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Demonstrates enhanced efficiency and stability in blue perovskite light-emitting diodes, highlighting polymer blend effectiveness.
Perovskite light-emitting diodes (PeLEDs) are promising low-cost, solution-processable, and color-pure optoelectronic devices for display and lighting applications. However, blue PeLEDs continue to lag their green and red counterparts in terms of luminance and operational lifetime, limiting their practical implementation. The performance disparity primarily arises from the imbalanced charge injection, which accelerates degradation at the perovskite/hole transport layer (HTL) interface under electrical bias. Here, we design a polymer blend HTL composing poly(N-vinyl-2,7-difluoro-carbazole) (PVK-F) and poly(bis(4-phenyl)(2,4,6-trimethylphenyl)amine) (PTAA), in which strengthened van der Waals interactions promote denser molecular packing. This optimized microstructure simultaneously enhances hole mobility and wettability, enabling high-quality perovskite film formation. Consequently, PeLEDs emitting at 485 nm achieve an external quantum efficiency of 24.1% and luminance exceeding 26,000 cd m-2. Moreover, the improved hole injection mitigates interfacial degradation, yielding an operational half-lifetime exceeding 700 minutes at an initial luminance of 100 cd m-2. This work establishes polymer blending as an effective strategy for advancing the performance and stability of blue PeLEDs.
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Gu et al. (2026) studied this question.
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