New Anderson‐Based Polyoxometalate Covalent Organic Frameworks as Electrodes for Energy Storage Boosted Through Keto‐Enol Tautomerization

The unique electrochemical properties of polyoxometalates (POMs) render them ideal components for the fabrication of next‐generation high‐performance energy storage systems. However, their practical applications have been hindered by their high solubility in common electrolytes. This problem can be overcome by the effective hybridization of POMs with other materials. Here we present the design and synthesis of two novel polyoxometalate‐covalent organic frameworks (POCOF) via one‐pot solvothermal strategy between an amino‐functionalized Anderson‐type POM and a trialdehyde‐based building unit. We show that structural and functional complexity can be enriched by adding hydroxyl groups in the 2,4,6 position to the benzene‐1,3,5‐tricarbaldehyde allowing to exploit for the first time in POCOFs the keto‐enol tautomerization as additional feature to impart greater chemical stability to the COFs and enhanced properties leading to large specific surface area (347 m2/g) and superior electrochemical performance of the POCOF‐1 electrodes, when compared with POCOF‐2 electrodes that possess only imine‐type linkage and with pristine POM electrodes. Specifically, POCOF‐1 electrodes display remarkable specific, areal, and volumetric capacitance (125 F/g, 248 mF/cm2 and 41.9 mF/cm3, respectively) at a current density of 0.5 A/g, a maximum energy density (56.2 Wh/kg), a maximum power density (3.7 kW/kg) and an outstanding cyclability (90 % capacitance retention after 5000 cycles). The engineering of novel nanostructured electrode materials represents a viable strategy to obtain devices with high energy and power density. We present the synthesis of two novel polyoxometalate‐covalent organic frameworks (POCOF) with superior electrochemical performance in terms of specific capacitance (125 F/g), energy and power density (56.2 Wh/kg and 3.7 kW/kg, respectively) and high cyclability (5000 cycles).