Mixed-halide blue perovskites CsPb(Br/Cl)3 are considered promising candidates for developing efficient deep-blue perovskite light-emitting diodes (PeLEDs), but their low photoluminescence quantum yield (PLQY), environmental instability, and poor device performance gravely inhibit their future development. Here, we employ a heteroatomic Cu2+ doping strategy combined with post-treatment Br- anion exchange to prepare high-performance deep-blue perovskites CsPb(Br/Cl)3. The Cu2+ doping strategy significantly decreases the intrinsic chlorine defects, ensuring that the inferior CsPbCl3 quantum dots are transformed into two-dimensional nanosheets with enhanced violet photoluminescence and increased exciton binding energy. Further, with the post-treatment Br- anion exchange, the as-prepared CsPb(Br/Cl)3 nanosheets with more radiation recombination and less ion migration present an enhanced PLQY of 94% and better humidity stability of 30 days. Based on the optimized CsPb(Br/Cl)3, we fabricated deep-blue PeLEDs with luminescence emission at 462 nm, a maximum luminance of 761 cd m-2, and a current density of 205 mA cm-2. This work puts forward a feasible synthesis strategy to prepare efficient and stable mixed-halide blue perovskite CsPb(Br/Cl)3 and related blue PeLEDs, which may promote the further application of mixed-halide perovskites in the blue light range.
Keywords: Defect passivation; Light-emitting diodes; Metal doping; Mixed-halide perovskites; Two-dimensional nanosheets.
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