Supported Ru Single Atoms and Clusters on P-Doped Carbon Nitride as an Efficient Photocatalyst for H2O2 Production

被引:18
作者
Bai, Lulu [1 ]
Sun, Hao [1 ]
Wu, Qiang [1 ]
Yao, Weifeng [1 ,2 ,3 ]
机构
[1] Shanghai Univ Elect Power, Coll Environm & Chem Engn, Shanghai Key Lab Mat Protect & Adv Mat Elect Powe, Shanghai 200090, Peoples R China
[2] Shanghai Inst Pollut Control & Ecol Secur, Shanghai 200092, Peoples R China
[3] Shanghai Univ Elect Power, Shanghai Engn Res Ctr Heat Exchange Syst & Energy, Shanghai 200090, Peoples R China
基金
上海市自然科学基金;
关键词
hydrogen peroxide; oxygen reduction; P-doped carbon nitride; photocatalytic; ruthenium; HYDROGEN-PEROXIDE; CHARGE SEPARATION; G-C3N4; PERFORMANCE; EVOLUTION; CATALYSTS; AU;
D O I
10.1002/cctc.202101954
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
Photocatalytic H2O2 evolution via two-electron oxygen reduction is a promising path for renewable and on-the-spot H2O2 production compared with the traditional anthraquinone method. However, the efficiency of photocatalytic production of H2O2 is usually very low. Herein, P-doped carbon nitride loaded with ruthenium single atoms and clusters (Ru-atom/P-CN) is reported as an efficient photocatalyst for H2O2 production. The yield of H2O2 over Ru-atom/P-CN (385.8 mmol g(-1) h(-1)) is about 4.3 times higher than that of P-CN (88.9 mmol g(-1) h(-1)) and 3.6 times higher than that of ruthenium nanoparticles loaded P-CN (105.9 mmol g(-1) h(-1)). Further mechanistic study indicates that the presence of Ru in the form of single atoms and clusters not only improves the separation efficiency of photogenerated carriers and inhibits the recombination of photogenerated electron-hole pairs, but also increases the reactive sites of this catalytic system. This study breaks through people's understanding that precious metal loading is not conducive to H2O2 selectivity and provides a new way to prepare low-metal loading, high-activity photocatalysts for H2O2 production.
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页数:8
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