{"title":"通过基于铟的电解质和锂金属表面改性提高固态锂金属电池性能:机理认识与优化","authors":"Zhongkai Wu, Chen Liu, Ziling Jiang, Lin Li, Siwu Li, Chaochao Wei, Qiyue Luo, Xia Chen, Long Zhang, Shijie Cheng, Chuang Yu","doi":"10.1007/s11426-024-2275-2","DOIUrl":null,"url":null,"abstract":"<p>Argyrodite-based solid-state lithium metal batteries exhibit significant potential as next-generation energy storage devices. However, their practical applications are constrained by the intrinsic poor stability of argyrodite towards Li metal and exposure to air/moisture. Therefore, an indium-involved modification strategy is employed to address these issues. The optimized doping yields a high Li-ion conductivity of 7.5 mS cm<sup>−1</sup> for Li<sub>5.54</sub>In<sub>0.02</sub>PS<sub>4.47</sub>O<sub>0.03</sub>Cl<sub>1.5</sub> electrolyte, accompanied by enhanced endurance against air/moisture and bare Li metal. It retains 92.0% of its original conductivity after exposure to air at a low dew point of −60 °C in dry room. Additionally, a composite layer comprising Li–In alloy and LiF phases is generated on the surface of lithium metal anode via the reaction between InF<sub>3</sub> and molten Li. This layer effectively mitigates Li dendrite growth by creating a physical barrier from the robust LiF phase, while the Li–In alloy induces uniform Li-ion deposition and accelerates Li transport dynamics across the interphase between the solid electrolyte/Li metal. Moreover, the In-doped electrolyte facilitates the <i>in-situ</i> generation of Li–In alloy within its voids, reducing local current density and further inhibiting lithium dendrite growth. Consequently, the combination of the Li<sub>5.54</sub>In<sub>0.02</sub>PS<sub>4.47</sub>O<sub>0.03</sub>Cl<sub>1.5</sub> electrolyte and the InF<sub>3</sub>@Li anode provides exceptional electrochemical performances in both symmetric cells and solid-state lithium metal batteries across different operating temperatures. Specifically, the LiNbO<sub>3</sub>@LiNi<sub>0.7</sub>Co<sub>0.2</sub>Mn<sub>0.1</sub>O<sub>2</sub>/Li<sub>5.54</sub>In<sub>0.02</sub>PS<sub>4.47</sub>O<sub>0.03</sub>Cl<sub>1.5</sub>/InF<sub>3</sub>@Li cell delivers a high discharge capacity of 167.8 mAh g<sup>−1</sup> at 0.5 C under 25 °C and retains 80.0% of its initial value after 400 cycles. This work offers a viable strategy for designing functional interfaces with enhanced stability for sulfide-based solid-state lithium batteries.</p>","PeriodicalId":772,"journal":{"name":"Science China Chemistry","volume":"87 1","pages":""},"PeriodicalIF":10.4000,"publicationDate":"2024-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Enhancing solid-state lithium metal battery performance via indium-based modification of electrolytes and lithium metal surfaces: mechanistic insights and optimization\",\"authors\":\"Zhongkai Wu, Chen Liu, Ziling Jiang, Lin Li, Siwu Li, Chaochao Wei, Qiyue Luo, Xia Chen, Long Zhang, Shijie Cheng, Chuang Yu\",\"doi\":\"10.1007/s11426-024-2275-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Argyrodite-based solid-state lithium metal batteries exhibit significant potential as next-generation energy storage devices. However, their practical applications are constrained by the intrinsic poor stability of argyrodite towards Li metal and exposure to air/moisture. Therefore, an indium-involved modification strategy is employed to address these issues. The optimized doping yields a high Li-ion conductivity of 7.5 mS cm<sup>−1</sup> for Li<sub>5.54</sub>In<sub>0.02</sub>PS<sub>4.47</sub>O<sub>0.03</sub>Cl<sub>1.5</sub> electrolyte, accompanied by enhanced endurance against air/moisture and bare Li metal. It retains 92.0% of its original conductivity after exposure to air at a low dew point of −60 °C in dry room. Additionally, a composite layer comprising Li–In alloy and LiF phases is generated on the surface of lithium metal anode via the reaction between InF<sub>3</sub> and molten Li. This layer effectively mitigates Li dendrite growth by creating a physical barrier from the robust LiF phase, while the Li–In alloy induces uniform Li-ion deposition and accelerates Li transport dynamics across the interphase between the solid electrolyte/Li metal. Moreover, the In-doped electrolyte facilitates the <i>in-situ</i> generation of Li–In alloy within its voids, reducing local current density and further inhibiting lithium dendrite growth. Consequently, the combination of the Li<sub>5.54</sub>In<sub>0.02</sub>PS<sub>4.47</sub>O<sub>0.03</sub>Cl<sub>1.5</sub> electrolyte and the InF<sub>3</sub>@Li anode provides exceptional electrochemical performances in both symmetric cells and solid-state lithium metal batteries across different operating temperatures. Specifically, the LiNbO<sub>3</sub>@LiNi<sub>0.7</sub>Co<sub>0.2</sub>Mn<sub>0.1</sub>O<sub>2</sub>/Li<sub>5.54</sub>In<sub>0.02</sub>PS<sub>4.47</sub>O<sub>0.03</sub>Cl<sub>1.5</sub>/InF<sub>3</sub>@Li cell delivers a high discharge capacity of 167.8 mAh g<sup>−1</sup> at 0.5 C under 25 °C and retains 80.0% of its initial value after 400 cycles. This work offers a viable strategy for designing functional interfaces with enhanced stability for sulfide-based solid-state lithium batteries.</p>\",\"PeriodicalId\":772,\"journal\":{\"name\":\"Science China Chemistry\",\"volume\":\"87 1\",\"pages\":\"\"},\"PeriodicalIF\":10.4000,\"publicationDate\":\"2024-09-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Science China Chemistry\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://doi.org/10.1007/s11426-024-2275-2\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science China Chemistry","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1007/s11426-024-2275-2","RegionNum":1,"RegionCategory":"化学","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
基于箭石的固态锂金属电池作为下一代储能设备具有巨大的潜力。然而,由于箭石对锂金属和暴露于空气/湿气中的内在稳定性较差,其实际应用受到限制。因此,我们采用了铟参与的改性策略来解决这些问题。通过优化掺杂,Li5.54In0.02PS4.47O0.03Cl1.5 电解质的锂离子电导率高达 7.5 mS cm-1,同时还增强了对空气/湿气和裸锂金属的耐受性。在-60 °C的低露点干燥室内暴露于空气中时,它仍能保持 92.0% 的原始电导率。此外,通过 InF3 与熔融锂的反应,在锂金属阳极表面生成了由 Li-In 合金和 LiF 相组成的复合层。该层通过与坚固的 LiF 相形成物理屏障,有效地减缓了锂枝晶的生长,而 Li-In 合金则诱导了锂离子的均匀沉积,并加速了锂在固体电解质/锂金属间相的动态传输。此外,掺 In 电解质有利于在其空隙中原位生成 Li-In 合金,从而降低局部电流密度并进一步抑制锂枝晶的生长。因此,Li5.54In0.02PS4.47O0.03Cl1.5 电解质与 InF3@Li 阳极的组合在不同工作温度下的对称电池和固态锂金属电池中都具有优异的电化学性能。具体来说,LiNbO3@LiNi0.7Co0.2Mn0.1O2/Li5.54In0.02PS4.47O0.03Cl1.5/InF3@Li 电池在 25 °C 下 0.5 C 的温度条件下可提供 167.8 mAh g-1 的高放电容量,并在 400 次循环后保持其初始值的 80.0%。这项研究为硫化物固态锂电池设计稳定性更强的功能界面提供了一种可行的策略。
Enhancing solid-state lithium metal battery performance via indium-based modification of electrolytes and lithium metal surfaces: mechanistic insights and optimization
Argyrodite-based solid-state lithium metal batteries exhibit significant potential as next-generation energy storage devices. However, their practical applications are constrained by the intrinsic poor stability of argyrodite towards Li metal and exposure to air/moisture. Therefore, an indium-involved modification strategy is employed to address these issues. The optimized doping yields a high Li-ion conductivity of 7.5 mS cm−1 for Li5.54In0.02PS4.47O0.03Cl1.5 electrolyte, accompanied by enhanced endurance against air/moisture and bare Li metal. It retains 92.0% of its original conductivity after exposure to air at a low dew point of −60 °C in dry room. Additionally, a composite layer comprising Li–In alloy and LiF phases is generated on the surface of lithium metal anode via the reaction between InF3 and molten Li. This layer effectively mitigates Li dendrite growth by creating a physical barrier from the robust LiF phase, while the Li–In alloy induces uniform Li-ion deposition and accelerates Li transport dynamics across the interphase between the solid electrolyte/Li metal. Moreover, the In-doped electrolyte facilitates the in-situ generation of Li–In alloy within its voids, reducing local current density and further inhibiting lithium dendrite growth. Consequently, the combination of the Li5.54In0.02PS4.47O0.03Cl1.5 electrolyte and the InF3@Li anode provides exceptional electrochemical performances in both symmetric cells and solid-state lithium metal batteries across different operating temperatures. Specifically, the LiNbO3@LiNi0.7Co0.2Mn0.1O2/Li5.54In0.02PS4.47O0.03Cl1.5/InF3@Li cell delivers a high discharge capacity of 167.8 mAh g−1 at 0.5 C under 25 °C and retains 80.0% of its initial value after 400 cycles. This work offers a viable strategy for designing functional interfaces with enhanced stability for sulfide-based solid-state lithium batteries.
期刊介绍:
Science China Chemistry, co-sponsored by the Chinese Academy of Sciences and the National Natural Science Foundation of China and published by Science China Press, publishes high-quality original research in both basic and applied chemistry. Indexed by Science Citation Index, it is a premier academic journal in the field.
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