脱氢
过电位
析氧
电催化剂
塔菲尔方程
钴
电化学
化学
材料科学
无机化学
催化作用
电极
物理化学
有机化学
作者
Yan Liu,Shuangshuang Zhang,Chi Jiao,Huimei Chen,Gang Wang,Wenjie Wu,Zhiwen Zhuo,Junjie Mao
标识
DOI:10.1002/advs.202206107
摘要
Cobalt single atoms coordinated with planar four nitrogen atoms (Co1 N4 ) represent an efficient electrocatalyst for oxygen evolution reaction (OER), whereas the large energy barrier of CoOH dehydrogenation limits the OER activity. Herein, axial phosphate (PO4 ) coordination is incorporated in Co1 N4 single atoms of cobalt phthalocyanine@carbon nanotubes (P-CoPc@CNT), so as to boost the intrinsic OER performance through manipulating the reaction pathway. With a relative low mass loading of Co (2.7%), the P-CoPc@CNT shows remarkable alkaline OER activity with the overpotential of 300 mV and Tafel slope of 41.7 mV dec-1 , which dramatically outperforms the CoPc@CNT without axial PO4 coordination. Based on mechanistic analysis, the axial PO4 coordination directly participates in the OER cycle by the transformation of axial ligand. Specially, the CoOH dehydrogenation process is replaced by the dehydrogenation of HPO4 -Co1 N4 intermediate, which largely decreases the energy barrier and thus benefits the whole OER process.
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