过电位
镍黄铁矿
析氧
电子转移
自旋态
动力学
化学
自旋跃迁
化学物理
氧气
自旋(空气动力学)
吸附
化学工程
材料科学
光化学
纳米技术
物理化学
无机化学
结晶学
电化学
热力学
矿物学
有机化学
物理
量子力学
工程类
黄铁矿
磁黄铁矿
电极
作者
Zhengyan Du,Zeshuo Meng,Xiliang Gong,Zeyu Hao,Xin Li,Haoteng Sun,Xiaoying Hu,Shansheng Yu,Hongwei Tian
标识
DOI:10.1002/ange.202317022
摘要
Abstract Triggering rapid reconstruction reactions holds the potential to approach the theoretical limits of the oxygen evolution reaction (OER), and spin state manipulation has shown great promise in this regard. In this study, the transition of Fe spin states from low to high was successfully achieved by adjusting the surface electronic structure of pentlandite. In situ characterization and kinetic simulations confirmed that the high‐spin state of Fe promoted the accumulation of OH − on the surface and accelerated electron transfer, thereby enhancing the kinetics of the reconstruction reaction. Furthermore, theoretical calculations revealed that the lower d‐band center of high‐spin Fe optimized the adsorption of active intermediates, thereby enhancing the reconstruction kinetics. Remarkably, pentlandites with high‐spin Fe exhibited ultra‐low overpotential (245 mV @ 10 mA cm −2 ) and excellent stability. These findings provided new insights for the design and fabrication of highly active OER electrocatalysts.
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