98%
921
2 minutes
20
Artificial manipulation of charge separation and transfer are central issues dominating hydrogen evolution reaction triggered via photocatalysis. Herein, through elaborate designing on the architecture, band alignment, and interface bonding mode, a sulfur vacancy-rich ZnInS-based (Vs-ZIS) multivariate heterostructure ZnInS/MoSe/InSe (Vs-ZIS/MoSe/InSe) with specific Janus Z-scheme charge transfer mechanism is constructed through a two-step hydrothermal process. Steering by the Janus Z-scheme charge transfer mechanism, photogenerated electrons in the conduction band of MoSe transfer synchronously to the valence band of Vs-ZIS and InSe, resulting in abundant highly-active photogenerated electrons reserved in the conduction band of Vs-ZIS and InSe, therefore significantly enhancing the photocatalytic activity of hydrogen evolution. Under visible light irradiation, the optimized Vs-ZIS/MoSe/InSe with the mass ratio of MoSe and InSe to ZnInS at 3 % and 30 %, respectively, performs a high hydrogen evolution rate of 124.42 mmol·g·h, about 43.5-folds of the original ZIS photocatalyst. Besides, an apparent quantum efficiency (AQE) of 22.5 % at 420 nm and favorable durability are also achieved over Vs-ZIS/MoSe/InSe photocatalyst. This work represents an important development in efficient photocatalysts and donates a sound foundation for the design of regulating charge transfer pathways.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.jcis.2023.03.199 | DOI Listing |
Chem Rec
September 2025
Interdisciplinary Research Center for Hydrogen Technologies and Carbon Management (IRC-HTCM), King Fahd University of Petroleum & Minerals, KFUPM Box 5040, Dhahran, 31261, Saudi Arabia.
The synthesis of biomass-derived nanocarbons via ball milling has emerged as an innovative, sustainable, and cost-effective strategy in the field of nanotechnology. This review comprehensively explores the principles, mechanisms, and process parameters that influence the production of high-quality nanocarbons from biomass using ball milling. This process efficiently transforms biomass residues into nanoscale carbon, including graphene, carbon nanotubes, and nanofibers, with tunable physicochemical properties tailored for advanced applications.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Confucius Energy Storage Lab, School of Energy and Environment & Z Energy Storage Center, Southeast University, Nanjing 211189, China.
Developing efficient and durable catalysts for the oxygen evolution reaction (OER) in acidic media is essential for advancing proton exchange membrane water electrolysis (PEMWE). However, catalyst instability caused by lattice oxygen (O) depletion and metal dissolution remains a critical barrier. Here, we propose an oxophilic-site-mediated dynamic oxygen replenishment mechanism (DORM), in which O actively participates in O-O bond formation and is continuously refilled by water-derived species.
View Article and Find Full Text PDFNanoscale Adv
August 2025
School of Electronic Science, Odisha University of Technology and Research Bhubaneswar India.
A novel electrocatalyst, zirconium ferrite nanoparticles (NPs) (ZrFeO NPs), was synthesized through coprecipitation and calcination processes at 300 °C and 500 °C using iron rust. The ZrFeO NPs were used as catalysts for the hydrogen evolution reaction. Furthermore, these NPs in an alkaline medium exhibited superior properties of a fractional order supercapacitor, based on which a prototype device was fabricated to demonstrate its energy storage applications.
View Article and Find Full Text PDFChem Sci
September 2025
Tianjin Key Laboratory of Micro-scale Optical Information Science and Technology, Institute of Modern Optics and Centre of Single-Molecule Science, Nankai University Tianjin 300350 China
The keto-enol tautomerism, involving a reversible isomerization of the molecule, plays a critical role in organic synthesis, biological activity, and molecular-scale charge transport. It is therefore essential to manipulate the process of keto-enol tautomerism. Unlike typical ketones, β-diketones exist dominantly in the enol form and it is a great challenge to realize enol-keto tautomerism due to the formation of intramolecular hydrogen bonds in the enol form.
View Article and Find Full Text PDFElectrochem Energ Rev
September 2025
Institute of New Energy Materials and Engineering, College of Materials Science and Engineering, Fuzhou University, Fuzhou, 350108 Fujian China.
Unlabelled: Proton exchange membrane water electrolyzers (PEMWEs) are a promising technology for large-scale hydrogen production, yet their industrial deployment is hindered by the harsh acidic conditions and sluggish oxygen evolution reaction (OER) kinetics. This review provides a comprehensive analysis of recent advances in iridium-based electrocatalysts (IBEs), emphasizing novel optimization strategies to enhance both catalytic activity and durability. Specifically, we critically examine the mechanistic insights into OER under acidic conditions, revealing key degradation pathways of Ir species.
View Article and Find Full Text PDF