Synthesis of LiNi0.9Co0.05Mn0.05O2 and modification with co-doping of Zr4+ and W6+ using acid leaching solution from spent lithium-ion batteries

IF 2.6 4区 化学 Q3 CHEMISTRY, PHYSICAL Ionics Pub Date : 2024-09-30 DOI:10.1007/s11581-024-05856-z
Rui Zhu, Guanghui Guo, Tian Zhou, Yanjiang Chen, Yan Yang
{"title":"Synthesis of LiNi0.9Co0.05Mn0.05O2 and modification with co-doping of Zr4+ and W6+ using acid leaching solution from spent lithium-ion batteries","authors":"Rui Zhu,&nbsp;Guanghui Guo,&nbsp;Tian Zhou,&nbsp;Yanjiang Chen,&nbsp;Yan Yang","doi":"10.1007/s11581-024-05856-z","DOIUrl":null,"url":null,"abstract":"<div><p>Considering the increase in raw material prices and environmental pollution, the spent lithium-ion battery cathode material was leached with oxalic acid and sulfuric acid, and LiNi<sub>0.9</sub>Co<sub>0.05</sub>Mn<sub>0.05</sub>O<sub>2</sub> (NCM955) was prepared from the leaching solution. Then, the Ni-rich cathode material NCM955 was doped with ZrO<sub>2</sub> and WO<sub>3</sub>. The co-doping of Zr<sup>4+</sup> and W<sup>6+</sup> in Ni-rich NCM955 cathode exhibits exceptional cycle stability performance. Specifically, the Zr<sup>4+</sup> and W<sup>6+</sup> co-doped sample demonstrates a remarkable capacity retention improvement of 89.21% at 0.5 C after 100 cycles compared to the pristine sample (69.15%). Meanwhile, at a high rate of 5 C, the co-doped sample shows a significantly higher specific capacity of 125.37 mAh·g<sup>−1</sup> compared to the pristine sample’s value of only 63.98 mAh·g<sup>−1</sup>. The results of XRD, XPS, and SEM indicate that the co-doping of Zr<sup>4+</sup> and W<sup>6+</sup> can enhance the stability of the material. Electrochemical impedance spectroscopy (EIS) results show that the co-doping of Zr<sup>4+</sup> and W<sup>6+</sup> effectively reduces the electrochemical impedance, and galvanostatic intermittent titration technique (GITT) shows that the co-doping of Zr<sup>4+</sup> and W<sup>6+</sup> increases the diffusion rate of Li<sup>+</sup>. Therefore, dual doping modification with Zr<sup>4+</sup> and W<sup>6+</sup> is beneficial for enhancing both structural stability and electrochemical performance of Ni-rich layered oxide cathode materials.</p></div>","PeriodicalId":599,"journal":{"name":"Ionics","volume":"30 12","pages":"7891 - 7902"},"PeriodicalIF":2.6000,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ionics","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11581-024-05856-z","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Considering the increase in raw material prices and environmental pollution, the spent lithium-ion battery cathode material was leached with oxalic acid and sulfuric acid, and LiNi0.9Co0.05Mn0.05O2 (NCM955) was prepared from the leaching solution. Then, the Ni-rich cathode material NCM955 was doped with ZrO2 and WO3. The co-doping of Zr4+ and W6+ in Ni-rich NCM955 cathode exhibits exceptional cycle stability performance. Specifically, the Zr4+ and W6+ co-doped sample demonstrates a remarkable capacity retention improvement of 89.21% at 0.5 C after 100 cycles compared to the pristine sample (69.15%). Meanwhile, at a high rate of 5 C, the co-doped sample shows a significantly higher specific capacity of 125.37 mAh·g−1 compared to the pristine sample’s value of only 63.98 mAh·g−1. The results of XRD, XPS, and SEM indicate that the co-doping of Zr4+ and W6+ can enhance the stability of the material. Electrochemical impedance spectroscopy (EIS) results show that the co-doping of Zr4+ and W6+ effectively reduces the electrochemical impedance, and galvanostatic intermittent titration technique (GITT) shows that the co-doping of Zr4+ and W6+ increases the diffusion rate of Li+. Therefore, dual doping modification with Zr4+ and W6+ is beneficial for enhancing both structural stability and electrochemical performance of Ni-rich layered oxide cathode materials.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
废锂离子电池酸浸液合成LiNi0.9Co0.05Mn0.05O2并共掺杂Zr4+和W6+改性
考虑到原材料价格上涨和环境污染,采用草酸和硫酸对废锂离子电池正极材料进行浸出,由浸出液制备LiNi0.9Co0.05Mn0.05O2 (NCM955)。然后,在富镍正极材料NCM955中掺杂ZrO2和WO3。在富镍NCM955阴极中共掺杂Zr4+和W6+,表现出优异的循环稳定性。具体来说,Zr4+和W6+共掺杂样品在0.5 C循环100次后,与原始样品(69.15%)相比,其容量保留率提高了89.21%。同时,在5℃的高倍率下,共掺杂样品的比容量达到125.37 mAh·g−1,而原始样品的比容量仅为63.98 mAh·g−1。XRD、XPS和SEM的分析结果表明,Zr4+和W6+的共掺杂增强了材料的稳定性。电化学阻抗谱(EIS)结果表明,Zr4+和W6+共掺杂有效降低了电化学阻抗,恒流间歇滴定技术(git)结果表明,Zr4+和W6+共掺杂提高了Li+的扩散速率。因此,Zr4+和W6+双掺杂改性有利于提高富镍层状氧化物正极材料的结构稳定性和电化学性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Ionics
Ionics 化学-电化学
CiteScore
5.30
自引率
7.10%
发文量
427
审稿时长
2.2 months
期刊介绍: Ionics is publishing original results in the fields of science and technology of ionic motion. This includes theoretical, experimental and practical work on electrolytes, electrode, ionic/electronic interfaces, ionic transport aspects of corrosion, galvanic cells, e.g. for thermodynamic and kinetic studies, batteries, fuel cells, sensors and electrochromics. Fast solid ionic conductors are presently providing new opportunities in view of several advantages, in addition to conventional liquid electrolytes.
期刊最新文献
A tutorial review on solid oxide fuel cells: fundamentals, materials, and applications. Recycling methods for spent lithium iron phosphate cathode materials An updated review on the potential of V₂O₅-based materials for zinc-ion batteries Radical-oxidation coupled phosphate stabilization strategy: an aqueous and scalable route to mesoporous MnPO4∙H2O precursor for high-performance LiMnPO4 cathodes The coupled influence of multiple conditions on the performance and stability characteristics of PEMFCs
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1