Electrochemical carbon dioxide reduction reaction (ECORR) is a promising approach to synthesize fuels and value-added chemical feedstocks while reducing atmospheric CO levels. Here, high surface area cerium and sulfur-doped hierarchical bismuth oxide nanosheets (Ce@S-BiO) are develpoed by a solvothermal method. The resulting Ce@S-BiO electrocatalyst shows a maximum formate Faradaic efficiency (FE) of 92.5% and a current density of 42.09 mA cm at -1.16 V versus RHE using a traditional H-cell system. Furthermore, using a three-chamber gas diffusion electrode (GDE) reactor, a maximum formate FE of 85% is achieved in a wide range of applied potentials (-0.86 to -1.36 V vs RHE) using Ce@S-BiO. The density functional theory (DFT) results show that doping of Ce and S in BiO enhances formate production by weakening the OH* and H* species. Moreover, DFT calculations reveal that *OCHO is a dominant pathway on Ce@S-BiO that leads to efficient formate production. This study opens up new avenues for designing metal and element-doped electrocatalysts to improve the catalytic activity and selectivity for ECORR.
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http://dx.doi.org/10.1002/smll.202400913 | DOI Listing |
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