Abstract

Inorganic indium‐based halide double perovskites (DPs) are environmentally friendly alternatives to lead‐based halide perovskites in light‐emitting diodes, but commonly suffer from low quantum efficiency and harsh synthesis conditions. Herein, a large‐scale green method using water as solvent is developed for the synthesis of 3D Cs2NaInCl6 and 0D Cs2InCl5·H2O with/without Sb3+ dopant at room temperature. The transformation between Cs2InCl5·H2O and Cs2NaInCl6 products is controlled by the concentration of eco‐friendly NaCl, where excess Cl− and Na+ ions play important roles in inhibiting In3+ hydrolysis and promoting Cs2NaInCl6 crystallization, respectively. The obtained Cs2NaInCl6:Sb and Cs2InCl5·H2O:Sb exhibit highly luminescent self‐trapped exciton‐related blue (450 nm; photoluminescence quantum yield [PLQY] ≈85%) and yellow (610 nm; PLQY ≈88%) emissions, which are comparable to those obtained by previous methods. Tunable cold/warm white light with a PLQY of up to ≈73% is achieved by the rational assembly of two components with highly overlapped excitation wavelength ranges. Each component demonstrates remarkable stability against humidity and heat. This composite shows great potential in solid‐state lighting for general illumination.

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