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通过原位蚀刻将阳离子空位引入NiFe层状双氢氧化物以改善整体析水性能

Introduction of Cationic Vacancies into NiFe LDH by In Situ Etching To Improve Overall Water Splitting Performance.

作者信息

Zhang Baojie, Qiu Shipeng, Xing Yupeng, Zhao Gang, Liao Wenbo, Mu Lan, Zhao Ning

机构信息

School of Physics and Technology, University of Jinan, Jinan 250022, P. R. China.

State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410017, PR China.

出版信息

Langmuir. 2023 Dec 12;39(49):18152-18160. doi: 10.1021/acs.langmuir.3c03194. Epub 2023 Nov 29.

DOI:10.1021/acs.langmuir.3c03194
PMID:38019648
Abstract

Nickel-iron layered double hydroxide (NiFe LDH) is still one of the hot catalysts for electrochemical water decomposition applications, despite its drawbacks, such as intrinsic activity and poor stability. In this work, the NiFe LDH-D1 electrocatalyst with cationic vacancies is successfully prepared by alkaline etching of Zn ion-doped NiFe LDH. The tightly arranged flocculated nanosheet structure on its surface provided a large active area. The cationic vacancies formed by strong alkaline etching not only promote the conversion of active phases such as NiOOH but also strengthen the stability of the electrode and the binding ability with oxygen so that the material has excellent catalytic properties along with alkaline long-term stability. At a current density of 10 and 100 mA cm, NiFe LDH-D1 shows a small voltage of 1.56 and 1.94 V, and at a current density of 200 mA cm, it performs well in a 72 h electrochemical water decomposition stability test. The present work demonstrates a simple etching strategy for cation vacancy engineering and provides an example of the construction of efficient bifunctional electrocatalysts with long-term stability.

摘要

镍铁层状双氢氧化物(NiFe LDH)尽管存在诸如本征活性和稳定性差等缺点,但仍是电化学水分解应用中的热门催化剂之一。在这项工作中,通过对锌离子掺杂的NiFe LDH进行碱性蚀刻,成功制备了具有阳离子空位的NiFe LDH-D1电催化剂。其表面紧密排列的絮凝纳米片结构提供了较大的活性面积。强碱性蚀刻形成的阳离子空位不仅促进了诸如NiOOH等活性相的转化,还增强了电极的稳定性以及与氧的结合能力,从而使该材料具有优异的催化性能以及碱性长期稳定性。在电流密度为10和100 mA/cm²时,NiFe LDH-D1的电压分别为1.56和1.94 V,并且在电流密度为200 mA/cm²时,它在72小时的电化学水分解稳定性测试中表现良好。本工作展示了一种用于阳离子空位工程的简单蚀刻策略,并提供了构建具有长期稳定性的高效双功能电催化剂的示例。

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引用本文的文献

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