In this study, a TiO₂/(MA)₂SnCl₄ nanocomposite film was synthesized using a sustainable, sunlight-driven approach, demonstrating enhanced photocatalytic performance for environmental remediation. TiO₂ nanoparticles (TiO₂-NPs) were dispersed in ethanol and mixed with a methylammonium (MA) and SnCl₂ precursor solution, followed by drop-casting onto a glass substrate and exposure to direct sunlight for 2 h. Sunlight served as an energy source, facilitating in situ structural modifications and leading to the formation of a well-integrated TiO₂/(MA)₂SnCl₄ hybrid structure, where TiO₂ was effectively encapsulated. Characterization revealed a band gap reduction from 3.1 eV (TiO₂-NPs) to 2.6 eV in the nanocomposite, extending light absorption into the visible range. The formation of Sn–O–Ti interactions enhanced charge separation, minimized electron–hole recombination, and improved charge carrier dynamics. Photocatalytic degradation tests using methylene blue (MB) under sunlight showed that the nanocomposite film achieved 90% MB degradation within 60 min, outperforming TiO₂-NPs, which achieved only 75% degradation. The presence of oxygen vacancies (OVs) generated during sunlight exposure further enhanced photocatalytic efficiency by acting as charge traps and reaction sites. This study introduces a green synthesis strategy leveraging sunlight as a renewable energy source, marking the first integration of (MA)₂SnCl₄ with TiO₂-NPs for enhanced photocatalysis. The synergistic effects of extended visible-light absorption, defect engineering, and efficient charge separation make TiO₂/(MA)₂SnCl₄ nanocomposite films a scalable, cost-effective solution for water purification applications, offering a promising solar-driven approach to addressing global water contamination challenges.

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.

Magnetic nanomaterials (MNMs), particularly magnetically recoverable systems with efficient regeneration capability, have emerged as highly efficient nanoadsorbents for water purification owing to their high surface area, tunable surface chemistry, and facile magnetic separation. This review critically analyzes recent advances (2022–2025) in the multi-cycle use of MNMs, with particular emphasis on regeneration strategies. The major syn-thesis approaches and adsorption mechanisms are discussed in relation to their influence on long-term stability. Recent studies demonstrate that many MNMs retain 85–90% of their removal efficiency over 3–6 cycles, although performance degradation due to aggregation, leaching, and surface passivation remains a key challenge. Regeneration techniques, including chemical, solvent-based, and thermal methods, are evaluated in terms of efficiency and feasibility. Moreover, bibliometric analysis reveals the increasing research focus on recyclable nanomaterial design. Overall, this review elucidates the structure–performance–stability relationships governing multi-cycle operation, with a particular focus on reusable and magnetically separable systems and provides insights into the economic feasibility of regenerable MNMs along with future perspectives for sustainable and scalable water treatment applications.

Nanomaterials have emerged as key platforms for environmental remediation owing to their tunable surface chemistry, high specific surface area, and multifunctional physicochemical properties. This review provides a critical comparison between conventional nanomaterials (CNMs) and phyto-mediated nanomaterials (PMNs), with particular emphasis on material design, surface chemistry, pollutant removal mechanisms, environmental performance, and sustainability. CNMs, including metal and metal oxide nanoparticles, carbon-based nanomaterials, and hybrid nanocomposites, offer excellent adsorption, photocatalytic, redox, and antimicrobial performance but remain constrained by concerns regarding toxicity, environmental persistence, and energy-intensive synthesis. PMNs provide a greener alternative by integrating plant-derived surface chemistry with nanomaterial functionality, potentially reducing reliance on hazardous synthesis reagents while modifying interfacial interactions relevant to environmental remediation. The review critically discusses the mechanistic roles of adsorption, surface complexation, photocatalytic degradation, electron-transfer processes, and reactive oxygen species (ROS) generation in pollutant removal. Recent advances in water purification, soil and groundwater remediation, carbon sequestration, and climate-related environmental applications are comprehensively summarized. Finally, current challenges associated with reproducibility, scalability, environmental safety, life-cycle assessment, and regulatory considerations are critically analyzed, together with future perspectives toward the rational design of sustainable nanomaterials for next-generation environmental remediation technologies.

The global transition toward sustainable energy systems has intensified interest in renewable hydrogen as a key pathway for reducing greenhouse gas emissions and decarbonizing hard-to-abate sectors. This review critically examines major renewable hydrogen production routes, including alkaline water electrolysis (AWE), proton exchange membrane (PEM) electrolysis, solid oxide electrolysis cells (SOEC), biomass-based conversion, photoelectrochemical water splitting, and biological processes. Particular emphasis is placed on recent advances in catalytic and electrocatalytic materials and their influence on hydrogen-production efficiency, durability, operating flexibility, cost, and scalability. Noble-metal and non-noble-metal catalyst systems, electrode materials, and emerging catalytic strategies are discussed in relation to their suitability for different hydrogen-production technologies and renewable-energy operating conditions. The review further compares the major production pathways in terms of technological maturity, system efficiency, scalability, and compatibility with intermittent renewable energy. Key limitations associated with catalyst degradation, critical-material dependence, hydrogen storage, infrastructure development, and system integration are critically assessed. Current research gaps include the need for more durable and earth-abundant catalysts, improved long-term performance under realistic operating conditions, and stronger integration between materials development and system-level techno-economic requirements. Overall, this review highlights the importance of linking catalytic innovation with electrolyzer design, renewable-energy integration, infrastructure readiness, and sustainability considerations to enable economically viable and scalable renewable hydrogen production.

Sunlight-assisted plant-mediated synthesis of silver nanoparticles (AgNPs) is well established, yet the complementary use of fluorescence spectroscopy to examine the optical response of complex phytochemical-containing media remains of interest. Here, Cucurbita pepo peel extract (CPE) was used for rapid AgNP formation under natural sunlight using single-step (A-Sun) and dropwise (B-Sun) addition strategies. The characteristic localized surface plasmon resonance (LSPR) band developed near 445–450 nm within 5 min, while corresponding dark controls showed negligible nanoparticle formation over the same period. Both dispersions retained their characteristic LSPR response during six months of optical monitoring. Steady-state photoluminescence (PL) measurements at excitation wavelengths of 300–350 nm and excitation–emission matrix (EEM) fluorescence mapping revealed lower recorded fluorescence intensities in the order CPE > A-Sun > B-Sun, with the principal emission region remaining broadly preserved near 435–440 nm. These observations provide complementary fluorescence fingerprints of the investigated preparations; however, inner-filter effects and light scattering may contribute to the measured attenuation, preventing its exclusive assignment to molecular quenching. FTIR revealed changes in oxygen-containing functional-group vibrations, while TEM showed predominantly spherical to quasi-spherical AgNPs, with mean particle diameters of 11.88 ± 3.60 nm for A-Sun and 9.77 ± 3.43 nm for B-Sun. The resulting dispersions also exhibited antibacterial activity against the six investigated bacterial strains. Overall, integrating PL and EEM with conventional characterization provides additional information on fluorescence changes accompanying sunlight-assisted AgNP formation without directly establishing the individual phytochemical reducing species, electron-transfer steps, or molecular surface-capping mechanisms.