Stable and Highly Active Single Atom Configurations for Photocatalytic H2 Generation

被引:10
|
作者
Wang, Yue [1 ]
Denisov, Nikita [1 ]
Qin, Shanshan [1 ]
Goncalves, Danielle Santos [2 ]
Kim, Hyesung [1 ]
Sarma, Bidyut Bikash [3 ,4 ]
Schmuki, Patrik [1 ,5 ]
机构
[1] Friedrich Alexander Univ Erlangen Nurnberg, Chair Surface Sci & Corros WW4 LKO, Dept Mat Sci & Engn, Martensstr 7, D-91058 Erlangen, Germany
[2] Karlsruhe Inst Technol, Inst Catalysis Res & Technol, D-76344 Eggenstein Leopoldshafen, Germany
[3] Karlsruhe Inst Technol, Inst Catalysis Res & Technol, D-76131 Karlsruhe, Germany
[4] Karlsruhe Inst Technol, Inst Chem Technol & Polymer Chem, D-76131 Karlsruhe, Germany
[5] Reg Ctr Adv Technol & Mat, Slechtitelu 27, Olomouc 78371, Czech Republic
基金
欧盟地平线“2020”;
关键词
photocatalytic H-2 generation; Pt co-catalyst; single atom configurations; sputtered anatase layers; HYDROGEN EVOLUTION; TIO2; CATALYSTS; SIZE; NANOPARTICLES; SITES; RECOMBINATION; REDISPERSION; TEMPERATURE; REDUCTION;
D O I
10.1002/adma.202400626
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The employment of single atoms (SAs), especially Pt SAs, as co-catalysts in photocatalytic H-2 generation has gained significant attention due to their exceptional efficiency. However, a major challenge in their application is the light-induced agglomeration of these SAs into less active nanosized particles under photocatalytic conditions. This study addresses the stability and reactivity of Pt SAs on TiO2 surfaces by investigating various post-deposition annealing treatments in air, Ar, and Ar-H-2 environments at different temperatures. It is described that annealing in an Ar-H-2 atmosphere optimally stabilizes SA configurations, forming stable 2D rafts of assembled SAs approximate to 0.5-1 nm in diameter. These rafts not only resist light-induced agglomeration but also exhibit significantly enhanced H-2 production efficiency. The findings reveal a promising approach to maintaining the high reactivity of Pt SAs while overcoming the critical challenge of their stability under photocatalytic conditions.
引用
收藏
页数:11
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