{"title":"自愈,Ga-Sb合金限制锡阳极在Glyme基电解质中稳定的na离子存储","authors":"Dimpal Deori, Madhurja Buragohain, Youhyun Son, Sooraj Kunnikuruvan, Ashok Kumar Nanjundan, Philipp Adelhelm, Thangavelu Palaniselvam","doi":"10.1002/smll.202504185","DOIUrl":null,"url":null,"abstract":"In this contribution, the development of a self-healable GaSb alloy featuring a confined Sn (core-shell) structure is reported for stable Na<sup>+</sup> storage in an ether-based electrolyte. The core-shell architecture of GaSb@Sn has been validated through high-angle annular dark field-scanning transmission electron microscopy (HAADF-STEM) paired with electron energy loss spectroscopy (EELS) analysis. The GaSb@Sn support on carbon electrode has delivered specific capacity of 560 mAh g<sub>electrode</sub><sup>−1</sup> at 50 mA g<sup>−1</sup> with 89% retention capacity after 1200 cycles and specific capacity of 449 mAh g<sub>electrode</sub><sup>−1</sup> at 2 Ag<sup>−1</sup> with 82% retention capacity after 2000 cycles. The GaSb@Sn/C electrode stores Na<sup>+</sup> by forming Na-Sn, Na-Sb-O, and Na-Ga-O intermetallic compounds, as confirmed by operando XRD studies. Operando electrochemical dilatometry studies reveal that the self-healable electrode expands by 33% at the electrode level during Na<sup>+</sup> insertion, significantly lower than the theoretically predicted expansion of Sn, which is 420%. DFT calculations show that the adsorption of diglyme on GaSb@Sn (−0.4 eV) is weaker than that on bulk Sn (−5.1 eV). The weaker interaction between diglyme and GaSb@Sn could be responsible for the thinner SEI formation on the edges of GaSb@Sn, thereby resulting in the high initial coulombic efficiency (GaSb@Sn- 81%, Bulk Sn-62%) and stable cycle life.","PeriodicalId":228,"journal":{"name":"Small","volume":"10 1","pages":""},"PeriodicalIF":13.0000,"publicationDate":"2025-06-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Self-Healing, Ga-Sb Alloy Confined Sn Anode for Stable Na-Ion Storage in Glyme Based Electrolytes\",\"authors\":\"Dimpal Deori, Madhurja Buragohain, Youhyun Son, Sooraj Kunnikuruvan, Ashok Kumar Nanjundan, Philipp Adelhelm, Thangavelu Palaniselvam\",\"doi\":\"10.1002/smll.202504185\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In this contribution, the development of a self-healable GaSb alloy featuring a confined Sn (core-shell) structure is reported for stable Na<sup>+</sup> storage in an ether-based electrolyte. The core-shell architecture of GaSb@Sn has been validated through high-angle annular dark field-scanning transmission electron microscopy (HAADF-STEM) paired with electron energy loss spectroscopy (EELS) analysis. The GaSb@Sn support on carbon electrode has delivered specific capacity of 560 mAh g<sub>electrode</sub><sup>−1</sup> at 50 mA g<sup>−1</sup> with 89% retention capacity after 1200 cycles and specific capacity of 449 mAh g<sub>electrode</sub><sup>−1</sup> at 2 Ag<sup>−1</sup> with 82% retention capacity after 2000 cycles. The GaSb@Sn/C electrode stores Na<sup>+</sup> by forming Na-Sn, Na-Sb-O, and Na-Ga-O intermetallic compounds, as confirmed by operando XRD studies. Operando electrochemical dilatometry studies reveal that the self-healable electrode expands by 33% at the electrode level during Na<sup>+</sup> insertion, significantly lower than the theoretically predicted expansion of Sn, which is 420%. DFT calculations show that the adsorption of diglyme on GaSb@Sn (−0.4 eV) is weaker than that on bulk Sn (−5.1 eV). The weaker interaction between diglyme and GaSb@Sn could be responsible for the thinner SEI formation on the edges of GaSb@Sn, thereby resulting in the high initial coulombic efficiency (GaSb@Sn- 81%, Bulk Sn-62%) and stable cycle life.\",\"PeriodicalId\":228,\"journal\":{\"name\":\"Small\",\"volume\":\"10 1\",\"pages\":\"\"},\"PeriodicalIF\":13.0000,\"publicationDate\":\"2025-06-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Small\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/smll.202504185\",\"RegionNum\":2,\"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":"Small","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/smll.202504185","RegionNum":2,"RegionCategory":"材料科学","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
在这篇贡献中,报道了一种具有限制Sn(核壳)结构的自修复GaSb合金的开发,用于在醚基电解质中稳定存储Na+。通过高角环形暗场扫描透射电子显微镜(HAADF-STEM)和电子能量损失谱(EELS)分析,验证了GaSb@Sn的核壳结构。碳电极上的GaSb@Sn载体在50 mA g−1下的比容量为560 mAh,在1200次循环后保持89%的容量,在2 Ag−1下的比容量为449 mAh,在2000次循环后保持82%的容量。GaSb@Sn/C电极通过形成Na- sn、Na- sb - o和Na- ga - o金属间化合物来储存Na+,这被operando XRD研究证实。Operando电化学膨胀测量研究表明,在Na+插入过程中,自愈电极在电极水平上的膨胀率为33%,显著低于Sn的理论预测膨胀率420%。DFT计算表明,二lyme在GaSb@Sn(−0.4 eV)上的吸附弱于在本体Sn(−5.1 eV)上的吸附。二lyme与GaSb@Sn之间较弱的相互作用可能是GaSb@Sn边缘较薄的SEI形成的原因,从而导致高的初始库仑效率(GaSb@Sn- 81%, Bulk Sn-62%)和稳定的循环寿命。
Self-Healing, Ga-Sb Alloy Confined Sn Anode for Stable Na-Ion Storage in Glyme Based Electrolytes
In this contribution, the development of a self-healable GaSb alloy featuring a confined Sn (core-shell) structure is reported for stable Na+ storage in an ether-based electrolyte. The core-shell architecture of GaSb@Sn has been validated through high-angle annular dark field-scanning transmission electron microscopy (HAADF-STEM) paired with electron energy loss spectroscopy (EELS) analysis. The GaSb@Sn support on carbon electrode has delivered specific capacity of 560 mAh gelectrode−1 at 50 mA g−1 with 89% retention capacity after 1200 cycles and specific capacity of 449 mAh gelectrode−1 at 2 Ag−1 with 82% retention capacity after 2000 cycles. The GaSb@Sn/C electrode stores Na+ by forming Na-Sn, Na-Sb-O, and Na-Ga-O intermetallic compounds, as confirmed by operando XRD studies. Operando electrochemical dilatometry studies reveal that the self-healable electrode expands by 33% at the electrode level during Na+ insertion, significantly lower than the theoretically predicted expansion of Sn, which is 420%. DFT calculations show that the adsorption of diglyme on GaSb@Sn (−0.4 eV) is weaker than that on bulk Sn (−5.1 eV). The weaker interaction between diglyme and GaSb@Sn could be responsible for the thinner SEI formation on the edges of GaSb@Sn, thereby resulting in the high initial coulombic efficiency (GaSb@Sn- 81%, Bulk Sn-62%) and stable cycle life.
期刊介绍:
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