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Thermal Plasma Synthesis of Li2S Nanoparticles for Application in Lithium-Sulfur Batteries.

Authors :
Nava-AvendaƱo, J.
Nussbaum, M.
Veilleux, J.
Source :
Plasma Chemistry & Plasma Processing; Jul2021, Vol. 41 Issue 4, p1149-1167, 19p
Publication Year :
2021

Abstract

Inductively-coupled thermal plasma processes were used to produce nanosized Li<subscript>2</subscript>S. Prior to the syntheses, the feasibility of forming Li<subscript>2</subscript>S was first evaluated using FactSage by considering the phase diagrams of sulfur and different lithium precursors in reducing atmospheres; Li<subscript>2</subscript>O, LiOH·H<subscript>2</subscript>O, Li<subscript>2</subscript>CO<subscript>3</subscript> and Li<subscript>2</subscript>SO<subscript>4</subscript>·H<subscript>2</subscript>O all showed promises in producing Li<subscript>2</subscript>S nanoparticles, as confirmed by experiments. Argon and hydrogen mixtures were used as plasma gases, and a carbothermal reduction was implemented for Li<subscript>2</subscript>SO<subscript>4</subscript>·H<subscript>2</subscript>O. In addition, carbon-coated Li<subscript>2</subscript>S nanoparticles were synthesized with downstream injection of methane. Carbon was shown to stabilize Li<subscript>2</subscript>S upon contact with ambient air. The Li<subscript>2</subscript>S nanoparticles were electrochemically tested in half-cells using electrolytes containing LiNO<subscript>3</subscript> or Li<subscript>2</subscript>S<subscript>6</subscript> as additives. It was found that adding LiNO<subscript>3</subscript> to the electrolyte was detrimental to the electrochemical performance of Li<subscript>2</subscript>S, whereas the combination of Li<subscript>2</subscript>S<subscript>6</subscript> and LiNO<subscript>3</subscript> as additives doubled the charge and discharge capacities of the half-cell over 10 cycles. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02724324
Volume :
41
Issue :
4
Database :
Complementary Index
Journal :
Plasma Chemistry & Plasma Processing
Publication Type :
Academic Journal
Accession number :
150747291
Full Text :
https://doi.org/10.1007/s11090-021-10168-5