{"title":"镁修饰P2/O3双相结构增强钠离子电池阴极阴离子氧化还原稳定性","authors":"Yichen He, Yonglin Huo, Maowen Xu, Yuruo Qi","doi":"10.1002/adfm.202509099","DOIUrl":null,"url":null,"abstract":"Layered cathode materials for sodium ion batteries (SIBs) have garnered significant attention due to their high theoretical capacity and tunable crystal structure. However, they still confront severe structural attenuation at high voltages, especially those undergoing anionic redox reactions. To mitigate these limitations and elucidate the underlying mechanism, herein, a biphasic cathode material, Na<sub>0.67</sub>Fe<sub>0.3</sub>Mn<sub>0.5</sub>Li<sub>0.1</sub>Mg<sub>0.1</sub>O<sub>2</sub>, comprising 76.6% P2 and 23.4% O3 phases is proposed. The “Na─O─Mg” structure with robust Mg─O bonds enhances oxygen redox activity but also suppresses lattice oxygen evolution at elevated voltages, enabling a high initial discharge capacity of 187.8 mA h g⁻¹ at 0.1C. Moreover, the biphasic structure suppresses O/P structural rearrangement and mitigates harmful phase changes via forming OP2 phase at high-voltage, resulting in excellent cycling stability with a capacity retention of 96.6% after 100 cycles at 1C within an extended voltage window of 1.8–4.3 V. These findings deepen the understanding in the interlocking effect of biphasic materials and offer valuable insights for designing high-performance cathode materials.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"147 1","pages":""},"PeriodicalIF":18.5000,"publicationDate":"2025-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Enhanced Anionic Redox Stability for Sodium Ion Battery Cathodes via Mg-Modified P2/O3 Biphasic Architecture\",\"authors\":\"Yichen He, Yonglin Huo, Maowen Xu, Yuruo Qi\",\"doi\":\"10.1002/adfm.202509099\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Layered cathode materials for sodium ion batteries (SIBs) have garnered significant attention due to their high theoretical capacity and tunable crystal structure. However, they still confront severe structural attenuation at high voltages, especially those undergoing anionic redox reactions. To mitigate these limitations and elucidate the underlying mechanism, herein, a biphasic cathode material, Na<sub>0.67</sub>Fe<sub>0.3</sub>Mn<sub>0.5</sub>Li<sub>0.1</sub>Mg<sub>0.1</sub>O<sub>2</sub>, comprising 76.6% P2 and 23.4% O3 phases is proposed. The “Na─O─Mg” structure with robust Mg─O bonds enhances oxygen redox activity but also suppresses lattice oxygen evolution at elevated voltages, enabling a high initial discharge capacity of 187.8 mA h g⁻¹ at 0.1C. Moreover, the biphasic structure suppresses O/P structural rearrangement and mitigates harmful phase changes via forming OP2 phase at high-voltage, resulting in excellent cycling stability with a capacity retention of 96.6% after 100 cycles at 1C within an extended voltage window of 1.8–4.3 V. These findings deepen the understanding in the interlocking effect of biphasic materials and offer valuable insights for designing high-performance cathode materials.\",\"PeriodicalId\":112,\"journal\":{\"name\":\"Advanced Functional Materials\",\"volume\":\"147 1\",\"pages\":\"\"},\"PeriodicalIF\":18.5000,\"publicationDate\":\"2025-05-29\",\"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.202509099\",\"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.202509099","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
钠离子电池层状正极材料由于具有较高的理论容量和可调的晶体结构而备受关注。然而,它们在高压下仍然面临严重的结构衰减,特别是那些经历阴离子氧化还原反应的。为了消除这些限制并阐明其潜在的机制,本文提出了一种双相阴极材料Na0.67Fe0.3Mn0.5Li0.1Mg0.1O2,由76.6%的P2相和23.4%的O3相组成。具有坚固的Mg─O键的“Na─O─Mg”结构增强了氧氧化还原活性,但也抑制了高电压下的晶格氧演化,使0.1C时的高初始放电容量达到187.8 mA h g⁻¹。此外,双相结构抑制O/P结构重排,并通过在高压下形成OP2相来减轻有害的相位变化,从而在1.8-4.3 V的扩展电压窗口内,在1C下循环100次后,其容量保持率为96.6%,具有优异的循环稳定性。这些发现加深了对双相材料联锁效应的理解,并为高性能正极材料的设计提供了有价值的见解。
Enhanced Anionic Redox Stability for Sodium Ion Battery Cathodes via Mg-Modified P2/O3 Biphasic Architecture
Layered cathode materials for sodium ion batteries (SIBs) have garnered significant attention due to their high theoretical capacity and tunable crystal structure. However, they still confront severe structural attenuation at high voltages, especially those undergoing anionic redox reactions. To mitigate these limitations and elucidate the underlying mechanism, herein, a biphasic cathode material, Na0.67Fe0.3Mn0.5Li0.1Mg0.1O2, comprising 76.6% P2 and 23.4% O3 phases is proposed. The “Na─O─Mg” structure with robust Mg─O bonds enhances oxygen redox activity but also suppresses lattice oxygen evolution at elevated voltages, enabling a high initial discharge capacity of 187.8 mA h g⁻¹ at 0.1C. Moreover, the biphasic structure suppresses O/P structural rearrangement and mitigates harmful phase changes via forming OP2 phase at high-voltage, resulting in excellent cycling stability with a capacity retention of 96.6% after 100 cycles at 1C within an extended voltage window of 1.8–4.3 V. These findings deepen the understanding in the interlocking effect of biphasic materials and offer valuable insights for designing high-performance cathode materials.
期刊介绍:
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