Redox flow batteries (RFBs) provide an attractive solution
for
large-scale energy buffering and storage. This report describes the
development of nonaqueous RFBs based on trimetallic coordination cluster
compounds: [Ru2M(μ3-O)(CH3CO2)6(py)3] (M = Ru, Mn, Co, Ni, Zn). The
all-ruthenium complex exhibited stable battery cycles in anolyte–catholyte
symmetric operation, with rarely observed multielectron storage in
a single molecule. Moreover, the complex holds modularly tunable synthetic
handles for systematic improvements in solubility and redox potentials.
An optimized battery stack containing [Ru3(μ3-O)(CH3CO2)6(py)3]+ anolyte and [Ru2Co(μ3-O)(CH3CO2)6(py)3] catholyte yielded
stable cycles with a discharge voltage of 2.4 V, comparable to the
state-of-the-art nonaqueous RFBs. Explanation for the exceptional
stability of the charged states and prediction of systematic tunability
of the redox potentials of the cluster compounds were assisted by
DFT calculations.