Multielectron Cycling of a Low-Potential Anolyte in Alkali Metal Electrolytes for Nonaqueous Redox Flow Batteries

被引:74
|
作者
Hendriks, Koen H. [1 ,2 ]
Sevov, Christo S. [1 ,2 ]
Cook, Monique E. [1 ,2 ]
Sanford, Melanie S. [1 ,2 ]
机构
[1] Univ Michigan, Dept Chem, 930 North Univ Ave, Ann Arbor, MI 48109 USA
[2] JCESR, Argonne, IL 60439 USA
来源
ACS ENERGY LETTERS | 2017年 / 2卷 / 10期
关键词
LIPF6-BASED ELECTROLYTES; ELECTROCHEMICAL PROPERTIES; ENERGY-STORAGE; FLUORINATION; DECOMPOSITION; DENSITY; IMPACT;
D O I
10.1021/acsenergylett.7b00559
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Recent efforts have led to the design of new anolytes for nonaqueous flow batteries that exhibit reversible redox couples at low potentials. However, these molecules generally cycle through just a single electron-transfer event, which limits the overall energy density of resulting batteries on account of the undesirably high equivalent weight (i.e., ratio of anolyte/supporting electrolyte molecular weight to electrons transferred). In addition, these anolytes generally require expensive alkylammonium salts as supporting electrolytes for stable cycling, which further increases the equivalent weight of the system. The current work describes the multielectron redox cycling of a low-potential anolyte using alkali metal salts as supporting electrolytes. These studies reveal that potassium hexafluorophosphate (KPF6) dramatically lowers the equivalent weight of the anolyte system while supporting flow cell cycling through two redox events at low potentials for 150 cycles with no detectable degradation.
引用
收藏
页码:2430 / 2435
页数:6
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