Quantification of activated carbon functional groups and active surface area by TPD-MS and their impact on supercapacitor performance

IF 18.9 1区 材料科学 Q1 CHEMISTRY, PHYSICAL
Bénédicte Réty, Hui-Yi Yiin, Camélia Matei Ghimbeu
{"title":"Quantification of activated carbon functional groups and active surface area by TPD-MS and their impact on supercapacitor performance","authors":"Bénédicte Réty, Hui-Yi Yiin, Camélia Matei Ghimbeu","doi":"10.1016/j.ensm.2024.103963","DOIUrl":null,"url":null,"abstract":"Carbon oxygenated functional groups and active sites play an important role in the interactions with the electrolytes in aqueous supercapacitors. For the first time, correlations between each type of O-surface groups and electrochemical performance are established by means of thermodesorption coupled with mass spectrometry (TPD-MS). A set of five activated carbons and one soft-salt templated carbon, were studied in three different pH electrolytes, 1M H<sub>2</sub>SO<sub>4</sub>, 1M KOH and 1M Na<sub>2</sub>SO<sub>4</sub>. Linear correlations between surface groups and capacitance were found: acidic groups such as carboxylic acid and phenol-ether groups improve capacitance, whereas carbonyl-quinone groups are detrimental. Moreover, active surface area (ASA) is for the first time measured for activated carbons thanks to a new protocol, which minimises material burn-off during oxygen chemisorption. In addition, a new approach consisting in the quantification of the ASA is proposed. It has been highlighted that certain active sites are linearly correlated to an improvement of capacitance. Although the oxygen surface groups and ASA improve the capacitance via pseudo-capacitance phenomena, the capacitive mechanisms, governed by the porosity of the activated carbons, are shown to be predominant. Among all materials, the soft-salt templated carbon gives the best electrochemical performance. Indeed, it combines a large quantity of carboxylic acid and phenol-ether surface groups as well as appropriate ASA. Moreover, it has a high specific surface area (2556 m²·g<sup>-1</sup>) and optimal pore size (0.88 nm). All these characteristics, provide a high capacitance, a high rate capability and a high capacitance retention after 10,000 cycles.","PeriodicalId":306,"journal":{"name":"Energy Storage Materials","volume":"40 1","pages":""},"PeriodicalIF":18.9000,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy Storage Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1016/j.ensm.2024.103963","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Carbon oxygenated functional groups and active sites play an important role in the interactions with the electrolytes in aqueous supercapacitors. For the first time, correlations between each type of O-surface groups and electrochemical performance are established by means of thermodesorption coupled with mass spectrometry (TPD-MS). A set of five activated carbons and one soft-salt templated carbon, were studied in three different pH electrolytes, 1M H2SO4, 1M KOH and 1M Na2SO4. Linear correlations between surface groups and capacitance were found: acidic groups such as carboxylic acid and phenol-ether groups improve capacitance, whereas carbonyl-quinone groups are detrimental. Moreover, active surface area (ASA) is for the first time measured for activated carbons thanks to a new protocol, which minimises material burn-off during oxygen chemisorption. In addition, a new approach consisting in the quantification of the ASA is proposed. It has been highlighted that certain active sites are linearly correlated to an improvement of capacitance. Although the oxygen surface groups and ASA improve the capacitance via pseudo-capacitance phenomena, the capacitive mechanisms, governed by the porosity of the activated carbons, are shown to be predominant. Among all materials, the soft-salt templated carbon gives the best electrochemical performance. Indeed, it combines a large quantity of carboxylic acid and phenol-ether surface groups as well as appropriate ASA. Moreover, it has a high specific surface area (2556 m²·g-1) and optimal pore size (0.88 nm). All these characteristics, provide a high capacitance, a high rate capability and a high capacitance retention after 10,000 cycles.

Abstract Image

求助全文
约1分钟内获得全文 求助全文
来源期刊
Energy Storage Materials
Energy Storage Materials Materials Science-General Materials Science
CiteScore
33.00
自引率
5.90%
发文量
652
审稿时长
27 days
期刊介绍: Energy Storage Materials is a global interdisciplinary journal dedicated to sharing scientific and technological advancements in materials and devices for advanced energy storage and related energy conversion, such as in metal-O2 batteries. The journal features comprehensive research articles, including full papers and short communications, as well as authoritative feature articles and reviews by leading experts in the field. Energy Storage Materials covers a wide range of topics, including the synthesis, fabrication, structure, properties, performance, and technological applications of energy storage materials. Additionally, the journal explores strategies, policies, and developments in the field of energy storage materials and devices for sustainable energy. Published papers are selected based on their scientific and technological significance, their ability to provide valuable new knowledge, and their relevance to the international research community.
×
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