化学
活动站点
还原(数学)
自旋态
自旋(空气动力学)
氧气
氧还原反应
中心(范畴论)
国家(计算机科学)
活动中心
无机化学
结晶学
物理化学
催化作用
热力学
有机化学
物理
几何学
数学
电极
算法
计算机科学
电化学
作者
Ki-Won Kim,Gyuchan Kim,Tae-Young Jeong,Won Young Lee,Yi-Lin Yang,Byung‐Hyun Kim,Bubryur Kim,Byeongyong Lee,Joonhee Kang,Myeongjin Kim
摘要
The ligand engineering for single-atom catalysts (SACs) is considered a cutting-edge strategy to tailor their electrocatalytic activity. However, the fundamental reasons underlying the reaction mechanism and the contemplation for which the actual active site for the catalytic reaction depends on the pyrrolic and pyridinic N ligand structure remain to be fully understood. Herein, we first reveal the relationship between the oxygen reduction reaction (ORR) activity and the N ligand structure for the manganese (Mn) single atomic site by the precisely regulated pyrrolic and pyridinic N
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