Search Results (127)

Electric-field-sensitive dielectrics play a crucial role in electric field induction sensing and related capacitive conversion, with interfacial polarization and charge accumulation largely determining the signal output. This paper introduces graphene/transition metal dichalcogenide (TMD) (MoSe₂, MoS₂, and WS₂) heterojunctions as functional fillers to enhance the dielectric response and electric-field-induced voltage output of flexible polydimethylsiloxane (PDMS) composites. Density functional theory (DFT) calculations were used to evaluate the stability of the heterojunctions and interfacial electronic modulation, including binding behavior, charge redistribution, and Fermi level-referenced band structure/total density of states (TDOS) characteristics. The calculations show that the graphene/TMD interface is primarily controlled by van der Waals forces, exhibiting negative binding energy and significant interfacial charge rearrangement. Based on these theoretical results, graphene/TMD heterojunction powders were synthesized and incorporated into polydimethylsiloxane (PDMS). Structural characterization confirmed the presence of face-to-face interfacial contacts and consistent elemental co-localization within the heterojunction filler. Dielectric spectroscopy analysis revealed an overall improvement in the dielectric constant of the composite materials while maintaining a stable loss trend within the studied frequency range. More importantly, calibrated electric field induction tests (based on pure PDMS) showed a significant enhancement in the voltage response of all heterojunction composite materials, with the WS₂-G/PDMS system exhibiting the best performance, exhibiting an electric-field-induced voltage amplitude 7.607% higher than that of pure PDMS. This work establishes a microscopic-to-macroscopic correlation between interfacial electronic modulation and electric-field-sensitive dielectric properties, providing a feasible interface engineering strategy for high-performance flexible dielectric sensing materials. Full article

Y-branched TiO₂ nanotubes (NTs) were produced by anodizing titanium plates derived from aerospace production leftovers and subsequently engineered to develop an enhanced TiO₂-based photocatalytic system. The NTs were electrochemically reduced to obtain reduced TiO₂ nanotubes (rTN) with a narrowed bandgap, followed by surface modification with polydopamine (PD) and silk fibroin-derived quantum dots (QDs) to promote enhanced UV and visible-light photocatalysis for wastewater treatment. The QDs were hydrothermally synthesized from Bombyx mori silk fibroin. Scanning Electron Microscopy (SEM) revealed spherical QD agglomerates encapsulated within the PD layer, while Energy Dispersive X-ray Spectroscopy (EDX) confirmed the presence of carbon and nitrogen originating from both PD and QD. The resulting rNT/PD/QD photocatalyst exhibited a significantly reduced bandgap (1.03 eV), increased Urbach energy (1.35 eV), and moderate hydrophilicity. A high double-layer capacitance (C_dl) indicated an enlarged electrochemically active surface due to the combination of treatments. Electrochemical characterization demonstrated reduced electrical resistance, higher charge density, and lower electron–hole recombination, leading to improved interfacial charge transfer efficiency and electrochemical stability during multi-cycle cyclic voltammetry measurements. Preliminary photocatalytic tests show that the rNT/PD/QD photocatalyst achieved a degradation efficiency of 79.26% for methyl orange (MO) and 35% for tetracycline (TC). Full article

We report the synthesis and multifunctional characterization of copper-reinforced Ba_0.85Sr_0.15TiO₃ (BST) ceramic composites with Cu contents ranging from 0 to 40 wt%, prepared by a sol–gel route and densified using spark plasma sintering (SPS). X-ray diffraction and FT-IR analyses confirm the coexistence of cubic and tetragonal BST phases, while Cu remains as a chemically separate metallic phase without detectable interfacial reaction products. Microstructural observations reveal abnormal grain growth induced by localized liquid-phase-assisted sintering and progressive Cu agglomeration at higher loadings. Scanning electron microscopy reveals abnormal grain growth, with the average BST grain size increasing from approximately 3.1 µm in pure BST to about 5.2 µm in BST–Cu40% composites. Optical measurements show a continuous reduction in the effective optical bandgap (apparent absorption edge) from 3.10 eV for pure BST to 2.01 eV for BST–Cu40%, attributed to interfacial electronic states, defect-related absorption, and enhanced scattering rather than Cu lattice substitution. Electrical characterization reveals a percolation threshold at approximately 30 wt% Cu, where AC conductivity and dielectric permittivity reach their maximum values. Impedance spectroscopy and equivalent-circuit analysis demonstrate strong Maxwell–Wagner interfacial polarization, yielding a maximum permittivity of ~1.2 × 10⁵ at 1 kHz for BST–Cu30%. At higher Cu contents, conductivity and permittivity decrease due to disrupted Cu connectivity and increased porosity. These findings establish BST–Cu composites as tunable ceramic–metal systems with enhanced dielectric and optical responses, demonstrating potential for specialized high-capacitance decoupling applications where giant permittivity is prioritized over low dielectric loss. Full article

The surface morphology of lithium metal electrodes evolves markedly during cycling, modulating interfacial kinetics and increasing the risk of dendrite-driven internal short circuits. Here, we infer this morphological evolution from direct-current (DC) signals by analyzing open-circuit voltage (OCV) transients after constant current interruptions. The OCV exhibits a rapid initial decay followed by a transition to a slower long-time decay. With repeated plating, this transition shifts to earlier times, thereby increasing the contribution of long-term relaxation. We quantitatively analyze this behavior using an equivalent circuit with a transmission-line model (TLM) representing the electrolyte-accessible interfacial region of the electrode, discretized into ten depth-direction segments. Tracking segment-wise changes in resistances and capacitances with cycling enables morphology estimation. Repeated plating strongly increases the double-layer area near the current collector, while the charge-transfer-active surface shifts toward the separator side, showing progressively smaller and eventually negative changes toward the current-collector side. Together with the segment-resolved time constants, these trends indicate that lithium deposition becomes increasingly localized near the separator-facing surface, while the interior becomes more tortuous, consistent with post-mortem observations. Overall, the results demonstrate that DC voltage-relaxation analysis combined with a TLM framework provides a practical route to track lithium metal electrode surface evolution in Li-metal-based cells. Full article

The rapid advancement of humanoid robotics has spurred researchers’ interest in flexible sensors for wide linear range detection. In response, we report a capacitive flexible pressure sensor based on a multi-walled carbon nanotubes/titanium dioxide/polydimethylsiloxane (MWCNTs/TiO₂/PDMS) composite. A micro-hemispherical structure array formed on the composite surface via a templating method reduces the initial capacitance value. Modified carbon nanotubes (F-MWCNTs) were prepared using 2 wt%, 5 wt% and 10 wt% γ-aminopropyltriethoxysilane (APTES), significantly enhancing dispersion and interfacial bonding strength. The synergistic effect of microstructures and MWCNTs surface functionalization further enhances sensing performance. The F-MWCNTs/TiO₂/PDMS pressure sensor modified with 2 wt% APTES exhibits outstanding sensing capabilities: it demonstrates dual-stage sensitivity across a broad linear range of 0–95 kPa (0–13 kPa segment: 1.89 ± 0.49 kPa⁻¹; 13–95 kPa segment: 7.08 ± 0.63 kPa⁻¹), with a response time of 200 milliseconds, maintaining stability over 2500 cyclic loadings. In practical application exploration, this sensor has demonstrated strong adaptability, confirming its significant potential in micro-pressure detection, wearable electronics, and array sensing applications. Full article

This review critically examines photoresponsive supercapacitors based on TiO₂/graphene hybrids, with a particular focus on their emerging dual role as energy-storage devices and environmental sensors. We first provide a concise overview of the electronic structure of TiO₂ and the key attributes of graphene and related nanocarbons that enable efficient charge separation, transport, and interfacial engineering. We then summarize and compare reported device architectures and electrode designs, highlighting how morphology, graphene integration strategies, and illumination conditions govern specific capacitance, cycling stability, rate capability, and light-induced enhancement in performance. Particular attention is given to the underlying mechanisms of photo-induced capacitance enhancement—including photocarrier generation, interfacial polarization, and photodoping—and to how these processes can be exploited to embed sensing functionality in working supercapacitors. We review representative studies in which TiO₂/graphene systems operate as capacitive sensors for humidity, gases, and volatile organic compounds, emphasizing quantitative figures of merit such as sensitivity, response/recovery times, and stability under repeated cycling. Finally, we outline current challenges in materials integration, device reliability, and benchmarking, and propose future research directions toward scalable, multifunctional TiO₂/graphene platforms for self-powered and environmentally aware electronics. This work is intended as a state-of-the-art summary and critical guide for researchers developing next-generation photoresponsive supercapacitors with integrated sensing capability. Full article

This study introduces a modified Laser Ablation Synthesis in Solution (LASiS), a surfactant-free and rapid synthesis approach that enables uniform MOF nucleation on graphene oxide (GO) and precise control over crystallinity, for fabricating graphene oxide (GO)-integrated cobalt-based ZIF-67 hybrid nanocomposites tailored for supercapacitor applications. By tuning LASiS parameters, we precisely controlled framework size, morphology, and crystallinity, enabling sustainable and scalable production. The incorporation of GO during synthesis markedly enhances the uniform dispersion of ZIF-67 frameworks, minimizing aggregation and establishing interconnected conductive pathways via strong $\pi$-$\pi$ stacking interactions. Following thermal reduction at 250 °C, the Co/ZIF-67–rGO composites exhibit outstanding electrochemical performance, achieving a specific capacitance of 1152 Fg⁻¹ at 1 Ag⁻¹ in a three-electrode configuration, driven by the synergistic combination of pseudocapacitive cobalt centers and double-layer capacitance from rGO. Structural analyses confirm the preservation of ZIF crystallinity and robust interfacial integration with the graphene sheets. Embedding these nanocomposites into fully 3D-printed supercapacitors yields a specific capacitance of 875 Fg⁻¹, demonstrating their suitability for additive manufacturing despite minor increases in interfacial resistance. The 3D-printed supercapacitor devices delivered an energy density of 77.7 Wh/kg at a power density of 399.6 W/kg. Collectively, these results highlight the potential of LASiS-engineered MOF-based nanocomposites as scalable, high-performance materials for next-generation energy storage devices. Full article

This study presents a dual surfactant-assisted hydrothermal approach for the synthesis of Co₃V₂O₈ (CoVO) nanostructures and their surfactant-modified derivatives, PVP-assisted Co₃V₂O₈ (P-CoVO) and PVP–SDS co-assisted Co₃V₂O₈ (P/S-CoVO), which were directly grown on nickel foam. The use of PVP and SDS enabled controlled nucleation and growth, yielding a hierarchical nanoflower-like morphology in P/S-CoVO with increased porosity, a higher surface area, and uniform structural features. Comprehensive physicochemical characterization confirmed that surfactant incorporation effectively modulated particle size, dispersion, and active-site availability. Electrochemical measurements demonstrated that P/S-CoVO exhibited superior performance, with the largest CV area, low equivalent series resistance (0.52 Ω), and a maximum areal capacitance of 13.71 F cm⁻² at 8 mA cm⁻², attributable to rapid redox kinetics and efficient ion transport. The electrode also showed excellent cycling stability, retaining approximately 83.7% of its initial capacitance after 12,000 charge–discharge cycles, indicating robust structural integrity and interfacial stability. Additionally, an asymmetric supercapacitor device (P/S-CoVO//AC) delivered a high energy density of 0.082 mWh cm⁻², a power density of 1.25 mW cm⁻², and stable operation within a 1.5 V potential window. These results demonstrate that cooperative surfactant engineering provides an effective and scalable strategy to enhance the morphology, electrochemical kinetics, and durability of Co₃V₂O₈-based electrodes for next-generation high-performance supercapacitors. Full article

Acquiring reliable thermal data during the high-pressure die-casting (HPDC) process remains a significant challenge due to its complexity and rapidly evolving thermal environment. In industrial settings, the influence of process parameters is typically evaluated after solidification by examining the final casting quality, as direct temperature measurements within the die during operation are difficult to obtain. Additionally, most casting simulation tools lack accurate correlations for the interfacial heat transfer coefficient (IHTC) as a function of process parameters. To address this limitation, a laboratory-scale hot chamber die-casting (HCDC) apparatus was developed to replicate the fluid flow and the thermal conditions of industrial HPDC operation while enabling direct thermal measurements inside the die cavity using embedded thermocouples. The molten metal temperature was estimated using the lumped capacitance method, and the IHTC was determined through a custom inverse heat conduction algorithm incorporating an adaptive forward time-stepping scheme. This algorithm was validated by solving the forward heat conduction problem using the ANSYS 2025 R1 Transient Thermal solver. The experimentally obtained IHTC values showed good agreement with those measured during industrial HPDC trials, with a maximum deviation of about 14% in the peak value, while the full width at half maximum (FWHM) differed by less than 12%. These results confirm that the developed HCDC setup can reliably reproduce industrial thermal conditions and generate high-quality thermal data that can be used in numerical casting simulations. Full article

We report an interracially engineered Co₃O₄@Ti₃C₂T_x MXene hybrid as a high-rate charge-storage electrode. Low-temperature assembly under inert conditions preserves the MXene carbide while anchoring nanocrystalline Co₃O₄ on conductive, ion-permeable sheets. XRD and FTIR confirm the structural integrity of MXene without TiO₂ formation. Electrochemically, cyclic voltammetry, Dunn analysis, and galvanostatic tests reveal mixed storage with a dominant pseudocapacitive contribution, while EIS fitting shows reduced charge-transfer resistance for the hybrid compared with either parent. Within a 0.6 V window in 2 M KOH, the composite delivers high specific charge and excellent rate retention, attributable to shortened diffusion paths and fast electron transport at the oxide–MXene interface. These results establish Co₃O₄@MXene as a robust, mechanism-consistent platform for high-power supercapacitors. Full article

Metal-oxide heterostructures represent an effective strategy to overcome the limitations of pristine TiO₂, including its ultraviolet-only light absorption and rapid electron–hole recombination, which hinder its performance in solar-driven applications. Among various configurations, coupling TiO₂ with tungsten oxide (WO_x) forms a favorable type-II band alignment that enhances charge separation. However, a comprehensive understanding of how WO_x overlayer thickness affects the optical and photoelectrochemical (PEC) behavior of device-grade thin films remains limited. In this study, bilayer TiO₂/WO_x heterostructures were fabricated via reactive DC magnetron sputtering, with controlled variation in WO_x thickness to systematically investigate its influence on the structural, optical, and PEC properties. Adjusting the WO_x deposition time enabled precise tuning of light absorption, interfacial charge transfer, and donor density, resulting in markedly distinct PEC responses. The heterostructure obtained with 30 min of WO_x deposition demonstrated a significant enhancement in photocurrent density under AM 1.5G illumination, along with reduced charge-transfer resistance and improved capacitive behavior, indicating efficient charge separation and enhanced charge storage at the electrode–electrolyte interface. These findings underscore the potential of sputtered TiO₂/WO_x bilayers as advanced photoanodes for solar-driven hydrogen generation and light-assisted energy storage applications. Full article

Poly(5-indolylboronic acid) was synthesized electrochemically via cyclic voltammetry using various electrodes, including screen-printed carbon electrodes, glassy carbon electrodes, highly oriented pyrolytic graphite, and 304 stainless steel. This study provides a thorough analysis of the resulting conducting polymer’s electrochemical behavior, morphological and structural characteristics, and potential applications. The following techniques were employed: cyclic voltammetry, electrochemical impedance spectroscopy, Fourier-transform infrared spectroscopy, Raman spectroscopy, and field-emission scanning electron microscopy. The polymer exhibits pH-dependent redox activity within the pH range of 4–10, displaying Nernstian behavior and achieving a specific areal capacitance of 0.234 mF∙cm⁻² on an SPCE electrode. This result highlights the electrode’s efficiency in terms of charge storage. Impedance data indicate that the modified electrodes demonstrate a substantial decrease in charge transfer resistance and improved interfacial conductivity compared to bare electrodes. Contact angle measurements show that the presence of boronic acid groups makes the polymer hydrophilic. However, when 5PIBA was incubated in the presence of molecules containing hydroxyl groups or certain proteins, such as casein, no adsorption was observed. This suggests limited interaction with functional groups such as amino, hydroxide, and carboxyl groups present in these molecules, indicating the potential application of the polymer in biocorrosion. 5PIBA forms homogeneous, stable, and electroactive coatings on various substrates, making it a promising and versatile material for electrochemical technologies, and paving the way for future functionalization strategies. Full article

Electrolyte-gated transistors (EGTs) have emerged as a highly promising platform for neuromorphic computing and bioelectronics, offering potential solutions to overcome the limitations of the von Neumann architecture. This comprehensive review examines recent advancements in EGT technology, focusing on three critical dimensions: materials, device configurations, and external field regulation strategies. We systematically analyze the development and properties of diverse electrolyte materials, including liquid electrolyte, polymer-based electrolytes, and inorganic solid-state electrolytes, highlighting their influence on ionic conductivity, stability, specific capacitance, and operational characteristics. The fundamental operating mechanisms of EGTs and electric double layer transistors (EDLTs) based on electrostatic modulation and ECTs based on electrochemical doping are elucidated, along with prevalent device configurations. Furthermore, the review explores innovative strategies for regulating EGT performance through external stimuli, including electric fields, optical fields, and strain fields/piezopotentials. These multi-field regulation capabilities position EGTs as ideal candidates for building neuromorphic perception systems and energy-efficient intelligent hardware. Finally, we discuss the current challenges such as material stability, interfacial degradation, switching speed limitations, and integration density. Furthermore, we outline future research directions, emphasizing the need for novel hybrid electrolytes, advanced fabrication techniques, and holistic system-level integration to realize the full potential of EGTs in next-generation computing and bio-interfaced applications. Full article

Skin irritation testing is transitioning toward non-animal alternatives that can replicate the functional properties of the human stratum corneum (SC). To address this need, we report a capacitive biosensing platform that integrates a lanolin-based artificial SC (aSC) for rapid, indicator-free detection of chemical irritants. The approach leverages a membrane-bound lipid matrix to detect changes in interfacial capacitance caused by chemical exposure. Among candidate materials, lanolin emerged as the most effective SC mimic, showing reproducible baseline stability and responsive dielectric shifts. The system quantifies barrier integrity through the capacitance change rate (ΔC/Δt), which serves as a real-time indicator of irritation potential. By positioning the biosensor as an analog of the SC and monitoring the dielectric environment during short exposures (7.5 min), we shift the paradigm from endpoint-based biochemical assays to rapid, physicochemical screening. This concept supports the advancement of ethical, scalable testing platforms that reduce reliance on animal or cellular models while maintaining sensitivity to barrier-compromising agents. Full article

The integration of microstructured current collectors offers a potential pathway to enhance interface properties in solid-state battery architectures. In this work, we investigate the influence of surface morphology on the electrochemical performance of Zn/Na_2.99Ba_0.005OCl/Cu electrodeless pouch cells by fabricating copper thin films on microstructured parylene-C substrates using a combination of colloidal lithography and reactive ion etching. O₂ plasma etching times ranging from 0 to 15 min were used to tune the surface topography, resulting in a systematic increase in root-mean-square roughness and a surface area enhancement of up to ~30% for the longest etching duration, measured via AFM. Kelvin probe force microscopy-analyzed surface potential showed maximum differences of 270 mV between non-etched and 12-minute-etched Cu collectors. The results revealed that the chemical potential is the property that relates the surface of the Cu current collector/electrode with the cell’s ionic transport performance, including the bulk ionic conductivity, while four-point sheet resistance measurements confirmed that the copper layers’ resistivity maintained values close to those of bulk copper (1.96–4.5 µΩ.cm), which are in agreement with electronic mobilities (−6 and −18 cm²V⁻¹s⁻¹). Conversely, the charge carrier concentrations (−1.6 to −2.6 × 10²³ cm⁻³) are indirectly correlated with the performance of the cell, with the samples with lower CCC_bulk (fewer free electrons) performing better and showing higher maximum discharge currents, interfacial capacitance, and first-cycle discharge plateau voltage and capacity. The data were further consolidated with Scanning Electron Microscopy and X-ray Photoelectron Spectroscopy analyses. These results highlight that the correlation between the surface morphology and the cell is not straightforward, with the microstructured current collectors’ surface chemical potential and the charge carriers’ concentration being determinant in the performance of all-solid-state electrodeless sodium battery systems. Full article