Optimizing Pt Electronic States through Formation of a Schottky Junction on Non-reducible Metal-Organic Frameworks for Enhanced Photocatalysis

被引:120
作者
Sun, Zi-Xuan [1 ]
Sun, Kang [1 ]
Gao, Ming-Liang [1 ]
Metin, Onder [2 ]
Jiang, Hai-Long [1 ]
机构
[1] Univ Sci & Technol China, Dept Chem, Hefei 230026, Anhui, Peoples R China
[2] Koc Univ, Coll Sci, Dept Chem, TR-34450 Istanbul, Turkey
基金
中国国家自然科学基金;
关键词
GOLD NANOPARTICLES; ENERGY; CHARGE; EFFICIENT; IMMOBILIZATION; HYDROGENATION; INTEGRATION; SEPARATION; CHEMISTRY; MECHANISM;
D O I
10.1002/anie.202206108
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Charge transfer between metal sites and supports is crucial for catalysis. Redox-inert supports are usually unfavorable due to their less electronic interaction with metal sites, which, we demonstrate, is not always correct. Herein, three metal-organic frameworks (MOFs) are chosen to mimic inert or active supports for Pt nanoparticles (NPs) and the photocatalysis is studied. Results demonstrate the formation of a Schottky junction between Pt and the MOFs, leading to the electron-donation effect of the MOFs. Under light irradiation, both the MOF electron-donation effect and Pt interband excitation dominate the Pt electron density. Compared with the "active" UiO-66 and MIL-125 supports, Pt NPs on the "inert" ZIF-8 exhibit higher electron density due to the higher Schottky barrier, resulting in superior photocatalytic activity. This work optimizes metal catalysts with non-reducible supports, and promotes the understanding of the relationship between the metal-support interaction and photocatalysis.
引用
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页数:7
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