Highly Efficient MAPbI3‐Based Quantum Dots Exhibiting Unusual Nonblinking Single Photon Emission at Room Temperature

Author:

Chuang Yung‐Tang1,Lin Tzu‐Yu1,Tan Guang‐Hsun1,Jan Pei‐En1,Lin Hao‐Cheng1,Chen Hung‐Ming1,Hsiao Kai‐Yuan1,Chen Bo‐Han2,Lu Chih‐Hsuan2,Lee Chi‐Hsuan3,Pao Chun‐Wei4,Yang Shang‐Da2,Lu Ming‐Yen1,Lin Hao‐Wu1ORCID

Affiliation:

1. Department of Materials Science and Engineering National Tsing Hua University Hsinchu 30013 Taiwan

2. Institute of Photonics Technologies National Tsing Hua University Hsinchu 30013 Taiwan

3. Institute of Atomic and Molecular Sciences Academia Sinica Taipei 106319 Taiwan

4. Research Center for Applied Sciences Academia Sinica Taipei 11529 Taiwan

Abstract

AbstractHighly emissive semiconductor nanocrystals, or so‐called quantum dots (QDs) possess a variety of applications from displays and biology labeling, to quantum communication and modern security. Though ensembles of QDs have already shown very high photoluminescent quantum yields (PLQYs) and have been widely utilized in current optoelectronic products, QDs that exhibit high absorption cross‐section, high emission intensity, and, most important, nonblinking behavior at single‐dot level have long been desired and not yet realized at room temperature. In this work, infrared‐emissive MAPbI3‐based halide perovskite QDs is demonstrated. These QDs not only show a ≈100% PLQY at the ensemble level but also, surprisingly, at the single‐dot level, display an extra‐large absorption cross‐section up to 1.80 × 10−12 cm2 and non‐blinking single photon emission with a high single photon purity of 95.3%, a unique property that is extremely rare among all types of quantum emitters operated at room temperature. An in‐depth analysis indicates that neither trion formation nor band‐edge carrier trapping is observed in MAPbI3 QDs, resulting in the suppression of intensity blinking and lifetime blinking. Fluence‐dependent transient absorption measurements reveal that the coexistence of non‐blinking behavior and high single photon purity in these perovskite QDs results from a significant repulsive exciton‐exciton interaction, which suppresses the formation of biexciton, and thus greatly reduces photocharging. The robustness of these QDs is confirmed by their excellent stability under continuous 1 h electron irradiation in high‐resolution transmission electron microscope inspection. It is believed that these results mark an important milestone in realizing nonblinking single photon emission in semiconductor QDs.

Publisher

Wiley

Subject

Biomaterials,Biotechnology,General Materials Science,General Chemistry

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