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  4. Synthesis and Characterization of Na3SbS4 Solid Electrolytes via Mechanochemical and Sintered Solid-State Reactions: A Comparative Study

Synthesis and Characterization of Na3SbS4 Solid Electrolytes via Mechanochemical and Sintered Solid-State Reactions: A Comparative Study

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Author(s)
Thairiyarayar, Celastin Bebina
•
Huang, Chia-Hung
•
Gandomi, Yasser Ashraf
•
Hsieh, Chien-Te
•
Liu, Wei-Ren
Date Issued
November 6, 2023
Publisher
Multidisciplinary Digital Publishing Institute
Citation
Sustainability 15 (21): 15662 (2023)
Version
Final published version
Abstract
A sulfide-based solid electrolyte is an enticing non-organic solid-state electrolyte developed under ambient conditions. Na3SbS4, a profoundly enduring substance capable of withstanding exceedingly elevated temperatures and pressures, emerges as a focal point. Within this investigation, we employ dual distinct techniques to fabricate Na3SbS4, encompassing ball milling and the combination of ball milling with sintering procedures. A remarkable ionic conductivity of 3.1 × 10−4 S/cm at room temperature (RT), coupled with a meager activation energy of 0.21 eV, is achieved through a bifurcated process, which is attributed to the presence of tetragonal Na3SbS4 (t-NSS). Furthermore, we delve into the electrochemical performance and cyclic longevity of the Na2/3Fe1/2Mn1/2O2|t-NSS|Na system within ambient environs. It reveals 160 mAh/g initial charge and 106 mAh/g discharge capacities at 0.01 A/g current density. Furthermore, a cycle life test conducted at 0.01 A/g over 30 cycles demonstrates stable and reliable performance. The capacity retention further highlights its enduring energy storage capabilities. This study underscores the sustainable potential of Na3SbS4 as a solid-state electrolyte for advanced energy storage systems.
MIT Department
Massachusetts Institute of Technology. Department of Chemical Engineering
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Creative Commons Attribution
https://creativecommons.org/licenses/by/4.0/
Persistent DSpace Link
https://hdl.handle.net/1721.1/152965
DOI of Published Version
https://doi.org/10.3390/su152115662
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