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Surface passivation for highly active, selective, stable, and scalable CO2 electroreduction

Abstract:
Electrochemical conversion of CO2 to formic acid using Bismuth catalysts is one the most promising pathways for industrialization. However, it is still difficult to achieve high formic acid production at wide voltage intervals and industrial current densities because the Bi catalysts are often poisoned by oxygenated species. Herein, we report a Bi3S2 nanowire-ascorbic acid hybrid catalyst that simultaneously improves formic acid selectivity, activity, and stability at high applied voltages. Specifically, a more than 95% faraday efficiency was achieved for the formate formation over a wide potential range above 1.0 V and at ampere-level current densities. The observed excellent catalytic performance was attributable to a unique reconstruction mechanism to form more defective sites while the ascorbic acid layer further stabilized the defective sites by trapping the poisoning hydroxyl groups. When used in an all-solid-state reactor system, the newly developed catalyst achieved efficient production of pure formic acid over 120 hours at 50 mA cm–2 (200 mA cell current)
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41467-023-40342-6
Publication website:
https://discovery.ucl.ac.uk/10174814/1/s41467-023-40342-6.pdf

Authors

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Role:
Author
ORCID:
0000-0003-1629-240X
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Role:
Author
ORCID:
0000-0001-8405-5962
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Role:
Author
ORCID:
0000-0003-3476-1628
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Role:
Author
ORCID:
0000-0002-8299-4517


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Funder identifier:
10.13039/501100001809
Grant:
51832004


Publisher:
Nature Research
Journal:
Nature Communications More from this journal
Volume:
14
Issue:
1
Pages:
4670-4670
Article number:
4670
Publication date:
2023-08-03
DOI:
EISSN:
2041-1723
ISSN:
2041-1723


Language:
English
Keywords:
Pubs id:
1510281
Local pid:
pubs:1510281
Source identifiers:
W4385515842
Deposit date:
2026-05-12
ARK identifier:
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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