{"title":"与超高镍阴极耦合的基于 LaCl3 的固体电解质的界面降解","authors":"Ye-Chao Wu, Feng Li, Xiaobin Cheng, Yihong Tan, Xin Huang, Jin-Da Luo, Shu Chen, Ruijun Pan, Yi-Chen Yin, Zheng Liang, Hong-Bin Yao","doi":"10.1021/acs.nanolett.4c03502","DOIUrl":null,"url":null,"abstract":"Despite competitive compatibility with high-nickel cathodes, chloride solid electrolytes (SEs) still experience inevitable side reactions at the cathode/SE interface, causing capacity decay in all-solid-state lithium batteries (ASSLBs) during cycling. Herein, a three-electrode ASSLB testing device is developed to comprehensively reveal the interface failure mechanisms of the ultrahigh-nickel LiNi<sub>0.92</sub>Co<sub>0.05</sub>Mn<sub>0.03</sub>O<sub>2</sub> (NCM92) cathode paired with LaCl<sub>3</sub>-based chloride SE Li<sub>0.447</sub>La<sub>0.475</sub>Zr<sub>0.059</sub>Ta<sub>0.179</sub>Cl<sub>3</sub> (LLZTC). Distribution of relaxation time (DRT) analysis clearly shows the ASSLB degradation accompanied by a significant NCM92/LLZTC interface impedance increase, which becomes more pronounced at the higher cutoff charging voltage of 4.8 V <i>vs</i> Li<sup>+</sup>/Li. Furthermore, time-of-flight secondary ion mass spectrometry (ToF-SIMS) and focused ion beam scanning electron microscopy (FIB-SEM) analysis also confirm the deterioration arising from active lattice oxygen and loss of physical contact at the NCM92/LLZTC interface. These findings reveal both electrochemical degradation and physical contact failure at the cathode/SE interface as key causes of the ASSLBs’ capacity decay.","PeriodicalId":53,"journal":{"name":"Nano Letters","volume":"62 1","pages":""},"PeriodicalIF":9.1000,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Interface Degradation of LaCl3-Based Solid Electrolytes Coupled with Ultrahigh-Nickel Cathodes\",\"authors\":\"Ye-Chao Wu, Feng Li, Xiaobin Cheng, Yihong Tan, Xin Huang, Jin-Da Luo, Shu Chen, Ruijun Pan, Yi-Chen Yin, Zheng Liang, Hong-Bin Yao\",\"doi\":\"10.1021/acs.nanolett.4c03502\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Despite competitive compatibility with high-nickel cathodes, chloride solid electrolytes (SEs) still experience inevitable side reactions at the cathode/SE interface, causing capacity decay in all-solid-state lithium batteries (ASSLBs) during cycling. Herein, a three-electrode ASSLB testing device is developed to comprehensively reveal the interface failure mechanisms of the ultrahigh-nickel LiNi<sub>0.92</sub>Co<sub>0.05</sub>Mn<sub>0.03</sub>O<sub>2</sub> (NCM92) cathode paired with LaCl<sub>3</sub>-based chloride SE Li<sub>0.447</sub>La<sub>0.475</sub>Zr<sub>0.059</sub>Ta<sub>0.179</sub>Cl<sub>3</sub> (LLZTC). Distribution of relaxation time (DRT) analysis clearly shows the ASSLB degradation accompanied by a significant NCM92/LLZTC interface impedance increase, which becomes more pronounced at the higher cutoff charging voltage of 4.8 V <i>vs</i> Li<sup>+</sup>/Li. Furthermore, time-of-flight secondary ion mass spectrometry (ToF-SIMS) and focused ion beam scanning electron microscopy (FIB-SEM) analysis also confirm the deterioration arising from active lattice oxygen and loss of physical contact at the NCM92/LLZTC interface. These findings reveal both electrochemical degradation and physical contact failure at the cathode/SE interface as key causes of the ASSLBs’ capacity decay.\",\"PeriodicalId\":53,\"journal\":{\"name\":\"Nano Letters\",\"volume\":\"62 1\",\"pages\":\"\"},\"PeriodicalIF\":9.1000,\"publicationDate\":\"2024-11-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nano Letters\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.nanolett.4c03502\",\"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":"Nano Letters","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acs.nanolett.4c03502","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}
Interface Degradation of LaCl3-Based Solid Electrolytes Coupled with Ultrahigh-Nickel Cathodes
Despite competitive compatibility with high-nickel cathodes, chloride solid electrolytes (SEs) still experience inevitable side reactions at the cathode/SE interface, causing capacity decay in all-solid-state lithium batteries (ASSLBs) during cycling. Herein, a three-electrode ASSLB testing device is developed to comprehensively reveal the interface failure mechanisms of the ultrahigh-nickel LiNi0.92Co0.05Mn0.03O2 (NCM92) cathode paired with LaCl3-based chloride SE Li0.447La0.475Zr0.059Ta0.179Cl3 (LLZTC). Distribution of relaxation time (DRT) analysis clearly shows the ASSLB degradation accompanied by a significant NCM92/LLZTC interface impedance increase, which becomes more pronounced at the higher cutoff charging voltage of 4.8 V vs Li+/Li. Furthermore, time-of-flight secondary ion mass spectrometry (ToF-SIMS) and focused ion beam scanning electron microscopy (FIB-SEM) analysis also confirm the deterioration arising from active lattice oxygen and loss of physical contact at the NCM92/LLZTC interface. These findings reveal both electrochemical degradation and physical contact failure at the cathode/SE interface as key causes of the ASSLBs’ capacity decay.
期刊介绍:
Nano Letters serves as a dynamic platform for promptly disseminating original results in fundamental, applied, and emerging research across all facets of nanoscience and nanotechnology. A pivotal criterion for inclusion within Nano Letters is the convergence of at least two different areas or disciplines, ensuring a rich interdisciplinary scope. The journal is dedicated to fostering exploration in diverse areas, including:
- Experimental and theoretical findings on physical, chemical, and biological phenomena at the nanoscale
- Synthesis, characterization, and processing of organic, inorganic, polymer, and hybrid nanomaterials through physical, chemical, and biological methodologies
- Modeling and simulation of synthetic, assembly, and interaction processes
- Realization of integrated nanostructures and nano-engineered devices exhibiting advanced performance
- Applications of nanoscale materials in living and environmental systems
Nano Letters is committed to advancing and showcasing groundbreaking research that intersects various domains, fostering innovation and collaboration in the ever-evolving field of nanoscience and nanotechnology.