Unknown

Dataset Information

0

Copper-on-nitride enhances the stable electrosynthesis of multi-carbon products from CO2.


ABSTRACT: Copper-based materials are promising electrocatalysts for CO2 reduction. Prior studies show that the mixture of copper (I) and copper (0) at the catalyst surface enhances multi-carbon products from CO2 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 CO2 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 C2+ products. We achieve a 40-fold enhancement in the ratio of C2+ to the competing CH4 compared to the case of pure copper. We further show that the copper-on-nitride catalyst performs stable CO2 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 CO2 reduction to multi-carbon products.

SUBMITTER: Liang ZQ 

PROVIDER: S-EPMC6148248 | biostudies-literature | 2018 Sep

REPOSITORIES: biostudies-literature

altmetric image

Publications


Copper-based materials are promising electrocatalysts for CO<sub>2</sub> reduction. Prior studies show that the mixture of copper (I) and copper (0) at the catalyst surface enhances multi-carbon products from CO<sub>2</sub> 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<sub>2</sub> reduction through the use of copper nitride as an underlying copper (I) species. We synthesize  ...[more]

Similar Datasets

| S-EPMC8121866 | biostudies-literature
| S-EPMC6772073 | biostudies-literature
| S-EPMC4664948 | biostudies-literature
| S-EPMC8706010 | biostudies-literature
| S-EPMC9278094 | biostudies-literature
| S-EPMC6755511 | biostudies-literature
| S-EPMC5772509 | biostudies-literature
| S-EPMC6218481 | biostudies-literature
| S-EPMC6710288 | biostudies-literature
| S-EPMC8347895 | biostudies-literature