Strong Interfacial Interaction Research Articles

Fabrication of Two-Dimensional Bi2MoO6 Nanosheet-Decorated Bi2MoO6/Bi4O5Br2 Type II Heterojunction and the Enhanced Photocatalytic Degradation of Antibiotics

This article successfully synthesized a series of Bi2MoO6/Bi4O5Br2 heterojunctions using a two-step solvothermal method followed by calcination, and the photocatalytic activity by degradation of tetracycline hydrochloride (TC) was investigated. Compared with pure Bi4O5Br2 and Bi2MoO6, a series of Bi2MoO6/Bi4O5Br2 heterojunctions exhibit higher photocatalytic activity, which can be attributed to the heterostructures with strong interfacial interaction, improving the charge separation. The 2% Bi2MoO6/Bi4O5Br2 heterojunction shows the best photocatalytic activity under visible light irradiation, which is 1.9 times and 1.8 times that of Bi2MoO6 and Bi4O5Br2, respectively. In addition, cyclic experiments have shown that 2% Bi2MoO6/Bi4O5Br2 heterojunction has high stability, with a degradation efficiency only decreasing by 3% after 5 cycles. From the capture agent experiment and ESR test, it can be seen that ·O2− and h+ are the main active species. A possible photocatalytic mechanism of 2% Bi2MoO6/Bi4O5Br2 heterojunction under visible light irradiation was proposed.

Self-Assembled Controllable Cu-Based Perovskite/Calcium Oxide Hybrids with Strong Interfacial Interactions for Enhanced CH4 Electrosynthesis.

Cu-based perovskite oxide catalysts show promise for CO2 electromethanation, but suffer from unsatisfactory CH4 selectivity and poor stability. Here, we report self-assembled, controllable Cu-based perovskite/calcium oxide hybrids with strongly interacting interfaces for high-performance CH4 electrosynthesis. As proof-of-concept catalysts, the La2CuO4/(CaO)x (x from 0.2 to 1.2) series has tunable CaO phase concentrations and thus controllable interface sizes. The La2CuO4 and CaO components are intimately connected at the interface, leading to strong interfacial interactions mainly manifested by marked electron transfer from Ca2+ to Cu2+. In CH4 electrosynthesis, their activity and selectivity show a volcano-type dependence on the CaO phase concentrations and are positively correlated with the interface sizes. Among them, the La2CuO4/(CaO)0.8 delivers the optimal activity and selectivity for CH4, together with good stability, much better than those of a physical-mixture counterpart and most reported Cu-based perovskite oxides. Moreover, La2CuO4/(CaO)0.8 stands out as one of the most effective Cu-based catalysts for CH4 electrosynthesis, achieving a high CH4 selectivity of 77.6% at 300 mA cm-2. Our experiments and theoretical calculations highlight the significant role of self-assembly-induced strong interfacial interactions in promoting *CO adsorption/hydrogenation, intensifying resistance to structural degradation, and consequently underpinning the achievement of such optimized performance.

Fabrication of a Partial Encapsulation Architecture on S-Scheme Heterojunctions toward Durable Selective Photocatalytic CO2 Reduction.

It remains a challenging issue to achieve durably stable photocatalytic CO2 reduction over heterojunctions owing to their inherent structural assembly features. Herein, a unique partial encapsulation architecture is fabricated on the 3D/2D CoWO4/C3N5 heterojunction by embedding CoWO4 microspheres on C3N5 nanosheets, which achieves efficient, durable, stable, and selective photocatalytic CO2 reduction. For the optimal 5%-CoWO4/C3N5 heterojunction, the yield of selective CO2 reduction to CO is 7.70 and 3.82 times higher than those of CoWO4 and C3N5 in 4 h, respectively, and it maintains a stable CO generation rate within 20 cycles over 80 h. A series of characterization experiments and density functional theory calculations reveal that the structural stability is reinforced significantly via strong interfacial interaction owing to the unique partial encapsulation architecture fabricated on the 3D/2D CoWO4/C3N5 heterojunction, the separation efficiency of photogenerated carriers is improved by inducing a built-in electric field and triggering the S-scheme charge-transport path, and the high CO product selectivity is attributed to the much lower free energy required for the generation path of CO compared to that for CH4.

In Situ Generatable and Recyclable Oxygen Vacancy-Modified Fe2O3-Decorated WO3 Nanowires with Super Stability for ppb-Level H2S Sensing.

Detecting hydrogen sulfide (H2S) odor gas in the environment at parts-per-billion-level concentrations is crucial. However, a significant challenge is the rapid deactivation caused by SO42- deposition. To address this issue, we developed a sensing material comprising Fe2O3-decorated WO3 nanowires (FWO) with strong interfacial interaction. During the H2S sensing process, important oxygen vacancies (OVs) are generated in situ and are recyclable on the surface of the Fe2O3 cluster. This sensor achieves a response of 140 (Ra/Rg) toward 50 ppm of H2S at 250 °C, with an experimentally measured detection limit of 1 ppb. It also exhibits remarkable stability, with no significant change observed over a long period of 150 days. Based on a combination of in situ DRIFT and DFT calculations, we have identified that the overactivation of O2 is the key step in the formation of SO42-. This overactivation can be partially modulated by the synergistic effect of Fe2O3 decoration and the in situ generated OVs, regulating the oxidation product to SO2 rather than the toxic SO42-. Furthermore, the continuous generation of OVs compensates for the loss of active sites pertaining to SO42- deposition, thereby contributing to the excellent stability of the sensor. This study underscores the beneficial impact of in situ OV generation in FWO for H2S sensing, offering a dynamic strategy to enhance sensor performance, particularly in terms of stability.

Efficient charge abstraction and oriented accumulation driven by strong interfacial interaction facilitate photocatalytic selective oxidation of furfuralcohol coupled with H2 evolution

S-scheme heterostructures are promising strategies for photogenerated charge transport and spatial separation, yet the intrinsic mechanism of interfacial interaction on carrier dynamics remains under exploration. Herein, an S-scheme NiTiO3/Cd0.6Zn0.4S (NTO/CZS) heterostructure with strong interfacial interaction was fabricated to synchronously drive redox half-reactions. The KPFM, SPV, in-situ ESR, in-situ XPS, and fs-TA combined with and DFT simulation confirmed the reinforced IEF’s role in efficient charge abstraction and oriented accumulation on RP and OP surfaces, respectively, thereby synchronously triggering redox half-reactions. In addition, the furfuryl alcohol (FOL) to furfural (FAL) conversion was driven by αC-H bond cleavage, with H2O playing a crucial role in achieving efficient photocatalytic selective oxidation of FOL coupled with H2 evolution reaction (HER). The optimized 35 % NTO/CZS exhibited exceptional photocatalytic performance, achieving FOL selective oxidation coupled with HER, surpassing that of CZS and NTO for HER of 3.3 mmol g−1 h−1 by 6 times and 50 times, respectively. The present work provides new insights into constructing S-scheme heterostructures with strong interfacial electric field (IEF) for efficient charge abstraction and oriented accumulation to synchronously facilitate redox half-reactions.

Preparation of rGO/CAU-10 anchored PdPbBi composites and their electrocatalytic ethylene glycol properties

An effective method to improve the catalytic performance of electrocatalytic alcohol oxidation by establishing strong interfacial interactions through novel carrier materials and polymetallic alloys. In this paper, novel polyhedral metal–organic framework Al-based [Al(OH)(mBDC)] (CAU-10) composites with PdPbBi trimetallic particles embedded in folded graphene oxide (rGO) modified by a simple hydrothermal reaction were prepared and applied to the electrocatalytic oxidation reaction of ethylene glycol. The results of electrochemical tests showed that the trimetallic catalysts exhibited excellent electrocatalytic activity compared to commercial Pd/C. In particular, PdPbBi@rGO/CAU-10 has the highest peak current density of 241.82 mA cm−2, which is 8.97 times higher than that of Pd/C (26.92 mA cm−2), and the largest electrochemical active area (ECSA) value of 88.12 mA cm−2, which is 2.40 times higher than that of Pd/C (36.75 mA cm−2). This outstanding electrocatalytic activity is mainly attributed to the polyhedral structure of CAU-10 composite carriers and the abundance of oxygen-containing atoms, which is conducive to the homogeneous loading of metals, at the same time, the strong electronic effect between Pd, Pb and Bi and the abundance of oxygen-containing species provide significant enhancement of electrocatalytic activity and stability, which provides an important reference for the development of electrocatalysts for ethylene glycol fuel cells.

Improved HER/OER Performance of NiS2/MoS2 Composite Modified by CeO2 and LDH.

In recent years, there has been significant interest in transition-metal sulfides (TMSs) due to their economic affordability and excellent catalytic activity. Nevertheless, it is difficult for TMSs to achieve satisfactory performance due to problems such as low conductivity, limited catalytic activity, and inadequate stability. Therefore, a catalyst with a heterostructure constituted of a nickel-iron-layered double hydroxide, nickel sulfide, molybdenum disulfide, and cerium dioxide was designed. At the current density of 10 mA cm-2 in an alkaline solution, the catalyst exhibits a HER overpotential of 116 mV. In addition, an overpotential of 235 mV@150 mA cm-2 was displayed for OER. The catalyst showed a good retention rate (94.7% for HER, 98.6% for OER) after 160 h stability tests. The excellent electrochemical performance is attributed to the following points: 1. The self-supporting three-dimensional hierarchical structure provides abundant sites, fast ion diffusion channels, and electron transfer paths, and ensures structural stability. 2. The strong interfacial electron interaction between Ni3S2/MoS2 heterojunction and NiFe-LDH improves the OER reaction kinetics. 3. The Ce3+ and oxygen vacancies in CeO2 promote the dissociation of H2O and promote the HER reaction kinetics. This approach paves the way for developing highly efficient electrocatalysts for various electrochemical applications.

Photoelectrocatalytic degradation of organic contaminants by spray coated Z-scheme TiO2/Bi2WO6 heterostructure electrode under solar light

This study demonstrates that spray deposited layered TiO2/Bi2WO6 heterostructure photoelectrodes exhibit strong interfacial interactions, leading to significant enhancements in photoelectrochemical performance. Time-resolved photoluminescence (TRPL) spectra indicated a prolonged lifetime of photoinduced carriers. The red shift in the absorption edge of TiO2/Bi2WO6 improved the visible light harvesting capability of Bi2WO6. Nyquist plots showed effective charge separation, and the TiO2 layer at the bottom significantly influenced the flat band potential compared to pristine Bi2WO6, as evidenced by Mott-Schottky analysis. This configuration improved the separation of photogenerated charge carriers via a Z-scheme charge transfer mechanism. The TiO2/Bi2WO6 electrode demonstrated a higher efficiency of 94% for methylene blue degradation within 160 min, compared to pure Bi2WO6. Quenching experiments confirmed the Z-scheme charge transfer mechanism in the coupled TiO2/Bi2WO6 heterojunction during degradation reactions. This study highlights the benefits of semiconductor coupling with different band potentials, promoting large-scale applications of solar-driven TiO2/Bi2WO6 photoelectrodes for environmental remediation.

Silicone rubber nanocomposites: Optimal graphene dosing for mechanical and electrical enhancements

The combination of lightweight, durable, and flexible elastomer nanocomposites presents a unique set of features that make them highly promising for a range of several engineering applications. Present work investigates the performance of the mechanical and electrical characteristics of a nanocomposite produced by combining silicon rubber (SR) with nano-Graphene, copper oxide (CuO). Two roll mixing followed by compression moulding is used to manufacture different configurations of Graphene/CuO/SR nano composite. Nano composites specimens are fabricated with 1, 2, 4, and 8 wt % of graphene with fixed 1 % CuO. There has been a discernible improvement of 146.52 % in the mechanical properties and 18.1 % in electrical performance. This improvement is supported by the FESEM morphological analysis of fractured surfaces. It has been observed that the optimized loading of 8 wt % of Graphene gives the best performance. The strong interfacial interaction between the Graphene/CuO and SR is responsible for the performance gain.

Porous TiO2 microspheres containing MgO nanoparticles/epoxy composite with superior thermal conductivity, EMI shielding, and electrical insulation

With the continuous advancement of electronic devices, the amounts of heat as well as electromagnetic (EM) waves generated have increased. Materials with high thermal conductivity and excellent EM interference shielding effectiveness (EMI SE) can be utilized to address this issue. In this work, we synthesized hollow anatase TiO2 microspheres. Through a reaction, MgO nanoparticles were incorporated into the interior of TiO2 microspheres. (H-TiO2/MgO). The heterostructure of the fillers contributed to performance enhancement. TiO2 and MgO particles formed a dual thermal-conduction pathway. H-TiO2/MgO effectively weakened the energy of EM waves upon contact. Additionally, TiO2, MgO, and epoxy all exhibited hydrophilicity. Consequently, the interfacial compatibility between H-TiO2/MgO and epoxy was excellent. They formed strong interfacial interactions by hydrogen bonding. Because of the excellent electrical insulation properties of H-TiO2 and MgO, the composites exhibited superior insulation performance (over 1010 Ω·cm). Our H-TiO2/MgO/Epoxy composites exhibited a maximum thermal conductivity of 7.52 W/m·K, an EMI SE of 64.92 dB, and a tensile strength of 79.10 MPa. Our composites are expected to effectively manage heat and EM waves generated by electronic devices

Synergistic Interactions of Bulk Polarization and Built-In Electric Field Inducing 2D/2D S-Scheme Homojunction Toward Enhanced Photocatalytic Performance.

The rational design of S-scheme photocatalysts, achieved by serially integrating two different semiconductors, represents a promising strategy for efficient charge separation and amplified photocatalytic performance, yet it remains a challenge. Herein, ZnIn2S4 (ZIS) and oxygen-doped ZnIn2S4 (O-ZIS) nanosheets are chosen to construct a homojunction catalyst architecture. Theoretical simulations alongside comprehensive in situ and ex situ characterizations confirm that ZIS and O-ZIS with noncentrosymmetric layered structures can generate a polarization-induced bulk-internal electric field (IEF) within the crystal. A robust interface-IEF is also created by the strong interfacial interaction between O-ZIS and ZIS with different work functions. Owing to these features, the O-ZIS/ZIS homojunction adopts an S-scheme directional charge transfer route, wherein photoexcited electrons in ZIS and holes in O-ZIS concurrently migrate to their interface and subsequently recombine. This enables spatial charge separation and provides a high driving force for both reduction and oxidation reactions simultaneously. Consequently, such photocatalyst exhibits an H2 evolution rate up to 142.9µmol h-1 without any cocatalysts, which is 4.6- and 3.4-fold higher than that of pristine ZIS and O-ZIS, respectively. Benzaldehyde is also produced as a value-added oxidation product with a rate of 146.9µmol h-1. This work offers a new perspective on the design of S-scheme systems.

Chameleon‐Inspired, Dipole Moment‐Increasing, Fire‐Retardant Strategies Toward Promoting the Practical Application of Radiative Cooling Materials

AbstractToward addressing the aesthetic demand, IR emissivity, and fire hazards of radiative cooling materials in the practical application, chameleon‐inspired is tactfully employed, dipole moment‐increasing, and fire‐retardant strategies to manufacture an advanced polyurea‐based composite coating through incorporating thermochromic microcapsules, boron nitride nanosheets, and montmorillonite nanosheets. The chameleon‐inspired thermochromic microcapsules and admirable IR emissivity (supported by the original IR emittance spectra) realized by the increasing dipole moment allow the composite coatings to spontaneously adjust the solar absorption and reflection during hot daytime, while enabling high‐efficiency radiative cooling throughout the day. The IR emissivity higher than most literature is attributed to the strong interfacial interactions within polyurea composite coatings which improve the dipole moment of C─O─C, Si─O, and B─N bonds by increasing the distance between the centers of positive and negative charges, thus producing more IR emissions. Furthermore, the thermally melted montmorillonite nanosheets can form a ceramic protective layer enhanced by boron nitride nanosheets, further suppressing combustion behavior to improve the fire safety performance of polyurea coatings. The integration of thermochromic functionality, high fire safety, and admirable IR emissivity not only contribute to promoting the practical application of radiative cooling materials, but also provide a precious reference route to design high IR emissivity.

An innovative strategy to enhance the interfacial interaction and effective contribution of BN in thermal conductivity in aramid based composites films

With the escalating concern over electronic device overheating, BN/polymer based thermal conductive composites have experienced remarkable growth in the field of heat dissipation. However, it is challenging to enhance the thermal conductivity of composites while preserving strong interfacial interaction due to the dilemma of chemical inertness of BN, interfacial thermal resistance and filler-polymer interaction. Herein, we utilized the adjustable surface charge of polydopamine under varying pH to fabricate composite films comprising polydopamine-modified boron nitride nanosheets and aramid sheets (BNNS@PDA/ANFS) by electrostatic assembly. The thermal conductivity of the composite rose to 36.9 W/m⋅K−1 with only 20 wt% filler. According to Density functional theory (DFT) simulation and interface thermal resistance calculation, the electrostatic assembly enhanced interface interactions and greatly reduced thermal resistance barrier. Furthermore, the optimal tensile strength of 304 MPa, is 2.32 times higher than pure ANFS film, accompanied by toughness of 33.2 MJ/m−3. These superior performances are the results of a synergistic strategy, combining interfacial and topological enhancements. This work provides an innovative approach to enhance effective filler contribution in matrix and underscores the significant potential of BNNS@PDA/ANFS composite films in applications related to heat management.

Interfacial properties and mechanical performance of hybrid graphene/carbon fibre composites

The interaction zone between the matrix and the reinforcing component within carbon fibre (CF) composites plays a crucial role in influencing their performance characteristics, as extensively documented in scientific literature. Building on this fundamental knowledge, this research focuses to the investigation of the interface of fibrous composites and the effect of the incorporation of graphene nanoplatelets (GNPs) into the epoxy matrix. Through the utilization of laser Raman spectroscopy, a significant increase of over 60 % in interfacial strength with just a 2 % weight fraction of GNPs, as expressed by the enhanced shear-lag parameter observed in single fibre model composites, has been observed on model composites indicating a stronger interfacial interaction between the matrix and fibres. The effect of the incorporation of GNPs on CF-graphene interaction has been also investigated on a macroscopic level. Hybrid carbon fibre epoxy resin composite produced, by the introduction of GNPs into the polymer matrix. A series of mechanical tests were conducted, including extensive tensile testing of epoxy/graphene nanocomposite films, thorough examination of bending characteristics, and meticulous measurement of interlaminar shear strength for hybrid GNP/carbon fibre composites. These evaluations provided a clearer understanding of how the GNP integration affects the interface parameters that govern the mechanical behaviour of both the resin and carbon fibre composites.

Efficient degradation of methylene blue at near neutral pH based on heterogeneous Fenton-like system catalyzed by Fe2O3/MnO2

The contamination of aquatic environments by organic dye contaminants in industrial wastewater has attracted widespread global attention. The heterogeneous Fenton-like process presents an attractive method for degrading dye pollutants, especially when such reactions are conducted under neutral pH. In this study, Fe2O3/MnO2 composite was employed as a novel heterogeneous catalyst for activating hydrogen peroxide (H2O2) to oxidize and subsequently degrade methylene blue (MB) under neutral pH. Multiple characterization results have confirmed the presence of MnO2 and Fe2O3 as the primary phases of the synthesized compound catalyst. Degradation experiments have demonstrated that the degradation efficiency of MB approaches 100% under the conditions of H2O2 concentration of 0.30% and Fe2O3/MnO2 amount of 0.888 g/L. Furthermore, the Fe2O3/MnO2 catalyst exhibits consistent and outstanding catalytic activity within a broad pH range from 5 to 9 benefiting from the strong interface interaction in Fe2O3/MnO2. The investigation into the kinetics of the Fenton-like reaction indicates that the catalytic degradation of MB by Fe2O3/MnO2 in conjunction with H2O2 follows pseudo-first-order kinetics. Moreover, supplementary scavenging experiments have demonstrated the crucial role played by hydroxyl radicals (·OH) in the catalytic oxidation mechanism of MB. This study offers a promising catalyst for the treatment of dye-containing wastewater under neutral pH condition.

Confined interfacial self-assembly of graphene-like carbon/MXene composite electrodes for capacitive deionization

Electrodes that have high desalting capacity, fast desalting rates and stable desalination performance are needed in capacitive deionization (CDI) technologies for water security. Herein, confined interfacial self-assembly of lignin-based graphene-like carbon (GC) precursors in Ti3C2-MXene interlayers was developed for forming GC/MXene composites. The formation of GC was generated in-situ by KHCO3-assisted pyrolytic carbonization which leads to exfoliation of multilayered MXene thereby forming GC/MXene heterostructures having strong interfacial interactions. GC/MXene exhibited tremella-like nanosheets morphology, accompanied by the formation of a TiO2 phase at the interface of GC and MXene hybridization, which confirmed formation of a heterostructure. Crystallographic phase identification of GC/MXene showed the exfoliation of MXene. GC/MXene had an ultra-negative surface charge of −39.3 mV, making it favorable for application as a cathode for Na+ removal. The GC/MXene heterostructure had high desalting capacity (54.2 mg g−1), high desalting rate (2.7 mg g−1 min−1), and stable cycling performance (90 % SAC retention after 30 cycles). The interfacial self-assembly strategy developed in this work is expected to enable green synthesis routes for graphene/MXene-based composite materials that allow construction of 2D/2D heterostructures for multilayer MXene and their analogues.

Hollow Cobalt Selenide-Carbon polyhedron sandwiched between reduced graphene oxide nanosheets: A superior anode material for lithium-ion batteries

In this work, a double carbon-confined sandwich-like CoSe/NCP/rGO composite was fabricated using an self-assembled method combined with a selenization treatment. In the composite, cobalt selenide (CoSe) nanoparticles were embedded in N‑doped hollow carbon polyhedrons (NCP) and sandwiched between reduced graphene oxide (rGO) nanosheets. The kinetics of electron/ion transport along with the structural stability of the composite were significantly enhanced by the layer-by-layer sandwiched hollow structure and the strong cohesive interface interaction between various components. The CoSe/NCP/rGO, when serving as LIB’s anode material, exhibited excellent performance. It demonstrated a high specific capacity with the value of 843 mAh/g at 1 A/g, superior high-rate capability with capacity remaining at 309 mAh/g at 10 A/g, long-term cycling stability with no noticeable capability fading over 1000 loops. More importantly, these results were achieved without additional conductive agents.

N, S, Se-Codoped dual carbon encapsulation and Se substitution in pyrite-type FeS2 for high-rate and long-life sodium-ion batteries

The use of metal sulfides as anodes in sodium-ion batteries (SIBs) faces significant challenges due to slow reaction kinetics and extensive shuttling of sodium polysulfides (NaPSs). In response, a selenium-substituted iron disulfide encapsulated in a nitrogen-sulfur-selenium-codoped dual carbon framework (Se-FeS2@NSSC) has been engineered for high-performance SIBs. Selenium substitution within the FeS2 lattice improves electrical conductivity, facilitates favorable redox kinetics that reducing the possibility of NaPSs generation. Moreover, the dual NSSC encapsulation promotes Na+/electron transport and efficiently manages volume expansion during electrochemical processes. Strong interfacial interaction (Fe-S-C bonding) between Se-FeS2 and NSSC further suppress NaPSs shuttling, significantly alleviating the cell failure and thus prolonging its lifespan. Consequently, Se-FeS2@NSSC demonstrates a top-notch performance, achieving a notable capacity of 725 mAh g-1 at 0.5 A g-1, unparalleled rate capability (355.1 mAh g-1 at 30 A g-1), and sustained cyclic stability (89.6 % capacity is retained after 1250 cycles). Theoretical analyses underscore the critical role of selenium in diminishing bulk stress–strain energies, lowering energy barriers for Na+ diffusion, and decreasing Gibbs free energy for conversion reactions, thereby markedly bolstering electrochemical kinetics and overall performance of Se-FeS2@NSSC. The insights gleaned from this research foster advancements in developing next-generation anodes with high capacity and durability, representing a promising response to the existing hurdles in SIBs technology.

Graphene-based hierarchical structure for significantly enhancing thermal conductivity of composites with high mechanical reinforcement

Significant enhancement in out-of-plane thermal conductivity of carbon fiber/epoxy laminated composites without sacrificing mechanical strength is of great challenge for advanced composites. In this study, a novel graphene-based hierarchical structure was constructed by combining graphene foams (GrFs) with graphene nanoplatelets (GNPs) together and laminating with carbon fiber (CF) fabrics. The GrFs acted as thermally-conductive skeletons in bridging CF fabrics together to remarkably increase out-of-plane thermal conductivity of composites, while the GNPs were helpful to further increasing heat-transfer paths and effectively transferring stress between continuous CFs for high mechanical reinforcement. The hierarchical composites exhibited extremely high out-of-plane thermal conductivity of 2.64 W/m·K, increasing by 158.8 % than that of CF/Ep composites, and they also showed satisfactory tensile, flexural, and interlaminar shear strength. Such high performance is mainly due to the hierarchical structure, continuous heat-transfer paths, synergetic enhancement of GrFs with GNPs, and strong interfacial interactions between components for high-efficiency heat and stress transfer.

The Influence of Molecular Weights on Dispersion and Thermoelectric Performance of Alkoxy Side-Chain Polythiophene/Carbon Nanotube Composite Materials.

In the development of wearable electronic devices, the composite modification of conductive polymers and single-walled carbon nanotubes (SWCNTs) has become a burgeoning research area. This study presents the synthesis of a novel polythiophene derivative, poly(3-alkoxythiophene) (P3(TEG)T), with alkoxy side chains. Different molecular weight variants of P3(TEG)T (P1-P4) were prepared and combined with SWCNTs to form composite materials. Density functional theory (DFT) calculations revealed a reduced bandgap for P3(TEG)T. Raman spectroscopy demonstrated π-π interactions between P3(TEG)T and SWCNTs, facilitating the dispersion of single-walled carbon nanotubes and the formation of a continuous conductive network. Among the composite films, P4/SWCNTs-0.9 exhibited the highest thermoelectric performance, with a power factor (PF) value of 449.50 μW m-1 K-2. The fabricated flexible thermoelectric device achieved an output power of 3976.92 nW at 50 K, with a tensile strength of 59.34 MPa for P4/SWCNTs. Our findings highlight the strong interfacial interactions between P3(TEG)T and SWCNTs in the composite material, providing an effective charge transfer pathway. Furthermore, an improvement in the tensile performance was observed with an increase in the molecular weight of the polymer used in the composite, offering a viable platform for the development of high-performance flexible organic thermoelectric materials.