Feng Jin, Ingeborg Sellæg Ellingsen, Laras Fadillah, Quoc Hung Nguyen, Henrik Rotvær Bratlie, Daniel Knez, Gerald Kothleitner, Mir Mehraj Ud Din, Sverre M. Selbach, Günther J. Redhammer, Daniel Rettenwander
{"title":"LiBF4-Derived Coating on LiCoO2 for 4.5 V Operation of Li6PS5Cl-Based Solid-State Batteries","authors":"Feng Jin, Ingeborg Sellæg Ellingsen, Laras Fadillah, Quoc Hung Nguyen, Henrik Rotvær Bratlie, Daniel Knez, Gerald Kothleitner, Mir Mehraj Ud Din, Sverre M. Selbach, Günther J. Redhammer, Daniel Rettenwander","doi":"10.1002/eem2.70047","DOIUrl":null,"url":null,"abstract":"<p>Solid-state batteries are attracting considerable attention for their high-energy density and improved safety over conventional lithium-ion batteries. Among solid-state electrolytes, sulfide-based options like Li<sub>6</sub>PS<sub>5</sub>Cl are especially promising due to their superior ionic conductivity. However, interfacial degradation between sulfide electrolytes and high-voltage cathodes, such as LiCoO<sub>2</sub>, limits long-term performance. This study demonstrates that a LiBF<sub>4</sub>-derived F-rich coating on LiCoO<sub>2</sub>, applied by immersing LiCoO<sub>2</sub> particles in a LiBF<sub>4</sub> solution followed by annealing, can significantly enhance performance in Li<sub>6</sub>PS<sub>5</sub>Cl-based solid-state batteries. This coating enables stable high-voltage (4.5 V vs Li<sup>+</sup>/Li) operation, achieving an initial specific capacity of 153.82 mAh g<sup>−1</sup> and 87.1% capacity retention over 300 cycles at 0.5C. The enhanced performance stems from the F-rich coating, composed of multiple phases including LiF, CoF<sub>2</sub>, Li<sub>x</sub>BF<sub>y</sub>O<sub>z</sub>, and Li<sub>x</sub>BO<sub>y</sub>, which effectively suppresses side reactions at the LiCoO<sub>2</sub>|Li<sub>6</sub>PS<sub>5</sub>Cl interface and improves lithium-ion diffusivity, thereby enabling greater Li capacity utilization. Our findings provide a practical pathway for advancing solid-state batteries with high-voltage LiCoO<sub>2</sub> cathodes, offering substantial promise for next-generation energy storage systems.</p>","PeriodicalId":11554,"journal":{"name":"Energy & Environmental Materials","volume":"8 5","pages":""},"PeriodicalIF":14.1000,"publicationDate":"2025-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/eem2.70047","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy & Environmental Materials","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/eem2.70047","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Solid-state batteries are attracting considerable attention for their high-energy density and improved safety over conventional lithium-ion batteries. Among solid-state electrolytes, sulfide-based options like Li6PS5Cl are especially promising due to their superior ionic conductivity. However, interfacial degradation between sulfide electrolytes and high-voltage cathodes, such as LiCoO2, limits long-term performance. This study demonstrates that a LiBF4-derived F-rich coating on LiCoO2, applied by immersing LiCoO2 particles in a LiBF4 solution followed by annealing, can significantly enhance performance in Li6PS5Cl-based solid-state batteries. This coating enables stable high-voltage (4.5 V vs Li+/Li) operation, achieving an initial specific capacity of 153.82 mAh g−1 and 87.1% capacity retention over 300 cycles at 0.5C. The enhanced performance stems from the F-rich coating, composed of multiple phases including LiF, CoF2, LixBFyOz, and LixBOy, which effectively suppresses side reactions at the LiCoO2|Li6PS5Cl interface and improves lithium-ion diffusivity, thereby enabling greater Li capacity utilization. Our findings provide a practical pathway for advancing solid-state batteries with high-voltage LiCoO2 cathodes, offering substantial promise for next-generation energy storage systems.
与传统锂离子电池相比,固态电池因其高能量密度和更高的安全性而备受关注。在固态电解质中,基于硫化物的选择,如Li6PS5Cl,由于其优异的离子导电性,尤其有前景。然而,硫化物电解质与高压阴极(如LiCoO2)之间的界面降解限制了其长期性能。本研究表明,通过将LiCoO2颗粒浸入LiBF4溶液中并进行退火处理,在LiCoO2表面涂覆LiBF4衍生的富f涂层,可以显著提高li6ps5cl基固态电池的性能。该涂层可实现稳定的高压(4.5 V vs Li+/Li)操作,在0.5C下实现153.82 mAh g - 1的初始比容量和超过300次循环的87.1%容量保持。性能的增强源于富f涂层,由LiF、CoF2、LixBFyOz和LixBOy等多相组成,有效抑制了LiCoO2|Li6PS5Cl界面的副反应,提高了锂离子的扩散率,从而提高了锂容量利用率。我们的发现为推进高压LiCoO2阴极固态电池提供了一条实用途径,为下一代储能系统提供了巨大的希望。
期刊介绍:
Energy & Environmental Materials (EEM) is an international journal published by Zhengzhou University in collaboration with John Wiley & Sons, Inc. The journal aims to publish high quality research related to materials for energy harvesting, conversion, storage, and transport, as well as for creating a cleaner environment. EEM welcomes research work of significant general interest that has a high impact on society-relevant technological advances. The scope of the journal is intentionally broad, recognizing the complexity of issues and challenges related to energy and environmental materials. Therefore, interdisciplinary work across basic science and engineering disciplines is particularly encouraged. The areas covered by the journal include, but are not limited to, materials and composites for photovoltaics and photoelectrochemistry, bioprocessing, batteries, fuel cells, supercapacitors, clean air, and devices with multifunctionality. The readership of the journal includes chemical, physical, biological, materials, and environmental scientists and engineers from academia, industry, and policy-making.