Selective photocatalytic oxidation of methane to methanol by enhancing H2O2 utilization over Au-Pd/In2O3

被引:16
作者
Zhou, Qiang [1 ,2 ]
Wang, Xinyu [1 ,2 ]
Xing, Tao [3 ]
Wang, Mingqing [3 ]
Wu, Mingbo [1 ,2 ]
Wu, Wenting [1 ,2 ]
机构
[1] China Univ Petr East China, Coll Chem & Chem Engn, State Key Lab Heavy Oil Proc, Qingdao 266580, Peoples R China
[2] China Univ Petr East China, Inst New Energy, Qingdao 266580, Peoples R China
[3] Shandong Energy Grp Co Ltd, Natl Engn Res Ctr Coal Gasificat & Coal Based Adv, Jinan 250101, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalysis; Methane oxidation; Radical regulation; Hydrogen peroxide activation; Nanomaterial; DECORATED ZINC-OXIDE; ROOM-TEMPERATURE; CARBON NITRIDE; CONVERSION; OXYGEN; CATALYST; O-2; CH4; AU;
D O I
10.1016/j.jcat.2024.115289
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
Hydrogen peroxide (H2O2) is widely used as an oxidant for photocatalytic oxidation of methane to value-added chemicals under mild conditions, but suffers from low utilization efficiency. Herein, we propose a comprehensive strategy for the proper amount of hydroxyl radicals (center dot OH) generation from H2O2 by regulating the Pd/Au molar ratios and the total Au-Pd contents loaded on In2O3. For the photocatalytic oxidation of methane at ambient temperature, the yield and selectivity of CH3OH over the optimized 1.0% AuPd0.5/In2O3 catalyst were as high as 2187.0 mu mol g-1 h-1 and 94.0% respectively, exceeding most reported literatures. Mechanism investigations revealed that the formation of Au-Pd alloys may contribute to the homolytic cleavage of H2O2 into center dot OH radicals and improve the selectivity of center dot OH generation. This work provides some guidance for the delicate design of photocatalysts to manipulate selective H2O2 activation and efficient photocatalytic methane oxidation.
引用
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页数:10
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