Singh Kaustub, Bondre Ameya, Petrov Kostadin V, Vermaas David A
Department of Chemical Engineering, Delft University of Technology, Van der Maasweg 9, 2629HZ Delft, The Netherlands.
ACS Appl Energy Mater. 2024 Dec 24;8(1):631-639. doi: 10.1021/acsaem.4c03032. eCollection 2025 Jan 13.
The decoupled power and energy output of a redox flow battery (RFB) offers a key advantage in long-duration energy storage, crucial for a successful energy transition. Iodide/iodine and hydrogen/water, owing to their fast reaction kinetics, benign nature, and high solubility, provide promising battery chemistry. However, H-I RFBs suffer from low open circuit potentials, iodine crossover, and their multiphase nature. We demonstrate a H-I operation with a combined neutral-pH catholyte (I /I) and an alkaline anolyte (KOH), producing an open circuit cell voltage of 1.28 V. Additionally, we incorporate a pressure-balanced gas diffusion electrode (GDE) to mitigate mass transport limitations at the anode. These improvements result in a maximum power density of 230 W/m when allowing a mild breakthrough of H through the GDE. While minimal crossover occurs, side reactions of permeating active species were found reversible, enabling long-term operation. Future work should address the stability of the GDE and optimization of the electrolyte thickness and concentration to fully leverage the potential unlocked by balancing the pressure and pH in the H-I RFB.
氧化还原液流电池(RFB)的功率和能量输出解耦,这在长时间储能方面具有关键优势,而长时间储能对于成功实现能源转型至关重要。碘化物/碘和氢/水由于其快速的反应动力学、良性性质和高溶解度,提供了有前景的电池化学体系。然而,氢 - 碘RFB存在开路电位低、碘交叉以及其多相性质等问题。我们展示了一种采用中性pH阴极电解液(I⁻/I₂)和碱性阳极电解液(KOH)组合的氢 - 碘运行方式,产生的开路电池电压为1.28V。此外,我们采用了压力平衡气体扩散电极(GDE)来减轻阳极处的传质限制。当允许氢气通过GDE有轻微穿透时,这些改进使得最大功率密度达到230W/m²。虽然碘交叉极少发生,但发现渗透活性物质的副反应是可逆的,从而实现了长期运行。未来的工作应解决GDE的稳定性以及电解液厚度和浓度的优化问题,以充分利用通过平衡氢 - 碘RFB中的压力和pH所释放的潜力。