Organic
electrodes have been identified as promising energy-storage
materials for aqueous zinc-ion batteries (AZIBs). Small molecular
materials have ideal redox properties, high specific capacity, and
structural diversity, making them a category of cathode candidates
for AZIBs. However, the instability and dissolution during the extraction
and insertion of H+/Zn2+ limit their application
of the long-cycle stability for AZIBs. Herein, a small-molecule nanosheet
(NI-DAQ, ∼14 nm in thickness) with imide linkage is designed
and synthesized by the condensation of anthraquinones and anhydrides.
It not only inhibits the dissolution of monomer electrodes but also
boosts the reactivity and conductivity of the whole molecule by the
introduction of π-conjugated imide groups and extended aromatic
planes. Therefore, the NI-DAQ electrode obtains a large initial capacity
of 191.9 mA h g–1 at 50 mA g–1 and superior cyclability after 3000 cycles at 500 mA g–1 with a minor average capacity fading rate of 0.01% per cycle. Moreover,
in situ Fourier transform infrared (FT-IR) and ex situ X-ray photoelectron
spectroscopy (XPS) characterization techniques have been implemented
to investigate the redox mechanism of CO units in AZIBs for
the NI-DAQ electrode. Thus, a promising conductive molecule is developed
and explored in this paper, which can provide insights into the application
of organic materials in AZIBs.