过电位
电催化剂
锰
法拉第效率
二氧化碳电化学还原
密度泛函理论
材料科学
催化作用
电化学
化学
无机化学
化学工程
电极
一氧化碳
物理化学
冶金
计算化学
有机化学
工程类
作者
Bingxing Zhang,Jianling Zhang,Jinbiao Shi,Dongxing Tan,Lifei Liu,Fanyu Zhang,Liang Cheng,Zhuizhui Su,Xiuniang Tan,Xiuyan Cheng,Buxing Han,Lirong Zheng,Jing Zhang
标识
DOI:10.1038/s41467-019-10854-1
摘要
Abstract Developing highly efficient electrocatalysts based on cheap and earth-abundant metals for CO 2 reduction is of great importance. Here we demonstrate that the electrocatalytic activity of manganese-based heterogeneous catalyst can be significantly improved through halogen and nitrogen dual-coordination to modulate the electronic structure of manganese atom. Such an electrocatalyst for CO 2 reduction exhibits a maximum CO faradaic efficiency of 97% and high current density of ~10 mA cm −2 at a low overpotential of 0.49 V. Moreover, the turnover frequency can reach 38347 h −1 at overpotential of 0.49 V, which is the highest among the reported heterogeneous electrocatalysts for CO 2 reduction. In situ X-ray absorption experiment and density-functional theory calculation reveal the modified electronic structure of the active manganese site, on which the free energy barrier for intermediate formation is greatly reduced, thus resulting in a great improvement of CO 2 reduction performance.
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