Author
Listed:
- Keyu Wei
(Nankai University)
- Tong Zhou
(Nankai University
Hubei University of Automotive Technology)
- Yuanzhi Jiang
(Nankai University
Haihe Laboratory of Sustainable Chemical Transformations)
- Changjiu Sun
(Nankai University)
- Yulong Liu
(Beijing Normal University)
- Saisai Li
(Nankai University)
- Siyu Liu
(Nankai University)
- Xinliang Fu
(Nankai University)
- Cejun Hu
(Nankai University)
- Shun Tian
(École Polytechnique Fédérale de Lausanne (EPFL))
- Yingguo Yang
(Fudan University)
- Xuewen Fu
(Nankai University)
- Najla AlMasoud
(Princess Nourah bint Abdulrahman University)
- Saif M. H. Qaid
(King Saud University)
- Mohammad Khaja Nazeeruddin
(École Polytechnique Fédérale de Lausanne (EPFL))
- Hsien-Yi Hsu
(City University of Hong Kong)
- Wen-Di Li
(The University of Hong Kong)
- Ji Tae Kim
(The University of Hong Kong)
- Run Long
(Beijing Normal University)
- Wei Zhang
(Nankai University
Haihe Laboratory of Sustainable Chemical Transformations)
- Jun Chen
(Nankai University
Haihe Laboratory of Sustainable Chemical Transformations)
- Mingjian Yuan
(Nankai University
Haihe Laboratory of Sustainable Chemical Transformations)
Abstract
Ultrasmall CsPbI3 perovskite quantum dots (QDs) are the most promising candidates for realizing efficient and stable pure-red perovskite light-emitting diodes (PeLEDs)1–5. However, it is challenging for ultrasmall CsPbI3 QDs to retain their solution-phase properties when they assemble into conductive films, greatly hindering their device application3,6. Here we report an approach for in situ deposit stabilized ultrasmall CsPbI3 QD conductive solids, by constructing CsPbI3 QD/quasi-two-dimensional (quasi-2D) perovskite heteroepitaxy. The well-aligned periodic array of edge-oriented ligands at heterointerface triggers a substantial octahedral tilting in a critical layer thickness of CsPbI3 QDs, which heightens the Gibbs free energy difference between the tilted-CsPbI3 and δ-CsPbI3 leading to thermodynamic stabilization of CsPbI3 QDs. The approach allows us to fabricate stabilized CsPbI3 QD conductive films with tunable emission covering the entire red spectral region from 600 nm to 710 nm. Here we report the pure-red PeLEDs with narrow electroluminescence peak centred at 630 nm, matching the Rec. 2100 standard for ultrahigh-definition display. The champion device exhibits a certified external quantum efficiency of 24.6% and a half-lifetime of 6,330 min, ranking as one of the most efficient and stable pure-red PeLED reported to date. The approach is also compatible with large-area manufacturing, enabling 1 cm2 PeLED to exhibit the best external quantum efficiency of 20.5% at 630 nm.
Suggested Citation
Keyu Wei & Tong Zhou & Yuanzhi Jiang & Changjiu Sun & Yulong Liu & Saisai Li & Siyu Liu & Xinliang Fu & Cejun Hu & Shun Tian & Yingguo Yang & Xuewen Fu & Najla AlMasoud & Saif M. H. Qaid & Mohammad Kh, 2025.
"Perovskite heteroepitaxy for high-efficiency and stable pure-red LEDs,"
Nature, Nature, vol. 638(8052), pages 949-956, February.
Handle:
RePEc:nat:nature:v:638:y:2025:i:8052:d:10.1038_s41586-024-08503-9
DOI: 10.1038/s41586-024-08503-9
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