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Macroscopic Displacement Reaction of Copper Sulfide in Lithium Solid‐State Batteries
- Source :
- Advanced Energy Materials. 10:2002394
- Publication Year :
- 2020
- Publisher :
- Wiley, 2020.
-
Abstract
- Copper sulfide (CuS) is an attractive electrode material for batteries, thanks to its intrinsic mixed conductivity, ductility and high theoretical specific capacity of 560 mAh g−1. Here, CuS is studied as cathode material in lithium solid-state batteries with an areal loading of 8.9 mg cm−2 that theoretically corresponds to 4.9 mAh cm−2. The configuration of the cell is LiLi3PS4[CuS (70 wt%) + Li3PS4 (30 wt%)]. No conductive additive is used. CuS undergoes a displacement reaction with lithium, leading to macroscopic phase separation between the discharge products Cu and Li2S. In particular, Cu forms a network of micrometer-sized, well-crystallized particles that seems to percolate through the electrode. The formed copper is visible to the naked eye. The initial specific discharge capacity at 0.1 C is 498 mAh g(CuS)−1, i.e., 84% of its theoretical value. The initial Coulomb efficiency (ICE) reaches 95%, which is higher compared to standard carbonate-based liquid electrolytes for the same cell chemistry (≈70%). After 100 cycles, the specific capacity reaches 310 mAh g(CuS)−1. With the current composition, the cell provides 58.2 Wh kg−1 at a power density of 7 W kg−1, which is superior compared to other transition metal sulfide cathodes.
- Subjects :
- high energy density
Materials science
Renewable Energy, Sustainability and the Environment
Solid-state
chemistry.chemical_element
displacement conversion reactions
Copper sulfide
chemistry.chemical_compound
Chemical engineering
chemistry
Energy density
solid-state batteries
General Materials Science
Lithium
Single displacement reaction
sulfide solid electrolytes
600 Technik
CuS
ddc:600
Subjects
Details
- ISSN :
- 16146840 and 16146832
- Volume :
- 10
- Database :
- OpenAIRE
- Journal :
- Advanced Energy Materials
- Accession number :
- edsair.doi.dedup.....31039d00dd430da66faae6618ce44c70
- Full Text :
- https://doi.org/10.1002/aenm.202002394