Probing the potential of type V Deep eutectic solvents as sustainable electrolytes

被引:0
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作者
de Araujo Lima e Souza, Giselle [1 ]
Pelegano-Titmuss, Emilia [1 ]
Muñoz, Miguel [2 ]
Gurkan, Burcu [2 ]
di Pietro, Maria Enrica [3 ]
Mele, Andrea [3 ]
Stallworth, Phillip [1 ]
Greenbaum, Steven [1 ]
机构
[1] Department of Physics & Astronomy, Hunter College of the City University of New York, New York, United States
[2] Department of Chemical and Biomolecular Engineering, Case Western Reserve University, Cleveland, United States
[3] Department of Chemistry, Materials and Chemical Engineering G. Natta, Politecnico di Milano, Milan, Italy
关键词
Electrolytes;
D O I
10.1016/j.molliq.2024.126526
中图分类号
学科分类号
摘要
The increasing interest within the scientific community in environmentally friendly solvents has led to a focus on Deep Eutectic Solvents (DES), which have natural components. DES are viewed as alternatives to traditional organic solvents and have the potential to be used as electrolytes. For the first time, transport properties of four Type V Deep Eutectic Salt Solutions (DESS) were accessed to investigate the potential of this technology, selecting precursors ranked as excellent in Eco-Scale metrics. The DESS were composed of terpene and trioctylphosphine oxide (TOPO), and varying concentrations of lithium bis(trifluoromethane)sulfonimide (LiTFSI), and their properties were assessed through self-diffusion, viscosity, density, and conductivity measurements. While Type V DESS are capable of dissolving significant amounts of LiTFSI (up to 30 % molar), their ionic conductivity is low, with values ranging from 3.6·10−3 to 9.3·10−2 mS·cm−1 at 25 °C, thus limiting their suitability as electrolytes, for instance, for lithium-ions batteries applications. Similar diffusion coefficients for Li+ and TFSI− ions suggest the formation of long-lived ion pairs moving as a neutral species. Therefore, future research aims to introduce additives to disrupt contact ion pairs and enhance transport properties, leveraging the sustainable appeal of DES and their use in advanced energy storage technologies. © 2024 Elsevier B.V.
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