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Crystalline CdS/Amorphous Cd(OH)2 Composite for Electrochemical CO2 Reduction to CO in a Wide Potential Window.
Hua, Zhixin; Qi, Kongsheng; Mi, Yulan; Zhao, Yuhua; Wu, Xinjie; Guo, Weiwei; Wan, Xiaoqi; Fan, Zixi; Yang, Dexin.
Affiliation
  • Hua Z; Green Catalysis Center, and College of Chemistry, Zhengzhou University, Zhengzhou, Henan, 450001, China.
  • Qi K; Green Catalysis Center, and College of Chemistry, Zhengzhou University, Zhengzhou, Henan, 450001, China.
  • Mi Y; Green Catalysis Center, and College of Chemistry, Zhengzhou University, Zhengzhou, Henan, 450001, China.
  • Zhao Y; Green Catalysis Center, and College of Chemistry, Zhengzhou University, Zhengzhou, Henan, 450001, China.
  • Wu X; Green Catalysis Center, and College of Chemistry, Zhengzhou University, Zhengzhou, Henan, 450001, China.
  • Guo W; Institute of Molecular Metrology, College of Chemistry and Chemical Engineering, Qingdao University, Qingdao, Shandong, 266071, China.
  • Wan X; Green Catalysis Center, and College of Chemistry, Zhengzhou University, Zhengzhou, Henan, 450001, China.
  • Fan Z; Henan Institute of Advanced Technology, Zhengzhou University, Zhengzhou, Henan, 450053, China.
  • Yang D; Green Catalysis Center, and College of Chemistry, Zhengzhou University, Zhengzhou, Henan, 450001, China.
Chemistry ; 30(39): e202400983, 2024 Jul 11.
Article in En | MEDLINE | ID: mdl-38747632
ABSTRACT
Electrochemical CO2 reduction is a promising method for converting atmospheric CO2 into valuable low-carbon chemicals. In this study, a crystalline cadmium sulfide/amorphous cadmium hydroxide composite was successfully deposited on the carbon paper substrate surface by in-situ chemical bath deposition (named as c-CdS/a-Cd(OH)2/CP electrodes) for the efficient electrochemical CO2 reduction to produce CO. The c-CdS/a-Cd(OH)2/CP electrode exhibited high CO Faradaic efficiencies (>90 %) under a wide potential window of 1.0 V, with the highest value reaching ~100 % at the applied potential ranging from -2.16 V to -2.46 V vs. ferrocene/ferrocenium (Fc/Fc+), superior to the crystalline counterpart c-CdS/CP and c-CdS/c-Cd(OH)2@CP electrodes. Meanwhile, the CO partial current density reached up to 154.7 mA cm-2 at -2.76 V vs. Fc/Fc+ on the c-CdS/a-Cd(OH)2/CP electrode. The excellent performance of this electrode was mainly ascribed to its special three-dimensional structure and the introduction of a-Cd(OH)2. These structures could provide more active sites, accelerate the charge transfer, and enhance adsorption of *COOH intermediates, thereby improving the CO selectivity. Moreover, the electrolytes consisting of 1-butyl-3-methylimidazolium tetrafluoroborate and acetonitrile also enhanced the reaction kinetics of electrochemical CO2 reduction to CO.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chemistry Journal subject: QUIMICA Year: 2024 Type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chemistry Journal subject: QUIMICA Year: 2024 Type: Article Affiliation country: China