Li-ion hopping conduction in highly concentrated lithium bis(fluorosulfonyl)amide/dinitrile liquid electrolytes. Issue 19 (1st May 2019)

• Record Type: Journal Article
• Authors: Ugata, Yosuke; Thomas, Morgan L.; Mandai, Toshihiko; Ueno, Kazuhide; Dokko, Kaoru; Watanabe, Masayoshi
• Is Part Of: Physical chemistry chemical physics. Volume 21:Issue 19(2019)
• Page Start: 9759
• Page End: 9768
• Publication Date: 2019-05-01
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c9cp01839e
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Li + ion hopping conduction through ligand (solvent and anion) exchange emerges in solvent-deficient liquid electrolytes of [Li salt]/[dinitrile] > 1. Abstract : Li + ion hopping conduction in highly concentrated solutions of lithium bis(fluorosulfonyl)amide (LiFSA) dissolved in dinitrile solvents, namely succinonitrile, glutaronitrile, and adiponitrile, was investigated. Phase behaviors of the LiFSA/dinitrile binary mixtures assessed by differential scanning calorimetry suggested that LiFSA and the dinitriles form stable solvates in a molar ratio of 1 : 2. For succinonitrile, a glass forming room temperature liquid is formed when [LiFSA]/[succinonitrile] > 1. The corresponding glutaronitrile and adiponitrile mixtures have melting points below 60 °C. The self-diffusion coefficients of Li +, FSA −, and dinitrile measured with pulsed field gradient NMR suggested that Li + ion diffuses faster than anion and dinitrile in the liquids of composition [LiFSA]/[dinitrile] = 1/0.8, indicating emergence of Li + ion hopping conduction. X-ray crystallography for the LiFSA–(dinitrile)2 solvates and Raman spectroscopy for the liquids with composition [LiFSA]/[dinitrile] > 1 revealed that the two cyano groups of the dinitrile coordinate to two different Li + ions and form solvent-bridged structures of (Li + –dinitrile–Li + ). In addition, the Raman spectra suggested that ionic aggregates (Li + –FSA − –Li + ) are formed in the liquids with composition [LiFSA]/[dinitrile] > 1. Although there is frequent ligand (dinitrile and/or anion) exchange for each Li + ion in the liquid state, the polymeric network structures (solvent-bridged structure and ionic aggregates) restrict the facile motion of ligands because each ligand is interacting with multiple Li + ions in the highly concentrated electrolytes. This induces the faster diffusion of the Li + ion than that of the ligands, i.e., hopping conduction of Li + through ligand exchange. Electrochemical measurements clarified that the [LiFSA]/[succinonitrile] = 1/0.8 electrolyte possesses a relatively high Li + transport ability (limiting current density > 7 mA cm −2 ) thanks to the Li + hopping conduction, regardless of its extremely high viscosity (3142 mPa s) and relatively low conductivity (0.26 mS cm −1 ) at room temperature. Furthermore, this electrolyte was shown to have a high Li + transference number (>0.6), exhibited reversible Li metal deposition/dissolution i.e. suppression of reductive decomposition of the solvent, and could be successfully applied to graphite and LiNi1/3 Mn1/3 Co1/3 O2 half-cells.