Identifying cathode and anode polarizations during practical high‐rate charging/discharging in different Li‐ion pouch batteries

阳极 石墨 阴极 材料科学 离子 电池(电) 光电子学 电气工程 分析化学(期刊) 化学工程 复合材料 物理 工程类 化学 电极 色谱法 物理化学 功率(物理) 有机化学 量子力学
作者
Li Wang,Leqiong Xie,Yaqin Song,Xiaomei Liu,Hao Zhang,Xiangming He
出处
期刊:Battery energy 卷期号:2 (1) 被引量:12
标识
DOI:10.1002/bte2.20220025
摘要

Abstract Cell design is effective to improve the performances of lithium‐ion batteries (LIBs). For identifying the bottleneck of a full battery used for high‐rate charging/discharging, we developed a simple method, by a reference electrode in practical pouch cells, to quick obtain the polarizations of the cathode and the anode. For a Li(Ni 0.6 Co 0.2 Mn 0.2 )O 2 /graphite full cell, 63.9% and 97.0% of the polarizations originate from the anode at 50% state of charge (SOC) during 2.0 C charging and discharging rates, respectively. While for LiFePO 4 /graphite system, 62.5% and 55.8% of the polarizations originate from the anode at the same charging and discharging conditions. These indicate that the anode is the limitation during fast charging/discharging, which is consistent with the common understanding but in contrary to the results obtained by coin cells reported previously. While the rate limitation from anode in LiFePO 4 /graphite system during fast charging/discharging is significantly changed to both cathode and anode compared with Li(Ni 0.6 Co 0.2 Mn 0.2 )O 2 /graphite. Besides, graphite anodes in LiFePO 4 /graphite cells more readily dive to the Li‐metal plating potential at high charging rate. This leads to safety concerns of LiFePO 4 /graphite cells during fast charging. This is a facile strategy for fast distinguishing polarizations from cathodes and anodes of high‐rate LIBs.
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
大幅提高文件上传限制,最高150M (2024-4-1)

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
超帅的小鸽子完成签到,获得积分10
2秒前
2秒前
WANGT完成签到,获得积分10
3秒前
领导范儿应助Regina采纳,获得10
4秒前
Orange应助zz采纳,获得10
5秒前
雁昔完成签到,获得积分10
6秒前
张大宝完成签到,获得积分10
6秒前
6秒前
启程牛牛完成签到,获得积分0
7秒前
张张发布了新的文献求助10
8秒前
失眠的梦之完成签到,获得积分10
9秒前
英姑应助像鱼采纳,获得10
9秒前
柳城完成签到,获得积分10
9秒前
10秒前
10秒前
大个应助GLY采纳,获得10
10秒前
10秒前
脑洞疼应助clearlove采纳,获得10
11秒前
Salt1222完成签到,获得积分10
11秒前
勇敢虫子不怕困难完成签到,获得积分10
12秒前
12秒前
12秒前
13秒前
123发布了新的文献求助10
13秒前
14秒前
迷路毛豆发布了新的文献求助10
17秒前
17秒前
17秒前
17秒前
CodeCraft应助LLLLL采纳,获得10
17秒前
18秒前
19秒前
优雅灵波发布了新的文献求助50
19秒前
zz发布了新的文献求助10
19秒前
123完成签到,获得积分10
19秒前
wangqiqi完成签到,获得积分10
20秒前
sxy发布了新的文献求助10
21秒前
温暖小猫咪完成签到,获得积分10
22秒前
mingjie完成签到,获得积分10
22秒前
22秒前
高分求助中
Sustainability in Tides Chemistry 2800
The Young builders of New china : the visit of the delegation of the WFDY to the Chinese People's Republic 1000
юрские динозавры восточного забайкалья 800
English Wealden Fossils 700
Foreign Policy of the French Second Empire: A Bibliography 500
Chen Hansheng: China’s Last Romantic Revolutionary 500
XAFS for Everyone 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 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3145115
求助须知:如何正确求助?哪些是违规求助? 2796489
关于积分的说明 7819996
捐赠科研通 2452771
什么是DOI,文献DOI怎么找? 1305202
科研通“疑难数据库(出版商)”最低求助积分说明 627448
版权声明 601449