of the synthesis medium on the electrochemical performance of the composite have been investigated. The investigation associated with conductivity measurement allowed us to determine the best conditions to reach a high specific capacitance of 465 F gr-1 measured by cyclic voltammetry with respect to the CCP synthesized at ambient temperature (220 F gr-1) and a 35% increase in capacity compared to its homologue synthesized in neutral conditions at a low temperature. These performances have been advantageously correlated both to the edge acidity of the host material and to the evolution of its conductivity according to the preparation conditions. The galvanostatic charge/discharge tests also confirm the stability of the obtained composite, and a capacitance of 325 F g-1 for the best CCP is recorded with a regime of 1 A g-1. In addition, the durability of the device shows that the proposed material has a relatively good stability during cycling.

Construction of a Conductive Polymer/AuNP/Cyanobacteria-Based Biophotovoltaic Cell Harnessing Solar Energy to Generate Electricity via Photosynthesis and Its Usage as a Photoelectrochemical Pesticide Biosensor: Atrazine as a Case Study.

In this research, a cyanobacteria (Leptolyngbia sp.)-based biological photovoltaic cell (BPV) was designed. This clean energy-friendly BPV produced a photocurrent as a result of illuminating the photoanode and cathode electrodes immersed in the aqueous medium with solar energy. For this purpose, both electrodes were first coated with conductive polymers with aniline functional groups on the gold electrodes. In the cell, the photoanode was first coated with a gold-modified poly 4-(2,5-di(thiophen-2-yl)-1H-pyrrol-1-yl)benzamine polymer, P(SNS-Aniline). Thioaniline-functionalized gold nanoparticles were used to provide a cross-link formation with bis-aniline conductive bonds with the conductive polymer using electrochemical techniques. Leptolyngbia sp., one of the cyanobacteria that can convert light energy into chemical energy, was attached to this layered electrode surface. The cathode of the cell was attached to the gold electrode surface with P(SNS-Aniline). Then, the bilirubin oxidase (BOx) enzyme was immobilized on this film surface with glutaraldehyde activation. This cell, which can use light, thanks to cyanobacteria, oxidized and split water, and oxygen was obtained at the photoanode electrode. At the cathode electrode, the oxygen gas was reduced to water by the bioelectrocatalytic method. To obtain a high photocurrent from the BPV, necessary optimizations were made during the design of the system to increase electron transport and strengthen its transfer. While the photocurrent value obtained with the designed BPV in optimum conditions and in the pseudosteady state was 10 mA/m2, the maximum power value obtained was 46.5 mW/m2. In addition to storing the light energy of the system, studies have been carried out on this system as a pesticide biosensor. Atrazine biosensing via the BPV system was analytically characterized between 0.1 and 1.2 μM concentrations for atrazine, and a very low detection limit was found as 0.024 μM. In addition, response time and recovery studies related to pesticide biosensor properties of the BPV were also investigated.

A high performance fireproof quasi-solid-state electrolyte enabled by multi-phase synergistic mechanism

Composite quasi-solid electrolytes usually suffer from reduced safety performance due to the presence of liquid plasticizers and an inherently unsafe polymer matrix. Adding inorganic fillers is an effective strategy to improve the safety performance of quasi-solid electrolytes, but excessive content may block ion transport channels, leading to a decrease in electrochemical performance. Therefore, it is proposed to construct a multi-phase synergistic non-flammable composite quasi-solid electrolyte (MS-NCQE) by combining an intrinsically safe porous composite framework with a Li+ conductive polymer through in-situ solidification technique. Thanks to multi-phase synergistic mechanism, a porous composite framework consisting of ceramic powder as well as a non-flammable polymer matrix enables MS-NCQE to exhibit significantly improved safety properties. At the same time, due to the interaction between the third-phase Li+ conductive polymer and ceramic powder, MS-NCQE presents excellent lithium ion transport performance (6.59×10−4 S cm−1 at 25 °C) and dendrite resistance (0.1 mA cm−2; 3000 h). Further, the as-prepared LiFePO4|Li and LiNi0.83Co0.12Mn0.05O2|Li batteries display outstanding cycling performance. In particular, the capacity retention rate of the LiFePO4|Li battery is approximately 98 % after 300 cycles at 0.5 C, and its average Coulombic efficiency is higher than 99.8 %. In addition, the pouch cell can work normally and safely under different abuse conditions. This work provides new insights into the design of composite quasi-solid electrolytes with high safety and excellent electrochemical properties.

Lithium Superionic Conductive Nanofiber-Reinforcing High-Performance Polymer Electrolytes for Solid-State Batteries.

Although composite solid-state electrolytes (CSEs) are considered promising ionic conductors for high-energy lithium metal batteries, their unsatisfactory ionic conductivity, low mechanical strength, poor thermal stability, and narrow voltage window limit their practical applications. We have prepared a new lithium superionic conductor (Li-HA-F) with an ultralong nanofiber structure and ultrahigh room-temperature ionic conductivity (12.6 mS cm-1). When it is directly coupled with a typical poly(ethylene oxide)-based solid electrolyte, the Li-HA-F nanofibers endow the resulting CSE with high ionic conductivity (4.0 × 10-4 S cm-1 at 30 °C), large Li+ transference number (0.66), and wide voltage window (5.2 V). Detailed experiments and theoretical calculations reveal that Li-HA-F supplies continuous dual-conductive pathways and results in stable LiF-rich interfaces, leading to its excellent performance. Moreover, the Li-HA-F nanofiber-reinforced CSE exhibits good heat/flame resistance and flexibility, with a high breaking strength (9.66 MPa). As a result, the Li/Li half cells fabricated with the Li-HA-F CSE exhibit good stability over 2000 h with a high critical current density of 1.4 mA cm-2. Furthermore, the LiFePO4/Li-HA-F CSE/Li and LiNi0.8Co0.1Mn0.1O2/Li-HA-F CSE/Li solid-state batteries deliver high reversible capacities over a wide temperature range with a good cycling performance.

Rationally coordinating polymer enabling effective Li-ion percolation network in composite electrolyte for solid-state Li-metal batteries

The sluggish lithium-ion mobility and inferior electrolyte/electrode interfacial compatibility of composite solid electrolytes greatly hinder the practical application of solid-state lithium-metal batteries. Here, a novel composite polymer electrolyte (CPE) with effective Li+ percolation network is synthesized based on single-ion conductive polymer lithiated polyvinyl formal (LiPVFM) and garnet Li6.4La3Zr2Ga0.2O12 (LLZGO) nanoparticles. The supramolecular interaction between the branched hydroxyl in LiPVFM and the lattice oxygen in LLZGO fillers endows CPE with a continuous percolation structure and improved toughness. Meanwhile, the rational O-Li+ coordination in the LiPVFM random polymer significantly enhances Li+ transfer within the percolation network. Therefore, this as-prepared CPE presents a lithium-ion transference number of 0.75 and an ionic conductivity of 0.527 mS cm−1 at 30 °C, alongside an electrochemical stability window of 4.6 V and a substantial suppression of Li dendrite growth. In addition, ultra-stable interfaces between this CPE and high-voltage LiNi0.6Mn0.2Co0.2O2 (NMC) cathode during cycling can be determined by in-situ electrochemical impedance spectroscopy and in-situ differential electrochemical mass spectrometry characterization. This work is a new exploration for the structural design of CPEs and highlights the importance of “rational coordination” of alkali cation in solid batteries.

Design and construction of conductive polymer PPy anchored NiCo bi-metal sulfide composite electrode materials for high-performance hybrid supercapacitor and electrochemical hydroquinone sensor

The development of green energy materials has a crucial role in the energy crisis and environmental issues. The dual-functional oriented strategy was used to prepare new electrode material PPy@NCS by using glycerol as a template. The electrode material PPy@NCS-5 exhibits a higher specific capacitance of 2011.6 F g−1 at 1 A g−1 and delivers excellent long-term cycling stability with 93.3 % of its specific capacitance retained at 20 Ag−1 after 5000 cycles. A hybrid supercapacitor (HSC) combining PPy@NCS-5 and activated carbon (AC) yields a high energy density of 44.6 Wh kg−1 at a power density of 15,005.6 W kg−1. Furthermore, the as-prepared PPy@NCS-5/GCE can be used as an HQ sensor, which displays high sensitivity (0.026 μA/μM), an extraordinary linear response ranging (0.5–1923 μM), and a low detection limit (0.026 μM).

Preparation of Highly Thermally Conductive Hexagonal Boron Nitride‐Polyvinyl Alcohol/Polydimethylsiloxane Composite Using Combined Freeze‐Drying and Spatial Confining Forced Network Assembly Method

With the rapid advancement of electronic products, an increasing number of electronic components are being integrated onto chips, leading to a higher power consumption per unit area. Consequently, effective heat dissipation has become increasingly important. To address this heat dissipation challenge, this article introduces and prepares a highly thermally conductive polymer composite based on freeze‐drying, coupled with the spatial confining forced network assembly (SCFNA) method. The freeze‐drying process is used to create a three‐dimensional thermal conductive network. This network provides a well‐defined heat path. The SCFNA method enhances the regularity of the thermal conductive network within the matrix. Ultimately, this results in the significant thermal conductivity enhancement of the polymer composite. After freeze‐drying, when the mass ratio of hexagonal boron nitride to polyvinyl alcohol is 4:1, the sample prepared by SCFNA presents 72.6% higher thermal conductivity than the one obtained through direct infiltration. This achievement holds significant value for the advancement of polymer composites with high‐thermal conductivity and excellent mechanical properties. It can improve the low‐dissipation performance of polymer thermal conductive composite systems, meet the needs of high‐performance and low‐dissipation use of thermal management materials, and reduce the working temperature of electronic chips.

Superlative and Selective Sensing of Serotonin in Undiluted Human Serum Using Novel Polystyrene Sulfonate Conductive Polymer.

In the past 5 years, real-time health monitoring has become ubiquitous with the development of watches and rings that can measure and report on the physiological state. As an extension, real-time biomarker sensors, such as the continuous glucose monitor, are becoming popular for both health and performance monitoring. However, few real-time sensors for biomarkers have been made commercially available; this is primarily due to problems with cost, stability, sensitivity, selectivity, and reproducibility of biosensors. Therefore, simple, robust sensors are needed to expand the number of analytes that can be detected in emerging and existing wearable platforms. To address this need, we present a simple but novel sensing material. In short, we have modified the already popular PEDOT/PSS conductive polymer by completely removing the PEDOT component and thus have fabricated a polystyrene sulfonate (PSS) sensor electrodeposited on a glassy carbon (GC) base (GC-PSS). We demonstrate that coupling the GC-PSS sensor with differential pulse voltammetry creates a sensor capable of the selective and sensitive detection of serotonin. Notably, the GC-PSS sensor has a sensitivity of 179 μA μM-1 cm-2 which is 36x that of unmodified GC and an interferent-free detection limit of 10 nM, which is below the concentrations typically found in saliva, urine, and plasma. Notably, the redox potential of serotonin interfacing with the GC-PSS sensor is at -0.188 V versus Ag/AgCl, which is significantly distanced from peaks produced by common interferants found in biofluids, including serum. Therefore, this paper reports a novel, simple sensor and polymeric interface that is compatible with emerging wearable sensor platforms.