Kinetic studies at carbon felt electrodes for vanadium redox-flow batteries under controlled transfer current density conditions

被引:23
作者
Becker, Maik [1 ,2 ]
Bredemeyer, Niels [3 ]
Tenhumberg, Nils [3 ]
Turek, Thomas [1 ,2 ]
机构
[1] Tech Univ Clausthal, Inst Chem & Electrochem Proc Engn, Leibnizstr 17, D-38678 Clausthal Zellerfeld, Germany
[2] Energy Res Ctr Lower Saxony EFZN, Stollen 19A, D-38640 Goslar, Germany
[3] Thyssenkrupp Ind Solut AG, Friedrich Uhde Str 15, D-44141 Dortmund, Germany
关键词
vanadium redox-flow battery; electrode kinetics; mathematical model; current density distribution; charge transfer coefficient; HIGH OVERPOTENTIALS; GRAPHITE ELECTRODE; ACIDIC-SOLUTIONS; MODEL; CELL; CONFIGURATION; REDUCTION; MECHANISM; MEMBRANE; STATE;
D O I
10.1016/j.electacta.2017.07.062
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this work we present a combination of mathematical modeling and experimental kinetic characterization of carbon felt electrodes in positive electrolyte (PE) and negative electrolyte (NE) of vanadium redox-flow batteries. The mathematical model is applied to check for homogeneous transfer current density within a radially connected carbon electrode intensively flown through by the electrolyte. Transfer current homogeneity depends mainly on electrolyte conductivity, electrode thickness and charge transfer coefficient. The transfer current inhomogeneity of the investigated electrode samples is below 5%, when single layers of carbon electrodes (415 mm thickness at 89% porosity and 210 mm thickness at 75% porosity) are applied and high electrolyte conductivities (>800 mS.cm(-1)) are maintained by low vanadium concentrations (< 15 mM). Experimental results show charge transfer coefficients for high overpotentials of 0.26 +/- 0.03 for the reduction reaction in NE and 0.37 +/- 0.04 for the oxidation reaction in NE. The charge transfer coefficients of the PE are 0.13 +/- 0.02 for reduction and 0.30 +/- 0.04 for the oxidation reaction. Application of the Butler-Volmer equation to describe the polarization behavior shows adequate agreement with the experimental results at states of charge between 25% and 75%. The rate constants for the PE reaction are nearly two times higher than for the NE reaction. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:12 / 24
页数:13
相关论文
共 32 条
[1]   Dramatic performance gains in vanadium redox flow batteries through modified cell architecture [J].
Aaron, D. S. ;
Liu, Q. ;
Tang, Z. ;
Grim, G. M. ;
Papandrew, A. B. ;
Turhan, A. ;
Zawodzinski, T. A. ;
Mench, M. M. .
JOURNAL OF POWER SOURCES, 2012, 206 :450-453
[2]   In Situ Kinetics Studies in All-Vanadium Redox Flow Batteries [J].
Aaron, Douglas ;
Sun, Che-Nan ;
Bright, Michael ;
Papandrew, Alexander B. ;
Mench, Matthew M. ;
Zawodzinski, Thomas A. .
ECS ELECTROCHEMISTRY LETTERS, 2013, 2 (03) :A29-A31
[3]   Identification of performance limiting electrode using asymmetric cell configuration in vanadium redox flow batteries [J].
Agar, Ertan ;
Dennison, C. R. ;
Knehr, K. W. ;
Kumbur, E. C. .
JOURNAL OF POWER SOURCES, 2013, 225 :89-94
[4]  
Bard A. J., 2012, ELECTROCHEMICAL DICT, P913
[5]   Mediated enzyme electrodes with combined micro- and nanoscale supports [J].
Barton, Scott Calabrese ;
Sun, Yuhao ;
Chandra, Bhupesh ;
White, Sean ;
Hone, James .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2007, 10 (05) :B96-B100
[6]   Polarization curve measurements combined with potential probe sensing for determining current density distribution in vanadium redox-flow batteries [J].
Becker, Maik ;
Bredemeyer, Niels ;
Tenhumberg, Nils ;
Turek, Thomas .
JOURNAL OF POWER SOURCES, 2016, 307 :826-833
[7]   BEHAVIOR OF A CARBON FELT FLOW BY ELECTRODES .1. MASS-TRANSFER CHARACTERISTICS [J].
CARTA, R ;
PALMAS, S ;
POLCARO, AM ;
TOLA, G .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1991, 21 (09) :793-798
[8]  
Corcuera S., 2012, European Chemical Bulletin, V1, P511, DOI [DOI 10.17628/ECB.2012.1.511-519, DOI 10.17628/ECB.2012.1.511]
[9]   The vanadium redox-battery:: an efficient storage unit for photovoltaic systems [J].
Fabjan, C ;
Garche, J ;
Harrer, B ;
Jörissen, L ;
Kolbeck, C ;
Philippi, F ;
Tomazic, G ;
Wagner, F .
ELECTROCHIMICA ACTA, 2001, 47 (05) :825-831
[10]   The electrochemical reduction of VO2+ in acidic solution at high overpotentials [J].
Gattrell, A ;
Qian, J ;
Stewart, C ;
Graham, P ;
MacDougall, B .
ELECTROCHIMICA ACTA, 2005, 51 (03) :395-407