析氧
过电位
催化作用
材料科学
化学工程
纳米技术
分解水
电化学
电极
光催化
化学
有机化学
物理化学
工程类
作者
Depei Liu,Yuandong Yan,Li Hu,Duanduan Liu,Yandong Yang,Taozhu Li,Yu Du,Shicheng Yan,Tao Yu,Wei Zhou,Peixin Cui,Zhigang Zou
标识
DOI:10.1002/adma.202203420
摘要
Substantial overpotentials and insufficient and unstable active sites of oxygen evolution reaction (OER) electrocatalysts limit their efficiency and stability in OER-related energy conversion and storage technologies. Here, a template editing strategy is proposed to graft highly active catalytic species onto highly conductive rigid frameworks to tackle this challenge. As a successful attempt, two types of NiO6 units of layered Ni BDC (BDC stands for 1,4-benzenedicarboxylic acid) metal organic frameworks are selectively edited by chemical etching-assisted electroxidation to create layered γ-NiOOH with intercalated Ni-O species. In such an interlayer-confined intercalated architecture, the large interlayer space with high ion permeability offers an ideal reaction region to sufficiently expose the OER active sites comprising high-density intercalated Ni-O species, which also suppresses the undesirable γ to β phase transformation, thus exhibiting efficient and durable OER activity. As a result, water oxidation can occur at an extremely low overpotential of 130 mV and affords 1000 h stability at 100 mA cm-2 . The strategy conceptually shows the possibility of achieving stable homogeneous-like catalysis in heterogeneous catalysis.
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