{"title":"富锂层状氧化物阴极的电压衰减和迟滞现象","authors":"Hongfei Zheng, Liguang Wang, Jun Lu","doi":"10.1002/adfm.202503578","DOIUrl":null,"url":null,"abstract":"Li‐rich layered oxide cathodes (LLOs) with anionic redox are promising to boost the energy density of lithium batteries beyond 500 Wh kg<jats:sup>−1</jats:sup>. However, their commercialization has long been hampered by inherent drawbacks, particularly voltage decay and hysteresis, which reduce energy density and efficiency, shorten battery life, and challenge battery management. To address these issues, a prerequisite is establishing a comprehensive understanding of voltage‐related phenomena correlated with anionic redox reactions (ARR), which remains elusive despite extensive research. Therefore, in this review, the proposed mechanisms are systematically summarized and the fundamental origins of voltage decay and hysteresis are identified, together with elucidating their relationship with ARR. Voltage decay is mainly attributed to irreversible TM migration and phase transition, whose driving force involves factors like lattice strain accumulation and oxygen loss. A relatively unified theory, the asymmetric non‐equilibrium reaction path during ARR, is identified as the fundamental origin of voltage hysteresis. This path includes sequential electrochemical reactions and chemical processes (sluggish electronic and atomic structural rearrangements, such as TM migration and ligand‐to‐metal charge transfer). Recent achievements and effective solutions for these voltage issues are also elaborated. After deeply understanding voltage decay and hysteresis, inspiring insights for mitigation strategies and forward‐looking remarks are provided.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"18 1","pages":""},"PeriodicalIF":18.5000,"publicationDate":"2025-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Understanding Voltage Decay and Hysteresis in Li‐Rich Layered Oxide Cathodes\",\"authors\":\"Hongfei Zheng, Liguang Wang, Jun Lu\",\"doi\":\"10.1002/adfm.202503578\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Li‐rich layered oxide cathodes (LLOs) with anionic redox are promising to boost the energy density of lithium batteries beyond 500 Wh kg<jats:sup>−1</jats:sup>. However, their commercialization has long been hampered by inherent drawbacks, particularly voltage decay and hysteresis, which reduce energy density and efficiency, shorten battery life, and challenge battery management. To address these issues, a prerequisite is establishing a comprehensive understanding of voltage‐related phenomena correlated with anionic redox reactions (ARR), which remains elusive despite extensive research. Therefore, in this review, the proposed mechanisms are systematically summarized and the fundamental origins of voltage decay and hysteresis are identified, together with elucidating their relationship with ARR. Voltage decay is mainly attributed to irreversible TM migration and phase transition, whose driving force involves factors like lattice strain accumulation and oxygen loss. A relatively unified theory, the asymmetric non‐equilibrium reaction path during ARR, is identified as the fundamental origin of voltage hysteresis. This path includes sequential electrochemical reactions and chemical processes (sluggish electronic and atomic structural rearrangements, such as TM migration and ligand‐to‐metal charge transfer). Recent achievements and effective solutions for these voltage issues are also elaborated. After deeply understanding voltage decay and hysteresis, inspiring insights for mitigation strategies and forward‐looking remarks are provided.\",\"PeriodicalId\":112,\"journal\":{\"name\":\"Advanced Functional Materials\",\"volume\":\"18 1\",\"pages\":\"\"},\"PeriodicalIF\":18.5000,\"publicationDate\":\"2025-05-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Functional Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/adfm.202503578\",\"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 Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adfm.202503578","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
具有阴离子氧化还原功能的富锂层状氧化物阴极(LLOs)有望将锂电池的能量密度提高到500 Wh kg - 1以上。然而,它们的商业化长期以来一直受到固有缺陷的阻碍,特别是电压衰减和滞后,这会降低能量密度和效率,缩短电池寿命,并给电池管理带来挑战。为了解决这些问题,一个先决条件是全面了解与阴离子氧化还原反应(ARR)相关的电压相关现象,尽管进行了广泛的研究,但这仍然是难以捉摸的。因此,在这篇综述中,本文系统地总结了所提出的机制,并确定了电压衰减和滞后的基本来源,并阐明了它们与ARR的关系。电压衰减主要归因于不可逆的TM迁移和相变,其驱动力涉及晶格应变积累和氧损失等因素。一种相对统一的理论认为,ARR过程中的不对称非平衡反应路径是电压滞后的根本原因。这条路径包括连续的电化学反应和化学过程(缓慢的电子和原子结构重排,如TM迁移和配体到金属的电荷转移)。本文还阐述了这些电压问题的最新成果和有效解决方案。在深入了解电压衰减和迟滞后,提供了缓解策略和前瞻性评论的鼓舞人心的见解。
Understanding Voltage Decay and Hysteresis in Li‐Rich Layered Oxide Cathodes
Li‐rich layered oxide cathodes (LLOs) with anionic redox are promising to boost the energy density of lithium batteries beyond 500 Wh kg−1. However, their commercialization has long been hampered by inherent drawbacks, particularly voltage decay and hysteresis, which reduce energy density and efficiency, shorten battery life, and challenge battery management. To address these issues, a prerequisite is establishing a comprehensive understanding of voltage‐related phenomena correlated with anionic redox reactions (ARR), which remains elusive despite extensive research. Therefore, in this review, the proposed mechanisms are systematically summarized and the fundamental origins of voltage decay and hysteresis are identified, together with elucidating their relationship with ARR. Voltage decay is mainly attributed to irreversible TM migration and phase transition, whose driving force involves factors like lattice strain accumulation and oxygen loss. A relatively unified theory, the asymmetric non‐equilibrium reaction path during ARR, is identified as the fundamental origin of voltage hysteresis. This path includes sequential electrochemical reactions and chemical processes (sluggish electronic and atomic structural rearrangements, such as TM migration and ligand‐to‐metal charge transfer). Recent achievements and effective solutions for these voltage issues are also elaborated. After deeply understanding voltage decay and hysteresis, inspiring insights for mitigation strategies and forward‐looking remarks are provided.
期刊介绍:
Firmly established as a top-tier materials science journal, Advanced Functional Materials reports breakthrough research in all aspects of materials science, including nanotechnology, chemistry, physics, and biology every week.
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