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. 2014 Feb 18;111(9):3205–3206. doi: 10.1073/pnas.1401033111

Fig. 2.

Fig. 2.

(A) In conventional nonaqueous electrolytes, Li+ is tightly solvated and slowed down in its migration by coordinating carbonate molecules, resulting in low t+. (B) In electrolytes based on highly fluorinated solvents, anion TFSI is solvated instead, thus freeing Li+ as the conducting species and resulting in almost unity t+.