Fabrication of 2D Cu-BDC MOF and its derived porous carbon as anode material for high-performance Li/K-ion batteries

阳极 材料科学 热解 锂(药物) 碳纤维 介孔材料 电流密度 化学工程 离子 化学 催化作用 复合材料 电极 物理化学 冶金 有机化学 复合数 内分泌学 工程类 物理 量子力学 医学
作者
Guojun Zheng,Zheng Xing,Xinran Gao,Chuanhao Nie,Zihan Xu,Zhicheng Ju
出处
期刊:Applied Surface Science [Elsevier BV]
卷期号:559: 149701-149701 被引量:79
标识
DOI:10.1016/j.apsusc.2021.149701
摘要

2D Cu-BDC MOF nanosheets were designed and synthesized by controlling the reaction time, and then annealed at different pyrolysis temperatures; the final MOF-derived carbons C500 (Final product at 500 °C) and C700 (Final product at 700 °C) were obtained by acid etching. Both carbon derivatives possessed abundant mesoporous structures which could facilitate ion migration and be conducive to the storage of lithium/potassium ions. C500 and C700 exhibited different dominant kinetic behaviors in lithium ion/potassium ion batteries. C500, which was controlled by diffusion process, showed better performance when used as anode material for lithium-ion batteries (LIBs). The C500 anode exhibited a reversible specific capacity of 690.4 mAhg−1 at a current density of 0.1 Ag−1. Even after 500 cycles at a current density of 5.0 Ag−1, the high specific capacity of 210.3 mAhg−1 was still maintained. C700, which was dominated by surface capacitance contribution, was a superior anode material for potassium-ion batteries (PIBs). The reversible specific capacity of C700 anode was maintained at 286.2 mAhg−1 at the current density of 0.1 Ag−1 after 100 cycles. Even after 500 cycles at a current density of 1.0 A g−1, C700 anode still maintained 170.8 mAhg−1.
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
we完成签到,获得积分10
1秒前
汉堡包应助ultramantaro采纳,获得10
1秒前
1秒前
2秒前
完美世界应助micett采纳,获得10
3秒前
我能私信骂你吗应助kang采纳,获得10
3秒前
脑洞疼应助胡质斌采纳,获得30
4秒前
勤恳的绿凝应助圆圆滚滚采纳,获得10
4秒前
4秒前
马界泡泡完成签到,获得积分10
4秒前
4秒前
端庄的傲易应助yide采纳,获得10
4秒前
xyz发布了新的文献求助10
4秒前
4秒前
6秒前
YJJJ0310发布了新的文献求助10
6秒前
852应助Swu采纳,获得10
6秒前
传统的傲菡完成签到,获得积分10
6秒前
6秒前
nly应助LXN采纳,获得10
7秒前
myn1990发布了新的文献求助10
7秒前
7秒前
7秒前
weixiao发布了新的文献求助10
7秒前
宝z发布了新的文献求助10
8秒前
Phd侯完成签到,获得积分10
8秒前
8秒前
1111发布了新的文献求助10
9秒前
9秒前
9秒前
9秒前
NexusExplorer应助坚强的笑天采纳,获得10
9秒前
9秒前
9秒前
乐观忆之完成签到 ,获得积分10
10秒前
10秒前
田様应助栗松琛采纳,获得10
10秒前
星辰大海应助AireenBeryl531采纳,获得10
10秒前
orixero应助伍号科研怪物采纳,获得10
10秒前
赏金猎人John_Wang完成签到,获得积分10
11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 7747466
求助须知:如何正确求助?哪些是违规求助? 9295763
关于积分的说明 20231203
捐赠科研通 7328333
什么是DOI,文献DOI怎么找? 3308523
关于科研通互助平台的介绍 2460324
邀请新用户注册赠送积分活动 2320418