Realizing efficient photoluminescence spectral modulation via Sb3+/Ln3+ co-doping in Cs2NaInCl6 double perovskites†
Abstract
The broad-band self-trapped exciton (STE) emission feature of lead-free halide double perovskites makes it challenging to realize emission with various wavelengths in a single material. Cs2NaInCl6:Sb3+ crystals with blue emission (440 nm) were synthesized by rationally introducing the Sb3+ ion into Cs2NaInCl6 with a photoluminescence quantum yield (PLQY) up to 99.35%. The Ln3+ (Tb3+ and Ho3+) ions were doped into Cs2NaInCl6:Sb3+ to achieve spectrally tunable emission from blue to green and pink emission owing to the energy transfer from the host STE to Ln3+ ions, with PLQY values of 90.68% and 61.87%, respectively. By carefully adjusting the doping level of Ln3+ ions, white light emission with a PLQY of 68.87% was achieved in the Tb3+ and Ho3+ co-doped Cs2NaInCl6:Sb3+ system. LED devices based on Sb3+/Ln3+ co-doped Cs2NaInCl6 with multicolor and white light emissions were fabricated based on these phosphors, which exhibit excellent spectral and environmental stability. The results show that double perovskite luminescence materials have potential for application in solid-state lighting and multi-color displays.