钴
催化作用
过电位
金属有机骨架
氧化钴
析氧
分解水
氧化物
无机化学
咪唑酯
材料科学
化学工程
双功能
钌
金属
化学
物理化学
电极
有机化学
电化学
吸附
光催化
工程类
作者
Yizhong Zou,Wenda Zhang,Ming Chen,Jiangyong Liu,Zhi‐Guo Gu,Xiaodong Yan
标识
DOI:10.1016/j.jcis.2023.09.040
摘要
The influence of the preorganized structure and chemical composition of metal-organic frameworks (MOFs) on the morphology, surface properties, and catalytic activity of the MOFs-derived metal oxides is yet to be revealed. In this work, two types of Co-MOFs with different coordination configurations are synthesized for the preparation of the structure-engineered ruthenium (Ru)-doped cobalt oxides. The effect of the preorganized coordination structure of the MOFs on the morphology and surface properties is investigated. Interestingly, the oxalate-based MOFs derived Ru-doped cobalt oxide (OX-Co3O4-Ru) exhibits much better surface wettability and more oxygen vacancies than the zeolitic imidazolate framework-67 derived Ru-doped cobalt oxide. As expected, the OX-Co3O4-Ru owns excellent catalytic properties towards both hydrogen evolution reaction and oxygen evolution reaction with an overpotential of 49 and 286 mV, respectively at a current density of 100 mA cm-2 in 1.0 M KOH. Importantly, the bifunctional OX-Co3O4-Ru catalyst offers an extremely high current density of 500 mA cm-2 at a cell voltage of 1.71 V for overall water splitting and as well demonstrates robust working stability.
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