posted on 2023-10-17, 12:07authored byJiali Wang, Heng Lv, Lulu Huang, Jiahao Li, Haijiao Xie, Gang Wang, Tiantian Gu
Organic materials with multiple active sites and flexible
structural
designs are becoming popular for use in aqueous zinc-ion batteries
(AZIBs). However, their applicability is limited due to the low specific
capacity and poor cycle stability originating from the introduction
of inactive units and high solubility. Herein, three organic molecules
with tunable redox properties were synthesized using anhydride (PMDA,
1,2,4,5-benzenetetracarboxylic anhydride-1,2-diaminoanthraquinone,
NTCDA, 1,4,5,8-naphthalenetetracarboxylic dianhydride-1,2-diaminoanthraquinone,
and PTCDA, 3,4,9,10-perylenetetracarboxylic dianhydride-1,2-diaminoanthraquinone,
referred to as PM12, NT12, and PT12) in the solid-phase method. Density
functional theory (DFT) simulations and experiments identified that
NT12 exhibits superior electrochemical performance compared with PM12
and PT12 because of the low energy gap and large aromatic conjugated
structure. They demonstrated specific capacities of 106.7, 192.9,
and 124.9 mA h g–1 at 0.05 A g–1, respectively. Especially, NT12 displayed excellent initial specific
capacity (85.4 mA h g–1 at 1 A g–1) and remarkable capacity retention (64.1% for 3000 cycles) due to
dual active centers (CN and CO). The all-NT12 full-cell
also had excellent performance (127.1 mA h g–1 under
1 A g–1 and 80.6% over 200 cycles). The organic
compounds synthesized in this work have potential applications of
AZIBs, highlighting the importance of molecular design to develop
the next generation of advanced materials.