Search Results (25)

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

Hydrogen and oxygen serve as energy carriers that can ease the transition of energy due to their high energy densities. Nonetheless, their production processes entail the development of efficient and low-cost storage and conversion technologies. In this regard, photoelectrocatalysts are materials based on the photoelectronic effect where electrons and holes interact with H₂O, producing H₂ and O_2, and in some cases, this is achieved with acceptable efficiency. Although there are several reviews on this topic, most of them focus on traditional semiconductors, such as TiO₂ and ZnO, neglecting others, such as those based on non-noble metals and organic ones. Herein, semiconductors like CdSe, NiWO₄, Fe₂O₃, and others have been investigated and compared in terms of photocurrent density, band gap, and charge transfer resistance. In addition, this brief review aims to discuss the mechanisms of overall water-splitting reactions from a photonic point of view and subsequently discusses the engineering of material synthesis. Advanced composites are also addressed, such as WO₃/BiVO₄/Cu₂O and CN-FeNiOOH-CoOOH, which demonstrate high efficiency by delivering photocurrent densities of 5 mAcm⁻² and 3.5 mA cm⁻² at 1.23 vs. RHE, respectively. Finally, the authors offer their perspectives and list the main challenges based on their experience in developing semiconductor-based materials applied in several fields. In this manner, this brief review provides the main advances in these topics, used as references for new directions in designing active materials for photoelectrocatalytic water splitting. Full article

In this work, Er-doped BiVO₄/BiFeO₃ composites are prepared using the sonochemical process with a difference of rare earth loading compositions. The crystallinity and chemical and morphological structure of as-synthesized samples were investigated via X-ray diffraction, Raman scattering, and electron microscopy, respectively. The diffuse reflectance technique was used to extract the optical property and calculate the optical band gap of the composite sample. The piezo-photocatalytic performance was evaluated according to the decomposition of a Rhodamine B organic compound. The decomposition of the organic compound was achieved under ultrasonic bath irradiation combined with light exposure. The Er-doped BiVO₄/BiFeO₃ composite heterojunction material exhibited significant enhancement of the piezo-photocatalytic activity under both ultrasonic and light irradiation due to the improvement in charge generation and separation. The result indicates that Er dopant strongly affects the phase transformation, change in morphology, and alternation in optical band gap of the BiVO₄ matrix. The incorporation of BiFeO₃ in the composite form with BiVO₄ doped with 1%Er can improve the photocatalytic performance of BiVO₄ via piezo-induced charge separation and charge recombination retardment. Full article

Wider application of BiVO₄ (BVO) for photocatalytic water treatment is primarily limited by its modest photocatalytic effectiveness, despite its appropriately narrow band gap for low-cost, sunlight-facilitated water treatment processes. In this study, we have photomodified an isotype BVO, consisting of a tetragonal zircon and monoclinic scheelite phase, with Fe (Fe@BVO) and Ag (Ag@BVO) ionic precursors under UV illumination in an aqueous ethanol solution in order to assess their effect on the opto-electronic properties and effectiveness for the removal of ciprofloxacin (CIP). Fe@BVO failed to demonstrate enhanced effectiveness over pristine BVO, whereas all Ag@BVO achieved improved CIP degradation, especially 1% Ag@BVO. At pH 4 and 6, 1% Ag@BVO demonstrated nearly 24% greater removal of CIP than BVO alone. Photomodification with Fe created surface oxygen vacancies, as confirmed by XPS and Mott–Schottky analysis, which facilitated improved electron mobility, although no distinct Fe-containing phase nor Fe-doping was detected. On the other hand, the introduction of mid-band gap states by oxygen vacancies decreased the reducing power of the photogenerated electrons as the flat band potentials were shifted to more positive values, thus likely negatively impacting superoxide formation. In contrast, Ag-photomodification (Ag@BVO) resulted in the formation of Ag₂O/AgO and Ag nanoparticles on the surface of BVO, which, under illumination, generated hot electrons by surface plasmon resonance and enhanced the mobility of photogenerated electrons. Our research underscores the pivotal role of photogenerated electrons for CIP degradation by BiVO₄-based materials and emphasizes the importance of appropriate band-edge engineering for optimizing contaminant degradation. Full article

Fe-BiOCl-V_o nanosheets with electron-capture centers of doped Fe and surface oxygen vacancies (V_o) for enhanced photocatalytic-Fenton performances were conducted. Compared with pristine BiOCl nanosheets, the band gap of the resulting Fe-BiOCl-V_o nanosheets was narrowed, and defective bands were introduced due to the Fe doping and V_o. Furthermore, the integrated electron trapping effect of V_o and doped Fe can efficiently drive charge transfer and separation. As a result, the photocatalytic-Fenton performances of phenol over Fe-BiOCl-V_o nanosheets were enhanced. The photocatalytic-Fenton performances of Fe-BiOCl-V_o nanosheets were enhanced two-fold and four-fold, respectively, as compared with the photocatalytic performances of Fe-BiOCl-V_o and pristine BiOCl nanosheets. During the photocatalytic-Fenton process, the multiple reactive species referring holes (h⁺), superoxide radicals (●O₂⁻), and hydroxyl radicals (●OH) induced by the efficiently separated charge carriers and Fenton reaction played synergetic roles in phenol degradation and mineralization. This work provides a sophisticated structure design of catalysts for efficient charge transfer and separation, promoting photocatalytic-Fenton performance. Full article

Bismuth vanadate (BiVO₄) has been investigated as a photocatalyst of great interest due to its ability to harvest photons efficiently in the visible spectral region. In addition, powdered BiVO₄ shows high photochemical stability, good dispersibility, and resistance to corrosion in oxidative conditions. Herein, we report the synthesis of monoclinic or tetragonal BiVO₄ particles using different methods, as well as the synthesis of hybrids materials through the combination of cobalt ferrite (CoFe₂O₄) and BiVO₄, and their application in the photodegradation of aqueous solutions of sulfamethoxazole (SMX) under simulated solar radiation. We demonstrate that high-crystallinity single-phase monoclinic BiVO₄ was synthesized fast and efficiently using a solid-state method and, in combination with magnetic CoFe₂O₄ particles, gives rise to a hybrid material that can be easily separated from the reaction medium, by applying an external magnetic field, without the need for further downstream treatments. Full article

Bismuth ferrite (BiFeO₃, BFO) is still widely investigated both because of the great diversity of its possible applications and from the perspective of intrinsic defect engineering in the perovskite structure. Defect control in BiFeO₃ semiconductors could provide a key technology for overcoming undesirable limitations, namely, a strong leakage current, which is attributed to the presence of oxygen vacancies (V_O) and Bi vacancies (V_Bi). Our study proposes a hydrothermal method for the reduction of the concentration of V_Bi during the ceramic synthesis of BiFeO₃.Using hydrogen peroxide (H₂O₂) as part of the medium, p-type BiFeO₃ ceramics characterized by their low conductivity were obtained. Hydrogen peroxide acted as the electron donor in the perovskite structure, controlling V_Bi in the BiFeO₃ semiconductor, which caused the dielectric constant and loss to decrease along with the electrical resistivity. The reduction of Bi vacancies highlighted by a FT-IR and Mott—Schottky analysis has an expected contribution to the dielectric characteristic. A decrease in the dielectric constant (with approximately 40%) and loss (3 times) and an increase of the electrical resistivity (by 3 times) was achieved by the hydrogen peroxide-assisted hydrothermal synthesized BFO ceramics, as compared with the hydrothermal synthesized BFOs. Full article

While metal oxides such as TiO₂, Fe₂O₃, WO₃, and BiVO₄ have been previously studied for their potential as photoanodes in photoelectrochemical (PEC) hydrogen production, their relatively wide band-gap limits their photocurrent, making them unsuitable for the efficient utilization of incident visible light. To overcome this limitation, we propose a new approach for highly efficient PEC hydrogen production based on a novel photoanode composed of BiVO₄/PbS quantum dots (QDs). Crystallized monoclinic BiVO₄ films were prepared via a typical electrodeposition process, followed by the deposition of PbS QDs using a successive ionic layer adsorption and reaction (SILAR) method to form a p-n heterojunction. This is the first time that narrow band-gap QDs were applied to sensitize a BiVO₄ photoelectrode. The PbS QDs were uniformly coated on the surface of nanoporous BiVO₄, and their optical band-gap was reduced by increasing the number of SILAR cycles. However, this did not affect the crystal structure and optical properties of the BiVO₄. By decorating the surface of BiVO₄ with PbS QDs, the photocurrent was increased from 2.92 to 4.88 mA/cm² (at 1.23 V_RHE) for PEC hydrogen production, resulting from the enhanced light-harvesting capability arising from the narrow band-gap of the PbS QDs. Moreover, the introduction of a ZnS overlayer on the BiVO₄/PbS QDs further improved the photocurrent to 5.19 mA/cm², attributed to the reduction in interfacial charge recombination. Full article

Carbon-protected BiVO₄ photoanode and Cu₂O photocathode tandem photoelectrochemical (PEC) system has been explored to reduce surface recombination and enhance the stability of the photoelectrodes. In addition to the carbon layer, the electrodeposited FeOOH nanolayer and drop-casted MoS₂ co-catalyst layer on the photoanode and photocathode, respectively improve the reaction kinetics. The optimized photoanode (Mo-BiVO₄/C/FeOOH) and photocathode (Cu₂O/C/MoS₂) produces current densities of ~1.22 mA cm⁻² at 1.23 V vs. RHE and ~−1.48 mA cm⁻² at 0 V vs. RHE, respectively. The obtained photocurrent is higher than bare photoelectrodes without a carbon layer. Finally, a tandem cell has been constructed, and an unassisted current density of ~0.107 mA cm⁻² is obtained for a carbon-protected BiVO₄–Cu₂O tandem PEC cell at zero bias. The improved stability and enhanced photocurrent of the carbon protective layer are attributed to its better charge transfer resistance and minimized surface defects. Carbon protective layer can be a viable option to improve the stability of photoelectrodes in aqueous media. Full article

A dual-mode lab-on-paper device based on BiVO₄/FeOOH nanocomposites as an efficient generating photoelectrochemical (PEC)/colorimetric signal reporter has been successfully constructed by integration of the lab-on-paper sensing platform and PEC/colorimetric detection technologies for sensitive detection of carcinoembryonic antigen (CEA). Concretely, the BiVO₄/FeOOH nanocomposites were in situ synthesized onto the paper-working electrode (PWE) through hydrothermal synthesis of the BiVO₄ layer on cellulose fibers (paper-based BiVO₄) which were initially modified by Au nanoparticles for improving the conductivity of three dimensional PWE, and then the photo-electrodeposition of FeOOH onto the paper-based BiVO₄ to construct the paper-based BiVO₄/FeOOH for the portable dual-mode lab-on-paper device. The obtained nanocomposites with an FeOOH needle-like structure deposited on the BiVO₄ layer exhibits enhanced PEC response activity due to its effective separation of the electron–hole pair which could further accelerate the PEC conversion efficiency during the sensing process. With the introduction of CEA targets onto the surface of nanocomposite-modified PWE assisted by the interaction with the CEA antibody from a specific recognition property, a signal-off PEC signal state with a remarkable photocurrent response decreasing trend can be achieved, realizing the quantitative detection of CEA with the PEC signal readout mode. By means of a smart origami paper folding, the colorimetric signal readout is achieved by catalyzing 3,3′,5,5′-tetramethylbenzidine (TMB) to generate blue oxidized TMB in the presence of H₂O₂ due to the satisfied enzyme-like catalytic activity of the needle-like structure, FeOOH, thereby achieving the dual-mode signal readout system for the proposed lab-on-paper device. Under the optimal conditions, the PEC and colorimetric signals measurement were effectively carried out, and the corresponding linear ranges were 0.001–200 ng·mL⁻¹ and 0.5–100 ng·mL⁻¹ separately, with the limit of detection of 0.0008 and 0.013 ng·mL⁻¹ for each dual-mode. The prepared lab-on-paper device also presented a successful application in serum samples for the detection of CEA, providing a potential pathway for the sensitive detection of target biomarkers in clinical application. Full article

In this study, 20Li₂O-60V₂O₅-(20 − x)B₂O₃-xBi₂O₃ (x = 5, 7.5, 10 mol%) glass materials have been prepared by the melt-quenching method, and the structure and morphology of the glass materials have been characterized by XRD, FTIR, Raman, and FE-SEM. The results show that the disordered network of the glass is mainly composed of structural motifs, such as VO₄, BO₃, BiO_3, and BiO₆. The electrochemical properties of the glass cathode material have been investigated by the galvanostatic charge-discharge method and cyclic voltammetry, and the results show that with the increases of Bi₂O₃ molar content, the amount of the VO₄ group increases, and the network structure of the glass becomes more stable. To further enhance the electrochemical properties, glass-ceramic materials have been obtained by heat treatment, and the effect of the heat treatment temperature on the structure and electrochemical properties of the glass has been studied. The results show that the initial discharge capacity of the glass-ceramic cathode obtained by heat treatment at 280 °C at a current density of 50 mA·g⁻¹ is 333.4 mAh·g⁻¹. In addition, after several cycles of charging and discharging at a high current density of 1000 mA·g⁻¹ and then 10 cycles at 50 mA·g⁻¹, its discharge capacity remains at approximately 300 mAh·g⁻¹ with a capacity retention rate of approximately 90.0%. The results indicate that a proper heat treatment temperature is crucial to improving the electrochemical properties of glass materials. This study provides an approach for the development of new glass cathode materials for lithium-ion batteries. Full article

Thin films of BiFeO₃, VO₂, and BiFeO₃/VO₂ were grown on SrTiO₃(100) and Al₂O₃(0001) monocrystalline substrates using radio frequency and direct current sputtering techniques. To observe the effect of the coupling between these materials, the surface of the films was characterized by profilometry, atomic force microscopy, and X-ray photoelectron spectroscopy. The heterostructures, monolayers, and bilayers based on BiFeO₃ and VO₂ grew with good adhesion and without delamination or signs of incompatibility between the layers. A good granular arrangement and RMS roughness between 1 and 5 nm for the individual layers (VO₂ and BiFeO₃) and between 6 and 18 nm for the bilayers (BiFeO₃/VO₂) were observed. Their grain size is between 20 nm and 26 nm for the individual layers and between 63 nm and 67 nm for the bilayers. X-ray photoelectron spectroscopy measurements show a higher proportion of V⁴⁺, Bi³⁺, and Fe³⁺ in the films obtained. The homogeneous ordering, low roughness, and oxidation states on the obtained surface show a good coupling in these films. The I-V curves show ohmic behavior at room temperature and change with increasing temperature. The effect of coupling these materials in a thin film shows the appearance of hysteresis cycles, I-V and R-T, which is typical of materials with high potential in applications, such as resistive memories and solar cells. Full article

Novel vitamin E chelate siderophore derivatives and their V^V and Fe^III complexes have been synthesised and the chemical and biological properties have been evaluated. In particular, the α- and δ-tocopherol derivatives with bis-methyldroxylamino triazine (α-tocTHMA) and (δ-tocDPA) as well their V^V complexes, [V₂^VO₃(α-tocTHMA)₂] and [V₂^IVO₃(δ-tocTHMA)₂], have been synthesised and characterised by infrared (IR), nuclear magnetic resonance (NMR), electron paramagnetic resonance (EPR) and ultra violet-visible (UV-Vis) spectroscopies. The dimeric vanadium complexes in solution are in equilibrium with their respefrctive monomers, H₂O + [V₂^VO₂(μ-O)]⁴⁺ = 2 [V^VO(OH)]²⁺. The two amphiphilic vanadium complexes exhibit enhanced hydrolytic stability. EPR shows that the complexes in lipophilic matrix are mild radical initiators. Evaluation of their biological activity shows that the compounds do not exhibit any significant cytotoxicity to cells. Full article

The review describes articles that provide data on the synthesis and study of the properties of catalysts for the oxidation of alkanes, olefins, and alcohols. These catalysts are polynuclear complexes of iron, copper, osmium, nickel, manganese, cobalt, vanadium. Such complexes for example are: [Fe₂(HPTB)(m-OH)(NO₃)₂](NO₃)₂·CH₃OH·2H₂O, where HPTB-¼N,N,N0,N0-tetrakis(2-benzimidazolylmethyl)-2-hydroxo-1,3-diaminopropane; complex [(PhSiO_1,5)₆]₂[CuO]₄[NaO_0.5]₄[dppmO₂]₂, where dppm-1,1-bis(diphenylphosphino)methane; (2,3-η-1,4-diphenylbut-2-en-1,4-dione)undecacarbonyl triangulotriosmium; phenylsilsesquioxane [(PhSiO_1.5)₁₀(CoO)₅(NaOH)]; bi- and tri-nuclear oxidovanadium(V) complexes [{VO(OEt)(EtOH)}₂(L²)] and [{VO(OMe)(H₂O)}₃(L³)]·2H₂O (L² = bis(2-hydroxybenzylidene)terephthalohydrazide and L³ = tris(2-hydroxybenzylidene)benzene-1,3,5-tricarbohydrazide); [Mn₂L2O3][PF6]2 (L = 1,4,7-trimethyl-1,4,7-triazacyclononane). For comparison, articles are introduced describing catalysts for the oxidation of alkanes and alcohols with peroxides, which are simple metal salts or mononuclear metal complexes. In many cases, polynuclear complexes exhibit higher activity compared to mononuclear complexes and exhibit increased regioselectivity, for example, in the oxidation of linear alkanes. The review contains a description of some of the mechanisms of catalytic reactions. Additionally presented are articles comparing the rates of oxidation of solvents and substrates under oxidizing conditions for various catalyst structures, which allows researchers to conclude about the nature of the oxidizing species. This review is focused on recent works, as well as review articles and own original studies of the authors. Full article