Effect of succinonitrile on ion transport in PEO-based lithium-ion battery electrolytes

被引:17
作者
Mohapatra, Sipra [1 ]
Sharma, Shubham [1 ]
Sriperumbuduru, Aman [1 ]
Varanasi, Srinivasa Rao [2 ]
Mogurampelly, Santosh [1 ]
机构
[1] Indian Inst Technol Jodhpur, Dept Phys, Karwar 342030, Rajasthan, India
[2] Sultan Qaboos Univ, Dept Phys, Muscat 123, Oman
关键词
MOLECULAR-DYNAMICS SIMULATION; POLYMER SOLID ELECTROLYTES; POLY(ETHYLENE OXIDE); FORCE-FIELD; INITIAL CONFIGURATIONS; SALT CONCENTRATION; TEMPERATURE; PHASE; CONDUCTIVITY; WEIGHT;
D O I
10.1063/5.0087824
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report the ion transport mechanisms in succinonitrile (SN) loaded solid polymer electrolytes containing polyethylene oxide (PEO) and dissolved lithium bis(trifluoromethane)sulphonamide (LiTFSI) salt using molecular dynamics simulations. We investigated the effect of temperature and loading of SN on ion transport and relaxation phenomenon in PEO-LiTFSI electrolytes. It is observed that SN increases the ionic diffusivities in PEO-based solid polymer electrolytes and makes them suitable for battery applications. Interestingly, the diffusion coefficient of TFSI ions is an order of magnitude higher than the diffusion coefficient of lithium ions across the range of temperatures and loadings investigated. By analyzing different relaxation timescales and examining the underlying transport mechanisms in SN-loaded systems, we find that the diffusivity of TFSI ions correlates excellently with the Li-TFSI ion-pair relaxation timescales. In contrast, our simulations predict distinct transport mechanisms for Li-ions in SN-loaded PEO-LiTFSI electrolytes. Explicitly, the diffusivity of lithium ions cannot be uniquely determined by the ion-pair relaxation timescales but additionally depends on the polymer segmental dynamics. On the other hand, the SN loading induced diffusion coefficient at a given temperature does not correlate with either the ion-pair relaxation timescales or the polymer segmental relaxation timescales. Published under an exclusive license by AIP Publishing.
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页数:14
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