Oxygen vacancies stabilized Ag+ to enhance the performance of an Ag/In2O3 photocatalyst for non-oxidative coupling of methane

被引:12
作者
Xiao, Mingquan [1 ,3 ]
Wang, Liang [1 ,2 ]
Wang, Hong [1 ,2 ]
Yuan, Jie [1 ,2 ]
Chen, Xun [1 ]
Zhang, Zizhong [1 ,3 ]
Fu, Xianzhi [1 ]
Dai, Wenxin [1 ,3 ]
机构
[1] Fuzhou Univ, Res Res Inst Photocatalysis, State Key Lab Photocatalysis Energy & Environm, Fuzhou 350108, Peoples R China
[2] Fuzhou Univ, Key Lab Ecomat Adv Technol, Fuzhou 350002, Fujian, Peoples R China
[3] Qingyuan Innovat Lab, Quanzhou 362801, Peoples R China
基金
中国国家自然科学基金;
关键词
SUPPORTED ZIRCONIUM-OXIDE; GALLIUM OXIDE; IN2O3; NANOPARTICLES; HYDROGEN EVOLUTION; PHOTOACTIVE SITES; ROOM-TEMPERATURE; ACTIVE-SITES; SILICA; CONVERSION; ETHANE;
D O I
10.1039/d3cy00515a
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
The photocatalytic non-oxidative coupling of methane (NOCM) process is a desirable reaction that uses solar energy to convert methane into an equal proportion of ethane and hydrogen. However, most current photocatalysts suffer from low product yields and selectivity due to the over-oxidation of methane or catalyst deactivation by coke deposition. In this study, a Ag/In2O3 photocatalyst was synthesized by a simple deposition precipitation method for the non-oxidative coupling of methane in a batch reactor under photoirradiation at room temperature and atmospheric pressure. Ethane yields of up to 450.26 & mu;mol g(-1) h(-1) with a high selectivity of 88% were achieved. The characterization results showed that Ag+ species were stably loaded in oxygen vacancies on the In2O3 carrier. The Ag+ accepted the photogenerated electrons from In2O3, which inhibited the recombination of the electrons and photogenerated holes, while the methane was oxidized by the holes to ethane. This study offers a new insight into the design of photocatalytic NOCM reactions.
引用
收藏
页码:4148 / 4155
页数:8
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