Hybrid Nanostructured Compounds of Mo2C on Vertical Graphene Nanoflakes for a Highly Efficient Hydrogen Evolution Reaction

催化作用 能量载体 化石燃料 石墨烯 材料科学 氢燃料 氢经济 碳纤维 碳化物 制氢 纳米技术 化学工程 自然资源经济学 化学 冶金 复合数 有机化学 复合材料 工程类 经济
作者
Stefanos Chaitoglou,Roger Amade,Rogelio Ospina,E. Bertrán
出处
期刊:ACS applied energy materials [American Chemical Society]
卷期号:6 (11): 6120-6131 被引量:30
标识
DOI:10.1021/acsaem.3c00625
摘要

Organizing a post-fossil fuel economy requires the development of sustainable energy carriers. Hydrogen is expected to play a significant role as an alternative fuel as it is among the most efficient energy carriers. Therefore, nowadays, the demand for hydrogen production is increasing. Green hydrogen produced by water splitting produces zero carbon emissions but requires the use of expensive catalysts. Therefore, the demand for efficient and economical catalysts is constantly growing. Transition-metal carbides, and especially Mo2C, have attracted great attention from the scientific community since they are abundantly available and hold great promises for efficient performance toward the hydrogen evolution reaction (HER). This study presents a bottom-up approach for depositing Mo carbide nanostructures on vertical graphene nanowall templates via chemical vapor deposition, magnetron sputtering, and thermal annealing processes. Electrochemical results highlight the importance of adequate loading of graphene templates with the optimum amount of Mo carbides, controlled by both deposition and annealing time, to enrich the available active sites. The resulting compounds exhibit exceptional activities toward the HER in acidic media, requiring overpotentials of 82 mV at -10 mA/cm2 and demonstrating a Tafel slope of 56 mV/dec. The high double-layer capacitance and low charge transfer resistance of these Mo2C on GNW hybrid compounds are the main causes of the enhanced HER activity. This study is expected to pave the way for the design of hybrid nanostructures based on nanocatalyst deposition on three-dimensional graphene templates.
最长约 10秒,即可获得该文献文件

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
脑洞疼应助搬乌龟采纳,获得10
刚刚
李健应助科研通管家采纳,获得10
刚刚
刚刚
充电宝应助科研通管家采纳,获得10
刚刚
Li完成签到,获得积分10
刚刚
顺心的大碗完成签到,获得积分10
1秒前
啥格式完成签到 ,获得积分10
1秒前
研友_VZG7GZ应助OsHTAS采纳,获得10
1秒前
2秒前
2秒前
2秒前
周玄完成签到 ,获得积分10
2秒前
NexusExplorer应助johnson7777采纳,获得10
2秒前
2秒前
诗和远方完成签到 ,获得积分10
3秒前
simpleboy完成签到,获得积分10
3秒前
我是老大应助blwd采纳,获得10
3秒前
火星上立果完成签到,获得积分10
4秒前
4秒前
淡淡曼安完成签到,获得积分10
5秒前
春锅锅完成签到,获得积分10
5秒前
5秒前
wanci应助doctor2023采纳,获得10
5秒前
背后的道天关注了科研通微信公众号
5秒前
5秒前
5秒前
元谷雪发布了新的文献求助10
5秒前
6秒前
7秒前
ZZZzzz发布了新的文献求助10
7秒前
尘中磨镜人完成签到,获得积分10
7秒前
8秒前
汉堡包应助micpeach采纳,获得10
8秒前
pu发布了新的文献求助10
8秒前
赘婿应助无语的饼干采纳,获得10
8秒前
ding应助jaywzz采纳,获得10
8秒前
8秒前
温柔如蓉完成签到 ,获得积分10
9秒前
aabbccc完成签到,获得积分10
9秒前
CipherSage应助Paper Maker采纳,获得30
9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
HYDROLYSE ACIDE DE QUELQUES DIOXASPIROCYCLANES 1314
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Navigating Normative Orders. Interdisciplinary Perspectives 800
1 Peter and Christ's Descent to the Dead in Its Early Christian Reception 700
Organizational Behavior 510
Management and the Arts 510
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 7747234
求助须知:如何正确求助?哪些是违规求助? 9295231
关于积分的说明 20228830
捐赠科研通 7327786
什么是DOI,文献DOI怎么找? 3308341
关于科研通互助平台的介绍 2460261
邀请新用户注册赠送积分活动 2320271