| Literature DB >> 31478325 |
Jessica J Hong1, Liangdong Zhu1, Cheng Chen1, Longteng Tang1, Heng Jiang1, Bei Jin1, Trenton C Gallagher1, Qiubo Guo1, Chong Fang1, Xiulei Ji1.
Abstract
Plating battery electrodes typically deliver higher specific capacity values than insertion or conversion electrodes because the ion charge carriers represent the sole electrode active mass, and a host electrode is unnecessary. However, reversible plating electrodes are rare for electronically insulating nonmetals. Now, a highly reversible iodine plating cathode is presented that operates on the redox couples of I2 /[ZnIx (OH2 )4-x ]2-x in a water-in-salt electrolyte. The iodine plating cathode with the theoretical capacity of 211 mAh g-1 plates on carbon fiber paper as the current collector, delivering a large areal capacity of 4 mAh cm-2 . Tunable femtosecond stimulated Raman spectroscopy coupled with DFT calculations elucidate a series of [ZnIx (OH2 )4-x ]2-x superhalide ions serving as iodide vehicles in the electrolyte, which eliminates most free iodide ions, thus preventing the consequent dissolution of the cathode-plated iodine as triiodides.Entities:
Keywords: aqueous batteries; dual-plating batteries; iodine batteries; water-in-salt electrolyte; zinc batteries
Year: 2019 PMID: 31478325 DOI: 10.1002/anie.201909324
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336