已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整的填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

Si nanoparticles confined within a conductive 2D porous Cu-based metal–organic framework (Cu3(HITP)2) as potential anodes for high-capacity Li-ion batteries

法拉第效率 阳极 材料科学 化学工程 阴极 金属有机骨架 纳米颗粒 多孔性 电极 导电体 电化学 纳米技术 复合材料 化学 吸附 有机化学 物理化学 工程类
作者
Aqsa Nazir,Hang T.T. Le,Arvind Kasbe,Chan-Jin Park
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:405: 126963-126963 被引量:45
标识
DOI:10.1016/j.cej.2020.126963
摘要

The utility of metal–organic frameworks (MOFs) as active agents in electronic appliances is beneficial owing to their outstanding properties, particularly their high porosity, high surface area, and unique chemical stability. Herein, we report the in-situ growth of Cu3(HITP)2, a two-dimensional (2D) conductive MOF with Cu at the center, around Si nanoparticles (SiNPs) at 27 °C. Enclosing the Si nanoparticles with the Cu-MOF yielded a desired buffer against the volume expansion and also effective electron- and ion-conducting channels for the SiNPs. Accordingly, the Cu-MOF-coated Si electrode exhibited high structural stability and low electrochemical degradation during lithiation/delithiation cycles. The electrode composed of SiNPs coated with 5% Cu-MOF exhibited an extremely high initial reversible capacity of 2511 mAh g−1 at the 0.1C rate with a coulombic efficiency of 78.5% in the first cycle and a capacity of 2483 mAh g−1 after 100 cycles. The reversible capacities during rate capability were 1303, 785, and 404 mAh g−1 at the rates of 5, 10, and 20C, respectively. The Cu-MOF (5%) delivered a reversible capacity of 1039 mAh g−1, even after 1000 cycles, at the high rate of 1C. The full-cell, composed of the Cu-MOF-coated Si anode and a LiCoO2 cathode, exhibited a remarkable rate capability and cyclability at 0.1C. This full-cell supplied a reversible (discharge) capacity of 1267 and 1105 mAh g−1 at rates of 0.5C and 1C, respectively. These results demonstrate the considerable potential of the synthesized Cu-MOF-encaged Si as a competitive anode material for next-generation LIBs in the near future.
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
不吃了完成签到 ,获得积分10
刚刚
11111完成签到 ,获得积分10
刚刚
核桃完成签到,获得积分10
2秒前
百里瓶窑完成签到,获得积分10
2秒前
bxsx完成签到,获得积分20
3秒前
小姚姚完成签到,获得积分10
4秒前
只如初完成签到,获得积分10
7秒前
英姑应助碧蓝的曼卉采纳,获得10
7秒前
Miracle完成签到,获得积分10
7秒前
8秒前
haha完成签到,获得积分10
8秒前
紫色翡翠完成签到,获得积分10
9秒前
科研通AI5应助lizhiqian2024采纳,获得10
9秒前
科研通AI5应助lizhiqian2024采纳,获得10
9秒前
hileborn完成签到,获得积分10
10秒前
嘉心糖完成签到,获得积分0
11秒前
想去烤地瓜关注了科研通微信公众号
11秒前
pegasus0802完成签到,获得积分10
11秒前
12秒前
zly完成签到 ,获得积分10
13秒前
lqqq完成签到 ,获得积分10
13秒前
卡戎529完成签到 ,获得积分10
14秒前
14秒前
cheng完成签到 ,获得积分10
14秒前
科研通AI5应助科研通管家采纳,获得10
14秒前
SciGPT应助科研通管家采纳,获得10
15秒前
所所应助科研通管家采纳,获得10
15秒前
YifanWang应助科研通管家采纳,获得20
15秒前
YifanWang应助科研通管家采纳,获得20
15秒前
搜集达人应助科研通管家采纳,获得10
15秒前
YifanWang应助科研通管家采纳,获得10
15秒前
冷酷的心情完成签到,获得积分10
16秒前
cxx完成签到 ,获得积分10
16秒前
eryday0完成签到 ,获得积分10
16秒前
小小飞xxf完成签到 ,获得积分10
16秒前
17秒前
科研通AI2S应助结实初翠采纳,获得10
17秒前
呜呼啦呼完成签到,获得积分10
18秒前
蜡笔小新完成签到,获得积分10
18秒前
安然完成签到 ,获得积分10
19秒前
高分求助中
Les Mantodea de Guyane Insecta, Polyneoptera 2500
Mobilization, center-periphery structures and nation-building 600
Introduction to Strong Mixing Conditions Volumes 1-3 500
Technologies supporting mass customization of apparel: A pilot project 450
China—Art—Modernity: A Critical Introduction to Chinese Visual Expression from the Beginning of the Twentieth Century to the Present Day 430
Multichannel rotary joints-How they work 400
A Field Guide to the Amphibians and Reptiles of Madagascar - Frank Glaw and Miguel Vences - 3rd Edition 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3795440
求助须知:如何正确求助?哪些是违规求助? 3340443
关于积分的说明 10300287
捐赠科研通 3057032
什么是DOI,文献DOI怎么找? 1677332
邀请新用户注册赠送积分活动 805385
科研通“疑难数据库(出版商)”最低求助积分说明 762491