4.7 Article

Elucidating the influence of structure and Ag+ -Na+ ion-exchange on crack-resistance and ionic conductivity of Na3Al1.8Si1.65 P1.8 O12 glass electrolyte

期刊

ACTA MATERIALIA
卷 227, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.actamat.2022.117745

关键词

Ion-exchange; Amorphous; Ionic-conductivity; Mechanical property; MD simulations

资金

  1. Science and Engineering Research Board (SERB), DST, Govt. of India, India [ECR/2018/000292]
  2. DST-SERB [ECR/2018/000292]
  3. Sao Paulo Research Foundation (FAPESP) [2021/06370-0]
  4. CeRTEV (Center for Research, Technology, and Education in Vitreous Materials-process FAPESP) [2013/07793-6]
  5. SERB [ECR/2018/002228]
  6. DST [DST/INSPIRE/04/2016/002774]

向作者/读者索取更多资源

This study improves the crack resistance of glass as a solid electrolyte for sodium-ion batteries through Na+-Ag+ ion exchange while maintaining its ionic conductivity. The study evaluates the structure, crack resistance, and conductivity of the glass using various techniques and concludes through experiments and simulations.
Glasses are emerging as promising and efficient solid electrolytes for all-solid-state sodium-ion batteries. However, they still suffer from poor ionic conductivity and crack-resistance, which need to be improved for better battery performance, reliability, and service life. The current study shows a significant enhancement in crack resistance (from 11.3 N to 32.9 N) for Na3Al (1.8) Si-1.65 P1.8O12 glass (Ag-0 glass) upon Na+ -Ag+ ion-exchange (IE) due to compressive stresses generated in the glass surface while the ionic conductivity values (similar to 10(-5) S/cm at 473 K) were retained. In this study, magic angle spinning-nuclear magnetic resonance (MAS-NMR), molecular dynamics (MD) simulations, Vickers micro hardness, and impedance spectroscopic techniques were used to evaluate the intermediate-range structure, atomic structure, crack resistance and conductivity of the glass. MAS-NMR and MD simulations confirm the presence of Si-OAl-O-P groups in the glass, thus enabling formation of Na percolated channel regions. AC-conductivity analysis for Ag-0 and ion-exchanged Ag-0 glass suggests that the mobility of Na+ ion increases with increasing temperature. It is observed that the measured mean square displacement (root < R-2(t(p))>) for sodium cations using AC-conductivity isotherms is nearly constant up to 448 K and then increases with increasing temperature up to 523 K. From the impedance spectra for ion-exchanged Ag-0 glass, it is identified that the increase in root < R-2 (t(nu))> and thereby, the mobility of sodium-ions for Ag-0 glass is due to the structural variations in the Ag-0 glass with increasing the temperature. Overall, the mechanisms presented in this article helps in formulating better glass based electrolyte materials for room temperature or high temperature sodium-ion batteries. (C) 2022 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

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