Low coordination number copper catalysts for electrochemical CO2 methanation in a membrane electrode assembly
Yi Xu,
Fengwang Li,
Aoni Xu,
Jonathan P. Edwards,
Sung-Fu Hung,
Christine M. Gabardo,
Colin P. O’Brien,
Shijie Liu,
Xue Wang,
Yuhang Li,
Joshua Wicks,
Rui Kai Miao,
Yuan Liu,
Jun Li,
Jianan Erick Huang,
Jehad Abed,
Yuhang Wang,
Edward H. Sargent () and
David Sinton ()
Additional contact information
Yi Xu: University of Toronto
Fengwang Li: University of Toronto
Aoni Xu: University of Toronto
Jonathan P. Edwards: University of Toronto
Sung-Fu Hung: University of Toronto
Christine M. Gabardo: University of Toronto
Colin P. O’Brien: University of Toronto
Shijie Liu: University of Toronto
Xue Wang: University of Toronto
Yuhang Li: University of Toronto
Joshua Wicks: University of Toronto
Rui Kai Miao: University of Toronto
Yuan Liu: University of Toronto
Jun Li: University of Toronto
Jianan Erick Huang: University of Toronto
Jehad Abed: University of Toronto
Yuhang Wang: University of Toronto
Edward H. Sargent: University of Toronto
David Sinton: University of Toronto
Nature Communications, 2021, vol. 12, issue 1, 1-7
Abstract:
Abstract The electrochemical conversion of CO2 to methane provides a means to store intermittent renewable electricity in the form of a carbon-neutral hydrocarbon fuel that benefits from an established global distribution network. The stability and selectivity of reported approaches reside below technoeconomic-related requirements. Membrane electrode assembly-based reactors offer a known path to stability; however, highly alkaline conditions on the cathode favour C-C coupling and multi-carbon products. In computational studies herein, we find that copper in a low coordination number favours methane even under highly alkaline conditions. Experimentally, we develop a carbon nanoparticle moderator strategy that confines a copper-complex catalyst when employed in a membrane electrode assembly. In-situ XAS measurements confirm that increased carbon nanoparticle loadings can reduce the metallic copper coordination number. At a copper coordination number of 4.2 we demonstrate a CO2-to-methane selectivity of 62%, a methane partial current density of 136 mA cm−2, and > 110 hours of stable operation.
Date: 2021
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-23065-4
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DOI: 10.1038/s41467-021-23065-4
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