磷化物
纳米线
分解水
材料科学
催化作用
化学工程
镍
过渡金属
电子转移
双功能
纳米技术
析氧
化学
光化学
冶金
电化学
电极
有机化学
物理化学
工程类
光催化
作者
Dongdong Wang,Yiwei Zhang,Ting Fei,Chunfeng Mao,Youchao Song,Yuming Zhou,Guomeng Dong
标识
DOI:10.1002/celc.202100487
摘要
Abstract The construction of a well‐defined metal‐organic framework (MOF) precursor structure is essential to obtain highly efficient transition metal phosphide electrocatalysts for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in water splitting. In this regard, we propose a novel strategy involving the in situ conversion of flake nickel‐cobalt hydroxide into NiCo MOF with a unique biomimetic architecture (i. e. Venus flytrap‐like morphology with dense 1D nanowires anchoring on 2D nanosheets), and further phosphating the precursor into NiCoP that possesses a similar, distinctive structure. Specifically, 1D nanowires afford effective electron transfer, while 2D nanosheets provide enhanced mechanical stability to the composite. The experimental results show that this material has an enormous amount of available active sites, accelerated charge/mass transfer, and a structural synergistic effect. As a result, the as‐prepared NiCoP/nickel foam (NF) catalyst only requires overpotentials of 78 and 262 mV to reach a current density of 10 mA cm −2 for the HER and OER in 1.0 M KOH, respectively. Furthermore, the application of NiCoP/NF as a bifunctional catalyst for the overall water splitting reaction yields current densities of 10 mA cm −2 at 1.60 V. Therefore, this is an effective strategy for the development of next‐generation electrocatalysts for solar‐energy conversion.
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