posted on 2017-06-14, 14:18authored byTing Ouyang, Cheng Hou, Jia-Wei Wang, Wen-Ju Liu, Di-Chang Zhong, Zhuo-Feng Ke, Tong-Bu Lu
Visible-light driven reduction of
CO2 into chemical
fuels has attracted enormous interest in the production of sustainable
energy and reversal of the global warming trend. The main challenge
in this field is the development of efficient, selective, and economic
photocatalysts. Herein, we report a Co(II)-based homogeneous catalyst,
[Co(NTB)CH3CN](ClO4)2 (1, NTB = tris(benzimidazolyl-2-methyl)amine), which shows high selectivity
and stability for the catalytic reduction of CO2 to CO
in a water-containing system driven by visible light, with turnover
number (TON) and turnover frequency (TOF) values of 1179 and 0.032
s–1, respectively, and selectivity to CO of 97%.
The high catalytic activity of 1 for photochemical CO2-to-CO conversion is supported by the results of electrochemical
investigations and DFT calculations.