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核壳型 NiFe-LDH@NiFe-B 纳米阵列:在近中性介质中高效水氧化电催化的原位电化学表面衍生制备。

Core-Shell NiFe-LDH@NiFe-B Nanoarray: In Situ Electrochemical Surface Derivation Preparation toward Efficient Water Oxidation Electrocatalysis in near-Neutral Media.

机构信息

College of Chemistry and Chemical Engineering, Qufu Normal University , Qufu 273165, Shandong, China.

Chengdu Institute of Geology and Mineral Resources , Chengdu 610064, China.

出版信息

ACS Appl Mater Interfaces. 2017 Jun 14;9(23):19502-19506. doi: 10.1021/acsami.7b01637. Epub 2017 Jun 1.

Abstract

The corrosion issue with acidic and alkaline water electrolyzers can be avoided by developing water oxidation catalysts performing efficiently under benign conditions. In this Letter, we report that a NiFe-borate layer can be generated on a NiFe-layered double hydroxide nanosheet array hydrothermally grown on carbon cloth via an in situ electrochemical surface derivation process in potassium borate (K-B) solution. The resulting 3D NiFe-LDH@NiFe-B nanoarray (NiFe-LDH@NiFe-B/CC) demonstrates high activity for water oxidation, demanding overpotentials of 444 and 363 mV to achieve 10 mA cm in 0.1 and 0.5 M K-B (pH: 9.2), respectively, rivaling the performances of most reported non-noble-metal catalysts in near-neutral media. Notably, this electrode also shows strong electrochemical durability with a high turnover frequency of 0.54 mol O s at overpotential of 600 mV. All these features promise its use as an efficient earth-abundant catalyst material for water oxidation under eco-friendly conditions.

摘要

通过开发在良性条件下高效工作的水氧化催化剂,可以避免酸性和碱性水电解槽的腐蚀问题。在本通讯中,我们报告了一种方法,即在硼酸钾(K-B)溶液中通过原位电化学表面衍生过程,可在水热生长在碳布上的 NiFe-层状双氢氧化物纳米片阵列上生成 NiFe-硼酸盐层。所得的 3D NiFe-LDH@NiFe-B 纳米阵列(NiFe-LDH@NiFe-B/CC)对水氧化表现出高活性,在 0.1 和 0.5 M K-B(pH:9.2)中分别需要 444 和 363 mV 的过电势才能达到 10 mA cm,可与大多数在近中性介质中报道的非贵金属催化剂的性能相媲美。值得注意的是,该电极在 600 mV 的过电势下还具有高的 0.54 mol O s 的周转频率,表现出很强的电化学耐久性。所有这些特性都预示着它在环保条件下作为一种高效的、丰富的地球催化剂材料在水氧化中的应用前景。

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