Efficient tunable white emission and multiple reversible photoluminescence switching in organic Tin(IV) chlorides via regulating the host lattice environment of antimony ions for multifunctional applications.

The host lattice environments of Sb3+ has a great influence on its photophysical properties. Here, we synthesized three zero-dimensional organic metal halides of (TPA)2 SbCl5 (1), Sb3+ -doped (TPA)SnCl5 (H2 O)·2H2 O (Sb3+ -2), and Sb3+ -doped (TPA)2 SnCl6 (Sb3+ -3). Compared with the intense orange emission of 1, Sb3+ -3 has smaller lattice distortion, thus effectively suppressing the exciton transformation from singlet to triplet self-trapped exciton (STE) states, which makes Sb3+ -3 has stronger singlet STE emission and further bring a white emission with a photoluminescence quantum efficiency (PLQE) of 93.4%. Conversely, the non-emission can be observed in Sb3+ -2 even though it has a similar [SbCl5 ]2- structure to 1, which should be due to its indirect bandgap characteristics and the effective non-radiative relaxation caused by H2 O in the lattice. Interestingly, the non-emission of Sb3+ -2 can convert into the bright emission of Sb3+ -3 under TPACl DMF solution treatment. Meanwhile, the white emission under 315 nm excitation of Sb3+ -3 can change into orange emission upon 365 nm irradiation, and the luminescence can be further quenched by the treatment of HCl. Therefore, a triple-mode reversible luminescence switch of off-onI -onII -off can be achieved. Finally, we demonstrated the applications of Sb3+ -doped compounds in single-component white light illumination, latent fingerprint detection, fluorescent anti-counterfeiting, and information encryption.