Tuning binding strength between single metal atoms and supports enhances electrochemical CO2 methanation

Linbo Li, Xin Lei, Zhilong Zheng, Yingjun Dong, Haohui Chen, Jun Chen, Yi Zhong, Yongping Zheng, Yongbing Tang (), Xiaolong Zhang () and Hui-Ming Cheng ()
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Linbo Li: Chinese Academy of Sciences
Xin Lei: Chinese Academy of Sciences
Zhilong Zheng: Chinese Academy of Sciences
Yingjun Dong: Chinese Academy of Sciences
Haohui Chen: Chinese Academy of Sciences
Jun Chen: Squires Way
Yi Zhong: Chinese Academy of Sciences
Yongping Zheng: Chinese Academy of Sciences
Yongbing Tang: Chinese Academy of Sciences
Xiaolong Zhang: Chinese Academy of Sciences
Hui-Ming Cheng: Chinese Academy of Sciences

Nature Communications, 2025, vol. 16, issue 1, 1-14

Abstract: Abstract Single-atom catalysts (SACs) with tunable site density and activity are promising for catalytic processes. However, the relationship between interacting sites and the catalytic mechanism, as well as the effect of the support on this relationship, remains incompletely understood. Here we report a support geometry engineering strategy to control the inter-site distance (dsite) of Cu–N–C (CuNC) SACs via strong interactions between CuNC and a secondary support (ss). This process allows tuning of the binding strength (that is Cu–N bond length) between individual Cu atoms and the N-doped primary supports, concomitantly suppressing defect formation and Cu atom detachment in the CuNC framework. The continuous optimization of the electronic and coordination structure of individual active Cu sites, achieved by reducing the dsite to approximately 0.7 nm, enhances their inherent CO2-to-methane selectivity and activity. As a result, the ss-engineered CuNC with a moderate dsite of 0.68 nm exhibits enhanced methane selectivity of 70% and a partial current density of 303.9 mA cm−2, over 1.5 times higher than that of unmodified CuNC.

Date: 2025
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DOI: 10.1038/s41467-025-63781-9

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