Mg-doped SrTiO3 photocatalyst with Ag-Co cocatalyst for enhanced selective conversion of CO2 to CO using H2O as the electron donor

被引:7
|
作者
Nakamoto, Takechi [1 ]
Iguchi, Shoji [1 ]
Naniwa, Shimpei [1 ]
Tanaka, Tsunehiro [1 ,2 ]
Teramura, Kentaro [1 ,2 ,3 ]
机构
[1] Kyoto Univ, Grad Sch Engn, Dept Mol Engn, Nishikyo Ku, Kyoto, Kyoto 6158510, Japan
[2] Kyoto Univ, Elements Strategy Initiat Catalysts & Batteries ES, 1-30 Goryo Ohara,Nishikyo Ku, Kyoto 6158245, Japan
[3] Kyoto Univ, Fukui Inst Fundamental Chem, Takano Nishibiraki Cho 34-4,Sakyo Ku, Kyoto 6068103, Japan
关键词
CARBON-DIOXIDE; WATER; REDUCTION; SURFACE; HYDROXIDE; LAYER; GA2O3;
D O I
10.1039/d3cy00576c
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 conversion of CO2 by H2O is a promising method for solving energy and environmental problems. In this context, efficient photocatalysts that facilitate the selective conversion of CO2 to the value-added chemical CO are essential. In this study, for the first time in the literature, we used an Mg-doped SrTiO3 photocatalyst (Mg-SrTiO3) for the photocatalytic conversion of CO2 to CO using H2O as the electron donor under monochromatic UV-light irradiation at 365 nm. Compared to pristine SrTiO3, Mg-SrTiO3, which was prepared via a flux method, exhibited dramatically enhanced conversion of CO2 to CO in the presence of an Ag-Co cocatalyst. Moreover, the selectivity toward CO evolution was >99%, which indicates suppression of the unnecessary and competitive H-2 evolution. Scanning electron microscopy of Mg-SrTiO3 revealed edge-shaved cubic particles, which were correlated to the anisotropic distribution of photogenerated electrons and holes and the consequent enhancement of photocatalytic activity. Furthermore, the Mg-doping temperature and amount used to prepare Mg-SrTiO3 influenced the substitution of Ti4+ sites by Mg2+ in the bulk of SrTiO3, thereby affecting the CO evolution. The apparent quantum efficiency of optimal Mg-SrTiO3 in the photocatalytic conversion of CO2 was determined to be 0.05%.
引用
收藏
页码:4534 / 4541
页数:8
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