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The bio-inspired heterogeneous single-cluster catalyst Ni100-FeS for enhanced electrochemical CO reduction to CH
Electrochemical conversion of CO 2 -to-CH 4 is a process of converting the inert greenhouse gas into energy molecules. It offers great promise for the transformation of carbon-neutral economy. However, achieving high CH 4 activity and selectivity remains a major challenge because the electrochemical...
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Published in: | Nanoscale 2023-02, Vol.15 (6), p.2756-2766 |
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Main Authors: | , , |
Format: | Article |
Language: | |
Online Access: | Get full text |
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Summary: | Electrochemical conversion of CO
2
-to-CH
4
is a process of converting the inert greenhouse gas into energy molecules. It offers great promise for the transformation of carbon-neutral economy. However, achieving high CH
4
activity and selectivity remains a major challenge because the electrochemical reduction of CO
2
-to-CH
4
is accompanied by various C
1
intermediates at the catalytic site, involving multiple proton-coupled electron transfer processes. Herein, different from the traditional designing strategy, we propose a bio-inspired theoretical design approach to construct a heterogeneous single-cluster catalyst Ni100-Fe
4
S
4
at the atomic level, which may show high CO
2
electroreduction performance. Combined with the crystallographic data and theoretical calculations, Ni100-Fe
4
S
4
and CO dehydrogenase exhibit highly similar catalytic geometric active centers and CO
2
binding modes. By exploring the origin of the catalytic activity of this biomimetic structure, we found that the activation of CO
2
on Ni100-Fe
4
S
4
theoretically exceeds that on natural CO dehydrogenase. Density functional theory calculations reveal that the dehydrogenase enzyme-liked Fe-Ni active site serves as an electron enrichment 'electro-bridge' (an electron-rich highly active catalytic site), which can activate CO
2
molecules efficiently and stabilize various intermediates in multistep elementary reactions to selectively produce CH
4
at a low overpotential (0.13 eV). The calculated CO
2
electroreduction pathways are well consistent with the nickel-based catalytic materials reported in experimental studies. Our work showcases and highlights the rational design of high-performance catalytic materials
via
the biomimetic methodology at the atomic level.
A heterogeneous single-cluster catalyst Ni100-Fe
4
S
4
via
bio-inspired design strategy exhibits excellent theoretical CO
2
electroreduction performance. |
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ISSN: | 2040-3364 2040-3372 |
DOI: | 10.1039/d2nr06665c |