The challenges of instability and surface defects in CsPbBr x I 3‐ x nanocrystals (NCs) pose significant limitations on their potential application in high‐performance pure‐red perovskite light‐emitting diodes (PeLEDs). Herein, a synergistic strategy of divalent cation (Zn 2+ ) doping and anion (Te 2− ) passivation is proposed to solve these issues. Density functional theory analysis reveals that the synergistic effect can not only reduce the formation energy of CsPbBr x I 3‐ x NCs but also increase theiodide vacancy defect formation energy of CsPbBr x I 3‐ x NCs. Consequently, the optimized Zn 2+ /Te 2− co‐modified CsPbBr x I 3‐ x NCs exhibit significantly enhanced stability with a near‐unity photoluminescence efficiency. Pure‐red PeLEDs based on these CsPbBr x I 3‐ x NCs possess outstanding spectral stability with a maximum external quantum efficiency and luminance of 16.1% and 1397.2 cd m −2 , respectively. This synergistic strategy provides a new approach for enhancing the performance of mixed halide perovskite NCs and the corresponding optoelectronic devices.
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Wang et al. (2024) studied this question.
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