Stimulus-responsive
long persistent luminescence (LPL) materials
have attracted wide attention due to their potential applications
in information storage, anti-counterfeiting, optoelectronic devices,
etc. However, LPL coordination polymers with room temperature afterglow
transition characteristics have not been explored. Herein, mellitic
acid and zinc ions were utilized to synthesize an acid–base
stable coordination polymer (1) by an organic solvent-free
hydrothermal method. 1 possesses a tightly stacked structure
and exhibits dual-emission peaks with blue luminescence and blue-green
afterglow. Upon exposure to heating, DMSO immersion, or vacuum, 1h, 1s, and 1v were obtained. The
original blue luminescence changes to blue-green, while the afterglow
turns yellow-green due to the loss of water molecules from the inner
cavity. This is the first example of an LPL coordination polymer that
can realize room temperature afterglow transition by dehydration operation.
Moreover, the emission spectra of 1 can be recovered
by exposing 1h, 1s, or 1v to
water vapor, suggesting a reversible dehydration/hydration process.
Experimental and density functional theory (DFT) results suggest that
the fluorescence of 1 originates from the mixing of intra-ligand
and ligand-to-metal charge transfer excited states. The triplet state
from intersystem crossing is responsible for the long persistent luminescence
of phosphorescence emission. The rational structural design along
with the conceptual model of anti-counterfeiting and information encryption
based on afterglow transition display the unique advantages of the
LPL coordination polymer in realizing convenient multiple stimuli-responsive
devices.