Promoting electrocatalytic CO2 reduction to formate via sulfur-boosting water activation on indium surfaces
Electrocatalytic reduction of CO 2 to fuels and chemicals is one of the most attractive routes for CO 2 utilization. Current catalysts suffer from low faradaic efficiency of a CO 2 -reduction product at high current density (or reaction rate). Here, we report that a sulfur-doped indium catalyst exhi...
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Published in | Nature communications Vol. 10; no. 1; pp. 892 - 10 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
21.02.2019
Nature Publishing Group Nature Portfolio |
Subjects | |
Online Access | Get full text |
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Summary: | Electrocatalytic reduction of CO
2
to fuels and chemicals is one of the most attractive routes for CO
2
utilization. Current catalysts suffer from low faradaic efficiency of a CO
2
-reduction product at high current density (or reaction rate). Here, we report that a sulfur-doped indium catalyst exhibits high faradaic efficiency of formate (>85%) in a broad range of current density (25–100 mA cm
−2
) for electrocatalytic CO
2
reduction in aqueous media. The formation rate of formate reaches 1449 μmol h
−1
cm
−2
with 93% faradaic efficiency, the highest value reported to date. Our studies suggest that sulfur accelerates CO
2
reduction by a unique mechanism. Sulfur enhances the activation of water, forming hydrogen species that can readily react with CO
2
to produce formate. The promoting effect of chalcogen modifiers can be extended to other metal catalysts. This work offers a simple and useful strategy for designing both active and selective electrocatalysts for CO
2
reduction.
CO
2
conversion to liquid fuels provides an appealing means to remove the greenhouse gas, although it is challenging to find materials that are both active and selective. Here, authors show sulfur-doped indium to be a highly active and selective electrocatalyst that transforms CO
2
into formate. |
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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/s41467-019-08805-x |