With growing environmental concerns and the need for sustainable energy, multifunctional materials that can simultaneously address water treatment and clean energy production are in high demand. In this study, we developed a cost-effective method to synthesize zinc oxide (ZnO) nanowires via the anodic oxidation of zinc foil. By carefully controlling the anodization time, we optimized the Zn/ZnO-5 min electrode to achieve impressive dual-function performance in terms of effective photoelectrocatalysis for water splitting and waste water treatment. The electrode exhibited a high photocurrent density of 1.18 mA/cm2 at 1.23 V vs. RHE and achieved a solar-to-hydrogen conversion efficiency of 0.55%. A key factor behind this performance is the presence of surface defects, such as oxygen vacancies (OVs), which enhanced charge separation and boosted electron transport. In tests for waste water treatment, the Zn/ZnO-5 min electrode demonstrated the highly efficient degradation of methylene blue (MB) dye, with a reaction rate constant of 0.4211 min−1 when exposed to light and a 1.0 V applied voltage significantly faster than using light or voltage alone. Electrochemical analyses, including impedance spectroscopy and voltammetry, further confirmed the superior charge transfer properties of the electrode under illumination, making it an excellent candidate for both energy conversion and pollutant removal. This study highlights the potential of using simple anodic oxidation to produce scalable and efficient ZnO-based photocatalysts. The dual-function capability of this material could pave the way for large-scale applications in renewable hydrogen production and advanced waste water treatment, offering a promising solution to some of today’s most pressing environmental and energy challenges.

Energy generation today heavily relies on the field of photocatalysis, with many conventional energy generation strategies now superseded by the conversion of solar energy into chemical or thermal energy for a variety of energy-related applications. Global warming has pointed to the urgent necessity of moving away from non-renewable energy sources, with a resulting emphasis on creating the best photocatalysts for effective solar conversion by investigating a variety of material systems and material combinations. The present study explores the influence of morphological changes on the photoelectrochemical activity of zinc oxide nanostructures by exploiting electrodeposition and capping agents to control the growth rates of different ZnO facets and obtain well-defined nanostructures and orientations. A zinc nitrate (Zn (NO₃)₂) bath was used to electrodeposit ZnO nanostructures on an indium tin oxide glass (ITO) substrate at 70 °C with an applied potential of −1.0 V. Ethylenediamine (EDA) or ammonium fluoride (NH₄F) were added as capping agents to the zinc nitrate bath. Extensive evaluation and characterization of the photoelectrochemical (PEC) capabilities of the resulting morphology-controlled zinc oxide nanostructures confirmed that altering the ZnO morphology can have positive impacts on PEC properties.

Energy generation now heavily relies on the field of photocatalysis. Many conventional research topics have been superseded by the conversion of solar energy into chemical or thermal energy for a variety of energy-related applications. The urgent necessity of moving away from non-renewable energy sources is a result of the problem of global warming. In an effort to create the best photocatalysts for effective solar conversion, scientists are investigating a variety of material systems and material combinations. By examining the influence of morphology changes on the photoelectrochemical activity of zinc oxide nanostructures, here electrodeposition was used to create the nanostructures. By using the proper capping agents, it is possible to control the growth rates of different ZnO facets and get well-defined nanostructures and orientation. In order to generate distinct ZnO morphologies, we report here the electrodeposition of ZnO nanostructured thin films in the presence of different capping agents. A zinc nitrate (Zn (NO₃)₂) bath was used to electrodeposit ZnO nanostructures on indium tin oxide glass (ITO) substrate at 70 °C with an applied potential of -1.0 V. Capping agents such as ethylenediamine (EDA) or ammonium fluoride (NH₄F) were added to this zinc nitrate bath. The photoelectrochemical capabilities of the morphology-controlled zinc oxide nanostructures were extensively evaluated and characterised. Thus various ZnO morphologies had an impact on the PEC properties.

The increasing global demand for energy and the environmental impact of greenhouse gas emissions have intensified interest in efficient catalytic processes for methane reforming. This study explores the dry reforming of methane (DRM), a reaction that utilizes methane (CH₄) and carbon dioxide (CO₂) to produce synthesis gas (H₂ and CO). A nanostructured catalyst featuring a Ni@Co core–shell architecture supported on ZnO–ZrO₂ was synthesized using a multi-step process involving hydrothermal treatment, metal impregnation, calcination, and hydrogen reduction. The choice of nickel and cobalt aimed to leverage potential synergistic effects, while ZnO and ZrO₂ served as thermally stable, high-surface-area supports to promote dispersion and structural durability. The catalyst was characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), and thermogravimetric analysis (TGA), confirming the successful formation of the intended structure. SEM images revealed well-dispersed nanoparticles, while TGA indicated good thermal stability under elevated temperatures. These findings demonstrate that the Ni@Co/ZnO–ZrO₂ catalyst is a viable platform for DRM, with promising structural and thermal properties that support further investigation into its long-term performance and potential applications in syngas production.