双功能
普鲁士蓝
氧化还原
材料科学
催化作用
分解水
析氧
化学工程
基质(水族馆)
镍
纳米技术
金属
无机化学
电化学
化学
电极
冶金
物理化学
有机化学
光催化
工程类
海洋学
地质学
作者
Shuang Wang,Jinguang Cai,Chao Lv,Cun Hu,Hongtai Guan,Junqiang Wang,Yan Shi,Jiangfeng Song,Akira Watanabe,Xingbo Ge
标识
DOI:10.1016/j.cej.2021.129972
摘要
Prussian blue analogs (PBA) and their derivatives show great application potentials in energy and environmental fields. However, the preparation of PBA and their derivatives on specific substrates are still far from practical use. Herein, we propose an innovative general and scalable strategy to grow PBA coatings on any conductive substrates including Ni, Co, stainless steel, Mo, W, Ti, Ta, Ni/carbon cloth (CC), and FTO with large sizes and high curvatures through spontaneous growth or electrodeposited seeds assisted epitaxial growth in solution. The potential difference between Fe3+/Fe2+ redox pair in the solution and metal ions/metal redox pair of the metal substrate may promote the release of metal ions from the substrate and induce the spontaneous growth. As a demonstration, PBA/Ni/CC samples prepared on Ni/CC substrates with this approach were transformed into nickel iron phosphides (NiFeP/CC) via a simple phosphidation process, which show excellent bifunctional electrocatalytic activities towards oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) due to the unique structures and desirable chemical compositions. It only requires very low overpotentials of 260 mV to achieve 200 mA cm−2 for OER and 129 mV to achieve 10 mA cm−2 for HER, respectively. Furthermore, the NiFeP/CC|| NiFeP/CC couple requires a low cell voltage of 1.57 V to reach 10 mA cm−2 and shows an ultralong lifetime with no obvious degradation after electrolyzing for 300 h, which is much superior to many other reported electrocatalysts. This work provides a facile strategy for designing efficient bifunctional electrocatalysts derived from spontaneously grown PBAs.
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