Editors' Choice—Lithium Primary Batteries Employing Multi-Electron Carbon-Fluorine Bond Cleavage in Perfluoroalkylated Reactants. Issue 3 (1st March 2022)

• Record Type: Journal Article
• Authors: Gao, Haining; Sevilla, Alejandro; Gallant, Betar M.
• Is Part Of: Journal of the Electrochemical Society. Volume 169:Issue 3(2022)
• Publication Date: 2022-03-01
• Subjects: Electrochemistry -- Periodicals; 541.3705
• DOI: 10.1149/1945-7111/ac5c09
• Languages: English
• ISSNs: 0013-4651

Abstract

Abstract : While Li−carbon monofluoride (CFx ) is the current energy leader among primary batteries, the technology is maturing, motivating further fundamental study of Li battery chemistry based on C−F redox. This study examines the possibility to conduct multi-electron carbon reduction using a candidate class of liquid CFx analogues, perfluoroalkyl iodides (Cn F2n+1 I, with F/C ratios of x > 2), in supporting electrolyte as catholytes for Li cells. The large, polarizable iodine supports electrochemical reduction with concerted F − ligand expulsion, forming lithium fluoride (LiF) as the main solid discharge product. Under initial conditions (1 M reactant and 0.3 mA cm −2 in dimethylsulfoxide), only limited defluorination (1.5 e − /molecule) is accessed. Governing factors for C−F bond redox are further investigated, including reactant concentration, discharge rate, temperature, and solvent properties (e.g. catholyte viscosity). A maximum of 8 e − /C6 F13 I, or 8/13 available F, is accessible in the voltage range 2.8−1.9 V vs Li/Li + with low reactant concentrations (0.1 M) and rates (20 μ A cm −2 ). The data indicate that multiple handles exist to tailor extended C−F bond activation in these reactants. However, premature reaction termination caused by deactivation of intermediates, which is particularly exacerbated at higher concentrations and/or rates, is likely to be a persistent challenge for practical applications.