Abstract
Compressing porous carbon electrodes is a common approach to improve flow battery performance, but the resulting impact on electrode structure, fluid dynamics, and cell performance is not well understood. Herein, microtomographic imaging, load cell testing, and flow cell diagnostics are employed to characterize how compression-induced changes impact pressure drop, polarization, and mass-transfer scaling. Five different compressions are tested, spanning ranges typically used in literature, for AvCarb 1071 cloth (0%, 9%, 20%, 25%, 32%) and Freudenberg H23 paper (0%, 8%, 12%, 17%, 22%). It is found that the two electrode structures have distinct responses to compression, resulting in differing optimal conditions identified for each material; specifically, the Freudenberg H23 exhibits lower combined ohmic, charge-transfer, and mass-transport values at 8% compression, resulting in improved electrochemical performance across all compressive values, as compared to the optimal AvCarb 1071 compression (20%). Overall, Freudenberg H23 exhibits a greater sensitivity to compression with peak electrochemical activity correlating with increased permeability, whereas AvCarb 1071 is insensitive to compressive loads but produces lower electrochemical performance. Herein, the trade-offs of mechanical robustness on fluid-dynamic and electrochemical performance between the two electrodes are demonstrated by the aforementioned findings, suggesting each could be used for specific operating environments.
Original language | English |
---|---|
Article number | 2101162 |
Number of pages | 11 |
Journal | Energy Technology |
Volume | 10 |
Issue number | 8 |
DOIs | |
Publication status | Published - Aug 2022 |
Bibliographical note
Funding Information:K.M.T. and K.V.G. contributed equally to this work. This work was supported by the Joint Center for Energy Storage Research, an Energy Innovation Hub funded by the US Department of Energy Office of Science, Basic Energy Sciences. K.M.T. and K.V.G. acknowledge additional financial support from the NSF Graduate Research Fellowship (Grant no. 1122374). Any opinion, findings, and conclusions or recommendations expressed in this material are those of the authors and do not necessarily reflect the views of the National Science Foundation. M.V.D.H. and A.F.‐C. acknowledge funding from the Dutch Research Council (NWO) for the Veni Grant (Grant no. 17324). A.M. acknowledges funding form the Swiss National Science Foundation (Grant no. 169913). We would like to thank Professor Leon E. Govaert for insightful comments and feedback throughout this work.
Funding
K.M.T. and K.V.G. contributed equally to this work. This work was supported by the Joint Center for Energy Storage Research, an Energy Innovation Hub funded by the US Department of Energy Office of Science, Basic Energy Sciences. K.M.T. and K.V.G. acknowledge additional financial support from the NSF Graduate Research Fellowship (Grant no. 1122374). Any opinion, findings, and conclusions or recommendations expressed in this material are those of the authors and do not necessarily reflect the views of the National Science Foundation. M.V.D.H. and A.F.‐C. acknowledge funding from the Dutch Research Council (NWO) for the Veni Grant (Grant no. 17324). A.M. acknowledges funding form the Swiss National Science Foundation (Grant no. 169913). We would like to thank Professor Leon E. Govaert for insightful comments and feedback throughout this work.
Keywords
- compression
- mass transfer
- microCT
- porous electrodes
- redox flow batteries