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脉冲电沉积超亲水且无粘结剂的Ni-Fe-P纳米结构作为用于析氢反应和析氧反应的高活性耐用型电催化剂

Pulse Electrodeposition of a Superhydrophilic and Binder-Free Ni-Fe-P Nanostructure as Highly Active and Durable Electrocatalyst for Both Hydrogen and Oxygen Evolution Reactions.

作者信息

Barati Darband Ghasem, Aliofkhazraei Mahmood, Hyun Suyeon, Shanmugam Sangaraju

机构信息

Department of Materials Engineering, Tarbiat Modares University, 14115-143 Tehran, Iran.

Materials and Metallurgical Engineering Department, Faculty of Engineering, Ferdowsi University of Mashhad, Mashhad 91775-1111, Iran.

出版信息

ACS Appl Mater Interfaces. 2020 Dec 2;12(48):53719-53730. doi: 10.1021/acsami.0c13648. Epub 2020 Nov 18.

DOI:10.1021/acsami.0c13648
PMID:33206495
Abstract

Development and fabrication of electrodes with favorable electrocatalytic activity, low-cost, and excellent electrocatalytic durability are one of the most important issues in the hydrogen production area using the electrochemical water splitting process. We use the pulse electrodeposition method as a versatile and cost-effective approach to synthesize three-dimensional Ni-Fe-P electrocatalysts on nickel nanostructures under various applied frequencies and duration times, in which nanostructures exhibit excellent intrinsic electrocatalytic activity. Benefiting from the three-dimensional structure, as well as the simultaneous presence of the three elements nickel, iron, and phosphorus, the electrode fabricated at the optimal conditions has indicated outstanding electrocatalytic activity with a η of 66 and 198 mV for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), respectively, in a 1.0 M KOH solution. Also, the water electrolysis cell constructed with this electrode and tested as a bifunctional electrode exhibited 1.508 V for 10 mA cm in overall water splitting. In addition, the lowest amount of potential change in 100 mA cm was observed for HER and OER, indicating excellent electrocatalytic stability. This study proposes a binder-free and economical technique for the synthesis of three-dimensional electrocatalysts.

摘要

开发和制造具有良好电催化活性、低成本且具有优异电催化耐久性的电极是电化学水分解制氢领域最重要的问题之一。我们采用脉冲电沉积法,这是一种通用且经济高效的方法,在不同的施加频率和持续时间下,在镍纳米结构上合成三维Ni-Fe-P电催化剂,其中纳米结构表现出优异的固有电催化活性。得益于三维结构以及镍、铁和磷这三种元素的同时存在,在最佳条件下制备的电极在1.0 M KOH溶液中对析氢反应(HER)和析氧反应(OER)分别表现出出色的电催化活性,η分别为66和198 mV。此外,用该电极构建并作为双功能电极测试的水电解槽在全水分解中,10 mA cm²时的电压为1.508 V。另外,在100 mA cm²时,HER和OER的电位变化量最低,表明具有优异的电催化稳定性。本研究提出了一种用于合成三维电催化剂的无粘结剂且经济的技术。

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