Reversible ketone hydrogenation and dehydrogenation for aqueous organic redox flow batteries
Engineering suitable redox molecules
In a flow battery, catholyte and anolyte are stored in separate tanks, and pumps are used to circulate the fluids into a stack with electrodes separated by a thin membrane. Such batteries are ideal for large-scale grid storage applications; however, suitable redox molecules are currently limited. Feng et al. used “molecular engineering” to modify an inexpensive precursor (9-fluorenone) as the basis for an organic-based redox flow battery (see the Perspective by Hu and Liu). The authors tested a series of variant molecules in a redox flow battery in which the reactions involve reversible ketone hydrogenation and dehydrogenation in an aqueous electrolyte. These reactions have advantageous features, including two-electron redox and operation in air and at elevated temperatures (50°C), that are more suitable for real-world applications.
Science, abd9795, this issue p. 836; see also abi5911, p. 788
Aqueous redox flow batteries with organic active materials offer an environmentally benign, tunable, and safe route to large-scale energy storage. Development has been limited to a small palette of organics that are aqueous soluble and tend to display the necessary redox reversibility within the water stability window. We show how molecular engineering of fluorenone enables the alcohol electro-oxidation needed for reversible ketone hydrogenation and dehydrogenation at room temperature without the use of a catalyst. Flow batteries based on these fluorenone derivative anolytes operate efficiently and exhibit stable long-term cycling at ambient and mildly increased temperatures in a nondemanding environment. These results expand the palette to include reversible ketone to alcohol conversion but also suggest the potential for identifying other atypical organic redox couple candidates.