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Cited 30 time in webofscience Cited 34 time in scopus
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A high-temperature tolerance solution for positive electrolyte of vanadium redox flow batteries

Authors
Kim, DonghyeonJeon, Joonhyeon
Issue Date
15-Sep-2017
Publisher
ELSEVIER SCIENCE SA
Keywords
Energy storage system; Redox flow battery; Vanadium redox flow battery; Sodium formate; Thermal stability
Citation
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, v.801, pp 92 - 97
Pages
6
Indexed
SCI
SCIE
SCOPUS
Journal Title
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
Volume
801
Start Page
92
End Page
97
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/23309
DOI
10.1016/j.jelechem.2017.07.037
ISSN
1572-6657
1873-2569
Abstract
Vanadium redox flow battery (VRFB) is attractive for energy storage applications, but there still remains a problem of preventing V-precipitation reaction (i.e., V2O5) to provide the thermal stability of electrolyte employed in VRFB. The V2O5 precipitation is accelerated in the positive electrolyte under high temperature, resulting in decreasing the charge capacity and energy efficiency of VRFB. So far, previous supporting materials, which are used to solve such precipitation problem, provide a disadvantage of decreasing voltage efficiency of VRFBs by increasing electrolyte resistance. This paper describes an advanced vanadium-positive electrolyte with high-temperature tolerance for high-efficiency VRFBs, which uses a sodium formate as a supporting material. The sodium formate plays a role as an agent capable of preventing precipitation reaction in the positive electrolyte and it also provides an effect of decreasing a viscosity of the positive electrolyte. The effectiveness of the proposed electrolyte solution is demonstrated through the following experiments: UVvis spectrometry, viscosity measurement, cyclic voltammetry (CV), VRFB operation and scanning electron microscopy (SEM) analysis. Then, for the performance comparison of high temperature stability, all experiments are carried out at 60 degrees C. Experimental results show that using the sodium formate leads to near 4.5 times increase of diffusion coefficient as compared to conventional electrolyte, and also provides 20.2% higher charge capacity (50th cycle) and 2.27% higher average energy efficiency (50 cycles) at the current density of 80 mA cm(-2). In addition, it appears that the precipitation of vanadium species is not observed in the electrolyte during VRFB operation. Therefore, this paper provides that new direction about effect of the additive in the positive electrolyte and the sodium formate can be considered as a promising additive for high-performance electrolyte of VRFBs
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