Title :
Investigation on Manganese (Mn²+/Mn³+) - Vanadium (V²+/V³+) Redox Flow Battery
Author :
Hong, Tao ; Xue, Fangqin
Author_Institution :
Sch. of Electron. & Inf. Eng., Beihang Univ., Beijing
Abstract :
A novel Mn2+/Mn3+- V2+/V3+redox flow battery has been designed. The electrochemical response of high concentration Mn2+/Mn3+ couple in H2SO4 solution were investigated via cyclic voltammetry, steady polarization curve, electrochemical impedance spectroscopy, and charge-discharge experiments. The electrochemical and the kinetic parameters for anodic oxidation of Mn2 and cathodic reduction of Mn3+ were measured. Performance of a RFB employing Mn2+/Mn3+ couple as anolyte active species and V2+/V3+ as catholyte ones was evaluated with constant-current charge-discharge tests. When the current density varies from 20 to 80 mA cm-2, the average coulombic efficiency varies from 81.5% to 92.5% and the voltage efficiency varies from 93.5% to 85.3%. Accordingly the whole energy efficiency varies from 76.2% to 81.2%. Energy efficiency is about 20% higher than that of the all-vanadium battery and average discharge voltage is 1.66 V, which is about 14% higher than that of the all-vanadium battery. The energy density is calculated to be 40.8 Wh/kg, which is 60% higher than that of the all-vanadium battery. The preliminary exploration shows that the Mn2+/Mn3+ couple is electrochemically promising for redox flow battery.
Keywords :
electrochemical electrodes; electrochemistry; oxidation; reduction (chemical); secondary cells; Mn-V; cathodic reduction; charge-discharge experiments; cyclic voltammetry; electrochemical impedance spectroscopy; electrochemical response; redox flow battery; voltage 1.66 V; Batteries; Current density; Electrochemical impedance spectroscopy; Energy efficiency; Kinetic theory; Manganese; Oxidation; Polarization; Testing; Voltage;
Conference_Titel :
Power and Energy Engineering Conference, 2009. APPEEC 2009. Asia-Pacific
Conference_Location :
Wuhan
Print_ISBN :
978-1-4244-2486-3
Electronic_ISBN :
978-1-4244-2487-0
DOI :
10.1109/APPEEC.2009.4918453