Single Atoms in Photocatalysis: Low Loading Is Good Enough!

被引:47
作者
Qin, Shanshan [1 ]
Will, Johannes [2 ,3 ]
Kim, Hyesung [1 ]
Denisov, Nikita [1 ]
Carl, Simon [2 ,3 ]
Spiecker, Erdmann [2 ,3 ]
Schmuki, Patrik [1 ,4 ,5 ,6 ]
机构
[1] Friedrich Alexander Univ Erlangen Nuremberg, Dept Mat Sci WW4 LKO, D-91058 Erlangen, Germany
[2] Univ Erlangen Nurnberg, Inst Micro & Nanostruct Res, IZNF, D-91058 Erlangen, Germany
[3] Univ Erlangen Nurnberg, Ctr Nanoanal & Electron Microscopy CENEM, IZNF, D-91058 Erlangen, Germany
[4] Friedrich Alexander Univ Erlangen Nuremberg, Olomouc 779 00, Jeddah 91058, Saudi Arabia
[5] Palacky Univ, Czech Adv Technol, Reg Ctr Adv Technol s & Mat, Olomouc 77900, Czech Republic
[6] Palacky Univ, Res Inst, Olomouc 77900, Czech Republic
关键词
HYDROGEN-PRODUCTION; ACTIVE-SITES; NOBLE-METAL; EVOLUTION; CATALYSTS; SIZE; SUPPORT;
D O I
10.1021/acsenergylett.2c02801
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We disperse Pt single atoms (SAs) with different loading densities on anatase TiO2 thin films and evaluate the photocatalytic H-2 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 similar to 10(5) atoms mu m(-2) (surface Pt content similar to 0.1 at.%) is sufficient to achieve a maximized H-2 production rate. This results in a maximum turnover frequency at a single Pt atom site of similar to 300 H-2 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.
引用
收藏
页码:1209 / 1214
页数:6
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