Pengfei Liu , Mingqian Wang , Wanfei Hu , Xiaoying Feng , Xing Gao , Wei Qian , Qiang Wang , Junying Zhang
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引用次数: 0
Abstract
The CC coupling of CO plays a crucial role in the reduction of CO/CO2 to C2+ compounds. Controlling the activity and active sites of the catalyst proves to be an effective method to achieve controllable CC coupling. By doping metals into fullerene to form endohedral metallofullerenes (EMF), a strategy emerges to achieve unique catalytic activity. Herein, we report that embedded nickel-metallofullerenes (Nin@C60) as an efficient catalyst can achieve controllable CC coupling of CO, thereby promoting the generation of C2 products. The results show that it is thermodynamically feasible for Nin clusters to embed into C60 to form Nin@C60, electronic structure analysis reveals that Nin clusters can activate C60 through electron transfer. Subsequently, research finds that the physically adsorbed CO on C60 and Nin@C60 surface can directly form O*C*CO intermediate through controllable CC coupling, with an extremely low activation energy barrier (0.10 ∼ 0.41 eV). Among them, Ni6@C60 has the lowest activation energy barrier, which is 0.10 eV. This work provides new theoretical insights into CC controllable coupling and the design of novel catalysts for efficient CO/CO2 conversion.
期刊介绍:
Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are:
Heterogeneous catalysis including immobilized molecular catalysts
Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis
Photo- and electrochemistry
Theoretical aspects of catalysis analyzed by computational methods