Search Results (167)

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

In recent years, biomass utilization has attracted extensive attention. Herein, hexagonal/cubic ZnIn₂S₄ (ZIS) heterojunction catalysts were synthesized via a solvothermal method for the selective oxidation of 5-hydroxymethylfurfural (HMF) to 2,5-diformylfuran (DFF). The results demonstrated that the constructed heterojunctions effectively promoted carrier separation. The optimal catalyst achieved an HMF conversion rate of 88.8% and a DFF yield of 86.6% within 1 h in the open air. X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) characterizations confirmed the successful fabrication of the composite phase structure and revealed a porous spherical morphology. Equivalent circuit fitting of electrochemical impedance spectroscopy (EIS) data indicated that the hexagonal/cubic heterojunctions possessed the lowest charge transfer resistance (Rct = 5825 Ω), which effectively reduced interfacial charge transfer resistance and accelerated the transport of photoinduced carriers. Radical quenching experiments and electron paramagnetic resonance (EPR) spectroscopy identified superoxide radicals (·O₂⁻) as the primary reactive species. Meanwhile, density functional theory (DFT) calculations elucidated the formation of the built-in electric field and the charge transfer mechanism. This work’s construction of Type-II ZIS heterojunctions effectively addressed the issue of rapid carrier recombination in pristine ZIS materials, providing a feasible strategy for biomass valorization. Full article

Defect engineering in semiconductor heterojunctions offers a promising route for enhancing the selectivity of photocatalytic CO₂ conversion. In this work, a ZnS/gel-derived TiO₂ photocatalyst featuring sulfur vacancies introduced via hydrazine hydrate (N₂H₄) treatment is developed. XRD, HRTEM, and XPS analyses confirm the formation of a crystalline heterointerface and a defect-rich ZnS surface, enabling effective interfacial electronic modulation. The optimized ZnS/gel-derived TiO₂-0.48 composite achieves CH₄ and CO yields of 6.76 and 14.47 μmol·g⁻¹·h⁻¹, respectively, with a CH₄ selectivity of 31.8% and an electron selectivity of 65.1%, clearly outperforming pristine TiO₂ and the corresponding single-component catalysts under identical conditions. Photoluminescence quenching, enhanced photocurrent response, and reduced charge-transfer resistance indicate significantly improved interfacial charge separation. Mott–Schottky analysis combined with optical bandgap measurements reveals pronounced interfacial charge redistribution in the composite system. Considering the intrinsic band structure of ZnS and gel-derived TiO₂, a Z-scheme-compatible interfacial charge migration model is proposed, in which photogenerated electrons with strong reductive power are preferentially retained on ZnS, while holes with strong oxidative capability remain on gel-derived TiO₂. This charge migration pathway preserves high redox potentials, facilitating multi-electron CO₂ methanation and water oxidation. Density functional theory calculations further demonstrate that sulfur vacancies stabilize *COOH and *CO intermediates and reduce the energy barrier for *COOH formation from +0.51 eV to +0.21 eV, thereby promoting CO₂ activation and CH₄ formation. These results reveal that sulfur vacancies not only activate CO₂ molecules but also regulate interfacial charge migration behavior. This work provides a synergistic strategy combining defect engineering and interfacial electronic modulation to enhance selectivity and mechanistic understanding in CO₂-to-CH₄ photoconversion. 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

Polyampholytes combine cationic and anionic groups in one macromolecular platform and are emerging as versatile components for energy storage and conversion. This review synthesizes how their charge balance, hydration, and architecture can be engineered to address ionic transport, interfacial stability, and safety across batteries, supercapacitors, solar cells, and fuel cells. We classify annealed, quenched, and zwitterionic systems, outline molecular design strategies that tune charge ratio, distribution, and crosslinking, and compare device roles as gel or solid electrolytes, eutectogels, ionogels, binders, separator coatings, and interlayers. Comparative tables summarize ionic conductivity, cation transference number, electrochemical window, mechanical robustness, and temperature tolerance. Across Li and Zn batteries, polyampholytes promote ion dissociation, homogenize interfacial fields, suppress dendrites, and stabilize interphases. In supercapacitors, antifreeze hydrogels and poly(ionic liquid) networks maintain conductivity and elasticity under strain and at subzero temperature. In solar cells, zwitterionic interlayers improve work function alignment and charge extraction, while ordered networks in fuel cell membranes enable selective ion transport with reduced crossover. Design rules emerge that couple charge neutrality with controlled hydration and dynamic crosslinking to balance conductivity and mechanics. Key gaps include brittleness, ion pairing with multivalent salts, and scale-up. Opportunities include soft segment copolymerization, ionic liquid and DES plasticization, side-chain engineering, and operando studies to guide translation. Full article

Metal halide perovskite (MHP)-based heterojunctions have become a forefront area in the research of optoelectronic functional materials due to their unique layered crystal structure, tunable band gaps, and exceptional optoelectronic properties. Recent studies have demonstrated that interface charge transfer is a crucial factor in determining the optoelectronic performance of the heterojunction devices. By constructing heterojunctions between MHPs and two-dimensional (2D) materials such as graphene, MoS₂, and WS₂, efficient electron–hole separation and transport can be achieved, significantly extending carrier lifetimes and suppressing non-radiative recombination. This results in enhanced response speed and energy conversion efficiency in photodetectors, photovoltaic devices, and light-emitting devices (LEDs). In these heterojunctions, the thickness of the MHP layer, interface defect density, and band alignment significantly influence carrier dynamics. Furthermore, techniques such as interface engineering, molecular passivation, and band engineering can effectively optimize charge separation efficiency and improve device stability. The integration of multilayer heterojunctions and flexible designs also presents new opportunities for expanding the functionality of high-performance optoelectronic devices. In this review, we systematically summarize the charge transfer mechanisms in MHP-based heterojunctions and highlight recent advances in their optoelectronic applications. Particular emphasis is placed on the influence of interfacial coupling on carrier generation, transport, and recombination dynamics. Furthermore, the ultrafast dynamic behaviors and band-engineering strategies in representative heterojunctions are elaborated, together with key factors and approaches for enhancing charge transfer efficiency. Finally, the potential of MHP heterojunctions for high-performance optoelectronic devices and emerging photonic systems is discussed. This review aims to provide a comprehensive theoretical and experimental reference for future research and to offer new insights into the rational design and application of flexible optoelectronics, photovoltaics, light-emitting devices, and quantum photonic technologies. Full article

In recent years, organic dye contamination has posed a significant threat to water safety. This study presents a novel composite photocatalyst comprising graphitic carbon nitride quantum dots (g-C3N4QDs) supported on a copper-based metal–organic framework (Cu-MOF) for efficient visible-light degradation of organic pollutants. The g-C₃N₄QDs were synthesized via a facile strategy and subsequently immobilized onto the Cu-MOF support. Comprehensive characterization including SEM, TEM, XRD, BET, UV-Vis DRS, PL, and EIS confirmed the successful formation of a heterostructure, revealing that an optimized loading of g-C₃N₄QDs significantly enhanced light absorption, facilitated charge separation, and increased the specific surface area, with the optimal composite exhibiting 273 m²/g compared to 112 m²/g for the pristine Cu-MOF. Electrochemical analyses indicated a 2.38-fold enhancement in photocurrent density and a reduced interfacial charge transfer resistance, reflecting superior electron–hole pair separation. Crucially, the optimized g-C₃N₄QDs/Cu-MOF composite demonstrated exceptional photocatalytic performance, achieving 96.6% degradation of Congo red (100 mg/L) within 30 min under visible light irradiation, substantially outperforming the 77.6% degradation attained by the pristine Cu-MOF. This enhancement is attributed to the synergistic effects of improved light harvesting, efficient interfacial charge transfer across the heterojunction, and an enlarged active surface area. The composite exhibits considerable potential as a high-performance and stable photocatalyst for purifying dye-contaminated wastewater. Full article

Photoelectrochemical water splitting (PEC-WS) provides a sustainable route to transform solar energy into hydrogen; however, its overall efficiency is constrained by the inherently slow kinetics of the oxygen evolution reaction. Bismuth vanadate (BiVO₄) is considered an attractive visible-light-responsive photoanode due to its suitable band gap (~2.4 eV) and chemical stability; however, its efficiency is restricted by limited charge transport and significant charge carrier recombination. To overcome these limitations, BiVO₄–MoS₂ (BVO–MS) heterostructures were synthesized through a simple in situ hydrothermal approach, ensuring robust interfacial coupling and uniform dispersion of MS nanosheets over BVO dendritic surfaces. This intimate contact promotes rapid charge transfer and improved light-harvesting capability. Structural and spectroscopic analyses confirmed the formation of monoclinic BVO with uniformly integrated amorphous MS. The optimized BVO–MS10 electrode delivered a photocurrent density of 4.72 mA cm⁻² at 0.6 V vs. SCE, approximately 5.3 times higher than pristine BVO, and achieved an applied bias photon-to-current efficiency of 0.49%. Mott–Schottky analysis revealed a distinct negative shift in the flat-band potential for BVO–MS10, indicative of an upward movement of its conduction band and the establishment of a strong internal electric field that enhances charge separation and interfacial electron transport. These synergistic effects collectively endow the in situ engineered BVO–MS heterostructure with superior PEC water oxidation performance and highlight its promise for efficient solar-driven hydrogen generation. 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

Photocatalytic antimicrobial materials represent a promising class of sustainable disinfection technologies, leveraging the generation of reactive oxygen species (ROS) under light irradiation for environmental and biomedical applications. Bismuth vanadate (BiVO₄), a visible-light-responsive semiconductor, has garnered considerable interest due to its suitable bandgap and chemical stability. However, its photocatalytic performance is critically limited by rapid charge carrier recombination and a relatively weak intrinsic built-in electric field. In this study, we report a novel composite strategy to address these limitations by coupling BiVO₄ with tourmaline, a naturally abundant piezoelectric mineral exhibiting spontaneous polarization. The integration of tourmaline induces a built-in electric field that synergistically aligns with and amplifies the internal field of BiVO₄, which substantially improves charge separation and carrier transport dynamics. The resulting tourmaline/BiVO₄ heterostructure demonstrates remarkedly enhanced antibacterial activity under visible-light irradiation against both Escherichia coli and Staphylococcus aureus, significantly outperforming pristine BiVO₄. Mechanistic investigations attribute this enhancement to the polarization-induced modulation of interfacial charge dynamics, which boosts ROS generation and accelerates microbial inactivation kinetics. This work presents a generalizable strategy for the rational design of high-efficiency photocatalytic antimicrobial systems, offering potential utility in water treatment, healthcare sterilization, and environmental remediation. Full article

Developing photoelectrochemical systems that couple pollutant removal with resource recovery is of great significance for sustainable wastewater treatment. In this study, a dual-function photocatalytic fuel cell (PFC) was developed using a TiO₂ nanotube photoanode modified with an amorphous CoOx cocatalyst, which markedly enhances charge separation and interfacial reaction kinetics. The optimized TiO₂@CoOx electrode achieves a twofold enhancement in photocurrent compared to pristine TiO₂. When applied to Cu²⁺-containing wastewater, the PFC achieved 91% Cu²⁺ removal under N₂-purged conditions, with metallic Cu identified as the sole reduction product. Although dissolved oxygen reduced metal recovery efficiency through competitive electron consumption, it simultaneously increased power generation and improved anodic organic degradation. Overall, the results demonstrate that amorphous-CoOx-modified TiO₂ photoanodes offer an effective platform for integrating sustainable energy production with wastewater remediation and valuable copper recovery. Full article

This review explores the pervasive role of water in generating, storing, and mediating electric charge across natural and artificial systems. Far from being a passive medium, water actively participates in electrostatic and electrochemical processes through its intrinsic ionization, interfacial polarization, and charge separation mechanisms. The Maxwell–Wagner–Sillars (MWS) effect is presented as a unifying framework explaining charge accumulation at air–water, water–ice, and water–solid interfaces, forming dynamic “electric mosaics” across Earth’s environments. The authors integrate diverse phenomena—triboelectricity, hygroelectricity, hydrovoltaic effects, elastoelectricity, and electric-field-driven phase transitions—showing that ambient water continually shapes the planet’s electrical landscape. Electrostatic shielding by humid air and hydrated materials is described, as well as the spontaneous electrification of sliding or dripping water droplets, revealing new pathways for clean energy generation. In addition, the review highlights how electric fields and interfacial charges alter condensation, freezing, and chemical reactivity, underpinning discoveries such as microdroplet chemistry, “on-water” reactions, and spontaneous redox processes producing hydrogen and hydrogen peroxide. Altogether, the paper frames water as a universal electrochemical medium whose interfacial electric imprint influences atmospheric, geological, and biological phenomena while offering novel routes for sustainable technologies based on ambient charge dynamics and water-mediated electrification. Full article

High-phosphorus iron ore can be utilized using a technical route of hydrogen-based shaft furnace reduction, followed by electric arc furnace (EAF) melting separation. In shaft furnace reduction, both pellet and lump ore could serve as feedstock. To optimize the charge pattern in the H₂-based shaft furnace, an investigation of the reduction behavior of high-phosphorus iron ore lumps and pellets under H₂ atmosphere was conducted. Results revealed distinct differences between the lumps and the pellets in terms of physicochemical characteristics, maximum reduction fractions, microstructure evolution, and reduction kinetics characteristics. The lumps exhibited a notable presence of oolitic structures with 60.08 wt.% total iron, 11.69 wt.%. Fe²⁺ ion, and 0.80 wt.% phosphorus. Under H₂ atmosphere, the lumps achieved a maximum reduction fraction of 0.80. During the reduction, fayalite formed in the early stage, and glassy phases appeared in the later stage. The rate-controlling steps included internal gas diffusion, interfacial chemical reaction, and solid-state diffusion of ions. In contrast, the oolitic structures were completely disrupted in the pellets. The pellets contained 56.01 wt.% total iron, 0.86 wt.% Fe²⁺ ions, and 0.73 wt.% phosphorus. The pellets reached a full reduction under H₂ atmosphere with negligible formation of fayalite and glassy phases. The rate-controlling steps included internal gas diffusion and interfacial chemical reaction. Full article

We report measurements of ultrafast photoinduced charge separation and recombination processes in the conjugated donor–acceptor (D-A) polymer PSBTBT, both as pure film and blended in various polymer matrices. Using time-resolved terahertz spectroscopy (TRTS), time-dependent photoconductivity is measured for samples with PSBTBT weight fractions (W_PSBTBT:W_PE/PEG/PS) of 2.0% dispersed in high-density polyethylene (HDPE), polyethylene glycol (PEG), and polystyrene (PS). Charge carrier generation is an intrinsic feature of conductive polymers that occurs on sub-picosecond and longer timescales and is attributed to initially generated dissociation of bound polaron pairs into free carriers that reside on polymer chains, or to adjacent interchain charge transfer and migration. Both interchain and interfacial charge transfer contribute to the measured photoconductivity of the samples, which is found to increase as a function of increasing local polarity and an increasingly hydrogen-bonded environment. Pure-PSBTBT polymer film, PSBTBT dispersed in PS, and PSBTST dispersed in HDPE were all found to exhibit shorter photoconductive free-carrier long-time signal decay than PSBTBT in a hydrogen-bonded, semi-crystalline PEG environment. Full article

Ultrafine bubbles (UFBs) have been proposed as interfacial agents that modulate colloidal interactions, yet their role in early-stage flocculation remains insufficiently quantified. Using amidine latex (AL) as a cationic model colloid under controlled end-over-end mixing, we combined flocculation kinetics with electrokinetic and interfacial measurements to elucidate the mechanism by which UFBs promote aggregation. Electrophoretic measurements show adsorption-driven charge regulation by bubbles; increasing the UFB-to-AL ratio progressively neutralizes the surface and at sufficient dose reverses its charge. The neutrality point occurs at a characteristic ratio that is only weakly sensitive to background sodium chloride (NaCl). Interfacial measurements reveal a thicker hydrodynamic layer at higher ionic strength, consistent with closer packing of adsorbed UFBs under double layer compression, and micrographs of particle dimers confirm a larger inter-particle separation that directly visualizes this layer. Aggregation accelerates at 10 mM sodium chloride but remains slow at 0.1 mM, indicating that electrolyte screening is required for efficient adsorption and bridging; pH modulated the process secondarily. Together, the results support a coherent picture in which UFB adsorption creates patchy, charge-compensated surfaces and a soft hydrodynamic layer that enlarges the effective collision cross-section, thereby enhancing early-stage flocculation. Full article