催化作用
过渡金属
单层
Atom(片上系统)
氧化还原
化学
碳纤维
吸附
材料科学
化学物理
纳米技术
无机化学
物理化学
有机化学
计算机科学
复合数
复合材料
嵌入式系统
作者
Hao Yuan,Zhenyu Li,Xiao Cheng Zeng,Jinlong Yang
标识
DOI:10.1021/acs.jpclett.0c00676
摘要
Single-atom catalysis has recently emerged as a promising approach for catalyzing the carbon dioxide reduction reaction (CO2RR). In this study, we present a principle for designing active single-atom catalysts (SACs) for CO2RR. We systematically examine totally 24 transition metals supported by a graphitic carbon nitride (g-CN) monolayer and find that their catalytic activities are highly correlated with the adsorption free energies of two intermediate species (OH and OCH). We then identify two important intrinsic descriptors, namely, the number of electrons in the outmost d-shell and the enthalpy of vaporization of the transition metal. Test calculations on transition metals supported by a C2N monolayer indicate that both descriptors are quite universal for SACs of CO2RR. Based on these results, we show that Ni@g-CN, Cu@g-CN, and Co@C2N are promising SACs for CO2RR. This study offers an effective principle for designing highly active SACs for CO2RR on the basis of intrinsic properties of transition metals.
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