論文 Pentagon‐Rich Caged Carbon Catalyst for the Oxygen Reduction Reaction in Acidic Electrolytes

Guoping Chen ; Miho Isegawa ; Taro Koide ; Yasuo Yoshida ; Koji Harano SAMURAI ORCID ; Kenji Hayashida ; Shusaku Fujita ; Kotaro Takeyasu ; Katsuhiko Ariga SAMURAI ORCID ; Junji Nakamura ORCID

コレクション

引用
Guoping Chen, Miho Isegawa, Taro Koide, Yasuo Yoshida, Koji Harano, Kenji Hayashida, Shusaku Fujita, Kotaro Takeyasu, Katsuhiko Ariga, Junji Nakamura. Pentagon‐Rich Caged Carbon Catalyst for the Oxygen Reduction Reaction in Acidic Electrolytes. Angewandte Chemie International Edition. 2024, 63 (49), . https://doi.org/10.1002/anie.202410747
SAMURAI

説明:

(abstract)

In this study, we present the successful synthesis of cage-like cubic carbon catalysts enriched with pentagon structures using pentagon ring-containing C60 and a NaCl template. The number of pentagons contained in the structure was increased by doping with nitrogen and annealing, and the number of electron spins also increased, thereby improving catalytic activity. The prepared catalyst exhibits remarkable activity in ORR under acidic electrolytes. Furthermore, we elucidate the correlation between the pentagon structure, the number of spin electrons, and catalytic activity, demonstrating that enhanced activity is contingent upon the presence of spin electrons. Density functional theory (DFT) calculations support the role of spin electrons in improving activity. The concept of spin electrons and the introduction of pentagon structures provide new design principles for carbon catalysts.

権利情報:

キーワード: Carbon catalyst, Oxygen reduction reaction, O2 absorption, Pentagon, Spin

刊行年月日: 2024-12-02

出版者: Wiley

掲載誌:

  • Angewandte Chemie International Edition (ISSN: 14337851) vol. 63 issue. 49

研究助成金:

  • Japan Society for the Promotion of Science JP23H05459
  • Japan Society for the Promotion of Science JP23H04874

原稿種別: 出版者版 (Version of record)

MDR DOI:

公開URL: https://doi.org/10.1002/anie.202410747

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更新時刻: 2024-12-05 12:47:18 +0900

MDRでの公開時刻: 2024-12-05 12:47:18 +0900

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