钙钛矿(结构)
材料科学
自旋态
协调球
自旋(空气动力学)
国家(计算机科学)
析氧
凝聚态物理
氧气
结晶学
化学物理
物理化学
热力学
冶金
物理
量子力学
化学
计算机科学
金属
电极
算法
电化学
作者
Di Yao,M. Y. Chai,Yunyun Lv,Enhui Wang,Tao Yang,Zhi Fang,Xinmei Hou
标识
DOI:10.1016/j.ceramint.2024.03.306
摘要
The evolution of oxygen evolution reaction (OER) remains a pivotal challenge in the realm of oxygen electrocatalysis. Recently, the proposition of regulating spin states has emerged as a novel avenue for enhancing the efficiency of electrocatalytic reactions. Presently, accurately modulating the metal active center into immediate spin (IS) remains a formidable challenge. Here, our research has achieved a breakthrough in precise spin state control and catalytic performance enhancement of Co3+ through the utilization of Ni-substituted LaCo1-xNixO3 perovskite. This achievement is primarily attributed to the fine regulation of both the secondary coordination sphere (SCS) and primary coordination sphere (PCS), i.e., Co6-y-[Co]-Niy (y = 0–6) and Co-O lengths, respectively. Our findings reveal that LaCo7/9Ni2/9O3 consisted of the SCS (y ≤ 2) with the eg1 fillings of IS Co3+ exhibits an optimal OER activity. Additionally, adjusting the Co-O bond length in PCS to approximately 1.89 Å proves to be more conducive to the transition of Co3+ spin states from high spin (HS) and low spin (LS) to IS. These discoveries present new approach to precisely modulating the spin state, offering promising prospects for the development of high-efficiency OER catalysts.
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