Abstract

Redox flow batteries (RFBs) are promising candidates for long-duration energy storage mainly due to the lower cost of improving the energy density compared to lithium-ion batteries. However, the full sustainability of RFBs has not been achieved yet, and there is a lot of room for further improvement. One of the main parameters showing a strong influence on the sustainability of RFBs is redox active materials. In this work, manganese was selected for electrochemical evaluation as it fulfills the sustainability requirements. Manganese is a non-toxic, low-cost and abundant material with sufficient aqueous solubility[1]. Moreover, the standard potential of manganese (1.51 V) is higher than that of vanadium (1.26 V).For electrochemical parameters, we have, through cyclic voltammetry (CVs) and polarization curves, estimated the diffusion coefficient (D0 ) and heterogeneous standard electron transfer rate (k 0) of manganese in an acidic electrolyte in the presence of titanium as an additive. In order to investigate the performance of an RFB system using a manganese electrolyte, a hybrid system was designed that uses hydrogen gas on the negative side and an acidic manganese electrolyte the positive side. We have studied the resistance behavior of the hybrid RFB through electrochemical impedance spectroscopy at different states of charge. From EIS data, cell ohmic resistance, and a general idea of the different processes taking place at different state of charge were obtained. Moreover, we studied the performance of the hybrid RFB during 70 cycles, obtaining an average coulombic efficiency of 98.1%, voltage efficiency of 77.8% and capacity retention of 97.7%. Carney, J.R., B.R. Dillon, and S.P. Thomas, Recent Advances of Manganese Catalysis for Organic Synthesis. European Journal of Organic Chemistry, 2016. 2016(23): p. 3912-3929.

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