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用于碱性溶液中电化学水分解的双功能自支撑NiFeP层包覆NiP棒材

Bifunctional and Self-Supported NiFeP-Layer-Coated NiP Rods for Electrochemical Water Splitting in Alkaline Solution.

作者信息

Diao Fangyuan, Huang Wei, Ctistis Georgios, Wackerbarth Hainer, Yang Yuan, Si Pengchao, Zhang Jingdong, Xiao Xinxin, Engelbrekt Christian

机构信息

Department of Chemistry, Technical University of Denmark, DK-2800 Kongens Lyngby, Denmark.

Department of Photonic Sensor Technology, Institut für Nanophotonik Göttingen, Hans-Adolf-Krebs-Weg 1, 37077 Göttingen, Germany.

出版信息

ACS Appl Mater Interfaces. 2021 May 26;13(20):23702-23713. doi: 10.1021/acsami.1c03089. Epub 2021 May 11.

DOI:10.1021/acsami.1c03089
PMID:33974401
Abstract

Designing efficient and robust nonprecious metal-based electrocatalysts for overall water electrolysis, which is mainly limited by the oxygen evolution reaction (OER), for hydrogen production remains a major challenge for the hydrogen economy. In this work, a bimetallic NiFeP catalyst is coated on nickel phosphide rods grown on nickel foam (NiFeP@NiP@NF). This self-supported and interfacially connected electrode structure is favorable for mass transfer and reducing electrical resistance during electrocatalysis. The preparation of NiFeP@NiP@NF is optimized in terms of (i) the coprecipitation time of the NiFe Prussian blue analogue layer that serves as phosphides precursor and (ii) the phosphidation temperature. The optimized sample exhibits excellent OER performance delivering current densities of 10 and 100 mA cm at low overpotentials of 227 and 252 mV in 1.0 M KOH, respectively, and maintaining 10 mA cm for more than 120 h without obvious degradation. Moreover, it can also be operated as a hydrogen evolution electrocatalyst, requiring an overpotential of 105 mV at 10 mA cm in the same medium. Thus, the as-prepared material was tentatively utilized as a bifunctional electrocatalyst in a symmetric electrolyzer, requiring a voltage bias of 1.57 V to afford 10 mA cm in 1.0 M KOH, while exhibiting outstanding stability.

摘要

设计用于全水解的高效且耐用的非贵金属基电催化剂仍然是氢经济面临的一项重大挑战,全水解主要受析氧反应(OER)限制,目的是制氢。在这项工作中,一种双金属NiFeP催化剂被涂覆在生长于泡沫镍上的磷化镍棒上(NiFeP@NiP@NF)。这种自支撑且界面连接的电极结构有利于传质并降低电催化过程中的电阻。NiFeP@NiP@NF的制备在以下方面进行了优化:(i)用作磷化物前驱体的NiFe普鲁士蓝类似物层的共沉淀时间,以及(ii)磷化温度。优化后的样品表现出优异的OER性能,在1.0 M KOH中,在227和252 mV的低过电位下分别提供10和100 mA cm²的电流密度,并在10 mA cm²下保持超过120小时而无明显降解。此外,它还可以用作析氢电催化剂,在相同介质中,在10 mA cm²下需要105 mV的过电位。因此,所制备的材料被初步用作对称电解槽中的双功能电催化剂,在1.0 M KOH中提供10 mA cm²需要1.57 V的电压偏置,同时表现出出色的稳定性。

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