| 1. |
- An, Xiaoqiang, et al.
(författare)
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Sodium-Directed Photon-Induced Assembly Strategy for Preparing Multisite Catalysts with High Atomic Utilization Efficiency
- 2023
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Ingår i: Journal of the American Chemical Society. - : AMER CHEMICAL SOC. - 0002-7863 .- 1520-5126. ; 145:3, s. 1759-1768
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Tidskriftsartikel (refereegranskat)abstract
- Integrating different reaction sites offers new prospects to address the difficulties in single-atom catalysis, but the precise regulation of active sites at the atomic level remains challenging. Here, we demonstrate a sodium-directed photon-induced assembly (SPA) strategy for boosting the atomic utilization efficiency of single-atom catalysts (SACs) by constructing multifarious Au sites on TiO2 substrate. Na+ was employed as the crucial cement to direct Au single atoms onto TiO2, while the light-induced electron transfer from excited TiO2 to Au(Na+) ensembles contributed to the self-assembly formation of Au nanoclusters. The synergism between plasmonic near-field and Schottky junction enabled the cascade electron transfer for charge separation, which was further enhanced by oxygen vacancies in TiO2. Our dual-site photocatalysts exhibited a nearly 2 orders of magnitude improvement in the hydrogen evolution activity under simulated solar light, with a striking turnover frequency (TOF) value of 1533 h(-1) that exceeded other Au/TiO2-based photocatalysts reported. Our SPA strategy can be easily extended to prepare a wide range of metal-coupled nanostructures with enhanced performance for diverse catalytic reactions. Thus, this study provides a well-defined platform to extend the boundaries of SACs for multisite catalysis through harnessing metal-support interactions.
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| 2. |
- Man, Zhang, et al.
(författare)
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Facile one-step synthesis and enhanced photocatalytic activity of WC/ferroelectric nanocomposite
- 2021
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Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry. - 2050-7488 .- 2050-7496. ; 9:40, s. 22861-22870
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Tidskriftsartikel (refereegranskat)abstract
- The development of noble-metal-free co-catalysts is seen as a viable strategy for improving the performance of semiconductor photocatalysts. Although the photocatalytic efficiency of ferroelectrics is typically low, it can be enhanced through the incorporation of a co-catalyst into nanocomposites. Here, we demonstrate the influence of ferroelectricity on the decolorization of rhodamine B under simulated solar light using RbBi2Ti2NbO10 and compared the performance with that of non-ferroelectric RbBi2Nb5O16. The decolorization rate for RbBi2Ti2NbO10 was 5 times greater than that of RbBi2Nb5O16. This behaviour can be explained in terms of ferroelectric polarization, which drives the separation of charge carriers. The photocatalytic activity of RbBi2Ti2NbO10 was further enhanced to over 30 times upon preparing a nanocomposite with tungsten carbide (WC) through high energy ball milling. This enhancement was attributed not only to the increased specific surface area, but also to the incorporated WC co-catalyst, which also serves as a source of plasmonic hot electrons and extends the photocatalytic activity into the visible light range. The WC/RbBi2Ti2NbO10 nanocomposite shows interesting water oxidation properties and evolves O-2 with a rate of 68.5 mu mol h(-1) g(-1) and a quantum yield of 3% at 420 nm. This work demonstrates a simple route for preparing WC containing nano-ferroelectric composites for solar energy conversion applications.
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