Realizing efficient broadband near-infrared emission and multimode photoluminescence switching via coordination structure modulation in Sb 3+ -doped 0D organic metal chlorides.

Recently, organic Sb(III)-based metal halides have achieved significant results in the visible light region due to their efficient emission. However, realizing efficient broadband near-infrared (NIR) emission in such materials is a great challenge. Herein, we developed three different NIR emitters via a coordination structure modulation strategy in Sb 3+ -doped zero-dimensional organic metal chlorides of (C 20 H 20 P) 2 MnCl 4 , (C 20 H 20 P) 2 ZnCl 4 , and (C 20 H 20 P) 2 CdCl 4 with tetrahedral structure. More specifically, after the dopant Sb 3+ is inserted into the host lattice, the coordination structures of Sb 3+ ions can change from [SbCl 5 ] 2- square-pyramidal configuration to [SbCl 4 ] - clusters, which will bring a larger lattice distortion degree to the excited state compared to the ground state, resulting in a larger Stokes shift. Thus, efficient NIR emission with near-unity photoluminescence quantum yield (PLQY) can be obtained in Sb 3+ -doped compounds under 365 nm excitation. Moreover, Sb 3+ -doped NIR emitters also show remarkable stabilities, which prompts us to fabricate NIR phosphor conversion light-emitting diodes (pc-LEDs) and demonstrate their application in night vision. More interestingly, the Sb 3+ -doped (C 20 H 20 P) 2 MnCl 4 shows tunable emission characteristics, which can be tuned from green to greenish-yellow, orange, red, and NIR emission under different external stimuli, and thus we can demonstrate the applications of this compound in quintuple-mode fluorescence anti-counterfeiting and information encryption.