Effect of Fe(III) on the positive electrolyte for vanadium redox flow battery

Author:

Ding Muqing1234ORCID,Liu Tao1234,Zhang Yimin12345,Cai Zhenlei1234,Yang Yadong1234,Yuan Yizhong1234

Affiliation:

1. School of Resource and Environmental Engineering, Wuhan University of Science and Technology, Wuhan 430081, Hubei Province, People's Republic of China

2. State Environmental Protection Key Laboratory of Mineral Metallurgical Resources Utilization and Pollution Control, Wuhan University of Science and Technology, Wuhan 430081, Hubei Province, People's Republic of China

3. Hubei Provincial Engineering Technology Research Center of Highly Efficient Cleaning Utilization for Shale Vanadium Resources, Wuhan University of Science and Technology, Wuhan 430081, Hubei Province, People's Republic of China

4. Hubei Collaborative Innovation Center for Highly Efficient Utilization of Vanadium Resources, Wuhan University of Science and Technology, Wuhan 430081, Hubei Province, People's Republic of China

5. School of Resource and Environmental Engineering, Wuhan University of Technology, Wuhan 430070, Hubei Province, People's Republic of China

Abstract

It is important to study the effect of Fe(III) on the positive electrolyte, in order to provide some practical guidance for the preparation and use of vanadium electrolyte. The effect of Fe(III) on the thermal stability and electrochemical behaviour of the positive electrolyte for the vanadium redox flow battery (VRFB) was investigated. When the Fe(III) concentration was above 0.0196 mol l −1 , the thermal stability of V(V) electrolyte was impaired, the diffusion coefficient of V(IV) species decreased from (2.06–3.33) × 10 −6 cm 2 s −1 to (1.78–2.88) × 10 −6 cm 2 s −1 , and the positive electrolyte exhibited a higher electrolyte resistance and a charge transfer resistance. Furthermore, Fe(III) could result in the side reaction and capacity fading, which would have a detrimental effect on battery application. With the increase of Fe(III), the collision probability of vanadium ions with Fe(III) and the competition with the redox reaction was aggravated, which would interfere with the electrode reaction, the diffusion of vanadium ions and the performance of VRFB. Therefore, this study provides some practical guidance that it is best to bring the impurity of Fe(III) below 0.0196 mol l −1 during the preparation and use of vanadium electrolyte.

Funder

the Project of National Natural Science Foundation of China

the Technical Innovation Special Major Project from Hubei Province of China

the Project of Natural Science Foundation of Hubei

Publisher

The Royal Society

Subject

Multidisciplinary

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