摘要
High-power operation of vanadium redox flow batteries (VRFBs) is still limited by sluggish interfacial charge transfer, insufficient electrolyte wettability, and concentration polarization within porous carbon electrodes. Herein, an iodine-functionalized reduced graphene oxide/graphite felt electrode (GF@rGO-V) was prepared through hydroiodic acid vapor treatment to regulate the solid–liquid interface of graphite felt while retaining its three-dimensional porous framework. Structural and surface analyses indicate that HI vapor treatment produces a less compact iodine-containing rGO interface with improved electrolyte accessibility. Electrochemical measurements further reveal enhanced apparent ion transport and reduced charge-transfer resistance toward both VO 2+ /VO 2 + and V 2+ /V 3+ redox couples. Temperature-dependent impedance analysis shows that the apparent activation energy for the positive reaction decreases from 40.2 kJ mol –1 on pristine graphite felt to 23.7 kJ mol –1 on GF@rGO-V, suggesting a more favorable interfacial kinetic environment. As a result, the assembled VRFB delivers an energy efficiency of 82.2% at 400 mA cm –2 , a peak power density of 1257.6 mW cm –2 , and stable cycling over 1500 cycles at 400 mA cm –2 . This work demonstrates an iodine-assisted interfacial engineering strategy for improving mass transport and charge-transfer kinetics in high-power aqueous flow batteries.
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