光催化
光电效应
锐钛矿
焊剂(冶金)
材料科学
Atom(片上系统)
反应速率
光化学
原子物理学
化学
光电子学
催化作用
物理
嵌入式系统
冶金
生物化学
计算机科学
作者
Shanshan Qin,Johannes Will,Hyesung Kim,Nikita Denisov,Simon Carl,Erdmann Spiecker,Patrik Schmuki
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-01-30
卷期号:8 (2): 1209-1214
被引量:26
标识
DOI:10.1021/acsenergylett.2c02801
摘要
We disperse Pt single atoms (SAs) with different loading densities on anatase TiO2 thin films and evaluate the photocatalytic H2 generation as a function of the incident light intensity. We show that under common illumination intensities (such as terrestrial solar illumination), a minuscule Pt SA loading of ∼105 atoms μm–2 (surface Pt content ∼0.1 at.%) is sufficient to achieve a maximized H2 production rate. This results in a maximum turnover frequency at a single Pt atom site of ∼300 H2 molecules s–1. For a vast majority of illumination conditions and a suitable surface configuration, it is not the density of co-catalytic sites that is rate-determining (a high loading is not needed!), but the charge carrier generation (and flux of photoelectrons to the co-catalytic centers) determines the overall reaction rate. This is in stark contrast to SA catalysis of classic chemical reactions where generally a maximum loading of reactive SA delivers a maximum activity.
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