Yashraj Soni , Sharad Dnyanu Pinjari , Yilan Wu , Purandas Mudavath , Mandala Rama Krishna , Hao Lu , Xiaoming Sun , Rohit Gaddam , X.S. Zhao
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This work aims to understand the origin of the unprecedented rate and cycling performance of sodium ions in diglyme solvent in carbon nanohorns with disordered graphitic domains and micropores. <em>Ex-situ</em> scanning electron microscope images reveal the formation of a uniformly thin solid electrolyte interphase on the surface of the carbon nanohorn electrode. The sodium-ion storage behavior is found to be closely related to the microstructure of the carbon nanohorns. In the diglyme-based electrolyte, the carbon nanohorn electrode displays a specific capacity of around 332 mA h<!--> <!-->g<sup>−1</sup> at the current density of 50 mA g<sup>−1</sup>, along with good rate tolerance and stable cycling stability over 500 cycles. The enhanced electrochemical performance is further elucidated through galvanostatic intermittent titration technique (GITT), <em>in-situ</em> electrochemical impedance spectroscopy (EIS), and distribution relaxation time (DRT) analysis. To the best of our knowledge, this is the first study to understand sodium-ion storage behavior in carbon nanohorns.</div></div>","PeriodicalId":100957,"journal":{"name":"Next Energy","volume":"9 ","pages":"Article 100408"},"PeriodicalIF":0.0000,"publicationDate":"2025-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sodium-ion storage behavior in carbon nanohorns in a diglyme-based electrolyte\",\"authors\":\"Yashraj Soni , Sharad Dnyanu Pinjari , Yilan Wu , Purandas Mudavath , Mandala Rama Krishna , Hao Lu , Xiaoming Sun , Rohit Gaddam , X.S. Zhao\",\"doi\":\"10.1016/j.nxener.2025.100408\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The interaction behavior of solvated sodium ions in ether-based electrolytes with graphite electrodes via the co-intercalation mechanism captures wide research interest due to the remarkable reversible sodium-ion storage capacity, which cannot be achieved in ester-based electrolytes. However, the understanding of the sodium-ion storage mechanism and the structure-performance correlation is not fully established. This work aims to understand the origin of the unprecedented rate and cycling performance of sodium ions in diglyme solvent in carbon nanohorns with disordered graphitic domains and micropores. <em>Ex-situ</em> scanning electron microscope images reveal the formation of a uniformly thin solid electrolyte interphase on the surface of the carbon nanohorn electrode. The sodium-ion storage behavior is found to be closely related to the microstructure of the carbon nanohorns. In the diglyme-based electrolyte, the carbon nanohorn electrode displays a specific capacity of around 332 mA h<!--> <!-->g<sup>−1</sup> at the current density of 50 mA g<sup>−1</sup>, along with good rate tolerance and stable cycling stability over 500 cycles. The enhanced electrochemical performance is further elucidated through galvanostatic intermittent titration technique (GITT), <em>in-situ</em> electrochemical impedance spectroscopy (EIS), and distribution relaxation time (DRT) analysis. 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引用次数: 0
摘要
醚基电解质中溶剂化钠离子通过共插层机制与石墨电极的相互作用引起了广泛的研究兴趣,因为它具有显著的可逆钠离子存储能力,这在酯基电解质中是无法实现的。然而,对钠离子的储存机理和结构-性能关系的认识尚未完全建立。本研究旨在了解钠离子在具有无序石墨畴和微孔的碳纳米角中史无前例的速率和循环性能的起源。非原位扫描电镜图像显示碳纳米角电极表面形成均匀薄的固体电解质界面。钠离子的储存行为与碳纳米角的微观结构密切相关。在二甘酸基电解质中,碳纳米角电极在电流密度为50 mA g−1时的比容量约为332 mA h g−1,并且具有良好的速率容忍度和500次以上的稳定循环稳定性。通过恒流间歇滴定技术(git)、原位电化学阻抗谱(EIS)和分布弛豫时间(DRT)分析进一步阐明了其增强的电化学性能。据我们所知,这是第一个了解碳纳米角中钠离子储存行为的研究。
Sodium-ion storage behavior in carbon nanohorns in a diglyme-based electrolyte
The interaction behavior of solvated sodium ions in ether-based electrolytes with graphite electrodes via the co-intercalation mechanism captures wide research interest due to the remarkable reversible sodium-ion storage capacity, which cannot be achieved in ester-based electrolytes. However, the understanding of the sodium-ion storage mechanism and the structure-performance correlation is not fully established. This work aims to understand the origin of the unprecedented rate and cycling performance of sodium ions in diglyme solvent in carbon nanohorns with disordered graphitic domains and micropores. Ex-situ scanning electron microscope images reveal the formation of a uniformly thin solid electrolyte interphase on the surface of the carbon nanohorn electrode. The sodium-ion storage behavior is found to be closely related to the microstructure of the carbon nanohorns. In the diglyme-based electrolyte, the carbon nanohorn electrode displays a specific capacity of around 332 mA h g−1 at the current density of 50 mA g−1, along with good rate tolerance and stable cycling stability over 500 cycles. The enhanced electrochemical performance is further elucidated through galvanostatic intermittent titration technique (GITT), in-situ electrochemical impedance spectroscopy (EIS), and distribution relaxation time (DRT) analysis. To the best of our knowledge, this is the first study to understand sodium-ion storage behavior in carbon nanohorns.