Alice RUINI

Pyrrolidinium-based (Pyr) ionic liquids (ILs) have been proposed as electrolyte components in lithium-ion batteries (LiBs), mainly due to their higher electrochemical stability and wider electrochemical window. Since they are not naturally electroactive, in order to allow their use in LiBs, it is necessary to mix the ionic liquids with lithium salts (Li). Li–PF6, Li–BF4, and Li–TFSI are among the lithium salts more frequently used in LiBs, and each anion, namely PF6 (hexafluorophosphate), BF4 (tetrafluoroborate), and TFSI (bis(trifluoromethanesulfonyl)azanide), has its own solvation characteristics and interaction profile with the pyrrolidinium ions. The size of Pyr cations, the anion size and symmetry, and cation–anion combinations influence the Li-ion solvation properties. In this work, we used molecular dynamics calculations to achieve a comprehensive view of the role of each cation–anion combination and of different fractions of lithium in the solutions to assess their relative advantage for Li-ion battery applications, by comparing the solvation and structural properties of the systems. This is the most-comprehensive work so far to consider pyrrolidinium-based ILs with different anions and different amounts of Li: from it, we can systematically determine the role of each constituent and its concentration on the structural and dynamic properties of the electrolyte solutions.