Abstract
Heteroaromatic-conjugated aromatic molecules have inspired numerous interests in rechargeable batteries like Li-ion batteries, but were limited by low conductivity and easy dissolution in electrolytes. Herein, we immobilize a nitrogen-rich aromatic molecule tricycloquinazoline (TQ) and CuO4 unit into a two-dimensional (2D) conductive metal-organic framework (MOF) to unlock their potential for Li+ storage. TQ was identified redox activity with Li+ for the first time. With a synergistic effect of TQ and CuO4 unit, the 2D conductive MOF, named Cu-HHTQ (HHTQ=2,3,7,8,12,13-hexahydroxytricycloquinazoline), can facilitate the Li+ /e- transport and ensure a resilient electrode, resulting in a high capacity of 657.6 mAh g-1 at 600 mA g-1 with extraordinary high-rate capability and impressive cyclability. Our findings highlight an efficient strategy of constructing electrode materials for energy storage with combining multiple redox-active moieties into conductive MOFs.
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