Self-supported film catalyst integrated with multifunctional carbon nanotubes and Ni-Ni(OH)2 heterostructure for promoted hydrogen evolution

IF 15.7 1区 化学 Q1 CHEMISTRY, APPLIED
Wancheng Zhao , Jiapeng Ma , Dong Tian , Baotao Kang , Fangquan Xia , Jing Cheng , Yajun Wu , Mengyao Wang , Gang Wu
{"title":"Self-supported film catalyst integrated with multifunctional carbon nanotubes and Ni-Ni(OH)2 heterostructure for promoted hydrogen evolution","authors":"Wancheng Zhao ,&nbsp;Jiapeng Ma ,&nbsp;Dong Tian ,&nbsp;Baotao Kang ,&nbsp;Fangquan Xia ,&nbsp;Jing Cheng ,&nbsp;Yajun Wu ,&nbsp;Mengyao Wang ,&nbsp;Gang Wu","doi":"10.1016/S1872-2067(24)60057-4","DOIUrl":null,"url":null,"abstract":"<div><p>In order to reduce energy consumption in water electrolysis, it is of great importance to design active and stable electrocatalysts for hydrogen evolution reaction (HER) in alkaline solution, especially based on earth-abundant metal. Here we integrate carbon nanotubes (CNTs) and Ni-Ni(OH)<sub>2</sub> heterostructure multifunctional components to design a self-supported 3D CNTs-Ni-Ni(OH)<sub>2</sub> catalyst for HER by composite deposition and subsequent <em>in-situ</em> oxidation. In alkaline solution, this designed CNTs-Ni-Ni(OH)<sub>2</sub> catalyst exhibits 0 mV onset overpotential, and overpotentials of 65 mV and 109 mV at 10 and 50 mA/cm<sup>2</sup> respectively. Electrochemical measurements, characterizations, and simulation results attribute the outstanding performance to the incorporation of CNTs and heterostructure. CNTs induce the formation 3D catalytic surface, enhance electrochemical active surface area, and more importantly weaken the adsorption of H. Moreover, the formation of heterostructure, especially reversible Ni(OH)<sub>2</sub>, supplies active sites and adjusts the adsorption strength of H atom to an optimal value. CNTs and heterostructure synergistically facilitate water adsorption, promote water dissociation, and accelerate H<sub>2</sub> desorption. Significantly, integration of multifunctional components supplies a distinct strategy for development of cost-effective electrocatalyst with outstanding performance.</p></div>","PeriodicalId":9832,"journal":{"name":"Chinese Journal of Catalysis","volume":"62 ","pages":"Pages 287-295"},"PeriodicalIF":15.7000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chinese Journal of Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1872206724600574","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0

Abstract

In order to reduce energy consumption in water electrolysis, it is of great importance to design active and stable electrocatalysts for hydrogen evolution reaction (HER) in alkaline solution, especially based on earth-abundant metal. Here we integrate carbon nanotubes (CNTs) and Ni-Ni(OH)2 heterostructure multifunctional components to design a self-supported 3D CNTs-Ni-Ni(OH)2 catalyst for HER by composite deposition and subsequent in-situ oxidation. In alkaline solution, this designed CNTs-Ni-Ni(OH)2 catalyst exhibits 0 mV onset overpotential, and overpotentials of 65 mV and 109 mV at 10 and 50 mA/cm2 respectively. Electrochemical measurements, characterizations, and simulation results attribute the outstanding performance to the incorporation of CNTs and heterostructure. CNTs induce the formation 3D catalytic surface, enhance electrochemical active surface area, and more importantly weaken the adsorption of H. Moreover, the formation of heterostructure, especially reversible Ni(OH)2, supplies active sites and adjusts the adsorption strength of H atom to an optimal value. CNTs and heterostructure synergistically facilitate water adsorption, promote water dissociation, and accelerate H2 desorption. Significantly, integration of multifunctional components supplies a distinct strategy for development of cost-effective electrocatalyst with outstanding performance.

集成了多功能碳纳米管和 Ni-Ni(OH)2 异质结构的自支撑薄膜催化剂用于促进氢气进化
为了降低电解水的能耗,设计活性稳定的碱性溶液中氢气进化反应(HER)电催化剂,尤其是基于富土金属的电催化剂具有重要意义。在此,我们整合了碳纳米管(CNTs)和镍-镍(OH)2 异质结构多功能成分,通过复合沉积和随后的原位氧化,设计了一种自支撑三维 CNTs-Ni-Ni(OH)2 催化剂,用于氢进化反应。在碱性溶液中,所设计的 CNTs-Ni-Ni(OH)2 催化剂的起始过电位为 0 mV,在 10 mA/cm2 和 50 mA/cm2 条件下的过电位分别为 65 mV 和 109 mV。电化学测量、表征和模拟结果表明,CNTs-镍(OH)2 催化剂的优异性能归功于 CNTs 的加入和异质结构。此外,异质结构的形成,尤其是可逆镍(OH)2 的形成,提供了活性位点,并将 H 原子的吸附强度调整到最佳值。碳纳米管和异质结构协同促进了水的吸附,促进了水的解离,并加速了 H2 的解吸。值得注意的是,多功能成分的集成为开发具有卓越性能的高性价比电催化剂提供了一种独特的策略。
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
Chinese Journal of Catalysis
Chinese Journal of Catalysis 工程技术-工程:化工
CiteScore
25.80
自引率
10.30%
发文量
235
审稿时长
1.2 months
期刊介绍: The journal covers a broad scope, encompassing new trends in catalysis for applications in energy production, environmental protection, and the preparation of materials, petroleum chemicals, and fine chemicals. It explores the scientific foundation for preparing and activating catalysts of commercial interest, emphasizing representative models.The focus includes spectroscopic methods for structural characterization, especially in situ techniques, as well as new theoretical methods with practical impact in catalysis and catalytic reactions.The journal delves into the relationship between homogeneous and heterogeneous catalysis and includes theoretical studies on the structure and reactivity of catalysts.Additionally, contributions on photocatalysis, biocatalysis, surface science, and catalysis-related chemical kinetics are welcomed.
×
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:481959085
Book学术官方微信