Reversible Conversion Reactions and Small First Cycle Irreversible Capacity Loss in Metal Sulfide-Based Electrodes Enabled by Solid Electrolytes

Authors
Kim, SanghyeonChoi, JaewonBak, Seong-MinSang, LingziLi, QunPatra, ArghyaBraun, Paul, V
Issue Date
2019-07
Publisher
WILEY-V C H VERLAG GMBH
Citation
ADVANCED FUNCTIONAL MATERIALS, v.29, no.27
Abstract
Solid-state batteries can potentially enable new classes of electrode materials which are unstable against liquid electrolytes. Here, SnS nanocrystals, synthesized by a wet chemical method, are used to fabricate a Li-ion electrode, and the electrochemical properties of this electrode are examined in both solid and liquid electrolyte designs. The SnS-based solid-state cell delivers a capacity of 629 mAh g(-1) after 100 cycles and exhibits an unprecedentedly small irreversible capacity in the first cycle (8.2%), while the SnS-based liquid cell shows a rapid capacity decay and large first cycle irreversible capacity (44.6%). Cyclic voltammetry (CV) experiments show significant solid electrolyte interphase (SEI) formation in the liquid cell during the first discharge while SEI formation by electrolyte reduction in the solid-state cell appears negligible. Along with CV, X-ray photoelectron spectroscopy and energy dispersive spectroscopy are used to investigate the differences between the solid-state and liquid cells. The reaction chemistry of SnS in solid-state cells is also studied in detail by ex situ X-ray diffraction and X-ray absorption spectroscopy. The overarching findings are that use of a solid electrolyte suppresses materials degradation and electrolyte reduction which leads to a small first cycle irreversible capacity and stable cycling.
Keywords
GRAPHENE OXIDE COMPOSITES; X-RAY-DIFFRACTION; ANODE MATERIAL; LITHIUM; PERFORMANCE; BATTERY; SNS; NANOCOMPOSITE; NANOSHEETS; CATHODE; all solid-state batteries; irreversible capacities; lithium-ion batteries; metal sulfides; reversible conversion reactions
ISSN
1616-301X
URI
https://pubs.kist.re.kr/handle/201004/119803
DOI
10.1002/adfm.201901719
Appears in Collections:
KIST Article > 2019
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