Modeling of Ion Crossover in Vanadium Redox Flow Batteries: A Computationally-Efficient Lumped Parameter Approach for Extended Cycling

被引:70
作者
Boettcher, Philipp A. [1 ]
Agar, Ertan [2 ]
Dennison, C. R. [3 ,4 ]
Kumbur, E. Caglan [4 ]
机构
[1] Drexel Univ, Dept Mech Engn & Mech, Philadelphia, PA 19104 USA
[2] Univ Massachusetts Lowell, Dept Mech Engn, Electrochem Energy Syst & Transport Lab, Lowell, MA 01854 USA
[3] Ecole Polytech Fed Lausanne Valais Wallis, Lab Electrochim Phys & Analyt, CH-1951 Sion, Switzerland
[4] Drexel Univ, Dept Mech Engn & Mech, Electrochem Energy Syst Lab, Philadelphia, PA 19104 USA
基金
美国国家科学基金会;
关键词
CAPACITY LOSS; EXCHANGE MEMBRANES; SOLVENT TRANSPORT; SULFURIC-ACID; DIFFUSION; ELECTRODES; STABILITY; CATIONS;
D O I
10.1149/2.0311601jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
070208 [无线电物理];
摘要
In this work, we have developed a zero-dimensional vanadium redox flow battery (VRFB) model which accounts for all modes of vanadium crossover and enables prediction of long-term performance of the system in a computationally-efficient manner. Using this model, the effects of membrane thickness on a 1000-cycle operation of a VRFB system have been investigated. It was observed that utilizing a thicker membrane significantly reduces the rate of capacity fade over time (up to similar to 15%) at the expense of reducing the energy efficiency (up to similar to 2%) due to increased ohmic losses. During extended cycling, the capacity of each simulated case was observed to approach an asymptote of similar to 60% relative capacity, as the concentrations in each half-cell reach a quasi-equilibrium state. Simulations also indicated that peak power density and limiting current density exhibit a similar asymptotic trend during extended cycling (i.e., an similar to 10-15% decrease in the peak power density and an similar to 20-25% decrease in the limiting current density is observed as quasi-equilibrium state is reached). (C) 2015 The Electrochemical Society. All rights reserved.
引用
收藏
页码:A5244 / A5252
页数:9
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