{"title":"通过调节离子和电子活性亚基实现高效储能:用于大量快速储存 Na+ 的 (SbS)1.15TiS2 超晶格","authors":"Baixin Peng, Tianxun Cai, Shaoning Zhang, Yuqiang Fang, Zhuoran Lv, Yusha Gao, Fuqiang Huang","doi":"10.1007/s11426-023-1699-x","DOIUrl":null,"url":null,"abstract":"<div><p>Alloying-type metal sulfides with high sodiation activity and theoretical capacity are promising anode materials for high energy density sodium ion batteries. However, the large volume change and the migratory and aggregation behavior of metal atoms will cause severe capacity decay during the charge/discharge process. Herein, a robust and conductive TiS<sub>2</sub> framework is integrated with a high-capacity SbS layer to construct a single phase (SbS)<sub>1.15</sub>TiS<sub>2</sub> superlattice for both high-capacity and fast Na<sup>+</sup> storage. The metallic TiS<sub>2</sub> sublayer with high electron activity acts as a robust and conductive skeleton to buffer the volume expansion caused by conversion and alloying reaction between Na<sup>+</sup> and SbS sublayer. Hence, high capacity and high rate capability can be synergistically realized in a single phase (SbS)<sub>1.15</sub>TiS<sub>2</sub> superlattice. The novel (SbS)<sub>1.15</sub>TiS<sub>2</sub> anode has a high charge capacity of 618 mAh g<sup>−1</sup> at 0.2 C and superior rate performance and cycling stability (205 mAh g<sup>−1</sup> at 35 C after 2,000 cycles). Furthermore, <i>in situ</i> and <i>ex situ</i> characterizations are applied to get an insight into the multi-step reaction mechanism. The integrity of robust Na-Ti-S skeleton during (dis)charge process can be confirmed. This superlattice construction idea to integrate the Na<sup>+</sup>-active unit and electron-active unit would provide a new avenue for exploring high-performance anode materials for advanced sodium-ion batteries.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":772,"journal":{"name":"Science China Chemistry","volume":"67 1","pages":"336 - 342"},"PeriodicalIF":10.4000,"publicationDate":"2023-08-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unlocking efficient energy storage via regulating ion and electron-active subunits: an (SbS)1.15TiS2 superlattice for large and fast Na+ storage\",\"authors\":\"Baixin Peng, Tianxun Cai, Shaoning Zhang, Yuqiang Fang, Zhuoran Lv, Yusha Gao, Fuqiang Huang\",\"doi\":\"10.1007/s11426-023-1699-x\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Alloying-type metal sulfides with high sodiation activity and theoretical capacity are promising anode materials for high energy density sodium ion batteries. However, the large volume change and the migratory and aggregation behavior of metal atoms will cause severe capacity decay during the charge/discharge process. Herein, a robust and conductive TiS<sub>2</sub> framework is integrated with a high-capacity SbS layer to construct a single phase (SbS)<sub>1.15</sub>TiS<sub>2</sub> superlattice for both high-capacity and fast Na<sup>+</sup> storage. The metallic TiS<sub>2</sub> sublayer with high electron activity acts as a robust and conductive skeleton to buffer the volume expansion caused by conversion and alloying reaction between Na<sup>+</sup> and SbS sublayer. Hence, high capacity and high rate capability can be synergistically realized in a single phase (SbS)<sub>1.15</sub>TiS<sub>2</sub> superlattice. The novel (SbS)<sub>1.15</sub>TiS<sub>2</sub> anode has a high charge capacity of 618 mAh g<sup>−1</sup> at 0.2 C and superior rate performance and cycling stability (205 mAh g<sup>−1</sup> at 35 C after 2,000 cycles). Furthermore, <i>in situ</i> and <i>ex situ</i> characterizations are applied to get an insight into the multi-step reaction mechanism. The integrity of robust Na-Ti-S skeleton during (dis)charge process can be confirmed. This superlattice construction idea to integrate the Na<sup>+</sup>-active unit and electron-active unit would provide a new avenue for exploring high-performance anode materials for advanced sodium-ion batteries.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":772,\"journal\":{\"name\":\"Science China Chemistry\",\"volume\":\"67 1\",\"pages\":\"336 - 342\"},\"PeriodicalIF\":10.4000,\"publicationDate\":\"2023-08-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Science China Chemistry\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11426-023-1699-x\",\"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://link.springer.com/article/10.1007/s11426-023-1699-x","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
合金型金属硫化物具有很高的钠化活性和理论容量,是很有前途的高能量密度钠离子电池阳极材料。然而,在充放电过程中,金属原子的大体积变化和迁移聚集行为会导致严重的容量衰减。在此,我们将坚固的导电 TiS2 框架与高容量的 SbS 层整合在一起,构建了单相 (SbS)1.15TiS2 超晶格,实现了高容量和快速 Na+ 储存。具有高电子活度的金属 TiS2 子层可作为坚固的导电骨架,缓冲 Na+ 与 SbS 子层之间的转换和合金化反应引起的体积膨胀。因此,在单相(SbS)1.15TiS2 超晶格中可以协同实现高容量和高速率能力。新型 (SbS)1.15TiS2 阳极在 0.2 摄氏度时的充电容量高达 618 mAh g-1,并具有优异的速率性能和循环稳定性(2,000 次循环后,在 35 摄氏度时的容量为 205 mAh g-1)。此外,为了深入了解多步反应机制,还采用了原位和非原位表征方法。在(放电)过程中,Na-Ti-S 骨架的完整性得到了证实。这种将 Na+ 活性单元和电子活性单元整合在一起的超晶格构造理念将为探索先进钠离子电池的高性能负极材料提供一条新途径。
Unlocking efficient energy storage via regulating ion and electron-active subunits: an (SbS)1.15TiS2 superlattice for large and fast Na+ storage
Alloying-type metal sulfides with high sodiation activity and theoretical capacity are promising anode materials for high energy density sodium ion batteries. However, the large volume change and the migratory and aggregation behavior of metal atoms will cause severe capacity decay during the charge/discharge process. Herein, a robust and conductive TiS2 framework is integrated with a high-capacity SbS layer to construct a single phase (SbS)1.15TiS2 superlattice for both high-capacity and fast Na+ storage. The metallic TiS2 sublayer with high electron activity acts as a robust and conductive skeleton to buffer the volume expansion caused by conversion and alloying reaction between Na+ and SbS sublayer. Hence, high capacity and high rate capability can be synergistically realized in a single phase (SbS)1.15TiS2 superlattice. The novel (SbS)1.15TiS2 anode has a high charge capacity of 618 mAh g−1 at 0.2 C and superior rate performance and cycling stability (205 mAh g−1 at 35 C after 2,000 cycles). Furthermore, in situ and ex situ characterizations are applied to get an insight into the multi-step reaction mechanism. The integrity of robust Na-Ti-S skeleton during (dis)charge process can be confirmed. This superlattice construction idea to integrate the Na+-active unit and electron-active unit would provide a new avenue for exploring high-performance anode materials for advanced sodium-ion 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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