Atomic-Scale Mechanisms of Li-Ion Transport Mediated by Li 10 GeP 2 S 12 in Composite Solid Poly(Ethylene Oxide) Electrolytes

作者
Syed Mustafa Shah,Musawenkosi K. Ncube,Mohammed Lemaalem,Selva Chandrasekaran Selvaraj,Naveen Kumar Dandu,Alireza Kondori,GaYoon Kim,Adel Azaribeni,Mohammad Asadi,Anh T. Ngo,Larry A. Curtiss
出处
期刊:Journal of Physical Chemistry C [American Chemical Society]
卷期号:130 (14): 5287-5296
标识
DOI:10.1021/acs.jpcc.6c00006
摘要

Polymer electrolytes incorporating Li 10 GeP 2 S 12 (LGPS) nanoparticles are promising for solid-state lithium batteries due to their potential for enhanced ionic conductivity; yet, the atomistic mechanisms driving this enhancement remain debated. Here, we systematically investigate the relationship between LGPS nanoparticle loading, poly(ethylene oxide) microstructure, and Li-ion transport using a combination of molecular dynamics (MD) simulations, experimental ionic conductivity measurements, and density functional theory (DFT) calculations. MD simulations and experiments reveal good agreement on ionic conductivity as a function of LGPS concentrations of up to 10 wt % ( x %), exhibiting a volcano-like curve with ionic conductivity increasing 5-fold from the low concentrations and can be accounted for by a classical transport mechanism governed by polymer segmental dynamics and interface effects. However, at more than 10% LGPS, experiments show further conductivity enhancement that cannot be accounted for by MD simulations, indicating a shift to another transport mechanism. DFT calculations elucidate that, at the polymer| LGPS interface, Li-ion migration proceeds via vacancy-driven hopping, with barriers sensitive to local atomic composition-low-barrier pathways are possible when S atoms dominantly occupy the sites on the interface to facilitate Li-hopping, while pathways involving Ge act as obstacles to Li transport. These results establish that optimized interfacial chemistry and electrolyte structure enable efficient, barrier-lowering migration channels that are distinct from bulk polymer or ceramic behavior. Our approach reconciles experiments with classical simulations at low LGPS concentrations and quantum chemical interface calculations, highlighting design criteria for maximizing the performance of these types of solid composite polymer electrolytes and guiding the development of advanced lithium batteries.

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
att的应助被QXS采纳,获得10
刚刚
CTY完成签到,获得积分10
刚刚
刚刚
忧心的曼凝的应助被兑为泽采纳,获得10
1秒前
伍若舟发布了新的文献求助10
1秒前
香菜完成签到 ,获得积分10
2秒前
无限若云完成签到,获得积分10
2秒前
思源的应助被DONG采纳,获得10
2秒前
2秒前
不是吹雪发布了新的文献求助10
2秒前
无骨鸡爪不长胖完成签到,获得积分10
3秒前
3秒前
4秒前
4秒前
华乐天完成签到,获得积分10
4秒前
似我完成签到,获得积分10
4秒前
4秒前
5秒前
吱呜猪发布了新的文献求助10
5秒前
顽固眩晕小洋葱完成签到,获得积分10
5秒前
虚心之玉发布了新的文献求助10
5秒前
6秒前
花灯王子发布了新的文献求助10
7秒前
千里毅发布了新的文献求助10
7秒前
8秒前
斯文败类的应助被大大的寄吧采纳,获得30
8秒前
8秒前
科研通AI6.2的应助被Ysczero采纳,获得10
9秒前
打打的应助被LRSDFJJ采纳,获得10
9秒前
科研阳完成签到,获得积分10
9秒前
搜集达人的应助被山复尔尔采纳,获得10
10秒前
10秒前
乐乐的应助被yang采纳,获得10
10秒前
XyM发布了新的文献求助10
10秒前
拉长的砖家完成签到,获得积分20
11秒前
科研通AI6.4的应助被太难了采纳,获得10
11秒前
核桃发布了新的文献求助10
11秒前
12秒前
aajhajkahna的应助被dodo采纳,获得10
12秒前
喔喔某人发布了新的文献求助10
12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
Energie-Contracting 1500
Klimaschutzrecht durch den Energiesektor im Mehrebenensystem – Ein Rechtsvergleich 1000
Stochastic Models in Operations Research,Vol. 2 600
桑白皮エキスの実験的, 臨床的育毛効果について 500
Qualitative Methodologies in Tourism Studies: Disrupting and Co-creating Critical Research 350
银行间市场数据报告库(上海)股份有限公司招聘笔试题库 350
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 工程类 有机化学 化学工程 生物化学 物理 复合材料 内科学 催化作用 光电子学 人工智能 细胞生物学 无机化学 物理化学 数学
热门帖子
关注 科研通微信公众号,转发送积分 8040114
求助须知:如何正确求助?哪些是违规求助? 9474147
关于积分的说明 21270941
捐赠科研通 7608616
什么是DOI,文献DOI怎么找? 3391058
关于科研通互助平台的介绍 2522549
邀请新用户注册赠送积分活动 2428683