Search Results (1,325)

Thermally conductive polymer composites are essential for effective heat dissipation in electronic packaging, where both thermal management and mechanical reliability are critical. Although diglycidyl ether of bisphenol-A (DGEBA)-based epoxies exhibit favorable properties, their intrinsically low thermal conductivity limits broader applications. Incorporating conductive fillers, such as expanded graphite (EG) and metal powders, enhances heat transport but often compromises mechanical strength due to poor filler–matrix compatibility. In this study, we address this trade-off by employing a titanate coupling agent to surface-modify aluminum (Al) fillers, thereby improving interfacial adhesion and dispersion within the DGEBA matrix. Our results show that incorporating 10 wt% untreated Al increases thermal conductivity from 7.35 to 9.60 W/m·K; however, this gain comes at the cost of flexural strength, which drops to 18.29 MPa. In contrast, titanate-modified Al (Ti@Al) not only preserves high thermal conductivity but also restores mechanical performance, achieving a flexural strength of 35.31 MPa (at 5 wt% Ti@Al) and increasing impact strength from 0.60 to 1.01 kJ/m². These findings demonstrate that interfacial engineering via titanate coupling offers a compelling strategy to overcome the thermal–mechanical trade-off in hybrid composites, enabling the development of high-performance materials for advanced thermal interface and structural applications. Full article

The shortage of tellurium and toxicity of lead are major obstacles to scaling mid-temperature thermoelectric generators. We engineer quaternary lead chalcogenides with composition (Pb_0.8Ge_0.2Te)_0.95-x(PbSe)_0.05(PbS)_x (0 ≤ x ≤ 0.25), where Pb is lead, Ge is germanium, Te is tellurium, Se is selenium, S is sulfur, and x denotes the molar fraction of lead sulfide (PbS). The primary novelty lies in achieving ultra-low thermal conductivity through controlled phase segregation induced by systematic PbS incorporation. X-ray diffraction analysis reveals single-phase solid solutions up to x ≈ 0.10, with secondary PbS precipitates forming beyond this threshold. These PbS-rich phases create hierarchical microstructures that scatter phonons across multiple length scales, suppressing total thermal conductivity to 0.6 Wm⁻¹K⁻¹ at x = 0.15—approximately 84% lower than pristine lead telluride (PbTe) and approaching glass-like thermal conductivity values. Electrical transport measurements demonstrate sulfur’s role as an electron donor, enabling carrier-type control from p-type to n-type conduction. Despite moderate electrical power factors, the optimized composition (x = 0.20) achieves a peak dimensionless figure of merit ZT ≈ 0.34 at 650 K. This work demonstrates an effective strategy for tellurium-lean, lead-reduced thermoelectric materials through sulfur-induced phase segregation, providing practical design guidelines for sustainable waste heat recovery applications. Full article

Under the accelerating global energy restructuring and the deepening carbon neutrality strategy, hydrogen energy has emerged with increasing strategic value as a zero-carbon secondary energy carrier. Water electrolysis technology based on renewable energy is regarded as an ideal pathway for large-scale green hydrogen production. However, polymer electrolyte membrane (PEM) conventional water electrolysis faces dual constraints in economic feasibility and scalability due to its high electrical energy consumption and reliance on noble metal catalysts. The mixed ionic-electronic conducting oxygen transport membrane (MIEC–OTM) reactor technology offers an innovative solution to this energy efficiency-cost paradox due to its thermo-electrochemical synergistic energy conversion mechanism and process integration. This not only overcomes the thermodynamic equilibrium limitations in traditional electrolysis but also reduces electrical energy demand by effectively coupling with medium- to high-temperature heat sources such as industrial waste heat and solar thermal energy. Therefore, this review, grounded in the physicochemical mechanisms of oxygen transport membrane reactors, systematically examines the influence of key factors, including membrane material design, catalytic interface optimization, and parameter synergy, on hydrogen production efficiency. Furthermore, it proposes a roadmap and breakthrough directions for industrial applications, focusing on enhancing intrinsic material stability, designing multi-field coupled reactors, and optimizing system energy efficiency. Full article

The simultaneous generation of hydrogen fuel and wastewater remediation via electrocatalytic urea oxidation has emerged as a promising approach for sustainable energy and environmental solutions. However, the practical application of this process is hindered by the limited active sites and high charge-transfer resistance of conventional anode materials. In this work, we introduce a novel CoP@P, N-CNTs/NF electrocatalyst, fabricated through a facile one-step thermal annealing technique. Comprehensive characterizations confirm the successful integration of CoP nanoparticles and phosphorus/nitrogen co-doped carbon nanotubes (P, N-CNTs) onto nickel foam, yielding a unique hierarchical structure that offers abundant active sites and accelerated electron transport. As a result, the CoP@P, N-CNTs/NF electrode achieves outstanding urea oxidation reaction (UOR) performance, delivering current densities of 158.5 mA cm⁻² at 1.5 V and 232.95 mA cm⁻² at 1.6 V versus RHE, along with exceptional operational stability exceeding 50 h with negligible performance loss. This innovative, multi-element-doped electrode design marks a significant advancement in the field, enabling highly efficient UOR and energy-efficient hydrogen production. Our approach paves the way for scalable, cost-effective solutions that couple renewable energy generation with effective wastewater treatment. Full article

Cubic phase SnSe-based materials have great potential in the field of thermoelectricity due to their reduced carrier scattering, increased band degeneracy, and ultra-low lattice thermal conductivity. Nevertheless, systematic studies on the influence of element doping on the thermoelectric properties of cubic SnSe-based materials are still relatively scarce. To enrich the research in this field, this work investigates the effects of Ge doping on the phase composition, electrical and thermal transport properties of cubic Sn_0.50Ag_0.25Bi_0.25Se_0.50Te_0.50 thermoelectric materials. X-ray diffraction (XRD) analysis confirmed that the Ge-doped samples exhibited a single cubic phase structure, while scanning electron microscopy (SEM) and energy-dispersive spectroscopy (EDS) revealed a uniform distribution of elements within the samples. The results indicate that increasing the Ge doping content substantially enhances their electrical conductivity, albeit at the expense of elevated thermal conductivity. By optimizing the content of Ge-doping, the thermoelectric figure of merit (ZT) reached 0.74 at 750 K. Notably, while moderate Ge doping enhances electrical transport properties, excessive doping leads to a significant rise in thermal conductivity, ultimately constraining further thermoelectric performance gains. Full article

The objective of this study is to examine the variations in the properties of cementitious materials subjected to bending loads in conjunction with dry and wet cycles of sulfate exposure. This investigation involved applying continuous bending loads at 0%, 20%, and 40% of the ultimate bending capacity to cementitious material specimens. Furthermore, three sets of mortars and concretes with differing water–cement ratios were formulated and analyzed using X-ray diffraction, scanning electron microscopy, and compressive strength tests. The findings indicated that while the flexural strength, compressive strength, and porosity of the specimens initially increased, they ultimately declined as the cementitious materials degraded over time within the sulfate solution. Additionally, it was observed that an increase in bending load corresponded with a decrease in flexural strength, alongside a rise in the internal sulfate ion concentration. By integrating an enhanced form of Fick’s second law with chemical reaction kinetics, a transport model for sulfate ions in cement-based materials was developed under the coupling effect of bending load and sulfate exposure, utilizing Comsol Multiphysics. The simulation results, which align well with the experimental observations, exhibit an error of approximately 5% at a depth of 5 mm. Full article

Drinking water biofilm ecosystems harbor complex and dynamic prokaryotic and eukaryotic microbial communities. However, little is known about the impact of copper corrosion on microbial community functions in metabolisms and resistance. This study was conducted to evaluate the impact of upstream Cu pipe materials on downstream viable community structures, pathogen populations, and metatranscriptomic responses of the microbial communities in drinking water biofilms. Randomly transcribed cDNA was generated and sequenced from downstream biofilm samples of either unplasticized polyvinylchloride (PVC) or Cu coupons. Diverse viable microbial organisms with enriched pathogen-like organisms and opportunistic pathogens were active in those biofilm samples. Cu-influenced tubing biofilms had a greater upregulation of genes associated with potassium (K) metabolic pathways (i.e., K-homeostasis, K-transporting ATPase, and transcriptional attenuator), and a major component of the cell wall of mycobacteria (mycolic acids) compared to tubing biofilms downstream of PVC. Other upregulated genes on Cu influenced biofilms included those associated with stress responses (various oxidative resistance genes), biofilm formation, and resistance to toxic compounds. Downregulated genes included those associated with membrane proteins responsible for ion interactions with potassium; respiration–electron-donating reactions; RNA metabolism in eukaryotes; nitrogen metabolism; virulence, disease, and defense; and antibiotic resistance genes. When combined with our previous identification of biofilm community differences, our studies reveal how microbial biofilms adapt to Cu plumbing conditions by fine-tuning gene expression, altering metabolic pathways, and optimizing their structural organization. This study offers new insights into how copper pipe materials affect the development and composition of biofilms in premise plumbing. Specifically, it highlights copper’s role in inhibiting the growth of many microbes while also contributing to the resistance of some microbes within the drinking water biofilm community. Full article

Titanium dioxide (TiO₂) is a wide-bandgap semiconductor material with broad application potential, known for its excellent photocatalytic performance, high chemical stability, low cost, and non-toxicity. These properties make it highly attractive for applications in photovoltaic energy, environmental remediation, and optoelectronic devices. For instance, TiO₂ is widely used as a photocatalyst for hydrogen production via water splitting and for degrading organic pollutants, thanks to its efficient photo-generated electron–hole separation. Additionally, TiO₂ exhibits remarkable performance in dye-sensitized solar cells and photodetectors, providing critical support for advancements in green energy and photoelectric conversion technologies. Boron-doped diamond (BDD) is renowned for its exceptional electrical conductivity, high hardness, wide electrochemical window, and outstanding chemical inertness. These unique characteristics enable its extensive use in fields such as electrochemical analysis, electrocatalysis, sensors, and biomedicine. For example, BDD electrodes exhibit high sensitivity and stability in detecting trace chemicals and pollutants, while also demonstrating excellent performance in electrocatalytic water splitting and industrial wastewater treatment. Its chemical stability and biocompatibility make it an ideal material for biosensors and implantable devices. Research indicates that the combination of TiO₂ nanostructures and BDD into heterostructures can exhibit unexpected optical and electrical performance and transport behavior, opening up new possibilities for photoluminescence and rectifier diode devices. However, applications based on this heterostructure still face challenges, particularly in terms of photodetector, photoelectric emitter, optical modulator, and optical fiber devices under high-temperature conditions. This article explores the potential and prospects of their combined heterostructures in the field of optoelectronic devices such as photodetector, light emitting diode (LED), memory, field effect transistor (FET) and sensing. TiO₂/BDD heterojunction can enhance photoresponsivity and extend the spectral detection range which enables stability in high-temperature and harsh environments due to BDD’s thermal conductivity. This article proposes future research directions and prospects to facilitate the development of TiO₂ nanostructured materials and BDD-based heterostructures, providing a foundation for enhancing photoresponsivity and extending the spectral detection range enables stability in high-temperature and high-frequency optoelectronic devices field. Further research and exploration of optoelectronic devices based on TiO₂-BDD heterostructures hold significant importance, offering new breakthroughs and innovations for the future development of optoelectronic technology. Full article

Highly efficient photocatalysts for solar energy conversion require effective charge carrier separation and rapid interfacial transport kinetics to maximize electron availability. Two-dimensional Ti₃CNT_x, a novel conductive material in the MXene family with exceptional electrical conductivity, has emerged as an ideal electron transfer mediator due to its large specific surface area and abundant active terminal groups. In this work, we strategically integrated the 2D multi-metal sulfide Cu-Zn-In-S (CZIS) with 2D Ti₃CNT_x nanosheets through physical mixture, constructing a heterostructured 2D/2D CZIS/Ti₃CNT_x composite photocatalyst for the hydrogen evolution reaction. The unique architecture significantly accelerates electron migration from CZIS to Ti₃CNT_x, while synergistically promoting the spatial separation and directional transfer of photogenerated electron–hole pairs (e⁻/h⁺). When the hydrogen evolution reaction is carried out under identical conditions, the hydrogen yield rate is 4.3 mmol g⁻¹ h⁻¹ with pristine CZIS but is improved dramatically to 14.3 mmol g⁻¹ h⁻¹ when the composite containing an adequate amount of 2D Ti₃CNT_x is used. This study offers new insight into the rational design and controllable synthesis of Ti₃CNT_x-based composite photocatalytic systems for efficient photocatalytic hydrogen production. Full article

Molybdenum disulfide (MoS₂) is a promising earth-abundant electrocatalyst for the hydrogen evolution reaction (HER), attributed to its favorable electronic structure and chemical stability. Nevertheless, its application is limited by poor electrical conductivity and low exposure of active sites. This review highlights recent progress in the synthesis and structural engineering of MoS₂-based catalysts to improve HER performance. Strategies such as morphology tuning, phase modulation, defect engineering, and heterostructure construction are systematically evaluated for their roles in enhancing charge transport, increasing active site density, and improving intrinsic catalytic activity. Additionally, the relationship between atomic structure, electronic properties, and HER kinetics is discussed to elucidate fundamental structure–activity correlations. These insights advance the development of MoS₂ as a cost-effective and scalable catalyst for hydrogen production and inform the rational design of future HER materials. Full article

The incorporation of commercial graphene oxide (GO) into composites offers significant improvements in mechanical, thermal, and electrical properties, making it a promising material for industrial applications. This study presents a comprehensive characterization analysis of five commercial GOs, using advanced techniques to evaluate their structural, chemical, and especially their behavior when submitted to thermal treatment. The aim is to enable the use of GO in industrial processes of particular technological importance, where its thermal stability/integrity is required, such as in polymer composites, electronic and energy storage devices, among others. Raman spectroscopy and attenuated total reflectance–Fourier-transform infrared (ATR-FTIR) spectroscopy are employed to examine the structural defects and functional groups of GOs, while X-ray diffraction (XRD) provides insight into the crystallinity and interlayer spacing. Thermogravimetric analysis (TGA) assesses the thermal stability, and X-ray photoelectron spectroscopy (XPS) offers detailed information on the surface chemistry and relevant elemental composition of GOs. Additionally, the temperature-dependent behavior of GOs is explored through temperature-dependent XRD and IR measurements to investigate the thermal expansion and functional group stability. The study highlights the critical role of oxygen-containing groups—such as epoxides, hydroxyls, and carboxyls—while variations in the type and concentration of these functional groups across commercial GOs could influence the compatibility and performance of nanocomposites. This research attempts to fill to some extent the gap in understanding how the unique properties of different commercial GOs can be strategically applied to meet specific industrial performance requirements, such as barrier properties, transport efficiency, or mechanical strength, among others. Full article

Although lithium-ion batteries are considered an ideal postulant for renewable energy harvesting, storage and applications, these batteries show promising performance; however, at the same time, these harvesting devices suffer from some major limitations, including scarce lithium resources, high cost, toxicity and safety concerns. Potassium ion batteries (PIBs) can be proven a favorable alternative to metal ion batteries because of their widespread potassium reserves, low costs and enhanced protection against sparks. In this study, DFT simulations were employed using the B3LYP/6-311⁺⁺g(d p) method to explore the application of graphene and its doped variants (N,B,P-graphene) as potential anode materials for PIBs. Various key parameters such as adsorption energy, Gibbs free energy, molecular orbital energies, non-covalent interactions, cell voltage, electron density distribution and density of states were computed as a means to evaluate the suitability of materials for PIB applications. Among the four structures, nitrogen- and phosphorus-doped graphene exhibited negative Gibbs free energy values of −0.020056 and −0.021117 hartree, indicating the thermodynamic favorability of charge transfer processes. Doping graphene with nitrogen and phosphorus decreases the HOMO-LUMO gap energy, facilitating efficient ion storage and charge transport. The doping of nitrogen and phosphorus increases the cell voltage from −1.05 V to 0.54 V and 0.57 V, respectively, while boron doping decreases the cell voltage. The cell voltage produced by graphene and its doped variants in potassium ion batteries has the following order: P-graphene (0.57 V) > N-graphene (0.54 V) > graphene (−1.05 V) > B-graphene (−1.54 V). This study illustrates how nitrogen- and phosphorus-doped graphene can be used as a propitious anode electrode for PIBs. Full article

The possibility of reinforcing polymeric matrices with multifunctional fillers for improving structural and functional properties is widely exploited. The compatibility between the filler and the polymeric matrix is crucial, especially for high filler content. In this paper, polymeric matrices of Nylon 6,6 with pyrene chains were successfully synthesized to improve the compatibility with carbonaceous fillers. The compatibility was proven using graphite as a carbonaceous filler. The different properties, including thermal stability, crystallinity, morphology, and local mechanical properties, have been evaluated for various filler contents, and the results have been compared to those of synthetic Nylon 6,6 without pyrene chain terminals. XRD results highlighted that the compatibilization of the composite matrix may lead to an intercalation of the polymeric chains among the graphite layers. This phenomenon leads to the protection of the polymer from thermal degradation, as highlighted by the thermogravimetric analysis (i.e., for a filler content of 20%, the beginning degradation temperature goes from 357 °C for the non-compatibilized matrix to 401 °C for the compatibilized one and the residual at 750 °C goes from 33% to 67%, respectively. A significant improvement in the interphase properties, as proven via Atomic Force Microscopy in Harmonix mode, leads to a considerable increase in local mechanical modulus values. Specifically, the compatibilization of the matrix hosting the graphite leads to a less pronounced difference in modulus values, with more frequent reinforcements that are quantitatively similar along the sample surface. This results from a significantly improved filler distribution with respect to the composite with the non-compatibilized matrix. The present study shows how the thermoplastic/filler compatibilization can sensitively enhance thermal and mechanical properties of the thermoplastic composite, widening its potential use for various high-performance applications, such as in the transport field, e.g., for automotive components (engine parts, gears, bushings, washers), and electrical and electronics applications (heat sinks, casing for electronic devices, and insulating materials). Full article

The global market for flame-retardant materials is expected to grow steadily, from USD 7.0 billion in 2022 to USD 16.6 billion in 2030, driven by increasing demand for environment-friendly fire safety solutions in transportation, construction, and electronics. Polylactic acid (PLA), a biodegradable polymer which possesses excellent mechanical properties, is increasingly being considered for future mobility applications. However, it is characterized by high heat release and toxic smoke during combustion, which are significant drawbacks. In order to address this, the chemical modification of Kraft lignin was achieved through a phenolation and subsequent silylation with tetraethoxysilane, aiming to mitigate the degradation of PLA’s mechanical properties while utilizing its inherent char-forming ability. The modified lignins were combined with ammonium polyphosphate (APP) and melt-mixed with PLA using an injection-mixing molder to prepare test specimens. Analysis by FT-IR, NMR spectroscopy, and SEM-EDS confirmed successful grafting of phenolic and silane functionalities, and thermogravimetric analysis demonstrated enhanced thermal stability of the modified lignins compared to unmodified ones. Vertical burning tests and limiting oxygen index (LOI) measurements showed that the PLA/APP/SPKL composite material achieved a V-0 UL-94 rating and 31.95% LOI, demonstrating the highest level of flame retardancy. This compares to the LOI of neat PLA, 19 to 21%. Despite the enhancement in flame retardancy to the V-0 level, the decline in tensile strength was limited, and the composite retained comparable mechanical strength to PLA-APP composites with V-2 flame retardancy. The findings indicate that the combination of phenolation and silylation of lignin with APP, a flame-retardant material, offers a viable and sustainable methodology for the fabrication of PLA composites that exhibit both flame retardancy and mechanical strength. Full article

The dielectric relaxation behavior of polymeric materials is critical to their performance in electronic, insulating, and energy storage applications. This study presents an electrical fractional model (EFM) based on fractional calculus and the complex electric modulus ($M^{*}\mathit{=}{M}^{\prime }\mathit{+}i{M}^{″}$) formalism to simultaneously describe two key relaxation phenomena: $\alpha$-relaxation and interfacial polarization (Maxwell–Wagner–Sillars effect). The model incorporates fractional elements (cap-resistors) into a modified Debye equivalent circuit to capture polymer dynamics and energy dissipation. Fractional differential equations are derived, with fractional orders taking values between 0 and 1; the frequency and temperature responses are analyzed using Fourier transform. Two temperature-dependent behaviors are considered: the Matsuoka model, applied to $\alpha$-relaxation near the glass transition, and an Arrhenius-type equation, used to describe interfacial polarization associated with thermally activated charge transport. The proposed model is validated using literature data for amorphous polymers, polyetherimide (PEI), polyvinyl chloride (PVC), and polyvinyl butyral (PVB), successfully fitting dielectric spectra and extracting meaningful physical parameters. The results demonstrate that the EFM is a robust and versatile tool for modeling complex dielectric relaxation in polymeric systems, offering improved interpretability over classical integer-order models. This approach enhances understanding of coupled relaxation mechanisms and may support the design of advanced polymer-based materials with tailored dielectric properties. Full article