亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

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
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

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
cjh发布了新的文献求助10
2秒前
情怀应助科研通管家采纳,获得10
4秒前
科目三应助科研通管家采纳,获得10
4秒前
归尘应助科研通管家采纳,获得10
4秒前
乐乐应助洪武采纳,获得10
11秒前
1777完成签到,获得积分10
23秒前
Letter完成签到 ,获得积分10
44秒前
pppcpppdpppy完成签到,获得积分10
46秒前
56秒前
阔达白凡完成签到,获得积分10
57秒前
HUNG发布了新的文献求助10
1分钟前
美丽的冰枫完成签到,获得积分10
1分钟前
义气的断秋完成签到,获得积分10
1分钟前
1分钟前
七人七发布了新的文献求助10
1分钟前
归尘应助科研通管家采纳,获得10
2分钟前
归尘应助科研通管家采纳,获得10
2分钟前
归尘应助科研通管家采纳,获得10
2分钟前
longh完成签到,获得积分10
2分钟前
唐泽雪穗应助女爰舍予采纳,获得10
2分钟前
走啊走应助难寻采纳,获得20
2分钟前
ggw完成签到 ,获得积分10
2分钟前
蜘蛛道理完成签到 ,获得积分10
2分钟前
linglingling完成签到 ,获得积分10
2分钟前
千寻未央完成签到,获得积分10
3分钟前
科研通AI5应助七人七采纳,获得30
3分钟前
聪明的云完成签到 ,获得积分10
3分钟前
3分钟前
七人七发布了新的文献求助30
3分钟前
走啊走应助七人七采纳,获得10
3分钟前
3分钟前
3分钟前
muhum完成签到 ,获得积分10
3分钟前
不安的冰枫092623完成签到,获得积分10
3分钟前
归尘应助科研通管家采纳,获得10
4分钟前
归尘应助科研通管家采纳,获得10
4分钟前
搜集达人应助科研通管家采纳,获得10
4分钟前
归尘应助科研通管家采纳,获得10
4分钟前
归尘应助科研通管家采纳,获得10
4分钟前
归尘应助科研通管家采纳,获得10
4分钟前
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
Zeolites: From Fundamentals to Emerging Applications 1500
Architectural Corrosion and Critical Infrastructure 1000
Early Devonian echinoderms from Victoria (Rhombifera, Blastoidea and Ophiocistioidea) 1000
Hidden Generalizations Phonological Opacity in Optimality Theory 1000
2026国自然单细胞多组学大红书申报宝典 800
Real Analysis Theory of Measure and Integration 3rd Edition 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 内科学 生物化学 物理 计算机科学 纳米技术 遗传学 基因 复合材料 化学工程 物理化学 病理 催化作用 免疫学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 4909965
求助须知:如何正确求助?哪些是违规求助? 4186014
关于积分的说明 12998951
捐赠科研通 3953257
什么是DOI,文献DOI怎么找? 2167844
邀请新用户注册赠送积分活动 1186297
关于科研通互助平台的介绍 1093258