Highly Active NaTaO3-Based Photocatalysts for CO2 Reduction to Form CO Using Water as the Electron Donor

被引:127
作者
Nakanishi, Haruka [1 ]
Iizuka, Kosuke [1 ]
Takayama, Tomoaki [1 ]
Iwase, Akihide [1 ,2 ]
Kudo, Akihiko [1 ,2 ]
机构
[1] Tokyo Univ Sci, Fac Sci, Dept Appl Chem, Shinjuku Ku, 1-3 Kagurazaka, Tokyo 1628601, Japan
[2] Tokyo Univ Sci, Res Inst Sci & Technol, Photocatalysis Int Res Ctr, 2641 Yamazaki, Noda, Chiba 2788510, Japan
关键词
alkali earth metals; carbon dioxide fixation; electron donor; energy conversion; photocatalysis; CARBON-DIOXIDE; ELECTROCHEMICAL REDUCTION; DOPED NATAO3; CONVERSION; EFFICIENT; DECOMPOSITION; SELECTIVITY; EVOLUTION; DOPANTS; H2O;
D O I
10.1002/cssc.201601360
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Doped NaTaO3 (NaTaO3 : A, where A= Mg, Ca, Sr, Ba, or La) has arisen as a highly active photocatalyst for CO2 reduction to simultaneously form CO, H-2, and O-2 using water as the electron donor when used with an Ag cocatalyst, under UV irradiation, and with 1 atm (0.1 MPa) of CO2. The ratio of the number of reacted electrons/holes was almost unity, indicating that water was consumed as the electron donor. A liquid-phase reduction method for loading of the Ag cocatalyst was superior to photodeposition and impregnation methods. The Ag cocatalystloaded NaTaO3: Ba was the most active photocatalyst in water with no required additives. The addition of bases, such as hydrogencarbonate, was effective to enhance the CO formation for Mg-, Ca-, Sr-, Ba-, and La-doped NaTaO3 photocatalysts with an Ag cocatalyst. Ca-and Sr-doped NaTaO3 photocatalysts showed especially high activity along with the Ba-doped photocatalyst in the aqueous NaHCO3 solution. The selectivity for the CO formation [CO/(CO+H-2)] on Ca-, Sr-, and Ba-doped NaTaO3 photocatalysts with Ag cocatalyst reached around 90%.
引用
收藏
页码:112 / 118
页数:7
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