Preparation and lithium-storage performance of (Ti1-x,Vx)3C2 MXene solid solutions

固溶体 锂(药物) 材料科学 阳极 相(物质) 电化学 化学工程 化学 物理化学 电极 冶金 有机化学 医学 工程类 内分泌学
作者
Han Liu,Yitong Guo,Ru Yang,Libo Wang,Yukai Chang,Aiguo Zhou
出处
期刊:Journal of Alloys and Compounds [Elsevier BV]
卷期号:976: 173204-173204 被引量:2
标识
DOI:10.1016/j.jallcom.2023.173204
摘要

Two-dimensional Ti3C2 MXene shows excellent lithium-storage performance as an anode of lithium-ion batteries. The replacement of Ti with V can enhance the lithium-storage performance, but decrease the stability of Ti3C2 MXene. To understand the impact of V replacement, in this study, a series of (Ti1-x,Vx)3C2 (x = 0, 0.1, 0.2…0.6) MXene solid solutions were prepared. The stability and lithium storage performance of the MXene solutions were investigated. The precursors to make (Ti1-x,Vx)3C2 MXene were MAX phase solid solutions of (Ti1-x,Vx)3AlC2, which were made from TiH2, V, Al and C powders at 1400 °C for 2 h under Ar atmosphere. Because of the replacement of > 60 at.% Ti by V destroys the stability of the (Ti1-x,Vx)3AlC2, the MAX solid solutions with x ≤ 0.6 were synthesized in this study. (Ti1-x,Vx)3C2 MXene was made from the corresponding MAX phases by the etching in mixed solutions of NaF + HCl. (Ti1-x,Vx)3C2 MXene (x = 0~0.4) were synthesized at 60 °C for 2 days, and the MXene (x = 0.5~0.6) were synthesized at 70 °C for 6 days. All (Ti1-x,Vx)3C2 solid solutions had better electrochemical performance than pure Ti3C2 MXene. Especially, (Ti0.7,V0.3)3C2 exhibited the best performance. The capacity of (Ti0.7,V0.3)3C2 was 183.5 mAh/g after 100 cycles at a current density of 500 mA/g, which was ~4.3 times of the capacity of the pure Ti3C2 (42.2 mAh/g at 500 mA/g). This is the first report to clarify the effect of V replacement on the stability and lithium performance on (Ti1-x,Vx)3C2 MXene solid solution. This work is critical for the synthesis of novel MXenes and MAX phases. It provides a way to make a MXene that is very close to V3C2 MXene, which is theoretically predicted but cannot be made. This work is vital for the enhancement of MXenes' electrochemical performance.
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
迷你的灵阳应助高求采纳,获得10
刚刚
pluto应助派大星采纳,获得10
刚刚
结实寒梦完成签到 ,获得积分10
1秒前
how发布了新的文献求助10
1秒前
黄坤发布了新的文献求助10
1秒前
大模型应助舒适静曼采纳,获得10
1秒前
不知人间烟火完成签到,获得积分20
1秒前
1秒前
研友_VZG7GZ应助默listening采纳,获得10
1秒前
秦刚发布了新的文献求助20
1秒前
缓舟行发布了新的文献求助10
2秒前
2秒前
无奈冥完成签到,获得积分10
2秒前
2秒前
v111发布了新的文献求助10
2秒前
笑点低易真完成签到,获得积分10
2秒前
3秒前
小马甲应助杨小辉采纳,获得10
3秒前
3秒前
打打应助junkround采纳,获得10
3秒前
朝文奕发布了新的文献求助10
3秒前
CipherSage应助无奈柚子采纳,获得10
4秒前
CodeCraft应助仵一采纳,获得10
4秒前
CodeCraft应助baiyuecheng采纳,获得10
4秒前
4秒前
瓜皮糖浆完成签到,获得积分10
5秒前
5秒前
科研通AI6.3应助小金鱼儿采纳,获得10
6秒前
YUEYUEHENCHEN完成签到 ,获得积分10
7秒前
7秒前
orixero应助王鑫采纳,获得10
7秒前
7秒前
郜kk完成签到,获得积分20
8秒前
秦刚完成签到,获得积分10
8秒前
Thouofsgs完成签到,获得积分10
8秒前
11发布了新的文献求助10
9秒前
俭朴忆雪发布了新的文献求助10
9秒前
顽石发布了新的文献求助10
9秒前
青青发布了新的文献求助80
9秒前
goKR完成签到,获得积分10
9秒前
高分求助中
Malcolm Fraser : a biography 700
Signals, Systems, and Signal Processing 610
天津市智库成果选编 600
Climate change and sports: Statistics report on climate change and sports 500
Forced degradation and stability indicating LC method for Letrozole: A stress testing guide 500
Organic Reactions Volume 118 400
A Foreign Missionary on the Long March: The Unpublished Memoirs of Arnolis Hayman of the China Inland Mission 400
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 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6463071
求助须知:如何正确求助?哪些是违规求助? 8270855
关于积分的说明 17632476
捐赠科研通 5534945
什么是DOI,文献DOI怎么找? 2906853
邀请新用户注册赠送积分活动 1883799
关于科研通互助平台的介绍 1730582