{"title":"通过富锂无序域释放无钴锂离子阴极的潜力。","authors":"Hao Liu,Hang Li,Weibo Hua,Bixian Ying,Karin Kleiner,Jing Lin,Hang Xu,Bijian Deng,Deniz Wong,Thomas Bergfeldt,Stefan Mangold,Peter Nagel,Stefan Schuppler,Michael Merz,Volodymyr Baran,Wei Xiang,Yongjian Li,Ning Li,Michael Knapp,Helmut Ehrenberg,Sylvio Indris","doi":"10.1021/acsnano.5c09233","DOIUrl":null,"url":null,"abstract":"High-voltage, low-nickel, cobalt-free layered oxides are promising candidates for high-energy-density lithium-ion batteries. However, their practical application is hindered by intrinsic cation disorder and structural degradation at high voltages, leading to a poor electrochemical performance. Here, we report a slightly lithium-enriched, cobalt-free layered oxide, Li1.05Ni0.43Mn0.52O2, featuring lithium-rich disorder domains achieved through chemical composition optimization. Advanced structural characterization demonstrates that nickel ions not only reside within the TM layers but also occupy the Li layers, acting as pinned ions. Theoretical calculations indicate that this in-plane and out-of-plane disorder enables reversible oxygen redox activity without oxygen release at high voltages. Moreover, this local structural framework preserves integrity even after extended cycling, ensuring chemical and structural stability during battery operation. Consequently, the cathode delivers an impressive discharge capacity of 202.2 mAh g-1 at C/10 and exceptional cycling stability, retaining 96.3% of its capacity after 200 cycles at C/3 within a voltage range of 2.5-4.55 V. Our findings provide valuable insights into the design of high-energy-density, cobalt-free layered cathodes.","PeriodicalId":21,"journal":{"name":"ACS Nano","volume":"116 1","pages":""},"PeriodicalIF":16.0000,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unlocking the Potential of Cobalt-Free Lithium-Ion Cathodes via Lithium-Rich Disorder Domains.\",\"authors\":\"Hao Liu,Hang Li,Weibo Hua,Bixian Ying,Karin Kleiner,Jing Lin,Hang Xu,Bijian Deng,Deniz Wong,Thomas Bergfeldt,Stefan Mangold,Peter Nagel,Stefan Schuppler,Michael Merz,Volodymyr Baran,Wei Xiang,Yongjian Li,Ning Li,Michael Knapp,Helmut Ehrenberg,Sylvio Indris\",\"doi\":\"10.1021/acsnano.5c09233\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"High-voltage, low-nickel, cobalt-free layered oxides are promising candidates for high-energy-density lithium-ion batteries. However, their practical application is hindered by intrinsic cation disorder and structural degradation at high voltages, leading to a poor electrochemical performance. Here, we report a slightly lithium-enriched, cobalt-free layered oxide, Li1.05Ni0.43Mn0.52O2, featuring lithium-rich disorder domains achieved through chemical composition optimization. Advanced structural characterization demonstrates that nickel ions not only reside within the TM layers but also occupy the Li layers, acting as pinned ions. Theoretical calculations indicate that this in-plane and out-of-plane disorder enables reversible oxygen redox activity without oxygen release at high voltages. Moreover, this local structural framework preserves integrity even after extended cycling, ensuring chemical and structural stability during battery operation. Consequently, the cathode delivers an impressive discharge capacity of 202.2 mAh g-1 at C/10 and exceptional cycling stability, retaining 96.3% of its capacity after 200 cycles at C/3 within a voltage range of 2.5-4.55 V. Our findings provide valuable insights into the design of high-energy-density, cobalt-free layered cathodes.\",\"PeriodicalId\":21,\"journal\":{\"name\":\"ACS Nano\",\"volume\":\"116 1\",\"pages\":\"\"},\"PeriodicalIF\":16.0000,\"publicationDate\":\"2025-10-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Nano\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1021/acsnano.5c09233\",\"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":"ACS Nano","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acsnano.5c09233","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
高电压、低镍、无钴的层状氧化物是高能量密度锂离子电池的有希望的候选者。然而,它们的实际应用受到固有阳离子无序和高压下结构降解的阻碍,导致其电化学性能较差。在这里,我们报告了一种略富锂,无钴的层状氧化物Li1.05Ni0.43Mn0.52O2,通过化学成分优化获得了富锂无序域。先进的结构表征表明,镍离子不仅存在于TM层中,而且还占据了Li层,作为钉住离子。理论计算表明,在高电压下,这种面内和面外无序可以实现可逆的氧氧化还原活性而不释放氧气。此外,这种局部结构框架即使在长时间循环后也能保持完整性,确保电池运行期间的化学和结构稳定性。因此,阴极在C/10下提供了令人印象深刻的202.2 mAh g-1的放电容量和出色的循环稳定性,在2.5-4.55 V电压范围内,在C/3下200次循环后保持了96.3%的容量。我们的发现为高能量密度、无钴层状阴极的设计提供了有价值的见解。
Unlocking the Potential of Cobalt-Free Lithium-Ion Cathodes via Lithium-Rich Disorder Domains.
High-voltage, low-nickel, cobalt-free layered oxides are promising candidates for high-energy-density lithium-ion batteries. However, their practical application is hindered by intrinsic cation disorder and structural degradation at high voltages, leading to a poor electrochemical performance. Here, we report a slightly lithium-enriched, cobalt-free layered oxide, Li1.05Ni0.43Mn0.52O2, featuring lithium-rich disorder domains achieved through chemical composition optimization. Advanced structural characterization demonstrates that nickel ions not only reside within the TM layers but also occupy the Li layers, acting as pinned ions. Theoretical calculations indicate that this in-plane and out-of-plane disorder enables reversible oxygen redox activity without oxygen release at high voltages. Moreover, this local structural framework preserves integrity even after extended cycling, ensuring chemical and structural stability during battery operation. Consequently, the cathode delivers an impressive discharge capacity of 202.2 mAh g-1 at C/10 and exceptional cycling stability, retaining 96.3% of its capacity after 200 cycles at C/3 within a voltage range of 2.5-4.55 V. Our findings provide valuable insights into the design of high-energy-density, cobalt-free layered cathodes.
期刊介绍:
ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.