Copper-on-nitride enhances the stable electrosynthesis of multi-carbon products from CO2
Copper-based materials are promising electrocatalysts for CO 2 reduction. Prior studies show that the mixture of copper (I) and copper (0) at the catalyst surface enhances multi-carbon products from CO 2 reduction; however, the stable presence of copper (I) remains the subject of debate. Here we rep...
Saved in:
Published in | Nature communications Vol. 9; no. 1; pp. 1 - 8 |
---|---|
Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
20.09.2018
Nature Publishing Group Nature Portfolio |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Copper-based materials are promising electrocatalysts for CO
2
reduction. Prior studies show that the mixture of copper (I) and copper (0) at the catalyst surface enhances multi-carbon products from CO
2
reduction; however, the stable presence of copper (I) remains the subject of debate. Here we report a copper on copper (I) composite that stabilizes copper (I) during CO
2
reduction through the use of copper nitride as an underlying copper (I) species. We synthesize a copper-on-nitride catalyst that exhibits a Faradaic efficiency of 64 ± 2% for C
2+
products. We achieve a 40-fold enhancement in the ratio of C
2+
to the competing CH
4
compared to the case of pure copper. We further show that the copper-on-nitride catalyst performs stable CO
2
reduction over 30 h. Mechanistic studies suggest that the use of copper nitride contributes to reducing the CO dimerization energy barrier—a rate-limiting step in CO
2
reduction to multi-carbon products.
While multi-carbon (C
2+
) products present high-value species attainable from emitted carbon dioxide, it is challenging to prepare stable, C
2+
selective catalysts. Here, authors support copper on copper nitride to improve copper’s electrocatalytic stability and selectivity toward C
2+
synthesis. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-018-06311-0 |