催化作用
吸附
化学
塔菲尔方程
同步加速器
酞菁
氧气
材料科学
物理化学
电极
物理
有机化学
电化学
核物理学
作者
Kejun Chen,Kang Liu,Pengda An,Huangjingwei Li,Yiyang Lin,Junhua Hu,Chuankun Jia,Junwei Fu,Hongmei Li,Lei Zhu,Zhang Lin,Wenzhang Li,Jiahang Li,Ying‐Rui Lu,Ting‐Shan Chan,Ning Zhang,Min Liu
标识
DOI:10.1038/s41467-020-18062-y
摘要
Abstract Iron phthalocyanine (FePc) is a promising non-precious catalyst for the oxygen reduction reaction (ORR). Unfortunately, FePc with plane-symmetric FeN 4 site usually exhibits an unsatisfactory ORR activity due to its poor O 2 adsorption and activation. Here, we report an axial Fe–O coordination induced electronic localization strategy to improve its O 2 adsorption, activation and thus the ORR performance. Theoretical calculations indicate that the Fe–O coordination evokes the electronic localization among the axial direction of O–FeN 4 sites to enhance O 2 adsorption and activation. To realize this speculation, FePc is coordinated with an oxidized carbon. Synchrotron X-ray absorption and Mössbauer spectra validate Fe–O coordination between FePc and carbon. The obtained catalyst exhibits fast kinetics for O 2 adsorption and activation with an ultralow Tafel slope of 27.5 mV dec −1 and a remarkable half-wave potential of 0.90 V. This work offers a new strategy to regulate catalytic sites for better performance.
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