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Formation of Enriched Vacancies for Enhanced CO2 Electrocatalytic Reduction over AuCu Alloys AITranslate

Tianjin University; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin); Tianjin University; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin); Tianjin University; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin); Tianjin University; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin); Tianjin University; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin); Tianjin University; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin); Tianjin University; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin); Tianjin University; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin)
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Publisher: ACS
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Abstract AITranslate

Electroreduction (ER) of carbon dioxide (CO2) is a promising way to curb excessive CO2 emission and produce value-added products. Gold–copper (AuCu) alloys are known to exhibit eminent CO production performance toward CO2ER. However, it still remains a grand challenge to balance *COOH and *CO bonding and to further decrease CO onset potential. This Letter describes the construction of Cu vacancies at an abrupt surface over a dealloyed AuCu catalyst to effectively decrease the overpotential and increase CO faradaic efficiency. Dealloyed Au3Cu exhibited a 90.2% CO faradaic efficiency at −0.38 V vs RHE and a 418.60 A/g CO mass current density at −0.8 V. vs RHE, achieving the record for CO production among AuCu catalysts. Combining the experimental and theoretical results, we concluded that the improved performance primarily results from the enhanced *COOH absorption.

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DOI:https://doi.org/10.1021/acsenergylett.8b01286

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Citation Information:

Electroreduction (ER) of carbon dioxide (CO2) is a promising way to curb excessive CO2 emission and produce value-added products. Gold–copper (AuCu) alloys are known to exhibit eminent CO production performance toward CO2ER. However, it still remains a grand challenge to balance *COOH and *CO bonding and to further decrease CO onset potential. This Letter describes the construction of Cu vacancies at an abrupt surface over a dealloyed AuCu catalyst to effectively decrease the overpotential and increase CO faradaic efficiency. Dealloyed Au3Cu exhibited a 90.2% CO faradaic efficiency at −0.38 V vs RHE and a 418.60 A/g CO mass current density at −0.8 V. vs RHE, achieving the record for CO production among AuCu catalysts. Combining the experimental and theoretical results, we concluded that the improved performance primarily results from the enhanced *COOH absorption.

quote

GB/T 7714-2015 [1] Wenjin Zhu, Lei Zhang, Piaoping Yang, et al. ACS Energy Letters, 2018(3). DOI:10.1021/acsenergylett.8b01286.
MLA [1] Wenjin Zhu, et al., ACS Energy Letters, no. 3, 2018, https://doi.org/10.1021/acsenergylett.8b01286.
APA [1] Wenjin Zhu, Lei Zhang, Piaoping Yang, Congling Hu, Hao Dong, ZhiJian Zhao, Rentao Mu, & Jinlong Gong. (2018). ACS Energy Letters(3). https://doi.org/10.1021/acsenergylett.8b01286
IEEE [1] Wenjin Zhu, Lei Zhang, Piaoping Yang, Congling Hu, Hao Dong, ZhiJian Zhao, Rentao Mu, and Jinlong Gong, ACS Energy Letters, no. 3, 2018, doi: 10.1021/acsenergylett.8b01286.