Search Results (254)

Despite significant progress in photoelectrochemical (PEC) water splitting, high fabrication costs and limited efficiency of photoanodes hinder practical applications. Bismuth vanadate (BiVO₄), with its low cost, non-toxicity, and suitable band structure, is a promising photoanode material but suffers from poor charge transport, sluggish surface kinetics, and photocorrosion. In this study, porous monoclinic BiVO₄ films are fabricated via a simplified successive ionic layer adsorption and reaction (SILAR) method, followed by borate treatment and PEC deposition of NiFeO_x. The resulting B/BiVO₄/NiFeO_x photoanode exhibits a significantly enhanced photocurrent density of 2.45 mA cm⁻² at 1.23 V vs. RHE—5.3 times higher than pristine BiVO₄. It also achieves an ABPE of 0.77% and a charge transfer efficiency of 79.5%. These results demonstrate that dual surface modification via borate and NiFeO_x is a cost-effective strategy to improve BiVO₄-based PEC water splitting performance. This work provides a promising pathway for the scalable development of efficient and economically viable photoanodes for solar hydrogen production. Full article

The rational design of photoanode materials is pivotal for advancing photoelectrochemical (PEC) water splitting toward sustainable hydrogen production. This review highlights recent progress in the machine learning (ML)-assisted development of nanostructured metal oxide photoanodes, focusing on bridging materials discovery and device-level performance optimization. We first delineate the fundamental physicochemical criteria for efficient photoanodes, including suitable band alignment, visible-light absorption, charge carrier mobility, and electrochemical stability. Conventional strategies such as nanostructuring, elemental doping, and surface/interface engineering are critically evaluated. We then discuss the integration of ML techniques—ranging from high-throughput density functional theory (DFT)-based screening to experimental data-driven modeling—for accelerating the identification of promising oxides (e.g., BiVO₄, Fe₂O₃, WO₃) and optimizing key parameters such as dopant selection, morphology, and catalyst interfaces. Particular attention is given to surrogate modeling, Bayesian optimization, convolutional neural networks, and explainable AI approaches that enable closed-loop synthesis-experiment-ML frameworks. ML-assisted performance prediction and tandem device design are also addressed. Finally, current challenges in data standardization, model generalizability, and experimental validation are outlined, and future perspectives are proposed for integrating ML with automated platforms and physics-informed modeling to facilitate scalable PEC material development for clean energy applications. Full article

This review presents a comprehensive overview of recent advances in TiO₂-based photoelectrocatalysis (PEC), with an emphasis on material design strategies to enhance visible-light responsiveness and charge carrier dynamics. Key approaches—including elemental doping, defect engineering, heterojunction construction, and plasmonic enhancement—are systematically discussed in relation to their roles in modulating energy band structures and promoting charge separation. Beyond fundamental mechanisms, the review highlights the broad environmental and energy-related applications of TiO₂-driven PEC systems, encompassing the degradation of persistent organic pollutants, microbial disinfection, heavy metal removal, photoelectrochemical water splitting for hydrogen production, and CO₂ reduction. Recent progress in integrating PEC systems with energy harvesting modules to construct self-powered platforms is critically examined. Current limitations and future directions are also outlined to guide the rational development of next-generation TiO₂-based photoelectrocatalytic systems for sustainable environmental remediation and solar fuel conversion. Full article

NiFe₂O₄ and TiO₂ are widely studied for photoelectrochemical (PEC) applications due to their unique properties. Nitrogen-doped graphene (NG) and metal–organic frameworks (MOFs), such as MIL-100(Fe) (where MIL stands for Materials of Lavoisier Institute), are commonly incorporated to enhance PEC performance by offering a high surface area and facilitating efficient charge transport. Composite systems are commonly employed to overcome the limitations of individual PEC catalysts. In this study, a highly efficient NiFe₂O₄/NG@MIL-100(Fe)/TiO₂ photoanode was developed to enhance photoelectrochemical water-splitting performance. The composite was synthesized via a hydrothermal method with a two-step heating process. X-ray diffraction confirmed the expected crystal structures, with peak broadening in NiFe₂O₄ indicating reduced crystallite size and increased lattice strain. X-ray photoelectron spectroscopy of the Ni 2p and Fe 2p regions validated the successful integration of NiFe₂O₄ into the composite. Electrochemical analysis demonstrated excellent performance, with linear sweep voltammetry achieving a peak photocurrent density of 3.5 mA cm⁻² at 1.23 V (vs RHE). Electrochemical impedance spectroscopy revealed a reduced charge-transfer resistance of 50 Ω, indicating improved charge transport. Optical and electronic properties were evaluated using UV-Vis spectroscopy and Tauc plots, revealing a direct bandgap of 2.1 eV. The composite exhibited stable photocurrent under amperometric J-t testing for 2000 s, demonstrating its durability. These findings underscore the potential of NiFe₂O₄/NG@MIL-100(Fe)/TiO₂ as a promising material for renewable energy applications, particularly in photoelectrochemical water splitting. Full article

Developing high-efficiency photoelectrodes plays an important role in the photoelectrocatalytic generation of hydrogen peroxide (H₂O₂) in the photoelectrochemical (PEC) water splitting field. In this work, an innovative strategy was proposed, the synergistic photocatalytic production of H₂O₂ using a bidirectional photoanode–photocathode coupling system under visible-light irradiation. Fe₂O₃-Ti, as the photoanode, which was built by way of Fe₂O₃ loaded on Ti-mesh using the hydrothermal-calcination method, was investigated in terms of the suitability of its properties for PEC H₂O₂ production after optimization of the bias voltage, the type of electrolyte solution, and the concentration of the electrolyte. Afterwards, a H-type double-electrode coupling system with an Fe₂O₃-Ti photoanode and a WO₃@Co₂SnO₄ photocathode was established for the bidirectional synergistic production of H₂O₂ under visible-light irradiation. The yield of H₂O₂ reached 919.56 μmol·L⁻¹·h⁻¹ in 2 h over −0.7 V with 1 mol·L⁻¹ of KHCO₃ as the anolyte and 0.1 mol·L⁻¹ Na₂SO₄ as the catholyte (pH = 3). It was inferred that H₂O₂ production on the WO₃@Co₂SnO₄ photocathode was in line with the 2e^- oxygen reduction reaction (ORR) principle, and on the Fe₂O₃-Ti photoanode was in line with the 2e^- water oxidation reaction (WOR) rule, or it was indirectly promoted by the electrolyte solution KHCO₃. This work provides an innovative idea and a reference for anode–cathode double coupling systems for the bidirectional production of H₂O₂. Full article

We prepared antimony metal films via electrodeposition, followed by the synthesis of Sb₂S₃ films through a chemical vapor phase reaction. Finally, an Sb₂O₃ film was deposited onto the Sb₂S₃ film using a chemical bath method, successfully constructing a heterojunction photocathode of Sb₂S₃/Sb₂O₃; the synthesized Sb₂S₃/Sb₂O₃ heterojunction is classified as a Type I heterostructure. The resulting Sb₂S₃/Sb₂O₃ heterojunction exhibited a photocurrent density of −0.056 mA cm⁻² at −0.15 V (vs. RHE), which is 1.40 times higher than that of Sb₂S₃ alone under simulated solar illumination. Additionally, the Sb₂S₃/Sb₂O₃ heterojunction demonstrated a lower carrier recombination rate and a faster charge transfer rate compared to Sb₂S₃, as evidenced by photoluminescence and electrochemical impedance spectroscopy tests. For these reasons, the Sb₂S₃/Sb₂O₃ heterojunction obtained a hydrogen precipitation rate of 0.163mL cm⁻² h⁻¹, which is twice the hydrogen precipitation rate of Sb₂S₃, under the condition of 60 min of light exposure. The significant enhancement in photoelectrochemical performance is attributed to the formation of the Sb₂S₃/Sb₂O₃ heterojunction, which improves both carrier separation and charge transfer efficiency. This heterojunction strategy holds promising potential for visible light-driven photoelectrochemical water splitting. Full article

In sustainable hydrogen generation, photoelectrochemical (PEC) water splitting stands as a crucial technology, offering solutions to the global energy crisis while tackling environmental challenges. PEC water splitting relies on metal oxide nanostructures due to their unique electronic and optical characteristics. This research highlights the development of a CuO-Fe₂O₃@g-C₃N₄ nanocomposite, created through the integration of three components and fabricated via a one-pot hydrothermal process, precisely engineered to enhance PEC water-splitting efficiency. The combination of CuO, Fe₂O₃, and g-C₃N₄ results in a unified heterojunction structure that efficiently mitigates issues associated with charge carrier recombination and structural stability. Additionally, the analyses of both the structure and composition confirmed the precise synthesis of the composite. The CuO-Fe₂O₃@g-C₃N₄ nanocomposite achieved a photocurrent density of 1.33 mA cm⁻² vs. Ag/AgCl upon exposure to light, demonstrating superior PEC performance and outperforming the individual CuO and Fe₂O₃ components. The enhanced performance is attributed to g-C₃N₄ acting as a photoactive material, generating charge carriers, while the combination of CuO-Fe₂O₃ enables efficient carrier separation and mobility. This synergistic interaction significantly enhances photocurrent generation and ensures long-term stability, positioning the material as a highly promising solution for sustainable hydrogen production. These results highlight the promise of hybrid nanocomposites in driving progress in renewable energy technologies, opening new avenues for the development of more efficient and long-lasting PEC systems. Full article

Hydrogen production via water splitting is a crucial strategy for addressing the global energy crisis and promoting sustainable energy solutions. This review systematically examines water-splitting mechanisms, with a focus on photocatalytic and electrochemical methods. It provides in-depth discussions on charge transfer, reaction kinetics, and key processes such as the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). Various electrode synthesis techniques, including hydrothermal methods, chemical vapor deposition (CVD), pulsed laser deposition (PLD), and radio frequency sputtering (RF), are reviewed for their advantages and limitations. The role of carbon-based materials such as graphene, biochar, and graphitic carbon nitride (g-C₃N₄) in photocatalytic and photoelectrochemical (PEC) water splitting is also highlighted. Their exceptional conductivity, tunable band structures, and surface functionalities contribute to efficient charge separation and enhanced light absorption. Further, advancements in heterojunctions, doped systems, and hybrid composites are explored for their ability to improve photocatalytic and PEC performance by minimizing charge recombination, optimizing electronic structures, and increasing active sites for hydrogen and oxygen evolution reactions. Key challenges, including material stability, cost, scalability, and solar spectrum utilization, are critically analyzed, along with emerging strategies such as novel synthesis approaches and sustainable material development. By integrating water splitting mechanisms, electrode synthesis techniques, and advancements in carbon-based materials, this review provides a comprehensive perspective on sustainable hydrogen production, bridging previously isolated research domains. Full article

Water photoelectrolysis cells based on photoelectrochemical water splitting seem to be an interesting alternative to other traditional green hydrogen generation processes (e.g., water electrolysis). Unfortunately, the practical application of this technology is currently hindered by several difficulties: low solar-to-hydrogen (STH) efficiency, expensive electrode materials, etc. A novel concept, based on a tandem photoelectrolysis cell configuration with an anion-conducting membrane separating the photoanode from the photocathode, has already been proposed in the literature. This approach allows the use of low-cost metal oxide electrodes and nickel-based co-catalysts. In this paper, we conducted a study to evaluate the economic and environmental sustainability of this technology, using the environmental life cycle cost. Preliminary results have revealed two main interesting aspects: the negligible percentage of externalities in the total cost (<0.15%), which means a positive environmental impact, and as evidenced by the net present value (NPV), there are potentially financial conditions that favour future investment. In fact, an NPV higher than 150,000 EUR can be achieved after 15 years. Full article

Delafossite CuFeO₂ has emerged as a promising earth-abundant p-type photocathode for solar fuel generation due to its stability in aqueous conditions and its favorable light absorption characteristics. However, practical photocurrent generation in CuFeO₂ has consistently fallen short of its theoretical potential. This limitation is attributed primarily to suboptimal practical visible light absorption, resulting in diminished incident photon-to-current conversion efficiency (IPCE). Challenges related to charge separation and transport, originating from low acceptor density and inherent low conductivity, further contribute to the reported suboptimal performance of delafossite CuFeO₂. Thus, the present review comprehensively documents the latest advancements in the field of CuFeO₂ photocathode research, with a particular emphasis on strategies to overcome the challenges currently being faced and on the illustration of pathways that may lead to the enhancement of critical performance parameters such as photocurrents, photovoltage, and fill factor. Full article

Dye-sensitization is a promising strategy to improve the light absorption and photoactivity abilities of wide-bandgap semiconductors, like TiO₂. For effective water-splitting photoanodes with no sacrificial agents, the electrochemical potential of the dye must exceed the thermodynamic threshold needed for the oxygen evolution reaction. This study investigates two promising organic cyanoacrylic dyes, designed to meet that criterion by means of theoretical calculations. Both yellow-colored dyes were synthesized and characterized by optical and photoelectrochemical techniques, demonstrating strong light absorption in the visible region, suitable experimental reduction potentials, and adsorption from the organic solvent onto mesoporous TiO₂ layers. In addition, to promote immobilization in aqueous electrolytes, the dyes were hybridized with graphene oxide or multi-walled carbon nanotubes. Photoelectrochemical analysis of the dye-sensitized photoelectrodes demonstrated efficient charge transfer from the dyes to the TiO₂ photoanode under simulated solar light. While the starting photocurrent notably surpassed the blank TiO₂, a subsequent decay points to kinetic obstacles that still need to be overcome. Full article

Considering the poor conductivity of Fe₂O₃ and the weak oxygen evolution reaction associated with it, surface hole accumulation leads to electron hole pair recombination, which inhibits the photoelectrochemical (PEC) performance of the Fe₂O₃ photoanode. Therefore, the key to improving the PEC water oxidation performance of the Fe₂O₃ photoanode is to take measures to improve the conductivity of Fe₂O₃ and accelerate the reaction kinetics of surface oxidation. In this work, the PEC performances of Fe₂O₃ photoanodes are synergistically improved by combining loaded an FeOOH cocatalyst and oxygen vacancy doping. Firstly, amorphous FeOOH layers are successfully prepared on Fe₂O₃ nanostructures through simple photoassisted electrodepositon. Then oxygen vacancies are introduced into FeOOH-Fe₂O₃ through plasma vacuum treatment, which reduces the content of Fe-O (O_L) and Fe-OH (-OH), jointly promoting the generation of oxygen vacancies. Oxygen vacancy can increase the concentration of most carriers in Fe₂O₃ and form photo-induced charge traps, promoting the separation of electron holes and enhancing the conductivity of Fe₂O₃. The other parts of -OH act as oxygen evolution catalysts to reduce the reaction obstacle of water oxidation and promote the transfer of holes to the electrode/electrolyte interface. The performance of FeOOH-Fe₂O₃ after plasma vacuum treatment has been greatly improved, and the photocurrent density is about 1.9 times higher than that of the Fe₂O₃ photoanode. The improvement in the water oxidation performance of PEC is considered to be the synergistic effect of the cocatalyst and oxygen vacancy. All outstanding PEC response characteristics show that the modification of the cocatalyst and oxygen vacancy doping represent a favorable strategy for synergistically improving Fe₂O₃ photoanode performance. Full article

Fibrous SiO₂-TiO₂ (FST) is one of the most promising materials for advancing photoelectrochemical water-splitting technology due to its cost-effectiveness and environmental friendliness. However, FST faces intrinsic limitations, including its low conductivity and wide bandgap. In this study, significant progress was made in modifying FST to overcome some of these limitations. This work involved synthesizing a new photoanode made of Ag-doped FST utilizing the microemulsion process. The Ag-doped FST was characterized using XRD, FTIR, UV–Vis, DRS, N₂ adsorption–desorption, FESEM, TEM, and XPS. The results confirmed the formation of a continuous concentric lamellar structure with a large surface area. The addition of Ag species into the FST matrix caused interactions that reduced the bandgap. The Ag-doped FST photoanode exhibited an impressive photocurrent density of 13.98 mA/cm² at 1.2 V (vs. RHE). This photocurrent density was notably higher than that of FST photoanodes, which was 11.65 mA/cm² at 1.2 V (vs. RHE). Furthermore, the conduction band of Ag-doped FST is positioned closer to the reduction potential of hydrogen compared to that of FST, SiO₂, and TiO₂, facilitating rapid charge transfer and enabling the spontaneous generation of H₂. The fabrication of Ag-doped FST provides valuable insights into the development of high-performance photoanodes for PEC water splitting. Full article

The modular photoelectrochemical (PEC) reactor accommodating eight photoelectrodes with a total active area of up to 46 cm² has been designed and manufactured using the fused deposition modeling method. The device was equipped with an electrolyte flow system, a relay module for the photoelectrode connection, and a feedback-loop module for switching between counter electrodes. The performance and durability of the system were tested within three case study experiments. The water splitting process was successfully combined with an in situ hydrogen storage in the form of metal hydride phases (confirmed by powder X-ray diffraction) using Fe₂O₃- or WO₃-based photoanodes and LaNi₅-based cathodes. The PEC water oxidation at the anodes was realized either in a strongly alkaline electrolyte (pH > 13.5) or in acidified synthetic seawater (pH < 2) for Fe₂O₃ and WO₃ electrodes, respectively. In the latter case, the photoresponse of the anodes decreased the cell charging voltage by 1.7 V at the current density of 60 mA∙g⁻¹. When the seawater was used as an anolyte, the oxygen evolution reaction was accompanied by the chlorine evolution reaction. The manufactured PEC-metal hydride reactor revealed mechanical and chemical stability during a prolonged operation over 300 h and in the broad range of pH values. Full article

Solar-driven hydrogen generation is one of the promising technologies developed to address the world’s growing energy demand in an sustainable way. While, for hydrogen generation (otherwise water splitting), photocatalytic, photoelectrochemical, and PV-integrated water splitting systems employing conventional semiconductor oxides materials and their electrodes have been under investigation for over a decade, lead (Pb)- halide perovskites (HPs) made their debut in 2016. Since then, the exceptional characteristics of these materials, such as their tunable optoelectronic properties, ease of processing, high absorption coefficients, and long diffusion lengths, have positioned them as a highly promising material for solar-driven water splitting. Like in solar photovoltaics, a solar-driven water splitting field is also dominated by Pb-HPs with ongoing efforts to improve material stability and hydrogen evolution/generation rate (HER). Despite this, with the unveiling potential of various Pb-free HP compositions in photovoltaics and optoelectronics researchers were inspired to explore the potential of these materials in water splitting. In this current review, we outlined the fundamentals of water splitting, provided a summary of Pb HPs in this field, and the associated issues are presented. Subsequently, Pb-free HP compositions and strategies employed for improving the photocatalytic and/or electrochemical activity of the material are discussed in detail. Finally, this review presents existing issues and the future potential of lead-free HPs, which show potential for enhancing productivity of solar-to-hydrogen conversion technologies. Full article