Apr 24, 2024
9:30am - 9:45am
Room 431, Level 4, Summit
Gan Chen1,Wenhao Zhang2,1,Yiping Li1,2,Kaushik Dey1,F. Dean Toste2,1,Brett Helms1
Lawrence Berkeley National Laboratory1,University of California, Berkeley2
Gan Chen1,Wenhao Zhang2,1,Yiping Li1,2,Kaushik Dey1,F. Dean Toste2,1,Brett Helms1
Lawrence Berkeley National Laboratory1,University of California, Berkeley2
Redox-flow batteries employ dissolved active materials separated by a semi-permeable membrane to store energy. Cell life and capacity are maximized when active materials can be sequestered in their respective cell compartments at high concentration. Here, I will discuss how the design of the semi-permeable membrane must be considered alongside that for the active materials, whose infinite miscibility with non-aqueous electrolytes allow for high volumetric capacity. The oligomeric design of these active materials makes them sufficiently large to be excluded by a microporous membrane, while maintaining substantially faster electron transfer kinetics than competing polymeric and colloidal active materials. I will discuss how these design features influence charge transfer with the electrode and other attributes that impact the efficiency of the flow cells as they relate to emerging applications in grid-scale energy storage.