NiMOF-derived MoSe2@NiSe2 heterostructure with hollow core-shell for efficient hydrogen evolution reaction

IF 6.3 2区 材料科学 Q2 CHEMISTRY, PHYSICAL
Feng-bo Guo , Xin-ya Zhao , Yi-miao Yu , Jing Cheng , Kan-kan Liu , Li-xin Zhang
{"title":"NiMOF-derived MoSe2@NiSe2 heterostructure with hollow core-shell for efficient hydrogen evolution reaction","authors":"Feng-bo Guo ,&nbsp;Xin-ya Zhao ,&nbsp;Yi-miao Yu ,&nbsp;Jing Cheng ,&nbsp;Kan-kan Liu ,&nbsp;Li-xin Zhang","doi":"10.1016/j.jallcom.2023.169513","DOIUrl":null,"url":null,"abstract":"<div><p><span>Hydrogen production by electrochemical water splitting is one of the best ways to store renewable energy. Metal organic framework (MOF)-derived non-precious metal catalysts are an effective idea for large-scale commercialization and electrolysis of water for hydrogen production. Herein, we have synthesized Ni,Mo bimetallic selenide MoSe</span><sub>2</sub>@NiSe<sub>2</sub><span> heterojunctions with hollow core-shell using a selenization reaction to combine MoSe</span><sub>2</sub> with NiMOF-derived NiSe<sub>2</sub>. The spherical clusters of MoSe<sub>2</sub> prevents the agglomeration and sintering of NiSe<sub>2</sub><span> and shorten the electron transfer distance form MoSe</span><sub>2</sub> to NiSe<sub>2</sub>. The electron flow between the transition metals Ni and Mo after the selenization reaction, which alters the electronic structure of NiMOF and MoSe<sub>2</sub>. NiSe<sub>2</sub><span><span><span> derived from NiMOF provides more active center as well as better conductivity to accelerate the electron transfer rate. Thus facilitating the </span>HER catalytic process. </span>Electrochemical analysis confirmed that the activity of Hydrogen evolution reaction (HER) of MoSe</span><sub>2</sub>@NiSe<sub>2</sub> was significantly increased in 0.5 M H<sub>2</sub>SO<sub>4</sub>, with an overpotential of 187 mV at 10 mA cm<sup>−2</sup> and a tafel slope of 71.43 mV dec<sup>−1</sup>. This work provides a new route for the design and preparation of the NiMOF-based catalysts in HER.</p></div>","PeriodicalId":344,"journal":{"name":"Journal of Alloys and Compounds","volume":"947 ","pages":"Article 169513"},"PeriodicalIF":6.3000,"publicationDate":"2023-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"10","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Alloys and Compounds","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0925838823008162","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 10

Abstract

Hydrogen production by electrochemical water splitting is one of the best ways to store renewable energy. Metal organic framework (MOF)-derived non-precious metal catalysts are an effective idea for large-scale commercialization and electrolysis of water for hydrogen production. Herein, we have synthesized Ni,Mo bimetallic selenide MoSe2@NiSe2 heterojunctions with hollow core-shell using a selenization reaction to combine MoSe2 with NiMOF-derived NiSe2. The spherical clusters of MoSe2 prevents the agglomeration and sintering of NiSe2 and shorten the electron transfer distance form MoSe2 to NiSe2. The electron flow between the transition metals Ni and Mo after the selenization reaction, which alters the electronic structure of NiMOF and MoSe2. NiSe2 derived from NiMOF provides more active center as well as better conductivity to accelerate the electron transfer rate. Thus facilitating the HER catalytic process. Electrochemical analysis confirmed that the activity of Hydrogen evolution reaction (HER) of MoSe2@NiSe2 was significantly increased in 0.5 M H2SO4, with an overpotential of 187 mV at 10 mA cm−2 and a tafel slope of 71.43 mV dec−1. This work provides a new route for the design and preparation of the NiMOF-based catalysts in HER.

nimof衍生的MoSe2@NiSe2具有高效析氢反应的空心核壳异质结构
电化学水分解制氢是储存可再生能源的最佳方法之一。金属有机骨架(MOF)衍生的非贵金属催化剂是实现大规模商业化和电解制氢用水的有效思路。本文利用硒化反应将MoSe2与nimof衍生的NiSe2结合,合成了具有空心核壳的Ni,Mo双金属硒化物MoSe2@NiSe2异质结。MoSe2的球形团簇防止了NiSe2的团聚和烧结,缩短了MoSe2到NiSe2的电子转移距离。硒化反应后过渡金属Ni和Mo之间的电子流动改变了NiMOF和MoSe2的电子结构。NiMOF衍生的nis2具有更强的活性中心和更好的导电性,可以加快电子传递速率。从而促进了HER催化过程。电化学分析证实,在0.5 M H2SO4溶液中,MoSe2@NiSe2的析氢反应(HER)活性显著提高,在10 mA cm−2下过电位为187 mV,塔非斜率为71.43 mV dec−1。本研究为纳米镍钼基催化剂的设计和制备提供了一条新的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Alloys and Compounds
Journal of Alloys and Compounds 工程技术-材料科学:综合
CiteScore
11.10
自引率
14.50%
发文量
5146
审稿时长
67 days
期刊介绍: The Journal of Alloys and Compounds is intended to serve as an international medium for the publication of work on solid materials comprising compounds as well as alloys. Its great strength lies in the diversity of discipline which it encompasses, drawing together results from materials science, solid-state chemistry and physics.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信