| Literature DB >> 32797719 |
Huijun Yang1,2, Yu Qiao1, Zhi Chang1,2, Han Deng1,2, Ping He3, Haoshen Zhou1,2,3.
Abstract
The introduction of the redox couple of triiodide/iodide (I3 - /I- ) into aqueous rechargeable zinc batteries is a promising energy-storage resource owing to its safety and cost-effectiveness. Nevertheless, the limited lifespan of zinc-iodine (Zn-I2 ) batteries is currently far from satisfactory owing to the uncontrolled shuttling of triiodide and unfavorable side-reactions on the Zn anode. Herein, space-resolution Raman and micro-IR spectroscopies reveal that the Zn anode suffers from corrosion induced by both water and iodine species. Then, a metal-organic framework (MOF) is exploited as an ionic sieve membrane to simultaneously resolve these problems for Zn-I2 batteries. The multifunctional MOF membrane, first, suppresses the shuttling of I3 - and restrains related parasitic side-reaction on the Zn anode. Furthermore, by regulating the electrolyte solvation structure, the MOF channels construct a unique electrolyte structure (more aggregative ion associations than in saturated electrolyte). With the concurrent improvement on both the iodine cathode and the Zn anode, Zn-I2 batteries achieve an ultralong lifespan (>6000 cycles), high capacity retention (84.6%), and high reversibility (Coulombic efficiency: 99.65%). This work not only systematically reveals the parasitic influence of free water and iodine species to the Zn anode, but also provides an efficient strategy to develop long-life aqueous Zn-I2 batteries.Entities:
Keywords: aqueous zinc-iodide batteries; electrolyte solvation regulation; metal-organic frameworks; triiodide/iodide redox couple; zinc electrodeposits
Year: 2020 PMID: 32797719 DOI: 10.1002/adma.202004240
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849