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用于在高电流密度下高效且超稳定析氧反应的原位重构锌掺杂铁镍羟基氧化物催化剂

In Situ Reconstructed Zn doped Fe Ni OOH Catalyst for Efficient and Ultrastable Oxygen Evolution Reaction at High Current Densities.

作者信息

Zhang Xian, Yi Hao, Jin Mengtian, Lian Qing, Huang Yu, Ai Zhong, Huang Runqing, Zuo Ziteng, Tang Chunmei, Amini Abbas, Jia Feifei, Song Shaoxian, Cheng Chun

机构信息

Department of Materials Science and Engineering, Southern University of Science and Technology, Shenzhen, 518055, China.

School of Resources and Environmental Engineering, Wuhan University of Technology, Luoshi Road 122, Wuhan, Hubei, 430070, China.

出版信息

Small. 2022 Sep;18(37):e2203710. doi: 10.1002/smll.202203710. Epub 2022 Aug 12.

Abstract

Developing FeOOH as a robust electrocatalyst for high output oxygen evolution reaction (OER) remains challenging due to its low conductivity and dissolvability in alkaline conditions. Herein, it is demonstrated that the robust and high output Zn doped NiOOH-FeOOH (Zn-Fe Ni )OOH catalyst can be derived by electro-oxidation-induced reconstruction from the pre-electrocatalyst of Zn modified Ni metal/FeOOH film supported by nickel foam (NF). In situ Raman and ex situ characterizations elucidate that the pre-electrocatalyst undergoes dynamic reconstruction occurring on both the catalyst surface and underneath metal support during the OER process. That involves the Fe dissolution-redeposition and the merge of Zn doped FeOOH with in situ generated NiOOH from NF support and NiZn alloy nanoparticles. Benefiting from the Zn doping and the covalence interaction of FeOOH-NiOOH, the reconstructed electrode shows superior corrosion resistance, and enhanced catalytic activity as well as bonding force at the catalyst-support interface. Together with the feature of superaerophobic surface, the reconstructed electrode only requires an overpotential of 330 mV at a high-current-density of 1000 mA cm and maintains 97% of its initial activity after 1000 h. This work provides an in-depth understanding of electrocatalyst reconstruction during the OER process, which facilitates the design of high-performance OER catalysts.

摘要

由于FeOOH在碱性条件下的低导电性和溶解性,将其开发成用于高输出析氧反应(OER)的稳健电催化剂仍然具有挑战性。在此,证明了通过对泡沫镍(NF)负载的Zn修饰的Ni金属/FeOOH薄膜的预电催化剂进行电氧化诱导重构,可以得到稳健且高输出的Zn掺杂NiOOH-FeOOH(Zn-Fe Ni)OOH催化剂。原位拉曼光谱和非原位表征表明,预电催化剂在OER过程中在催化剂表面和金属载体下方均发生动态重构。这涉及Fe的溶解-再沉积以及Zn掺杂的FeOOH与来自NF载体的原位生成的NiOOH和NiZn合金纳米颗粒的合并。得益于Zn掺杂以及FeOOH-NiOOH的共价相互作用,重构后的电极表现出优异的耐腐蚀性、增强的催化活性以及催化剂-载体界面处的结合力。连同超疏气表面的特性,重构后的电极在1000 mA cm的高电流密度下仅需要330 mV的过电位,并且在1000 h后仍保持其初始活性的97%。这项工作为深入理解OER过程中的电催化剂重构提供了依据,有助于高性能OER催化剂的设计。

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