Weakly Solvating Ether‐Based Electrolyte Constructing Anion‐Derived Solid Electrolyte Interface in Graphite Anode toward High‐Stable Potassium‐Ion Batteries

电解质 阳极 离子 材料科学 石墨 无机化学 化学工程 乙醚 化学 有机化学 电极 冶金 物理化学 工程类
作者
Qilin Feng,Jiangmin Jiang,Shuang Li,Gaoyu Zhou,Xiangkai Kong,Yaxin Chen,Quanchao Zhuang,Zhicheng Ju
出处
期刊:Small [Wiley]
卷期号:21 (9): e2406506-e2406506 被引量:16
标识
DOI:10.1002/smll.202406506
摘要

Low-cost graphite has emerged as the most promising anode material for potassium-ion batteries (PIBs). Constructing the inorganic-rich solid electrolyte interface (SEI) on the surface of graphite anode is crucial for achieving superior electrochemical performance of PIBs. However, the compositions of SEI formed by conventional strongly solvating electrolytes are mainly organic, leading to the SEI structure being thick and causing the co-intercalation behavior of ions with the solvent. Herein, a weakly solvating electrolyte is applied to weaken the cation-solvent interaction and alter the cation solvation sheath structures, conducing to the inorganic composition derived from anions also participating in the formation of SEI, together with forming a uniformly shaped SEI with superior mechanical properties, and thus improving the overall performance of PIBs. The electrolyte solvation structure rich in aggregated ion pairs (AGGs) (69%) enables remarkable potassium-ion intercalation behavior at the graphite anode (reversible capacity of 269 mAh g-1) and highly stable plating/stripping of potassium metal anode (96.5%). As a practical device application, the assembled potassium-ion full-battery (PTCDA//Graphite) displays superior cycle stability. The optimizing strategy of cation solvation sheath structures offers a promising approach for developing high-performance electrolytes and beyond.
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
小二郎应助平常的雨兰采纳,获得10
刚刚
爆炸头关注了科研通微信公众号
刚刚
香蕉觅云应助谢西瓜采纳,获得10
1秒前
qjm完成签到,获得积分10
1秒前
1秒前
1秒前
2秒前
2秒前
简简单单完成签到,获得积分10
2秒前
2秒前
3秒前
3秒前
毛欢发布了新的文献求助10
3秒前
zmn0419完成签到,获得积分10
3秒前
在水一方应助十四采纳,获得10
3秒前
3秒前
DW应助思考的河苇采纳,获得10
4秒前
hhh完成签到,获得积分10
5秒前
荒野风完成签到,获得积分20
5秒前
科研喵完成签到,获得积分10
5秒前
5秒前
小李冲冲完成签到,获得积分10
5秒前
星辰大海应助该饮茶了采纳,获得10
6秒前
糖发人发布了新的文献求助10
6秒前
6秒前
ddgd发布了新的文献求助10
6秒前
利威尔会长高完成签到,获得积分10
7秒前
南瓜博士发布了新的文献求助10
7秒前
molihuakai应助毛驴采纳,获得10
7秒前
科研通AI6.4应助Hyacinth采纳,获得10
7秒前
meng发布了新的文献求助10
7秒前
科研通AI6.4应助柳驰采纳,获得10
7秒前
8秒前
8秒前
EZ完成签到,获得积分10
8秒前
李爱国应助浮华乱世采纳,获得30
9秒前
9秒前
10秒前
该饮茶了发布了新的文献求助10
10秒前
南苏完成签到,获得积分20
10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
Organizational Behavior 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Rosenblum, Global Change Biology 500
CLSI VET01S-2024 Performance Standards for Antimicrobial Disk and Dilution Susceptibility Tests for Bacteria Isolated From Animals (7th Ed) 500
DIPPR Project 801 - Full Version 380
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 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7767444
求助须知:如何正确求助?哪些是违规求助? 9311073
关于积分的说明 20321479
捐赠科研通 7352460
什么是DOI,文献DOI怎么找? 3315318
关于科研通互助平台的介绍 2464693
邀请新用户注册赠送积分活动 2330011