Oxynitride photocatalysts hold promise for renewable solar hydrogen production via water splitting owing to their intense visible light absorption. Cocatalyst loading is essential for activation of such oxynitride photocatalysts. However, cocatalyst nanoparticles form aggregates and exhibit weak interaction with photocatalysts, which prevents eliciting their intrinsic photocatalytic performance. Here, we demonstrate efficient utilization of photoexcited electrons in a single-crystalline particulate BaTaON photocatalyst prepared with the assistance of RbCl flux for H evolution reactions via sequential decoration of Pt cocatalyst by impregnation-reduction followed by site-selective photodeposition. The Pt-loaded BaTaON photocatalyst evolves H over 100 times more efficiently than before, with an apparent quantum yield of 6.8% at the wavelength of 420 nm, from a methanol aqueous solution, and a solar-to-hydrogen energy conversion efficiency of 0.24% in Z-scheme water splitting. Enabling uniform dispersion and intimate contact of cocatalyst nanoparticles on single-crystalline narrow-bandgap particulate photocatalysts is a key to efficient solar-to-chemical energy conversion.
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http://dx.doi.org/10.1038/s41467-021-21284-3 | DOI Listing |
J Am Chem Soc
January 2025
Department of Chemistry, The University of Hong Kong, Hong Kong Island 000000, Hong Kong SAR, China.
Methanol (ME) is a liquid hydrogen carrier, ideal for on-site-on-demand H generation, avoiding its costly and risky distribution issues, but this "ME-to-H" electric conversion suffers from high voltage (energy consumption) and competitive oxygen evolution reaction. Herein, we demonstrate that a synergistic cofunctional PtPd/(Ni,Co)(OH) catalyst with Pt single atoms (Pt) and Pd nanoclusters (Pd) anchored on OH-vacancy(V)-rich (Ni,Co)(OH) nanoparticles create synergistic triadic active sites, allowing for methanol-enhanced low-voltage H generation. For MOR, OH* is preferentially adsorbed on Pd and then interacts with the intermediates (such as *CHO or *CHOOH) adsorbed favorably on neighboring Pt with the assistance of hydrogen bonding from the surface hydrogen of (Ni,Co)(OH).
View Article and Find Full Text PDFInorg Chem
January 2025
School of Chemistry and Chemical Engineering, School of Pharmacy, Jiangsu University, Zhenjiang 212013, P. R. China.
Electrochemical water splitting is a promising method for the generation of "green hydrogen", a renewable and sustainable energy source. However, the complex, multistep synthesis processes, often involving hazardous or expensive chemicals, limit its broader adoption. Herein, a nitrate (NO) anion-intercalated nickel-iron-cerium mixed-metal (oxy)hydroxide heterostructure electrocatalyst is fabricated on nickel foam (NiFeCeOH@NF) via a simple electrodeposition method followed by cyclic voltammetry activation to enhance its surface properties.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
School of Materials Science and Engineering, CNPC-CZU Innovation Alliance, Key Laboratory of Materials Surface Science and Technology of Jiangsu Province Higher Education Institutes, Changzhou University, Changzhou, 213164, Jiangsu, China.
Herein, NiFeP/TiC@NF was synthesized from a hydrothermal process and chemical conversion, and exhibited a low overpotential of 177 mV at = 50 mA cm, a low Tafel slope of 56 mV dec, and a very competitive stable activity in alkaline electrolyte, proposing a strategy for efficient OER and overall water splitting.
View Article and Find Full Text PDFRSC Adv
January 2025
School of Electronic Engineering, Guangxi Key Laboratory of Multidimensional Information Fusion for Intelligent Vehicles, Guangxi University of Science and Technology Liuzhou 545000 China
This study presents a novel approach to enhance photoelectrochemical (PEC) water oxidation by integrating cobalt phthalocyanine (CoPc) with bismuth vanadate (BVO) a direct solvothermal method. The as-prepared BVO@CoPc photoanode demonstrated a photocurrent density of 4.0 mA cm at 1.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
National Center for International Research on Photoelectric and Energy Materials, Yunnan Key Laboratory for Micro/Nano Materials & Technology, School of Materials and Energy, Yunnan University, Kunming 650091 China; Southwest United Graduate School, Kunming 650091 China. Electronic address:
Heterojunction materials for photocatalytic overall water splitting (POWS) become popular in recent times. However, even in the superior S-scheme heterojunction, the two semiconductor materials still do not have an efficient activity to separate and migrate photogenerated carriers. To further improve the charge separation and enhance the activity of POWS, a novel S-scheme heterojunction photocatalyst, Cu/ZnInS-V/TiO-V, was synthesized using solvothermal and calcination methods.
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