Optimization and scalability assessment of supercapacitor electrodes based on hydrothermally grown MoS2 on carbon cloth†

IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Jasna Mannayil, Olli Pitkänen, Minna Mannerkorpi and Krisztian Kordas
{"title":"Optimization and scalability assessment of supercapacitor electrodes based on hydrothermally grown MoS2 on carbon cloth†","authors":"Jasna Mannayil, Olli Pitkänen, Minna Mannerkorpi and Krisztian Kordas","doi":"10.1039/D4NA00368C","DOIUrl":null,"url":null,"abstract":"<p >MoS<small><sub>2</sub></small> is a well-known 2D transition metal dichalcogenide (TMD) with feasibility for energy storage applications due to its eco-friendliness and high electroactive surface area. Electrodes based on MoS<small><sub>2</sub></small> are typically made by either immobilizing its multiphase nanocomposites, having binders and conductive fillers, or by directly growing the materials on current collectors. In this work, we follow and optimize this latter approach by applying a hydrothermal route to directly synthesize MoS<small><sub>2</sub></small> nanostructures on carbon cloth (MoS<small><sub>2</sub></small>@CC) hence enabling binder-free current collector electrodes. Raman spectroscopy and electron microscopy analyses confirmed the formation of 2H MoS<small><sub>2</sub></small> nanosheets with hexagonal structure. The as-prepared electrodes were used to assemble symmetric supercapacitor cells, whose performance were tested in various types of electrolytes. Electrochemical measurements indicate that both precursor concentration and growth time significantly affect the device performance. Under optimized conditions, specific capacitance up to 226 F g<small><sup>−1</sup></small> (at 1 A g<small><sup>−1</sup></small> in 6 M KOH) was achieved, with corresponding energy and power densities of 5.1 W h kg<small><sup>−1</sup></small> and 2.1 W kg<small><sup>−1</sup></small>. The device showed good stability, retaining 85% capacitance after 1000 cycles. Furthermore, the electrodes assessed in PYR14-TFSI showed energy and power densities of up to 26.3 W h kg<small><sup>−1</sup></small> and 2.0 kW kg<small><sup>−1</sup></small>, respectively, indicating their feasibility not only in aqueous but also in ionic liquid electrolytes. In addition, galvanostatic charge/discharge measurements conducted on devices having footprint sizes from 1 cm<small><sup>2</sup></small> to 25 cm<small><sup>2</sup></small> show very similar specific capacitances, which proves scalability and thus the practical relevance of the binder-free electrodes demonstrated in this study.</p>","PeriodicalId":18806,"journal":{"name":"Nanoscale Advances","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/na/d4na00368c?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nanoscale Advances","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/na/d4na00368c","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

MoS2 is a well-known 2D transition metal dichalcogenide (TMD) with feasibility for energy storage applications due to its eco-friendliness and high electroactive surface area. Electrodes based on MoS2 are typically made by either immobilizing its multiphase nanocomposites, having binders and conductive fillers, or by directly growing the materials on current collectors. In this work, we follow and optimize this latter approach by applying a hydrothermal route to directly synthesize MoS2 nanostructures on carbon cloth (MoS2@CC) hence enabling binder-free current collector electrodes. Raman spectroscopy and electron microscopy analyses confirmed the formation of 2H MoS2 nanosheets with hexagonal structure. The as-prepared electrodes were used to assemble symmetric supercapacitor cells, whose performance were tested in various types of electrolytes. Electrochemical measurements indicate that both precursor concentration and growth time significantly affect the device performance. Under optimized conditions, specific capacitance up to 226 F g−1 (at 1 A g−1 in 6 M KOH) was achieved, with corresponding energy and power densities of 5.1 W h kg−1 and 2.1 W kg−1. The device showed good stability, retaining 85% capacitance after 1000 cycles. Furthermore, the electrodes assessed in PYR14-TFSI showed energy and power densities of up to 26.3 W h kg−1 and 2.0 kW kg−1, respectively, indicating their feasibility not only in aqueous but also in ionic liquid electrolytes. In addition, galvanostatic charge/discharge measurements conducted on devices having footprint sizes from 1 cm2 to 25 cm2 show very similar specific capacitances, which proves scalability and thus the practical relevance of the binder-free electrodes demonstrated in this study.

Abstract Image

基于碳布上水热生长的 MoS2 的超级电容器电极的优化和可扩展性评估
MoS2 是一种著名的二维过渡金属二掺杂物 (TMD),因其生态友好性和高电活性表面积而具有储能应用的可行性。基于 MoS2 的电极通常是通过固定其多相纳米复合材料(包括粘合剂和导电填料)或直接在集流器上生长材料而制成的。在这项工作中,我们沿用并优化了后一种方法,采用水热法在碳布上直接合成 MoS2 纳米结构(MoS2@CC),从而实现了无粘合剂集流电极。拉曼光谱和电子显微镜分析证实了具有六边形结构的 2H MoS2 纳米片的形成。制备的电极被用于组装对称超级电容器电池,并在各种类型的电解质中对其性能进行了测试。电化学测量结果表明,前驱体浓度和生长时间对器件性能有显著影响。在优化条件下,比电容高达 226 F/g(在 6 M KOH 中为 1 A/g 时),相应的能量密度和功率密度分别为 5.1 Wh/kg 和 2.1 W/kg。该装置显示出良好的稳定性,在 1000 次循环后仍能保持 85% 的电容。此外,在PYR14-TFSI 中评估的电极的能量密度和功率密度分别高达 26.3 Wh/kg 和 2.0 kW/kg,这表明它们不仅在水性电解质中可行,在离子液体电解质中也同样可行。此外,在占地面积从 1 平方厘米到 25 平方厘米的装置上进行的电静电充放电测量显示出非常相似的比电容,这证明了本研究中展示的无粘结剂电极的可扩展性和实用性。
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
Nanoscale Advances
Nanoscale Advances Multiple-
CiteScore
8.00
自引率
2.10%
发文量
461
审稿时长
9 weeks
文献相关原料
公司名称 产品信息 采购帮参考价格
×
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