4.6 Article

Influence of Additives on the Electrochemical and Interfacial Properties of SiOx-Based Anode Materials for Lithium-Sulfur Batteries

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LANGMUIR
卷 38, 期 8, 页码 2423-2434

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AMER CHEMICAL SOC
DOI: 10.1021/acs.langmuir.1c02342

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资金

  1. CSIR-HRDG, New Delhi [31/020(0179)/2019-EMR-I]
  2. National Research Foundation of Korea (NRF) [2020 H1D3A2A01103894]

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This study systematically investigated the influence of four different electrolyte additives on the electrochemical and interfacial properties of SiOx-based anodes in lithium-sulfur batteries. Among the additives, FEC was found to offer the lowest self-extinguishing time and interfacial resistance, leading to superior charge-discharge properties attributed to the formation of a stable solid electrolyte interface layer on the electrode surface.
The influence of electrolyte additives on the electrochemical and interfacial properties of SiOx-based anodes for lithium-sulfur batteries (Li-S) was systematically investigated. Four different electrolyte additives, namely, lithium nitrate, vinylene carbonate (VC), vinyl ethylene carbonate, and fluoroethylene carbonate (FEC), were added to the bare electrolyte comprising 1 M LiTFSI in tetraethylene glycol dimethyl ether/1,3 dioxolane in a ratio of 1:1 (v/v). The self-extinguishing time (SET) of the liquid electrolytes was measured. The 2032-type half-cells composed of Li/SiOx/Si/C were assembled, and their charge-discharge studies were analyzed at the 0.1 Crate. Upon cycling, the electrode materials were subjected to surface morphology and differential scanning calorimetry analyses. The interfacial properties of SiOx-based electrodes were investigated by electrochemical impedance spectroscopy, Fourier transform infrared, and X-ray photoelectron spectroscopy studies. Among the electrolytes examined, FEC-added electrolytes offered the lowest SET and interfacial resistance values. The superior charge-discharge properties of FEC-added electrolytes were attributed to the formation of a stable solid electrolyte interface layer on the electrode surface. The surface chemistry studies revealed the formation of Li2CO3 and ROCO2Li peaks on the electrode surface.

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