Yueyang Wang, Yulin Mao, Qinglu Yu, Guichuan Xing, Qingyuan Li and Guoxing Sun
{"title":"Core–shell structured carbon@tin sulfide@hard carbon spheres as high-performance anode for low voltage sodium-ion battery†","authors":"Yueyang Wang, Yulin Mao, Qinglu Yu, Guichuan Xing, Qingyuan Li and Guoxing Sun","doi":"10.1039/D4NJ04756G","DOIUrl":null,"url":null,"abstract":"<p >Transition metal sulfides (TMS) are promising candidates for sodium-ion battery anodes due to their high theoretical capacities. However, their practical application is limited by high operating voltages (<em>vs.</em> Na<small><sup>+</sup></small>/Na) and low initial Coulombic efficiency (ICE). In this study, we present the controlled synthesis of a core–shell structured composite, comprising tin sulfide (SnS) encapsulated within hard carbon microspheres (C@Sn<small><sub><em>x</em></sub></small>S<small><sub><em>y</em></sub></small>@HCS). This composite is prepared using a straightforward chemical bath deposition method followed by low-temperature annealing. The resulting material significantly lowers the average discharge voltage to 0.5 V <em>vs.</em> Na<small><sup>+</sup></small>/Na—a reduction of 71.4%—while achieving a relatively high ICE of 73.56%. The composite also exhibits excellent rate performance, delivering 212.5 mA h g<small><sup>−1</sup></small> at 5 A g<small><sup>−1</sup></small>, and remarkable cycling stability, maintaining 153.3 mA h g<small><sup>−1</sup></small> after 1000 cycles at the same current density. The core–shell architecture effectively mitigates the volume expansion typically associated with tin sulfides, ensuring a stable solid electrolyte interphase (SEI) and robust electrode interface. This work offers a promising design strategy for developing low-voltage, high-performance sodium-ion battery anodes.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 2","pages":" 579-588"},"PeriodicalIF":2.5000,"publicationDate":"2024-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d4nj04756g","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Transition metal sulfides (TMS) are promising candidates for sodium-ion battery anodes due to their high theoretical capacities. However, their practical application is limited by high operating voltages (vs. Na+/Na) and low initial Coulombic efficiency (ICE). In this study, we present the controlled synthesis of a core–shell structured composite, comprising tin sulfide (SnS) encapsulated within hard carbon microspheres (C@SnxSy@HCS). This composite is prepared using a straightforward chemical bath deposition method followed by low-temperature annealing. The resulting material significantly lowers the average discharge voltage to 0.5 V vs. Na+/Na—a reduction of 71.4%—while achieving a relatively high ICE of 73.56%. The composite also exhibits excellent rate performance, delivering 212.5 mA h g−1 at 5 A g−1, and remarkable cycling stability, maintaining 153.3 mA h g−1 after 1000 cycles at the same current density. The core–shell architecture effectively mitigates the volume expansion typically associated with tin sulfides, ensuring a stable solid electrolyte interphase (SEI) and robust electrode interface. This work offers a promising design strategy for developing low-voltage, high-performance sodium-ion battery anodes.
过渡金属硫化物(TMS)具有较高的理论容量,是钠离子电池阳极的理想材料。然而,它们的实际应用受到高工作电压(相对于Na+/Na)和低初始库仑效率(ICE)的限制。在这项研究中,我们提出了一种核壳结构复合材料的受控合成,该复合材料由包裹在硬碳微球(C@SnxSy@HCS)内的硫化锡(sn)组成。该复合材料采用简单的化学浴沉积法,然后进行低温退火制备。与Na+/Na相比,该材料显著降低了平均放电电压至0.5 V,降低了71.4%,同时获得了73.56%的相对较高的ICE。该复合材料还具有优异的倍率性能,在5 A g−1下可输出212.5 mA h g−1,并且具有出色的循环稳定性,在相同电流密度下循环1000次后仍能保持153.3 mA h g−1。核壳结构有效地减轻了通常与硫化锡相关的体积膨胀,确保了稳定的固体电解质界面(SEI)和坚固的电极界面。这项工作为开发低电压、高性能钠离子电池阳极提供了一种有前途的设计策略。