Abstract

Traditional static optical anti-counterfeiting technology can only output a single emission signal, which is easy to replicate and difficult to meet the needs in current high-tech fields. Multi-level stimuli-responsive luminescent materials with internal logical relationship can improve the degree of anti-counterfeiting and resist against the flood of counterfeiting. In this work, we propose to use force and acid dual stimuli to restrict the dissipation path of photogenerated free radicals, which further lead to the radical-actuated photochromic luminescence (PCL) performance. Based on this strategy, a zero-dimensional (0D) dinuclear zinc complex Zn2(9-AC)4(IM)2 (1) with blue luminescent properties (450 nm) was designed and synthesized. The interaction between 9-AC and IM (as 9-AC/IM exciplex) can be cut off by force-induced rearrangement of structural units in the spatial dimensions or acid-induced protonation of 9-AC, achieving the luminescent transformation from 9-AC/IM exciplex (447 nm) to 9-AC/9-AC excimer (480 nm) or 9-HAC (485 nm). At the same time, the PCL performance was activated and the emission intensity quenching rate increased from 4.77 % to 93.86 % or 44.93 % under UV light irradiation, respectively. The solid-state ultraviolet–visible absorption spectra, electron paramagnetic resonance spectra and theoretical calculation confirmed that the activation of PCL performance is due to the fact that the 9-AC• radicals are more difficult to dissipate upon force- or acid-induced stimuli. Combining mechanochromic luminescence (MCL) and PCL, a dynamic anti-counterfeiting quick response (QR) code with multi-level and fast-responsive logic sequence have been designed, which are promising for the application in time-resolved information encryption. This work provides an effective strategy to construct multi-level stimuli-responsive luminescence as novel anti-counterfeiting materials by changing the photogenerated free radical dissipation pathway to activate PCL properties.

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