Ruozhu Feng1,Ying Chen1,Xin Zhang1,Benjamin Rousseau2,Peiyuan Gao1,Ping Chen1,Sebastian Mergelsberg1,Lirong Zhong1,Aaron Hollas1,Yangang Liang1,Vijayakumar Murugesan1,Qian Huang1,Sharon Hammes-Schiffer2,Yuyan Shao1,Wei Wang1
Pacific Northwest National Laboratory1,Yale University2
Ruozhu Feng1,Ying Chen1,Xin Zhang1,Benjamin Rousseau2,Peiyuan Gao1,Ping Chen1,Sebastian Mergelsberg1,Lirong Zhong1,Aaron Hollas1,Yangang Liang1,Vijayakumar Murugesan1,Qian Huang1,Sharon Hammes-Schiffer2,Yuyan Shao1,Wei Wang1
Pacific Northwest National Laboratory1,Yale University2
Redox flow batteries have a unique architecture that potentially enables cost-effective long-duration energy storage to address the intermittency introduced by increased renewable integration for the decarbonization of the electric power sector. Targeted molecular engineering has demonstrated electrochemical reversibility in natively redox-inactive ketone molecules in aqueous electrolytes. Yet, the kinetics of fluorenone-based flow batteries continue to be limited by slow alcohol oxidation. We show how strategically designed principles can accelerate alcohol oxidation and thus enhance battery kinetics. Rationally designed fluorenone-based flow battery electrolytes demonstrate enhanced rate capability, high battery capacity, and record-breaking long cycling. This study opens a new avenue to improve the kinetics of aqueous organic flow batteries.