Abstract
The current obstacles for all-vanadium redox flow batteries (VRFBs) include the sluggish reaction kinetics of electrode materials and the overlapping potential range of the hydrogen evolution reaction (HER) with the negative redox couple. Bismuth (Bi) additives have exhibited tremendous enhancement of battery performance; however, the performance plateaus with concentration of Bi and the catalytic mechanism remains inconclusive and controversial. Quantified kinetic values from three electrochemical methodologies, including modelling, show that the performance plateau with Bi concentration was related to the kinetics of the vanadium redox reaction (VRR) instead of dissolution of Bi, and VRR reaction rate was improved three orders of magnitude with the addition of Bi, with the highest VRR reaction rate observed for electrolyte with 750 ppm Bi additive. Additionally, a competing relationship between VRR and the HER was explored via electrochemical methodologies. It was further confirmed that Bi effectively selectively catalysed VRR over HER via in-situ mass spectrometry measurements during battery cycling, which allows for a higher battery charging cut-off potential of 1.7 V without electrolyte imbalance caused by water electrolysis, achieving 86% of the theoretical electrolyte capacity at 110 mA cm−2 with 750 ppm Bi. The full battery performance with 750 ppm Bi additive is among the best in the literature to date.
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© 2023 The Authors. Published by Elsevier B.V.
