光催化
纳米片
催化作用
氟
材料科学
铂金
化学工程
反应性(心理学)
金属
纳米技术
化学
冶金
有机化学
工程类
医学
替代医学
病理
作者
Si‐Ming Wu,Imgon Hwang,Benedict Osuagwu,Johannes Will,Zhenni Wu,Bidyut Bikash Sarma,Fu‐Fei Pu,Liying Wang,Zdeňěk Baďura,Giorgio Zoppellaro,Erdmann Spiecker,Patrik Schmuki
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2022-12-09
卷期号:13 (1): 33-41
被引量:38
标识
DOI:10.1021/acscatal.2c04481
摘要
Trapping sites in single atom (SA) catalysts are critical to the stabilization and reactivity of isolated atoms. Herein, we show that anchoring of Pt SAs on TiO2 nanosheets is strongly aided by lattice incorporated fluorine species. Tailoring the speciation of fluorine on TiO2 nanosheets is a key factor for uniform and stable dispersion of the Pt SAs and high efficiency in Pt SA co-catalyzed photocatalytic H2 production. Fluorine-stabilized uniformly dispersed Pt SAs on the (001) surface of TiO2 can provide a remarkable photocatalytic activity (a H2 production rate of 45.3 mmol h–1 mg–1 Pt for 65 mW/cm2 365 nm light). This high (maximized) efficiency can be achieved with a remarkably low loading amount of Pt SAs on TiO2 nanosheets (0.03 wt %), which is far superior to Pt nanoparticles on a TiO2 nanosheet with the same or a higher loading amount. F-stabilized Pt SAs on TiO2 nanosheets also exhibit an excellent stability in long-term photocatalytic reactions.
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