Itaconic acid modified carboxylic-acid functionalized (002) faceted monoclinic WO3 nanorods for electrochemical hydrogen evolution reaction

IF 2.5 4区 材料科学 Q2 CHEMISTRY, APPLIED
Angelin Abraham, Abhishek T.K., M. Junaid Bushiri
{"title":"Itaconic acid modified carboxylic-acid functionalized (002) faceted monoclinic WO3 nanorods for electrochemical hydrogen evolution reaction","authors":"Angelin Abraham,&nbsp;Abhishek T.K.,&nbsp;M. Junaid Bushiri","doi":"10.1007/s10934-024-01672-y","DOIUrl":null,"url":null,"abstract":"<div><p>Design of strategies to modify the hydrogen evolution activity of electrocatalysts is vital for the commercial implementation of hydrogen production. Herein, we explore the surface modification of monoclinic WO<sub>3</sub> using itaconic acid (ITA) ligand via a facile hydrothermal synthesis route. Comprehensive XRD, HRTEM, FTIR, and Raman analyses confirmed the formation of (002) oriented monoclinic WO<sub>3</sub> and the successful incorporation of ITA coating on the WO<sub>3</sub> samples. The FESEM images illustrated the randomly coated ITA particles on the smooth nanorods of <i>m-</i>WO<sub>3</sub> nanorods. The ITA-coated <i>m-</i>WO<sub>3</sub> demonstrated an overpotential of 267 mV at 10 mA/cm<sup>2</sup> current density and exhibited a lower Tafel slope and charge transfer resistance in an acidic electrolyte medium. The carboxylic groups of itaconic acid promote proton transfer, which, along with the highly reactive (002) dominant facets of WO<sub>3</sub>, synergistically enhanced the HER activity. The (002) oriented WO<sub>3</sub> sample with the highest mass loading of itaconic acid (0.3 M) resulted in a tenfold increase in surface area, thereby enhancing the accessible active sites. The enhanced porosity and proton transfer properties of the itaconic acid on integration with WO<sub>3</sub> improved their potential as an HER electrocatalyst.</p></div>","PeriodicalId":660,"journal":{"name":"Journal of Porous Materials","volume":"31 6","pages":"2241 - 2249"},"PeriodicalIF":2.5000,"publicationDate":"2024-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Porous Materials","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s10934-024-01672-y","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
引用次数: 0

Abstract

Design of strategies to modify the hydrogen evolution activity of electrocatalysts is vital for the commercial implementation of hydrogen production. Herein, we explore the surface modification of monoclinic WO3 using itaconic acid (ITA) ligand via a facile hydrothermal synthesis route. Comprehensive XRD, HRTEM, FTIR, and Raman analyses confirmed the formation of (002) oriented monoclinic WO3 and the successful incorporation of ITA coating on the WO3 samples. The FESEM images illustrated the randomly coated ITA particles on the smooth nanorods of m-WO3 nanorods. The ITA-coated m-WO3 demonstrated an overpotential of 267 mV at 10 mA/cm2 current density and exhibited a lower Tafel slope and charge transfer resistance in an acidic electrolyte medium. The carboxylic groups of itaconic acid promote proton transfer, which, along with the highly reactive (002) dominant facets of WO3, synergistically enhanced the HER activity. The (002) oriented WO3 sample with the highest mass loading of itaconic acid (0.3 M) resulted in a tenfold increase in surface area, thereby enhancing the accessible active sites. The enhanced porosity and proton transfer properties of the itaconic acid on integration with WO3 improved their potential as an HER electrocatalyst.

Abstract Image

用于电化学氢进化反应的衣康酸修饰羧酸功能化 (002) 面状单斜 WO3 纳米棒
设计改变电催化剂氢进化活性的策略对于商业化制氢至关重要。在此,我们通过简便的水热合成路线,探索了使用衣康酸(ITA)配体对单斜 WO3 进行表面改性的方法。全面的 XRD、HRTEM、FTIR 和拉曼分析证实了 (002) 取向单斜 WO3 的形成,以及在 WO3 样品上成功加入了 ITA 涂层。FESEM 图像显示了在 m-WO3 纳米棒的光滑纳米棒上随机涂覆的 ITA 颗粒。在 10 mA/cm2 电流密度下,ITA 涂层 m-WO3 的过电位为 267 mV,并且在酸性电解质介质中表现出较低的塔菲尔斜率和电荷转移电阻。衣康酸的羧基促进了质子转移,这与 WO3 的高活性(002)主导面协同增强了 HER 活性。衣康酸质量负荷最高(0.3 M)的(002)取向 WO3 样品的表面积增加了十倍,从而增加了可访问的活性位点。衣康酸与 WO3 结合后,其孔隙率和质子转移特性得到增强,从而提高了其作为 HER 电催化剂的潜力。
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 Porous Materials
Journal of Porous Materials 工程技术-材料科学:综合
CiteScore
4.80
自引率
7.70%
发文量
203
审稿时长
2.6 months
期刊介绍: The Journal of Porous Materials is an interdisciplinary and international periodical devoted to all types of porous materials. Its aim is the rapid publication of high quality, peer-reviewed papers focused on the synthesis, processing, characterization and property evaluation of all porous materials. The objective is to establish a unique journal that will serve as a principal means of communication for the growing interdisciplinary field of porous materials. Porous materials include microporous materials with 50 nm pores. Examples of microporous materials are natural and synthetic molecular sieves, cationic and anionic clays, pillared clays, tobermorites, pillared Zr and Ti phosphates, spherosilicates, carbons, porous polymers, xerogels, etc. Mesoporous materials include synthetic molecular sieves, xerogels, aerogels, glasses, glass ceramics, porous polymers, etc.; while macroporous materials include ceramics, glass ceramics, porous polymers, aerogels, cement, etc. The porous materials can be crystalline, semicrystalline or noncrystalline, or combinations thereof. They can also be either organic, inorganic, or their composites. The overall objective of the journal is the establishment of one main forum covering the basic and applied aspects of all porous materials.
×
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