Abstract
The lack of a suitable ionic exchange membrane has retarded the development of organic nonaqueous redox flow batteries (RFBs). Membrane-free redox stratified batteries, wherein electroactive materials in immiscible nonaqueous and aqueous solvents as anolyte and catholyte, have emerged as a promising strategy to mitigate the high dependence of RFBs on battery separators. Here we report the exploration of the application of immiscible electrolytes, water and dichloromethane, in membrane-free redox stratified batteries. With 0.5 M phenothiazines in dichloromethane as the catholytes and zinc metal in aqueous electrolyte as the anolyte, the aqueous/nonaqueous stratified battery presents stable long cycling with a capacity retention of 79.1% over 202 cycles under ambient testing conditions. Study of phenothiazines with varying lengths of alkyl chains (C0, C3, C8, and C18) reveals that the hydrophobicity of the phenothiazine molecules greatly affects the solubility in dichloromethane and battery cyclability. Computation on free energy of solvation and molecular dynamics is also performed to elucidate the hydrophobicity effects. The results presented in this work lay a solid foundation for potential development of the membrane-free RFBs.
Original language | English |
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Pages (from-to) | 337-343 |
Number of pages | 7 |
Journal | ACS Materials Letters |
Volume | 3 |
Issue number | 4 |
DOIs | |
State | Published - Apr 5 2021 |
Externally published | Yes |
Funding
The authors acknowledge the University of Cincinnati for startup funding support and the Ohio Supercomputer Center for providing the computational resources. NMR experiments were performed on a Bruker AVANCE NEO 400 MHz NMR spectrometer funded by NSF-MRI Grant CHE-1726092. This material is based upon work partially supported by the National Science Foundation under Grant CHE-1955161 (T.L.B.).
Funders | Funder number |
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NSF-MRI | CHE-1726092 |
National Science Foundation | CHE-1955161 |