Freestanding three-dimensional graphene foam gives rise to beneficial electrochemical signatures within non-aqueous media

作者
Dale A. C. Brownson,Luiz C. S. Figueiredo‐Filho,Xiaobo Ji,María Gómez-Mingot,Jesús Iniesta,Orlando Fatibello‐Filho,Dimitrios K. Kampouris,Craig E. Banks
出处
期刊:Journal of materials chemistry. A, Materials for energy and sustainability [Royal Society of Chemistry]
卷期号:1 (19): 5962-5962 被引量:95
标识
DOI:10.1039/c3ta10727b
摘要

Freestanding three-dimensional (3D) graphene foam has been fabricated via a Chemical Vapour Deposition (CVD) methodology which has a macroscopic structure with microscopic (graphene) features. The 3D graphene macrostructure is characterised with SEM, EDX, XPS and Raman spectroscopy and is found to comprise pristine graphene (O/C of 0.05) which is in the range of mono- to few-layered graphene sheets and is thus termed quasi-graphene. This unique 3D graphene foam is electrochemically explored in both aqueous and non-aqueous solutions and compared to a freestanding 3D reticulated vitreous carbon (RVC) foam alternative. In aqueous solutions, the 3D graphene foam exhibits poor voltammetric responses. Contact angle measurements reveal the 3D graphene to exhibit a value of 120° representing quasi-super-hydrophobicity. Consequently the freestanding 3D graphene foam is found to give rise to significantly improved voltammetric signatures in non-aqueous media (ionic liquids) over that of a freestanding 3D RVC alternative. The 3D graphene foam provides a promising and beneficial architecture over 2D pristine graphene due to its ease of use and macroscopic/microscopic structure, which will have wide implementation in the field of electrochemistry.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
汉堡包应助科研通管家采纳,获得10
刚刚
传奇3应助科研通管家采纳,获得10
刚刚
李爱国应助科研通管家采纳,获得10
刚刚
NexusExplorer应助科研通管家采纳,获得10
刚刚
赘婿应助科研通管家采纳,获得10
刚刚
1秒前
1秒前
华仔应助蜡笔小新采纳,获得10
2秒前
Lancelot发布了新的文献求助10
3秒前
3秒前
3秒前
4秒前
5秒前
JamesPei应助Cheems采纳,获得10
7秒前
爱笑以山完成签到,获得积分10
7秒前
7秒前
gurdeva发布了新的文献求助10
7秒前
小张不慌发布了新的文献求助10
8秒前
伶俐小懒猪完成签到,获得积分10
8秒前
Tom完成签到,获得积分10
8秒前
xue发布了新的文献求助10
10秒前
11秒前
11秒前
往前走往前看完成签到,获得积分10
11秒前
阿航发布了新的文献求助10
12秒前
耀星发布了新的文献求助10
13秒前
英俊的铭应助一天吃八顿采纳,获得10
15秒前
可可不饿完成签到,获得积分20
16秒前
16秒前
李健的粉丝团团长应助TTT采纳,获得10
16秒前
博修发布了新的文献求助10
17秒前
852应助jennynnny采纳,获得10
17秒前
Owen应助随风守着她采纳,获得10
18秒前
19秒前
深情安青应助耀星采纳,获得10
20秒前
今夜有雨发布了新的文献求助10
23秒前
马洪雪发布了新的文献求助10
25秒前
儒雅向日葵关注了科研通微信公众号
26秒前
倔强完成签到,获得积分10
26秒前
Ava应助Feng5945采纳,获得10
28秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Römisch-Germanische Forschungen 1000
APA handbook of comparative psychology: Basic concepts, methods, neural substrate, and behavior 1000
China Pluperfect I: Epistemology of Past and Outside in Chinese Art 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
The fast track to determining transfer functions of linear circuits: The student guide 500
The Analytical and Numerical Solution of Electric and Magnetic Fields 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7610184
求助须知:如何正确求助?哪些是违规求助? 9185884
关于积分的说明 19678296
捐赠科研通 7183954
什么是DOI,文献DOI怎么找? 3270346
关于科研通互助平台的介绍 2434021
邀请新用户注册赠送积分活动 2265021