Improvement of optical properties of lead-free double perovskite Cs2AgInCl6 nanocrystals through Bi ion alloying

Lead-free double perovskite nanocrystals (NCs) have garnered significant attention due to their non-toxicity and excellent stability, offering vast potential applications in the field of optoelectronics. They are considered promising substitutes for lead-based perovskite NCs. Herein, we successfully synthesized monodisperse, uniformly sized, cubic-shaped Cs2AgIn1-xBixCl6 (0 ≤ x ≤ 1) NCs via a simple hot injection approach. The Cs2AgInCl6 NCs exhibit a lower photoluminescence quantum yield (PLQY) of 3.9 % due to the presence of parity-forbidden transitions. However, with the introduction of Bi3+ alloying, the parity-forbidden transitions are broken, transforming into direct transitions allowed by parity. This transformation leads to efficient bright yellow emission, with the highest PLQY reaching up to 31.6 % (Cs2AgIn0.90Bi0.10Cl6 NCs). Adjusting the Bi3+ alloying concentration allows tuning the NCs band gap from 3.62 eV to 2.88 eV, and the exciton lifetime can be extended from 5.99 ns to 24.88 ns. Temperature-dependent photoluminescence spectra and density functional theory calculations indicate that Bi3+ alloying increases the exciton binding energy, weakens the electron-phonon coupling, and breaks parity-forbidden transitions. Moreover, Cs2AgIn0.90Bi0.10Cl6 NCs display outstanding stability under ambient conditions, laying a solid foundation for their applications in optoelectronics. The results of this study open a new pathway to enhance the optical performance of lead-free double perovskite nanomaterials. •Monodisperse Bi3+ alloyed Cs2AgInCl6 nanocrystals were prepared.•Bi3+ alloyed Cs2AgInCl6 nanocrystals show a improved PLQY of 31.6 %.•Bi3+ alloyed Cs2AgInCl6 nanocrystals demonstrate a remarkable stability.