In Situ Active Site Refreshing of Electro-Catalytic Materials for Ultra-Durable Hydrogen Evolution at Elevated Current Density
2024
发表期刊ADVANCED ENERGY MATERIALS (IF:24.4[JCR-2023],27.2[5-Year])
ISSN1614-6832
EISSN1614-6840
卷号14期号:17
发表状态已发表
DOI10.1002/aenm.202304099
摘要

["Enhancing the durability of catalysts is of critical significance to industrialize green hydrogen production. Herein, a novel active site in situ refreshing strategy is proposed and demonstrated to fabricate highly active and ultra-durable hydrogen evolution reaction (HER) electro-catalytic material by HER activation. Briefly, a composite catalytic material is synthesized, which features Ni(PO3)2 active sites being embedded inside the amorphous Mo compound matrix (named NiMoO-P). The Mo compound matrix undergoes gradual dissolution during HER followed by a dynamic equilibrium between the dissolution and deposition of the amorphous matrix. This process promotes the continuous exposure of insoluble Ni(PO3)2 and Ni2P partially converted from Ni (PO3) 2 in situ on the surface during HER activation. Thus, activated catalyst exhibits excellent HER performance featuring an extremely high current density of 1500 mA cm-2 at a rather low overpotential of 340 mV, and more attractively, an ultra-long durability for hydrogen evolution for at least 1000 h at an industrial-applicable current density of 900 mA cm-2. The mechanisms for the especially high HER performance are attributed to the exposure and continuous refreshing of Ni(PO3)2 and the in situ formed Ni2P during the HER process based on the DFT calculations and quasi-in situ Raman spectroscopic monitoring.","An active site in situ refreshing strategy is proposed to fabricate highly active and ultra-durable hydrogen evolution reaction (HER) electro-catalytic material by HER activation, in which Mo compound matrix undergoes gradual dissolution during HER followed by a dynamic equilibrium between the dissolution and deposition, leading to the high HER performance and ultra-long durability at industrial-applicable current density.image"]

关键词durability HER in situ refreshing industrial current density
URL查看原文
收录类别SCI ; EI
语种英语
资助项目National Natural Science Foundation of China[
WOS研究方向Chemistry ; Energy & Fuels ; Materials Science ; Physics
WOS类目Chemistry, Physical ; Energy & Fuels ; Materials Science, Multidisciplinary ; Physics, Applied ; Physics, Condensed Matter
WOS记录号WOS:001147105600001
出版者WILEY-V C H VERLAG GMBH
EI入藏号20240415428845
EI主题词Current density
EI分类号522 Gas Fuels ; 701.1 Electricity: Basic Concepts and Phenomena ; 802.2 Chemical Reactions ; 802.3 Chemical Operations ; 803 Chemical Agents and Basic Industrial Chemicals ; 804 Chemical Products Generally
原始文献类型Journal article (JA)
引用统计
正在获取...
文献类型期刊论文
条目标识符https://kms.shanghaitech.edu.cn/handle/2MSLDSTB/349695
专题物质科学与技术学院
物质科学与技术学院_博士生
通讯作者Cui, Xiangzhi; Shi, Jianlin
作者单位
1.Shanghai Tech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
2.Chinese Acad Sci, Shanghai Inst Ceram, Shanghai 200050, Peoples R China
3.Univ Chinese Acad Sci, Hangzhou Inst Adv Study, Sch Chem & Mat Sci, Hangzhou 310024, Peoples R China
第一作者单位物质科学与技术学院
第一作者的第一单位物质科学与技术学院
推荐引用方式
GB/T 7714
Li, Qin,Chen, Chang,Luo, Wenshu,et al. In Situ Active Site Refreshing of Electro-Catalytic Materials for Ultra-Durable Hydrogen Evolution at Elevated Current Density[J]. ADVANCED ENERGY MATERIALS,2024,14(17).
APA Li, Qin.,Chen, Chang.,Luo, Wenshu.,Yu, Xu.,Chang, Ziwei.,...&Shi, Jianlin.(2024).In Situ Active Site Refreshing of Electro-Catalytic Materials for Ultra-Durable Hydrogen Evolution at Elevated Current Density.ADVANCED ENERGY MATERIALS,14(17).
MLA Li, Qin,et al."In Situ Active Site Refreshing of Electro-Catalytic Materials for Ultra-Durable Hydrogen Evolution at Elevated Current Density".ADVANCED ENERGY MATERIALS 14.17(2024).
条目包含的文件
文件名称/大小 文献类型 版本类型 开放类型 使用许可
个性服务
查看访问统计
谷歌学术
谷歌学术中相似的文章
[Li, Qin]的文章
[Chen, Chang]的文章
[Luo, Wenshu]的文章
百度学术
百度学术中相似的文章
[Li, Qin]的文章
[Chen, Chang]的文章
[Luo, Wenshu]的文章
必应学术
必应学术中相似的文章
[Li, Qin]的文章
[Chen, Chang]的文章
[Luo, Wenshu]的文章
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。