| Literature DB >> 29276817 |
Huicong Yang1,2, Lichang Yin1, Ji Liang1,3, Zhenhua Sun1, Yuzuo Wang1,4, Hucheng Li1, Kuang He1, Lipo Ma5, Zhangquan Peng5, Siyao Qiu6, Chenghua Sun7, Hui-Ming Cheng1,8,9, Feng Li1.
Abstract
The electrochemical performance of the aluminum-sulfur (Al-S) battery has very poor reversibility and a low charge/discharge current density owing to slow kinetic processes determined by an inevitable dissociation reaction from Al2 Cl7- to free Al3+ . Al2 Cl6 Br- was used instead of Al2 Cl7- as the dissociation reaction reagent. A 15-fold faster reaction rate of Al2 Cl6 Br- dissociation than that of Al2 Cl7- was confirmed by density function theory calculations and the Arrhenius equation. This accelerated dissociation reaction was experimentally verified by the increase of exchange current density during Al electro-deposition. Using Al2 Cl6 Br- instead of Al2 Cl7- , a kinetically accelerated Al-S battery has a sulfur utilization of more than 80 %, with at least four times the sulfur content and five times the current density than that of previous work.Entities:
Keywords: aluminum-sulfur battery; electrochemistry; energy storage; ionic liquid electrolytes; kinetics
Year: 2018 PMID: 29276817 DOI: 10.1002/anie.201711328
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336