Single Atom Iridium Decorated Nickel Alloys Supported on Segregated MoO2 for Alkaline Water Electrolysis

Author:

Wang Bin12,Li Jiangnan1,Li Dongze3,Xu Junyuan3,Liu Shoujie4,Jiang Qike1,Zhang Yashi1,Duan Zhiyao5,Zhang Fuxiang1ORCID

Affiliation:

1. State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian National Laboratory for Clean Energy The Collaborative Innovation Center of Chemistry for Energy Materials (iChEM) Zhongshan Road 457 Dalian 116023 P. R. China

2. Center for Advanced Materials Research School of Materials and Chemical Engineering Zhongyuan University of Technology Zhongyuan Road 41 Zhengzhou 450007 P. R. China

3. Laboratory of Advanced Spectro‐Electrochemistry and Li‐Ion Batteries, Dalian Institute of Chemical Physics Chinese Academy of Sciences Zhongshan Road 457 Dalian 116023 P. R. China

4. School of Materials Science and Engineering Anhui University Jiulong Road 111 Hefei 230601 P. R. China

5. State Key Laboratory of Solidification Processing School of Materials Science and Engineering Northwestern Polytechnical University Dongxiang Road 1 Xi'an 710072 P. R. China

Abstract

AbstractHetero‐interface engineering has been widely employed to develop supported multicomponent catalysts for water electrolysis, but it still remains a substantial challenge for supported single atom alloys. Herein a conductive oxide MoO2 supported Ir1Ni single atom alloys (Ir1Ni@MoO2 SAAs) bifunctional electrocatalysts through surface segregation coupled with galvanic replacement reaction, where the Ir atoms are atomically anchored onto the surface of Ni nanoclusters via the Ir‐Ni coordination accompanied with electron transfer from Ni to Ir is reported. Benefiting from the unique structure, the Ir1Ni@MoO2 SAAs not only exhibit low overpotential of 48.6 mV at 10 mA cm−2 and Tafel slope of 19 mV dec−1 for hydrogen evolution reaction, but also show highly efficient alkaline water oxidation with overpotential of 280 mV at 10 mA cm−2. Their overall water electrolysis exhibits a low cell voltage of 1.52 V at 10 mA cm−2 and excellent durability. Experiments and theoretical calculations reveal that the Ir‐Ni interface effectively weakens hydrogen binding energy, and decoration of the Ir single atoms boost surface reconstruction of Ni species to enhance the coverage of intermediates (OH*) and switch the potential‐determining step. It is suggested that this approach opens up a promising avenue to design efficient and durable precious metal bifunctional electrocatalysts.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Natural Science Foundation of Shaanxi Province

Natural Science Foundation of Henan Province

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials,General Materials Science

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3