Journal article
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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(Preview, Version of record, pdf, 3.6MB, Terms of use)
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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
+ National Natural Science Foundation of China
More from this funder
- 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:
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2041-1723
- ISSN:
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2041-1723
- Language:
-
English
- Keywords:
- Pubs id:
-
1510281
- Local pid:
-
pubs:1510281
- Source identifiers:
-
W4385515842
- Deposit date:
-
2026-05-12
- ARK identifier:
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Terms of use
- Copyright date:
- 2023
- Licence:
- CC Attribution (CC BY)
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