In-situ transformation obtained defect-rich porous hollow CuO@CoZn-LDH nanoarrays as self-supported electrode for highly efficient overall water splitting

分解水 材料科学 化学工程 电化学 电解质 咪唑酯 电极 双功能 电解 电解水 析氧 纳米线 电催化剂 多孔性 催化作用 纳米技术 光催化 化学 复合材料 生物化学 物理化学 工程类
作者
Leilei Yin,Xi Du,Chenze Di,Mingwen Wang,Kunmei Su,Zhenhuan Li
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:414: 128809-128809 被引量:97
标识
DOI:10.1016/j.cej.2021.128809
摘要

Driving the electrochemical water splitting is considered as a green and sustainable method to produce hydrogen energy. Herein, a novel strategy to fabricate the dual-metal zeolitic imidazolate framework (CoZn-ZIF) nanocrystals on Cu(OH)2 nanowires supported by Cu foam (CF) as a precursor to change the conventional LDH growth has been proposed. It can obtain highly ordered hollow [email protected] nanoarrays with defect-rich porous surface for efficient overall water splitting. Specifically, the appropriate adjustment of Co/Zn metal ratios in the ZIF precursor could lead to a well-defined morphology to create the defect-rich porous surface, which exposes more active sites and the accessibility of electrolyte to promote the electrocatalytic efficiency. The obtained hollow [email protected]/CF nanoarrays catalyst exhibits an excellent activity in alkaline media with the low overpotentials of 194 mV and 124 mV at the current density of 10 mA cm−2 for OER and HER, respectively. Remarkably, as bifunctional electrodes for overall water splitting, it displays an alkali-electrolyzer with a low cell voltage of 1.55 V at the current density of 10 mA cm−2, and can be comparable to commercial the IrO2@CF||Pt/[email protected] couple catalyst. The work provides a new prospect for the rational design and fabrication of advanced hierarchical multifunctional electrocatalysts in electrochemical energy device application.
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