Improvement of irreversible behavior of SiO anodes for lithium ion batteries by a solid state reaction at high temperature

法拉第效率 阳极 电化学 锂钴氧化物 材料科学 锂(药物) 阴极 电极 氧化钴 化学工程 锂离子电池 氧化物 离子 电池(电) 无机化学 分析化学(期刊) 化学 冶金 物理化学 色谱法 有机化学 热力学 功率(物理) 内分泌学 医学 物理 工程类
作者
Jee Ho Yom,Sun Woo Hwang,Sung Man Cho,Woo Young Yoon
出处
期刊:Journal of Power Sources [Elsevier BV]
卷期号:311: 159-166 被引量:79
标识
DOI:10.1016/j.jpowsour.2016.02.025
摘要

Herein, we describe a new simple method to improve the irreversible performance of a SiO anode during the initial cycle. The solid state-reacted SiO material was synthesized from bare SiO and lithium powders (three samples with weight ratios of 7:1, 8:1, and 9:1 were prepared) using a heat treatment process at 600 °C. Irreversible phases such as lithium silicates (Li4SiO4 and Li2SiO3) and Li2O were formed upon the solid state reaction with SiO. Electrochemical tests using half-cells were performed to confirm the effects of the solid state-reacted SiO material. The initial Coulombic efficiencies of the three samples were 82.12% (7:1), 79.81% (8:1), and 78.95% (9:1), which were far higher than that of a bare SiO cell (58.52%). Furthermore, the electrochemical performance of a full cell using a 7:1 wt% SiO anode and a lithium cobalt oxide cathode was evaluated. The full cell exhibited an initial Coulombic efficiency of 93.62% and a capacity retention of 74.70% after 15 cycles, which were also far higher than those of a bare SiO cell (66.4% and 55.72%, respectively). A comparison of the solid state-reacted and bare SiO electrodes demonstrated that the pre-formed irreversible phases prevented the consumption of lithium ions during the 1st cycle.

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
刚刚
鲸鱼完成签到,获得积分10
刚刚
willowei完成签到,获得积分10
刚刚
所所应助白白采纳,获得30
刚刚
1秒前
1秒前
1秒前
左丘寒烟完成签到 ,获得积分10
1秒前
文艺的青槐完成签到,获得积分10
2秒前
2秒前
佳佳完成签到,获得积分10
3秒前
严锦强完成签到,获得积分10
3秒前
orit发布了新的文献求助20
3秒前
志轩完成签到,获得积分10
3秒前
大胆幼枫发布了新的文献求助10
3秒前
2Rui完成签到,获得积分10
4秒前
所所应助段辉采纳,获得10
5秒前
wsy发布了新的文献求助10
5秒前
哈哈就哈哈完成签到,获得积分10
6秒前
叶问完成签到,获得积分10
6秒前
科研通AI6.2应助咸芋咸鱼采纳,获得10
7秒前
张铭娟发布了新的文献求助30
7秒前
小二郎应助nazi采纳,获得10
7秒前
8秒前
10秒前
11秒前
11秒前
11秒前
11秒前
11秒前
Lucas应助科研通管家采纳,获得10
11秒前
小蘑菇应助哈哈采纳,获得10
11秒前
wanci应助科研通管家采纳,获得10
11秒前
脑洞疼应助科研通管家采纳,获得10
11秒前
科研通AI6.4应助风清扬采纳,获得10
12秒前
12秒前
dd发布了新的文献求助10
12秒前
昀汐完成签到 ,获得积分10
12秒前
ws完成签到,获得积分10
13秒前
科研通AI6.1应助sgssm采纳,获得10
13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
Metallurgy at high pressures and high temperatures 2000
Tier 1 Checklists for Seismic Evaluation and Retrofit of Existing Buildings 1000
PowerCascade: A Synthetic Dataset for Cascading Failure Analysis in Power Systems 1000
The Organic Chemistry of Biological Pathways Second Edition 1000
Free parameter models in liquid scintillation counting 1000
Signals, Systems, and Signal Processing 610
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 6331150
求助须知:如何正确求助?哪些是违规求助? 8147587
关于积分的说明 17096964
捐赠科研通 5386797
什么是DOI,文献DOI怎么找? 2855965
邀请新用户注册赠送积分活动 1833364
关于科研通互助平台的介绍 1684781