Reduced graphene oxides prepared via mass loading-controlled non-explosive thermal reduction for high volumetric capacitance supercapacitors†

IF 9.5 2区 材料科学 Q1 CHEMISTRY, PHYSICAL Journal of Materials Chemistry A Pub Date : 2025-03-12 DOI:10.1039/D5TA01172H
Jianing Tan, Zhaoyuan Liu, Wei Wu, Gang Li and Wei Guo
{"title":"Reduced graphene oxides prepared via mass loading-controlled non-explosive thermal reduction for high volumetric capacitance supercapacitors†","authors":"Jianing Tan, Zhaoyuan Liu, Wei Wu, Gang Li and Wei Guo","doi":"10.1039/D5TA01172H","DOIUrl":null,"url":null,"abstract":"<p >Graphene oxide (GO) is known to undergo volume expansion during rapid and high-temperature heat treatment, resulting in a low packing density and thus a poor volumetric capacitance. This paper reports a non-explosive thermal reduction strategy (NET) to prepare compact thermally reduced graphene oxide (NE-TRGO) by controlling the mass loading of the GO film below a typical value (&lt;5 mg cm<small><sup>−2</sup></small>). On one hand, the NET strategy effectively inhibits the expansion of graphene sheets, and thus the optimized NE-TRGO exhibits a high packing density of 1.94 g cm<small><sup>−3</sup></small>. On the other hand, the NET strategy contributes to preserving the electrochemically active C–OH and C<img>O groups. Due to the high packing density and the abundance of electrochemically active groups, the gravimetric and volumetric capacitance of the optimized NE-TRGO were 314 F g<small><sup>−1</sup></small> and 609 F cm<small><sup>−3</sup></small> @ 0.1 A g<small><sup>−1</sup></small>, respectively, with excellent rate capability (160 F g<small><sup>−1</sup></small> and 310 F cm<small><sup>−3</sup></small> @ 10 A g<small><sup>−1</sup></small>) and significant cycling performance (∼99% capacitance retention after 9000 cycling at 5 A g<small><sup>−1</sup></small>). The assembled symmetric supercapacitor delivers an energy density of 9.5 W h L<small><sup>−1</sup></small> at a power density of 96.7 W L<small><sup>−1</sup></small> and 1.5 W h L<small><sup>−1</sup></small> at a power density of 1056.3 W L<small><sup>−1</sup></small>. This NET strategy represents a simple and feasible heat treatment approach to control the packing density and oxygen functional groups of graphene-based materials toward compact energy storage devices.</p>","PeriodicalId":82,"journal":{"name":"Journal of Materials Chemistry A","volume":" 16","pages":" 11330-11343"},"PeriodicalIF":9.5000,"publicationDate":"2025-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Materials Chemistry A","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/ta/d5ta01172h","RegionNum":2,"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

Graphene oxide (GO) is known to undergo volume expansion during rapid and high-temperature heat treatment, resulting in a low packing density and thus a poor volumetric capacitance. This paper reports a non-explosive thermal reduction strategy (NET) to prepare compact thermally reduced graphene oxide (NE-TRGO) by controlling the mass loading of the GO film below a typical value (<5 mg cm−2). On one hand, the NET strategy effectively inhibits the expansion of graphene sheets, and thus the optimized NE-TRGO exhibits a high packing density of 1.94 g cm−3. On the other hand, the NET strategy contributes to preserving the electrochemically active C–OH and CO groups. Due to the high packing density and the abundance of electrochemically active groups, the gravimetric and volumetric capacitance of the optimized NE-TRGO were 314 F g−1 and 609 F cm−3 @ 0.1 A g−1, respectively, with excellent rate capability (160 F g−1 and 310 F cm−3 @ 10 A g−1) and significant cycling performance (∼99% capacitance retention after 9000 cycling at 5 A g−1). The assembled symmetric supercapacitor delivers an energy density of 9.5 W h L−1 at a power density of 96.7 W L−1 and 1.5 W h L−1 at a power density of 1056.3 W L−1. This NET strategy represents a simple and feasible heat treatment approach to control the packing density and oxygen functional groups of graphene-based materials toward compact energy storage devices.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
通过质量负载控制非爆炸热还原法制备高容量电容超级电容器的还原氧化石墨烯
众所周知,氧化石墨烯(GO)在快速和高温热处理过程中会发生体积膨胀,导致填料密度低,因此体积电容很差。本文报道了一种非爆炸热还原策略(NET),通过控制氧化石墨烯薄膜的质量负荷低于典型值(<;5mg cm-2)。一方面,NET策略有效地抑制了石墨烯片的膨胀,因此优化后的NE-TRGO具有1.94 g cm-3的高堆积密度。另一方面,NET策略有助于保留电化学活性的C- oh和C=O基团。由于高密度的填料和丰富的电化学活性基团,优化后的NE-TRGO的重量和体积电容分别为314 F g-1和609 F cm-3 @ 0.1 A g-1,具有优异的倍率性能(160 F g-1和310 F cm-3 @ 10 A g-1)和显著的循环性能(在5 A g-1下循环9000次后电容保持率~ 99%)。当功率密度为96.7 W L-1时,对称超级电容器的能量密度为9.5 W h L-1;当功率密度为1056.3 W L-1时,对称超级电容器的能量密度为1.5 W h L-1。这种NET策略代表了一种简单可行的热处理方法,可以控制石墨烯基材料的包装密度和氧官能团,从而实现紧凑的储能装置。
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 去求助
来源期刊
Journal of Materials Chemistry A
Journal of Materials Chemistry A CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
19.50
自引率
5.00%
发文量
1892
审稿时长
1.5 months
期刊介绍: The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.
期刊最新文献
Static promise versus dynamic reality in a Z-scheme photocatalyst: nonadiabatic dynamics reveal a charge-separation bottleneck in MoSi2P4/WTe2 High capacity metal-rich copper sulfide as an intercalation-type cathode material for all solid-state batteries Mechanistic insights into defect-governed ion migration and phase instability in mixed-halide perovskites Engineering a dual-site CuO/Cu 2 O/CeO 2 heterostructure: synergistic Cu + /Cu 2+ and CeO 2 modulation for tandem ammonia electrosynthesis from nitrate Bifunctional Ni-TiO2 catalyst for the efficient glycolysis of polylactic acid: a selective route to obtain 2-hydroxyethyl lactate
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1