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具有由氧和不饱和金属空位诱导的定制表面电子构型的层状FeCoNi双氢氧化物,用于促进整体水分解过程。

Layered FeCoNi double hydroxides with tailored surface electronic configurations induced by oxygen and unsaturated metal vacancies for boosting the overall water splitting process.

作者信息

Zhai Zibo, Yan Wei, Zhang Jiujun

机构信息

Institute for Sustainable Energy/College of Sciences, Shanghai University, Shanghai, China 200444.

出版信息

Nanoscale. 2022 Mar 17;14(11):4156-4169. doi: 10.1039/d2nr00143h.

Abstract

Two-dimensional (2D) layered double hydroxides (LDH) with excellent hydrophilic ability and rapid hydroxyl insertion are regarded as one of the most promising electrocatalysts for both the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) for overall water splitting to produce hydrogen. However, the electrocatalytic HER/OER activities can be restricted by the inert basal plane due to the poor conductivity, deficient active sites and inferior durability despite there being efficient active sites in the material edge. Thus, capturing many more exposed reactive sites to facilitate the rapid reaction kinetics is a crucial strategy. In this paper, both oxygen and unsaturated metal vacancies with FeCoNi LDH materials are generated through a surface activation approach by pre-covering of fluoride and a post-boronizing process. Such a material is grown on Ni foam to form an F-FeCoNi-Ov LDH/NF electrocatalyst. The activated surface of the electrocatalyst with oxygen vacancies and unsaturated metal sites shows enhanced electroconductivity for regulating the surface electronic structure and optimizing the surface adsorption energy for intermediates during HER/OER processes. As a result, this electrocatalyst exhibits excellent electrocatalytic performance for both the HER and OER with low overpotentials, small Tafel slopes and long durability. The enhancement mechanism is also studied deeply for fundamental understanding. For performance validation, an F-FeCoNi-Ov LDH/NF∥F-FeCoNi-Ov LDH/NF water splitting cell is fabricated and needs only 1.54 V and 1.81 V to reach current densities of 10 and 100 mA cm, respectively. This work provides a practicable strategy to develop 2D LDH nanomaterials with boosted electrocatalytic activity for sustainable and clean energy storage systems.

摘要

具有优异亲水性和快速羟基插入能力的二维(2D)层状双氢氧化物(LDH)被认为是用于全水解制氢的析氧反应(OER)和析氢反应(HER)最有前景的电催化剂之一。然而,尽管材料边缘存在高效活性位点,但由于导电性差、活性位点不足和耐久性较差,惰性基面会限制电催化HER/OER活性。因此,捕获更多暴露的反应位点以促进快速反应动力学是一项关键策略。本文通过氟化物预覆盖和后硼化过程的表面活化方法,在FeCoNi LDH材料中产生了氧和不饱和金属空位。这种材料生长在泡沫镍上,形成F-FeCoNi-Ov LDH/NF电催化剂。具有氧空位和不饱和金属位点的电催化剂活化表面显示出增强的导电性,用于调节表面电子结构并优化HER/OER过程中中间体的表面吸附能。结果,这种电催化剂在HER和OER方面均表现出优异的电催化性能,具有低过电位、小塔菲尔斜率和长耐久性。还对增强机制进行了深入研究以获得基本理解。为了验证性能,制备了F-FeCoNi-Ov LDH/NF∥F-FeCoNi-Ov LDH/NF水电解槽,分别仅需1.54 V和1.81 V即可达到10和100 mA cm的电流密度。这项工作为开发具有增强电催化活性的二维LDH纳米材料以用于可持续和清洁能源存储系统提供了一种可行的策略。

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