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Sensitization of a wide-gap oxide semiconductor with a visible-light-absorbing dye has been studied for decades as a means of producing H from water. However, efficient overall water splitting using a dye-sensitized oxide photocatalyst has remained an unmet challenge. Here we demonstrate visible-light-driven overall water splitting into H and O using HCaNbO nanosheets sensitized by a Ru(II) tris-diimine type photosensitizer, in combination with a WO-based water oxidation photocatalyst and a triiodide/iodide redox couple. With the use of Pt-intercalated HCaNbO nanosheets further modified with amorphous AlO clusters as the H evolution component, the dye-based turnover number and frequency for H evolution reached 4580 and 1960 h, respectively. The apparent quantum yield for overall water splitting using 420 nm light was 2.4%, by far the highest among dye-sensitized overall water splitting systems reported to date. The present work clearly shows that a carefully designed dye/oxide hybrid has great potential for photocatalytic H production, and represents a significant leap forward in the development of solar-driven water splitting systems.
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http://dx.doi.org/10.1021/jacs.0c02053 | DOI Listing |
Electrophoresis
September 2025
School of Mechanical Engineering, Jiangsu Key Laboratory for Design and Manufacturing of Precision Medicine Equipment, Southeast University, Nanjing, China.
Electric droplet sorting is widely applied in the screening of target molecules, cells, drugs, and microparticles. Previous studies have made several optimizations on the electrode materials, structures, and arrangements. However, voltages of over 1 kV are required to realize droplet sorting, which causes the undesired droplet splitting.
View Article and Find Full Text PDFChemphyschem
September 2025
School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, China.
Excessive fossil fuel combustion has accelerated renewable energy development, with hydrogen energy emerging as a promising alternative due to its high energy density and environmental compatibility. Photocatalytic hydrogen production through solar energy conversion represents a viable approach for sustainable development. Metal-organic frameworks (MOFs) have garnered significant research interest owing to their structural tunability, well-defined catalytic sites, and post-synthetic modification capabilities.
View Article and Find Full Text PDFNano Lett
September 2025
School of Physical Science and Technology, Lanzhou University, Lanzhou 730000, China.
Multijunction photoelectrodes, which generate active photocarriers with sufficient energy to drive unassisted solar-fuel conversion, represent a promising avenue for sustainable energy applications. However, achieving controllable p/n-type doping and high-quality growth remains a challenge for most emerging metal oxide semiconductors. In this study, we demonstrate the creation of in-plane ferroelectric p/n homojunction superstructures in BiFeO (BFO) films, enabling bias-free photoelectrochemical (PEC) reactions.
View Article and Find Full Text PDFEcotoxicol Environ Saf
September 2025
Key Laboratory of Groundwater Resources and Environment, Ministry of Education, Jilin Provincial Key Laboratory of Water Resources and Environment, College of New Energy and Environment, Jilin University, Changchun 130012, China.
Liquid crystal monomers (LCMs) have emerged as novel endocrine disrupting chemicals that affect the growth, development, and metabolism of organisms by binding to nuclear hormone receptors (NHRs). However, the studies on the impact of LCMs' molecular features on their binding affinities remain limited. In this study, considering the challenge of activity cliffs in linear quantitative structure-activity relationship modeling, a multidimensional feature fusion model was developed to predict the binding affinities of 1173 LCMs to 15 NHRs.
View Article and Find Full Text PDFNano Lett
September 2025
Key Laboratory of Automobile Materials (Jilin University), Ministry of Education, and School of Materials Science and Engineering, Jilin University, Changchun 130022, China.
Developing highly active and stable nonprecious electrocatalysts toward sluggish alkaline oxygen evolution reaction (OER) is essential for large-scale green hydrogen production via electrochemical water splitting. Here we report phase and surface co-reconstruction of S-doped (NiCo)WC nanoparticles into (NiCo)C with amorphous electroactive NiCoOOH layer for highly efficient alkaline OER by W dissolution and NiCo surface oxidation. The W dissolution results in the formation of Brønsted base WO ions, which electrostatically accumulate around electrode to promote water dissociation into abundant OH* intermediates, in situ constructing a locally strong alkaline microenvironment to facilitate OH* adsorption on NiCoOOH sites and trigger lattice-oxygen oxidation path.
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