材料科学
氧还原反应
稀土
氧气
还原(数学)
纳米技术
能量(信号处理)
氧还原
化学工程
物理化学
冶金
有机化学
物理
化学
几何学
数学
电极
量子力学
工程类
电化学
作者
Liangde Dong,Cunhuai Yu,Bowen Yan,Jiawang Li,Bin Yang,Mingjie Lin,Ji Huang,Wanling Xiao,Jian Zhong,Pei Kang Shen,Zhi Qun Tian
标识
DOI:10.1002/adfm.202501884
摘要
Abstract Developing the new member of transition Metal‐nitrogen‐carbon (M‐N‐C) for oxygen reduction reaction (ORR) is critical to address the issues in 3d‐orbital metal M‐N‐C as noble metal‐free catalyst to achieve affordable fuel cells and metal‐air batteries. Herein, Gd‐N‐C nanosheets are developed by pyrolyzing the self‐polymerized compound of 2, 6‐diaminopyridine initiated by GdCl 3 . The Gd‐N‐C features a unique mixed structure of single GdN 5 moieties and Gd x N y O z atomic clusters, exhibiting excellent ORR performance with the half‐wave potentials of 0.89 and 0.76 V versus RHE in 0.1 M KOH and 0.5 M H 2 SO 4 , respectively, the ORR activity is confirmed by the high‐performance Zn‐air battery and proton exchange membrane fuel cell with a maximum power density of 191 and 370 mW cm −2 as cathodes, respectively. Moreover, the theoretical calculation verifies that the single GdN 5 moiety with specific f‐d hybridization facilitates the interaction with the intermediate OH* to produce the d‐p hybridization, which can significantly reduce the adsorption energy of OH*, while the existence of Gd x N y O z atomic clusters also can enhance the d‐p hybridization effect and effectively promote the ORR. The results confirm the atomic Gd‐N‐C as the new active site for ORR for the first time and extend the library of the M‐N‐C catalysts.
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