1. Stabilizing Undercoordinated Zn Active Sites through Confinement in CeO2 Nanotubes for Efficient Electrochemical CO2 Reduction.
- Author
-
Guo, Si‐Tong, Du, Yu‐Wei, Luo, Huihua, Zhu, Ziyin, Ouyang, Ting, and Liu, Zhao‐Qing
- Subjects
- *
ELECTROLYTIC reduction , *CATALYST structure , *DYNAMIC stability , *REDUCTION potential , *BINDING energy - Abstract
Zn‐based catalysts hold great potential to replace the noble metal‐based ones for CO2 reduction reaction (CO2RR). Undercoordinated Zn (Znδ+) sites may serve as the active sites for enhanced CO production by optimizing the binding energy of *COOH intermediates. However, there is relatively less exploration into the dynamic evolution and stability of Znδ+ sites during CO2 reduction process. Herein, we present ZnO, Znδ+/ZnO and Zn as catalysts by varying the applied reduction potential. Theoretical studies reveal that Znδ+ sites could suppress HER and HCOOH production to induce CO generation. And Znδ+/ZnO presents the highest CO selectivity (FECO 70.9 % at −1.48 V vs. RHE) compared to Zn and ZnO. Furthermore, we propose a CeO2 nanotube with confinement effect and Ce3+/Ce4+ redox to stabilize Znδ+ species. The hollow core–shell structure of the Znδ+/ZnO/CeO2 catalyst enables to extremely expose electrochemically active area while maintaining the Znδ+ sites with long‐time stability. Certainly, the target catalyst affords a FECO of 76.9 % at −1.08 V vs. RHE and no significant decay of CO selectivity in excess of 18 h. [ABSTRACT FROM AUTHOR]
- Published
- 2024
- Full Text
- View/download PDF