Mesoporous Iron Family Element (Fe, Co, Ni) Molybdenum Disulfide/Carbon Nanohybrids for High-Performance Supercapacitors

二硫化钼 介孔材料 超级电容器 化学 电极 化学工程 二硫化碳 碳纤维 无机化学 电化学 催化作用 材料科学 有机化学 物理化学 复合材料 复合数 工程类
作者
Shiyi Yao,Songtao Zhang,Guangxun Zhang,Yijian Tang,Rongmei Zhu,Yi Peng,Yong Chen,Huan Pang
出处
期刊:Inorganic Chemistry [American Chemical Society]
卷期号:62 (39): 16038-16046 被引量:24
标识
DOI:10.1021/acs.inorgchem.3c02167
摘要

As the demand for fuel continues to increase, the development of energy devices with excellent performance is crucial. Supercapacitors (SCs) are attracting attention for their advantages of high specific energy and a long cycle life. At present, the development of high-performance electrode materials is the main point for research and development of SCs. Transition metal sulfides have the advantages of a large interlayer space and high theoretical capacity, making them promising electrode materials. Herein, we reported a series of ultrathin mesoporous iron family element (Fe, Co, Ni) molybdenum disulfide (MxMo1-xS2/C, M = Fe, Co, and Ni) by a template method. The original monolayer mesoporous structure of MoS2/C was maintained, and accumulation and agglomeration of MoS2/C were avoided. Based on our investigations, the best performance was that of CoxMo1-xS2/C nanohybrids. Furthermore, the concentrations of Co and Mo ions were modulated to obtain the best performance, in which Mo and Co ions were released at 1:1, 1:2, and 1:3 ratios and they were named CoxMo1-xS2/C-1, CoxMo1-xS2/C-2, and CoxMo1-xS2/C-3, respectively. Overall, these materials represent a significant improvement and show promise as high-performance SC electrode materials due to their enhanced capacitance and stability. At a current density of 0.5 A g-1, CoxMo1-xS2/C-2 has the optimal specific capacitance of 184 F g-1. CoxMo1-xS2/C-2 as an SC electrode exhibited better reversible capacity and cycling stability than MoS2/C, which is an improvement over MoS2/C regarding reversible capacity and cycling stability.
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
你好包包完成签到,获得积分10
刚刚
项秋发布了新的文献求助10
1秒前
2秒前
Hello应助汪思显采纳,获得10
3秒前
3秒前
我刷的烧饼贼亮完成签到 ,获得积分10
4秒前
情怀应助加厚加大采纳,获得10
4秒前
hgg发布了新的文献求助10
4秒前
活泼烤鸡发布了新的文献求助10
5秒前
irisy发布了新的文献求助10
6秒前
Elaine2021完成签到 ,获得积分10
7秒前
Charlie完成签到,获得积分10
8秒前
8秒前
美好绝施发布了新的文献求助10
9秒前
汪思显完成签到,获得积分10
9秒前
无花果应助山野的雾采纳,获得10
10秒前
10秒前
研友_VZG7GZ应助小丁采纳,获得10
10秒前
molihuakai应助dip采纳,获得10
10秒前
hgg完成签到,获得积分10
11秒前
12秒前
12秒前
irisy完成签到,获得积分10
13秒前
muzili完成签到 ,获得积分10
13秒前
leammmm发布了新的文献求助10
13秒前
勤劳的寒烟完成签到,获得积分10
15秒前
我爱山之东完成签到,获得积分10
15秒前
lyz完成签到,获得积分10
15秒前
Mali完成签到,获得积分10
17秒前
17秒前
CipherSage应助只要两毛九采纳,获得30
17秒前
屾从完成签到 ,获得积分10
18秒前
疯子星应助我爱山之东采纳,获得20
18秒前
nonopanda发布了新的文献求助10
18秒前
18秒前
Cassiopeia完成签到,获得积分10
18秒前
加厚加大发布了新的文献求助10
19秒前
脑洞疼应助molihuakai采纳,获得10
19秒前
xiqianyangyi发布了新的文献求助10
19秒前
共享精神应助活泼烤鸡采纳,获得10
20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
Principles of town planning: translating concepts to applications 1000
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
Matrix Methods in Data Mining and Pattern Recognition Second Edition 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 7740783
求助须知:如何正确求助?哪些是违规求助? 9289329
关于积分的说明 20195239
捐赠科研通 7318946
什么是DOI,文献DOI怎么找? 3306525
关于科研通互助平台的介绍 2458797
邀请新用户注册赠送积分活动 2316770