Novel Binder with Cross-Linking Reconfiguration Functionality for Silicon Anodes of Lithium-Ion Batteries

阳极 材料科学 锂(药物) 化学工程 电池(电) 电极 酰胺 聚合物 锂离子电池 复合材料 有机化学 光电子学 化学 功率(物理) 物理化学 内分泌学 工程类 物理 医学 量子力学
作者
Ruilai Ye,Jiaxiang Liu,Jianling Tian,Yi Deng,Xueying Yang,Qichen Chen,Peng Zhang,Jinbao Zhao
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:16 (13): 16820-16829 被引量:33
标识
DOI:10.1021/acsami.4c00590
摘要

Silicon is expected to be used as a high theoretical capacity anode material in lithium-ion batteries with high energy densities. However, the huge volume change incurred when silicon de-embeds lithium ions, leading to destruction of the electrode structure and a rapid reduction in battery capacity. Although binders play a key role in maintaining the stability of the electrode structure, commonly used binders cannot withstand the large volume expansion of the silicon. To alleviate this problem, we propose a PGC cross-linking reconfiguration binder based on poly(acrylic acid) (PAA), gelatin (GN), and β-cyclodextrin (β-CD). Within PGC, PAA supports the main chain and provides a large number of carboxyl groups (-COOH), GN provides rich carboxyl and amide groups that can form a cross-linking network with PAA, and β-CD offers rich hydroxyl groups and a cone-shaped hollow ring structure that can alleviate stress accumulation in the polymer chain by forming a new dynamic cross-linking coordination conformation during stretching. In the half cell, the silicon negative prepared by the PGC binder exhibited a high specific capacity and capacity maintenance ratio, and the specific capacity of the silicon negative electrode prepared by the PGC binder is still 1809 mAh g-1 and the capacity maintenance ratio is 73.76% following 200 cycles at 2 A g-1 current density, indicating that PGC sufficiently maintains the silicon negative structure during the battery cycle. The PGC binder has a simple preparation method and good capacity retention ability, making it a potential reference for the further development of silicon negative electrodes.
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
小二郎应助危机的阁采纳,获得10
4秒前
5秒前
awaiskhan发布了新的文献求助20
6秒前
无极微光应助HaHa007采纳,获得20
7秒前
mr_beard完成签到 ,获得积分10
8秒前
8秒前
11秒前
12秒前
Jasper应助lkl采纳,获得10
12秒前
13秒前
上官若男应助扑通扑通通采纳,获得10
14秒前
念所三旬完成签到,获得积分10
14秒前
niufuking发布了新的文献求助10
14秒前
kelaier发布了新的文献求助10
16秒前
zzww发布了新的文献求助10
17秒前
周文凯发布了新的文献求助10
17秒前
小碗面完成签到,获得积分10
17秒前
学术小白完成签到,获得积分10
18秒前
苏苏完成签到 ,获得积分10
19秒前
小碗面发布了新的文献求助10
20秒前
20秒前
Orange应助云7采纳,获得10
24秒前
科研通AI6.2应助马以琳采纳,获得10
25秒前
asd1576562308完成签到 ,获得积分10
27秒前
一一给一一的求助进行了留言
27秒前
银角大王完成签到,获得积分10
29秒前
34秒前
科研通AI6.3应助yxl采纳,获得10
35秒前
科目三应助科研通管家采纳,获得10
38秒前
脑洞疼应助科研通管家采纳,获得10
38秒前
miss张应助科研通管家采纳,获得10
38秒前
miss张应助科研通管家采纳,获得10
38秒前
38秒前
38秒前
情怀应助科研通管家采纳,获得10
38秒前
英俊的铭应助科研通管家采纳,获得10
38秒前
ilugbh发布了新的文献求助10
38秒前
Pingouin应助科研通管家采纳,获得10
38秒前
38秒前
38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
PowerCascade: A Synthetic Dataset for Cascading Failure Analysis in Power Systems 2000
Research Handbook on the Law of the Paris Agreement 1000
Various Faces of Animal Metaphor in English and Polish 800
Superabsorbent Polymers: Synthesis, Properties and Applications 700
Signals, Systems, and Signal Processing 610
Photodetectors: From Ultraviolet to Infrared 500
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 6352700
求助须知:如何正确求助?哪些是违规求助? 8167549
关于积分的说明 17189858
捐赠科研通 5408826
什么是DOI,文献DOI怎么找? 2863411
邀请新用户注册赠送积分活动 1840825
关于科研通互助平台的介绍 1689766