Abstract In this report, a facile wet chemical method using acetonitrile combined with thermal annealing was used to prepare Li2S‐P2S5(LPS) based glass‐ceramic electrolytes with (1 wt%, 3 wt%, and 5 wt% Ce2S3) and without Ce2S3doping. The crystal structure, ionic conductivity, and chemical stability of Li7P3S11glass‐ceramic electrolytes were examined at varying temperatures (250–350°C). The results indicated that the highest ionic conductivity of 3.15 × 10−4S cm−1for pure Li7P3S11was observed at a temperature of 325°C. By incorporating 1 wt% Ce2S3and subjecting it to a heat treatment at 250°C, the glass ceramic electrolyte attained a remarkable ionic conductivity of 7.7 × 10−4(S cm−1) at 25°C. Furthermore, it exhibited a stable and extensive electrochemical potential range, reaching up to 5 volts when compared to the Li/Li+reference electrode. By tuning the glass transition and crystallization temperature, cerium doping seems to make Li7P3S11more chemically stable, compared to its original 70Li2S‐30P2S5counterpart. According to Raman and X‐ray photoelectron spectroscopy analyses, cerium doping inhibits the decomposition of highly conductive P2S74‐(pyro‐thiophosphate) to PS43−and P2S64−. Doped LPS has a greater crystallinity and more uniform microstructure than pure LPS, according to XRD, Raman spectroscopy, and scanning electron microscopy analysis. Consequently, Li7P2.9Ce0.1S11electrolyte shows great potential as a solid‐state electrolyte for constructing high‐performance sulfide‐based all‐solid‐state batteries.
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C 9 N 4 and C 2 N 6 S 3 monolayers as promising anchoring materials for lithium–sulfur batteries: weakening the shuttle effect via optimizing lithium bonds
The notorious polysulfide shuttle effect is a crucial factor responsible for the degradation of Li-S batteries. A good way to suppress the shuttle effect is to effectively anchor dissoluble lithium polysulfides (LPSs, Li 2 S n ) on appropriate substrates. Previous studies have revealed that Li of Li 2 S n is prone to interact with the N of N-containing materials to form Li–N bonds. In this work, by means of density functional theory (DFT) computations, we explored the possibility to form Li bonds on ten different N-containing monolayers, including BN, C 2 N, C 2 N 6 S 3 , C 9 N 4 , a covalent triazine framework (CTF), g -C 3 N 4 , p -C 3 N 4 , C 3 N 5 , S -N 2 S, and T -N 2 S, by examining the adsorption behavior of Li 2 S n ( n = 1, 2, 3, 4, 6, 8) on these two-dimensional (2D) anchoring materials (AMs), and investigated the performance of the formed Li bonds (if any) in inhibiting the shuttle effect. By comparing and analyzing the nitrogen content, the N-containing pore size, charge transfer, and Li bonds, we found that the N content and N-containing pore size correlate with the number of Li bonds, and the formed Li–N bonds between LPSs and AMs correspond well with the adsorption energies of the LPSs. The C 9 N 4 and C 2 N 6 S 3 monolayers were identified as promising AMs in Li-S batteries. From the view of Li bonds, this work provides guidelines for designing 2D N-containing materials as anchoring materials to reduce the shuttle effect in Li-S batteries, and thus improving the performance of Li-S batteries.
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- Award ID(s):
- 1849243
- PAR ID:
- 10321794
- Date Published:
- Journal Name:
- Physical Chemistry Chemical Physics
- Volume:
- 23
- Issue:
- 23
- ISSN:
- 1463-9076
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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