纳米片
电解
原位
离子交换
材料科学
膜
电极
电解水
离子
化学工程
电化学
纳米技术
无机化学
化学
电解质
有机化学
工程类
生物化学
物理化学
作者
Qi Song,Tongguang Xu,Chengxu Tu,Kaili Li,Qian Kong,Gang He,Linglong Yao,Yufan Wang,Hongyu Liu,Tao Wan,Xiaoping Dai,Xin Zhang
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2024-06-01
卷期号:18 (6): 94907487-94907487
被引量:2
标识
DOI:10.26599/nr.2025.94907487
摘要
Design of efficient non-precious metal electrodes for anion exchange membrane water electrolysis (AEMWE) is an ongoing challenge. We in-situ constructed a CoFe LDH nanosheet array (CoFe LDH NS array) on Nickel foam. Only 275 mV of low overpotential was required for the electrode to achieve a current density of 1000 mA cm-2 for OER and stable operation for over 200 hours. The high catalytic activity, mechanical stability as well as electrical conductivity could be ascribed to the intimate interfacial contact between NF substrate with NiS intermediate layer and CoFe LDH. Moreover, the unique superaerophobic surface of the nanosheet arrays promoted the release of the bubble and the re-engagement of the electrolyte with the active sites. In-situ Raman results certified that in the OER process, CoOOH was the true active phase of the catalyst. In AEMWE tests, CoFe LDH-NS arrays || Pt/C/CP arrays outperformed commercial IrO2 at 80 °C and 1.62 V to actuate 1 A cm-2, and stable operating over 1500 hours. This morphology-dependent enhancement strategy may lead to new references for efficient electrode design for the next generation of AEMWE.
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