{"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}
引用次数: 0
Abstract
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:
Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments.
With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology.
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