{"title":"绿色可持续深度共晶溶剂在环境条件下直接低温再生降解LiFePO₄阴极","authors":"Yixin Lin, Tiansheng Wang, Chaochao Gao, Xiaoxuan Zhang, Wen Yu, Mi Wang, Chao Yang, Jiaheng Zhang","doi":"10.1002/advs.202504683","DOIUrl":null,"url":null,"abstract":"<p><p>The definite lifespan of lithium iron phosphate (LiFePO<sub>4</sub>, LFP) batteries necessitates the advancement of cost-effective, nature-friendly, and productive recycling techniques for spent LFP batteries. In this study, ethylene glycol (C<sub>2</sub>H<sub>6</sub>O<sub>2</sub>), a sustainable and economical small organic molecule, is employed as a multifunctional hydrogen-bonding donor, along with lithium chloride (LiCl), a readily accessible Li source and hydrogen-bonding acceptor. Together, they form a novel Li-salt deep eutectic solvent (DES) through hydrogen bonding interactions. This DES directly repairs and rejuvenates the spent cathode material (S-LFP) at 80 °C. The Li-salt DES not only replenishes the depleted Li in S-LFP and reduces the adverse effects of Li-Fe antisite defects but also establishes a reducing environment that facilitates the reversion of degraded Fe(III) species in S-LFP back to their original Fe(II) state. Consequently, the regenerated LFP exhibits remarkable electrochemical behavior, delivering an initial capacity of 155.6 mAh g<sup>-1</sup> at 0.1 C and retaining 93% of its initial capacity after 300 cycles at 1 C. This approach can be scaled up to treat large quantities of LFP cathode material recovered from fully retired batteries, presenting a practical pathway toward large-scale recycling of spent LFP batteries in the future.</p>","PeriodicalId":117,"journal":{"name":"Advanced Science","volume":" ","pages":"e2504683"},"PeriodicalIF":14.3000,"publicationDate":"2025-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Direct and Low-Temperature Regeneration of Degraded LiFePO₄ Cathodes at Ambient Conditions Using Green and Sustainable Deep Eutectic Solvent.\",\"authors\":\"Yixin Lin, Tiansheng Wang, Chaochao Gao, Xiaoxuan Zhang, Wen Yu, Mi Wang, Chao Yang, Jiaheng Zhang\",\"doi\":\"10.1002/advs.202504683\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The definite lifespan of lithium iron phosphate (LiFePO<sub>4</sub>, LFP) batteries necessitates the advancement of cost-effective, nature-friendly, and productive recycling techniques for spent LFP batteries. In this study, ethylene glycol (C<sub>2</sub>H<sub>6</sub>O<sub>2</sub>), a sustainable and economical small organic molecule, is employed as a multifunctional hydrogen-bonding donor, along with lithium chloride (LiCl), a readily accessible Li source and hydrogen-bonding acceptor. Together, they form a novel Li-salt deep eutectic solvent (DES) through hydrogen bonding interactions. This DES directly repairs and rejuvenates the spent cathode material (S-LFP) at 80 °C. The Li-salt DES not only replenishes the depleted Li in S-LFP and reduces the adverse effects of Li-Fe antisite defects but also establishes a reducing environment that facilitates the reversion of degraded Fe(III) species in S-LFP back to their original Fe(II) state. Consequently, the regenerated LFP exhibits remarkable electrochemical behavior, delivering an initial capacity of 155.6 mAh g<sup>-1</sup> at 0.1 C and retaining 93% of its initial capacity after 300 cycles at 1 C. This approach can be scaled up to treat large quantities of LFP cathode material recovered from fully retired batteries, presenting a practical pathway toward large-scale recycling of spent LFP batteries in the future.</p>\",\"PeriodicalId\":117,\"journal\":{\"name\":\"Advanced Science\",\"volume\":\" \",\"pages\":\"e2504683\"},\"PeriodicalIF\":14.3000,\"publicationDate\":\"2025-05-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Science\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/advs.202504683\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Science","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/advs.202504683","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
磷酸铁锂(LiFePO4, LFP)电池的明确寿命要求提高成本效益、自然友好型和高效的废旧LFP电池回收技术。在本研究中,乙二醇(C2H6O2)是一种可持续和经济的小有机分子,与氯化锂(LiCl)一起作为多功能氢键供体,氯化锂(LiCl)是一种容易获得的锂源和氢键受体。它们通过氢键相互作用形成了一种新型的锂盐深共晶溶剂(DES)。这种DES在80°C下直接修复和恢复废阴极材料(S-LFP)。Li-salt DES不仅补充了S-LFP中耗尽的Li,减少了Li-Fe对位缺陷的不利影响,而且还建立了还原环境,促进了S-LFP中降解的Fe(III)物种恢复到原来的Fe(II)状态。因此,再生的LFP表现出卓越的电化学行为,在0.1 C下提供155.6 mAh g-1的初始容量,在1 C下循环300次后保持93%的初始容量。这种方法可以扩展到处理从完全退役的电池中回收的大量LFP正极材料,为未来大规模回收废旧LFP电池提供了一条实用的途径。
Direct and Low-Temperature Regeneration of Degraded LiFePO₄ Cathodes at Ambient Conditions Using Green and Sustainable Deep Eutectic Solvent.
The definite lifespan of lithium iron phosphate (LiFePO4, LFP) batteries necessitates the advancement of cost-effective, nature-friendly, and productive recycling techniques for spent LFP batteries. In this study, ethylene glycol (C2H6O2), a sustainable and economical small organic molecule, is employed as a multifunctional hydrogen-bonding donor, along with lithium chloride (LiCl), a readily accessible Li source and hydrogen-bonding acceptor. Together, they form a novel Li-salt deep eutectic solvent (DES) through hydrogen bonding interactions. This DES directly repairs and rejuvenates the spent cathode material (S-LFP) at 80 °C. The Li-salt DES not only replenishes the depleted Li in S-LFP and reduces the adverse effects of Li-Fe antisite defects but also establishes a reducing environment that facilitates the reversion of degraded Fe(III) species in S-LFP back to their original Fe(II) state. Consequently, the regenerated LFP exhibits remarkable electrochemical behavior, delivering an initial capacity of 155.6 mAh g-1 at 0.1 C and retaining 93% of its initial capacity after 300 cycles at 1 C. This approach can be scaled up to treat large quantities of LFP cathode material recovered from fully retired batteries, presenting a practical pathway toward large-scale recycling of spent LFP batteries in the future.
期刊介绍:
Advanced Science is a prestigious open access journal that focuses on interdisciplinary research in materials science, physics, chemistry, medical and life sciences, and engineering. The journal aims to promote cutting-edge research by employing a rigorous and impartial review process. It is committed to presenting research articles with the highest quality production standards, ensuring maximum accessibility of top scientific findings. With its vibrant and innovative publication platform, Advanced Science seeks to revolutionize the dissemination and organization of scientific knowledge.