{"title":"通过常压等离子处理获得星形氮化锂钝化层,用于可充电锂金属电池","authors":"Vijay Shankar Rangasamy , Bert Verheyde , Dirk Vangeneugden , Myrjam Mertens , Savitha Thayumanasundaram , Danny Havermans , Erwin Van Hoof , Pieter Lens , Annick Vanhulsel","doi":"10.1016/j.ssi.2024.116609","DOIUrl":null,"url":null,"abstract":"<div><p>Lithium metal anodes are indispensable to realize the maximum energy density in future generation batteries. However, the lithium surface must be ‘protected’ to suppress its high reactivity and to stabilize its deposition and dissolution. Here, we report a process to form a lithium nitride (Li<sub>3</sub>N) protective layer on lithium by a two-minute treatment in a dielectric barrier discharge (DBD) plasma. The process does not require low-pressure conditions or time-intensive post-treatments. The passivation layer is characterized by a unique, hexagonal bipyramid morphology, with α-Li<sub>3</sub>N crystals stacked to form pillar-like structures. Such an arrangement is shown to be favorable for fast Li<sup>+</sup> ion diffusion and dendrite prevention, as demonstrated by the stable Li plating/stripping of symmetric cells with passivated lithium (500 cycles compared to 150 cycles with bare lithium) at 1 mA/cm<sup>2</sup>. Full cells with LiNi<sub>0.33</sub>Mn<sub>0.33</sub>Co<sub>0.33</sub>O<sub>2</sub> (NMC111) cathode and passivated lithium anode retain 74% of their initial capacity after 300 cycles at 1C rate, by which time the cells with bare Li anode fail completely. This approach promises to be a practical solution for lithium passivation at industrial scale.</p></div>","PeriodicalId":431,"journal":{"name":"Solid State Ionics","volume":"413 ","pages":"Article 116609"},"PeriodicalIF":3.0000,"publicationDate":"2024-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Star-shaped lithium nitride passivation layer obtained by atmospheric-pressure plasma treatment for rechargeable lithium metal batteries\",\"authors\":\"Vijay Shankar Rangasamy , Bert Verheyde , Dirk Vangeneugden , Myrjam Mertens , Savitha Thayumanasundaram , Danny Havermans , Erwin Van Hoof , Pieter Lens , Annick Vanhulsel\",\"doi\":\"10.1016/j.ssi.2024.116609\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Lithium metal anodes are indispensable to realize the maximum energy density in future generation batteries. However, the lithium surface must be ‘protected’ to suppress its high reactivity and to stabilize its deposition and dissolution. Here, we report a process to form a lithium nitride (Li<sub>3</sub>N) protective layer on lithium by a two-minute treatment in a dielectric barrier discharge (DBD) plasma. The process does not require low-pressure conditions or time-intensive post-treatments. The passivation layer is characterized by a unique, hexagonal bipyramid morphology, with α-Li<sub>3</sub>N crystals stacked to form pillar-like structures. Such an arrangement is shown to be favorable for fast Li<sup>+</sup> ion diffusion and dendrite prevention, as demonstrated by the stable Li plating/stripping of symmetric cells with passivated lithium (500 cycles compared to 150 cycles with bare lithium) at 1 mA/cm<sup>2</sup>. Full cells with LiNi<sub>0.33</sub>Mn<sub>0.33</sub>Co<sub>0.33</sub>O<sub>2</sub> (NMC111) cathode and passivated lithium anode retain 74% of their initial capacity after 300 cycles at 1C rate, by which time the cells with bare Li anode fail completely. This approach promises to be a practical solution for lithium passivation at industrial scale.</p></div>\",\"PeriodicalId\":431,\"journal\":{\"name\":\"Solid State Ionics\",\"volume\":\"413 \",\"pages\":\"Article 116609\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2024-06-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Solid State Ionics\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0167273824001577\",\"RegionNum\":4,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Solid State Ionics","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0167273824001577","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Star-shaped lithium nitride passivation layer obtained by atmospheric-pressure plasma treatment for rechargeable lithium metal batteries
Lithium metal anodes are indispensable to realize the maximum energy density in future generation batteries. However, the lithium surface must be ‘protected’ to suppress its high reactivity and to stabilize its deposition and dissolution. Here, we report a process to form a lithium nitride (Li3N) protective layer on lithium by a two-minute treatment in a dielectric barrier discharge (DBD) plasma. The process does not require low-pressure conditions or time-intensive post-treatments. The passivation layer is characterized by a unique, hexagonal bipyramid morphology, with α-Li3N crystals stacked to form pillar-like structures. Such an arrangement is shown to be favorable for fast Li+ ion diffusion and dendrite prevention, as demonstrated by the stable Li plating/stripping of symmetric cells with passivated lithium (500 cycles compared to 150 cycles with bare lithium) at 1 mA/cm2. Full cells with LiNi0.33Mn0.33Co0.33O2 (NMC111) cathode and passivated lithium anode retain 74% of their initial capacity after 300 cycles at 1C rate, by which time the cells with bare Li anode fail completely. This approach promises to be a practical solution for lithium passivation at industrial scale.
期刊介绍:
This interdisciplinary journal is devoted to the physics, chemistry and materials science of diffusion, mass transport, and reactivity of solids. The major part of each issue is devoted to articles on:
(i) physics and chemistry of defects in solids;
(ii) reactions in and on solids, e.g. intercalation, corrosion, oxidation, sintering;
(iii) ion transport measurements, mechanisms and theory;
(iv) solid state electrochemistry;
(v) ionically-electronically mixed conducting solids.
Related technological applications are also included, provided their characteristics are interpreted in terms of the basic solid state properties.
Review papers and relevant symposium proceedings are welcome.