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Ni-Doped Pr0.7Ba0.3MnO3-δ Cathodes for Enhancing Electrolysis of CO2 in Solid Oxide Electrolytic Cells.
Shan, Fei; Chen, Tao; Ye, Lingting; Xie, Kui.
Afiliação
  • Shan F; College of Chemistry, Fuzhou University, Fuzhou 350108, China.
  • Chen T; Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou 350002, China.
  • Ye L; Fujian College, University of Chinese Academy of Sciences, Fuzhou 350002, China.
  • Xie K; College of Chemistry, Fuzhou University, Fuzhou 350108, China.
Molecules ; 29(18)2024 Sep 21.
Article em En | MEDLINE | ID: mdl-39339487
ABSTRACT
Solid Oxide Electrolysis Cells (SOECs) can electro-reduce carbon dioxide to carbon monoxide, which not only effectively utilizes greenhouse gases, but also converts excess electrical energy into chemical energy. Perovskite-based oxides with exsolved metal nanoparticles are promising cathode materials for direct electrocatalytic reduction of CO2 through SOECs, and have thus received increasing attention. In this work, we doped Pr0.7Ba0.3MnO3-δ at the B site, and after reduction treatment, metal nanoparticles exsolved and precipitated on the surface of the cathode material, thereby establishing a stable metal-oxide interface structure and significantly improving the electrocatalytic activity of the SOEC cathode materials. Through research, among the Pr0.7Ba0.3Mn1-xNixO3-δ (PBMNx = 0-1) cathode materials, it has been found that the Pr0.7Ba0.3Mn0.9Ni0.1O3-δ (PBMN0.1) electrode material exhibits greater catalytic activity, with a CO yield of 5.36 mL min-1 cm-2 and a Faraday current efficiency of ~99%. After 100 h of long-term testing, the current can still remain stable and there is no significant change in performance. Therefore, the design of this interface has increasing potential for development.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Molecules / Molecules (Basel) Assunto da revista: BIOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Molecules / Molecules (Basel) Assunto da revista: BIOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Suíça