Quantifying the impact of viscosity on mass-transfer coefficients in redox flow batteries
Quantifying the impact of viscosity on mass-transfer coefficients in redox flow batteries
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DOI:
10.1016/j.jpowsour.2018.07.046
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发表时间:
2018-09-30
影响因子:
9.2
通讯作者:
Brushett, Fikile R.
中科院分区:
文献类型:
--
作者:
Barton, John L.;Milshtein, Jarrod D.;Brushett, Fikile R.
Here, a model redox-active electrolyte (RAE) is fully characterized in terms of its transport properties, and subsequent flow cell polarization experiments enable extraction of mass-transfer coefficients. Specifically, experimental manipulation of flow rate and electrolyte viscosity are coupled with a 1-D polarization model in a flow cell to quantify the mass-transfer coefficients as a function of these material and operating parameters. Both flow-through and interdigitated flow fields are used to develop dimensionless correlations that describe mass transfer rates as a function of RAE properties. Experimental results and fitted model parameters illustrate and quantify the changes in limiting current and mass-transfer coefficient as a function of electrolyte velocity and viscosity. The resulting power-law correlations for the Sherwood (Sh) number, in terms of the Peclet (Pe) and Schmidt (Sc) numbers, are Sh = 0.0040Pe(0.75)Sc(-0.24) and Sh = 0.018Pe(0.68)Sc(-0.18) for the flow-through and inter digitated flow fields, respectively. These correlations provide quantitative estimates of mass-transfer coefficients within high-performance flow cell architectures as a function of geometry and RAE properties, enabling front-end screening in future RAE development campaigns, as well as performance benchmarking for potential redox flow batteries (RFBs).