Organic Metal HalogenideNetted Colloidal QuantumDot Superlattice

Abstract The bottom-up assembly of colloidal quantum dots (CQDs) into superlattice structures is attractive for leveraging nanocrystal quantum features into films and optoelectronic devices. However, current CQD superlattices often require tedious control of the assembly kinetics, and they suffer from either excessively long interfacial distances, which impede carrier transport, or facet fusion, which brings high defect density. These hinder CQD superlattice applications in optoelectronic devices, where low defect density and large carrier diffusion lengths are essential. Herein, inspired by the growth of a two-dimensional (2D) perovskite layer, a class of aromatic organic cation ligands is adopted to stabilize CQDs and induce close and ordered packing of CQDs into a superlattice netted by an organic metal halogenide (QD@OMH), giving rise to a high carrier diffusion length (>250 nm) for lead sulfide (PbS) CQD film. The superlattice-based infrared photodetectors achieve a responsivity of 0.663 A W–1 at 1560 nm and an order-of-magnitude reduction in noise current density, yielding a detectivity exceeding 1013 Jones. Furthermore, the infrared light-emitting diodes achieve a high radiance (22.4 W sr–1 m–2) and an operational T90 lifetime exceeding 200 h under continuous operation at peak luminance.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-08-14
DOI
https://doi.org/10.1021/jacs.6c12708
Primary Topic
Perovskite Materials and Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

Organic Metal HalogenideNetted Colloidal QuantumDot Superlattice

Zhiqiang Zou, Haobo Wu, W. M. Liu, Zhijun Ning et al.
Journal of the American Chemical Society
Perovskite Materials and Applications
article

Organic Metal HalogenideNetted Colloidal QuantumDot Superlattice

Zhiqiang Zou, Haobo Wu, W. M. Liu, Zhijun Ning, Wenjia Zhou, Yi Yu, Yue Lu, Baile Chen, Qingqing Ji, Francisco Pelayo García de Arquer, Jun Jiang, Jiahui Du, Xin Wen, Mingyu Ma, Hao Liang, Hao Wang, Ziyao Ma, Yaxin Zhao, Fan Zheng, Yu Chen, Wei Zhou, Zihao Wang
article en

Abstract

Abstract The bottom-up assembly of colloidal quantum dots (CQDs) into superlattice structures is attractive for leveraging nanocrystal quantum features into films and optoelectronic devices. However, current CQD superlattices often require tedious control of the assembly kinetics, and they suffer from either excessively long interfacial distances, which impede carrier transport, or facet fusion, which brings high defect density. These hinder CQD superlattice applications in optoelectronic devices, where low defect density and large carrier diffusion lengths are essential. Herein, inspired by the growth of a two-dimensional (2D) perovskite layer, a class of aromatic organic cation ligands is adopted to stabilize CQDs and induce close and ordered packing of CQDs into a superlattice netted by an organic metal halogenide (QD@OMH), giving rise to a high carrier diffusion length (>250 nm) for lead sulfide (PbS) CQD film. The superlattice-based infrared photodetectors achieve a responsivity of 0.663 A W–1 at 1560 nm and an order-of-magnitude reduction in noise current density, yielding a detectivity exceeding 1013 Jones. Furthermore, the infrared light-emitting diodes achieve a high radiance (22.4 W sr–1 m–2) and an operational T90 lifetime exceeding 200 h under continuous operation at peak luminance.

Journal of the American Chemical Society
University of Science and Technology of China (CN), Institute of Photonic Sciences (ES), ShanghaiTech University (CN)
Fundación Cellex, National Natural Science Foundation of China, Generalitat de Catalunya, Science and Technology Commission of Shanghai Municipality, ShanghaiTech University, FUNDACIÓ Privada MIR-PUIG, Agencia Estatal de Investigación, National Key Research and Development Program of China
Openalex Percentile: Top 18%
Perovskite Materials and Applications
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