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Confinement of ionomer for electrocatalytic CO2 reduction reaction via efficient mass transfer pathways.
Du, Xiaowei; Zhang, Peng; Zhang, Gong; Gao, Hui; Zhang, Lili; Zhang, Mengmeng; Wang, Tuo; Gong, Jinlong.
Affiliation
  • Du X; School of Chemical Engineering and Technology, Key Laboratory for Green Chemical Technology of the Ministry of Education, Tianjin University, Tianjin300072, China.
  • Zhang P; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin300072, China.
  • Zhang G; School of Chemical Engineering and Technology, Key Laboratory for Green Chemical Technology of the Ministry of Education, Tianjin University, Tianjin300072, China.
  • Gao H; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin300072, China.
  • Zhang L; National Industry-Education Platform of Energy Storage, Tianjin University, Tianjin300350, China.
  • Zhang M; School of Chemical Engineering and Technology, Key Laboratory for Green Chemical Technology of the Ministry of Education, Tianjin University, Tianjin300072, China.
  • Wang T; Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin300072, China.
  • Gong J; School of Chemical Engineering and Technology, Key Laboratory for Green Chemical Technology of the Ministry of Education, Tianjin University, Tianjin300072, China.
Natl Sci Rev ; 11(2): nwad149, 2024 Feb.
Article in En | MEDLINE | ID: mdl-38213529
ABSTRACT
Gas diffusion electrodes (GDEs) mediate the transport of reactants, products and electrons for the electrocatalytic CO2 reduction reaction (CO2RR) in membrane electrode assemblies. The random distribution of ionomer, added by the traditional physical mixing method, in the catalyst layer of GDEs affects the transport of ions and CO2. Such a phenomenon results in elevated cell voltage and decaying selectivity at high current densities. This paper describes a pre-confinement method to construct GDEs with homogeneously distributed ionomer, which enhances mass transfer locally at the active centers. The optimized GDE exhibited comparatively low cell voltages and high CO Faradaic efficiencies (FE > 90%) at a wide range of current densities. It can also operate stably for over 220 h with the cell voltage staying almost unchanged. This good performance can be preserved even with diluted CO2 feeds, which is essential for pursuing a high single-pass conversion rate. This study provides a new approach to building efficient mass transfer pathways for ions and reactants in GDEs to promote the electrocatalytic CO2RR for practical applications.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Natl Sci Rev Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Natl Sci Rev Year: 2024 Document type: Article Affiliation country: China