Fluorescence Resonance Energy Transfer Properties and Auger Recombination Suppression in Supraparticles Self-Assembled from Colloidal Quantum Dots

Author:

Tian Xinhua12ORCID,Chang Hao1ORCID,Dong Hongxing134,Zhang Chi35ORCID,Zhang Long1234

Affiliation:

1. Key Laboratory of Materials for High-Power Laser, Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Shanghai 201800, China

2. School of Physical and Technology, ShanghaiTech University, Shanghai 201210, China

3. School of Physics and Optoelectronic Engineering, Hangzhou Institute for Advanced Study, University of Chinese Academy of Sciences, Hangzhou 310024, China

4. CAS Center for Excellence in Ultra-Intense Laser Science, Shanghai 201800, China

5. Department of Mechanical and Aerospace Engineering, University of Missouri, Columbia, MO 65211, USA

Abstract

Colloid quantum dots (CQDs) are recognized as an ideal material for applications in next-generation optoelectronic devices, owing to their unique structures, outstanding optical properties, and low-cost preparation processes. However, monodisperse CQDs cannot meet the requirements of stability and collective properties for device applications. Therefore, it is urgent to build stable 3D multiparticle systems with collective physical and optical properties, which is still a great challenge for nanoscience. Herein, we developed a modified microemulsion template method to synthesize quantum dot supraparticles (QD-SPs) with regular shapes and a high packing density, which is an excellent research platform for ultrafast optical properties of composite systems. The redshift of the steady-state fluorescence spectra of QD-SPs compared to CQD solutions indicates that fluorescence resonance energy transfer (FRET) occurred between the CQDs. Moreover, we investigated the dynamic processes of energy transfer in QD-SPs by time-resolved ultrafast fluorescence spectroscopy. The dynamic redshift and lifetime changes of the spectra further verified the existence of rapid energy transfer between CQDs with different exciton energies. In addition, compared with CQD solutions, the steady-state fluorescence lifetime of SPs increased and the fluorescence intensity decreased slowly with increasing temperature, which indicates that the SP structure suppressed the Auger recombination of CQDs. Our results provide a practical approach to enhance the coupling and luminescence stability of CQDs, which may enable new physical phenomena and improve the performance of optoelectronic devices.

Funder

China Postdoctoral Science Foundation

Shanghai Sailing Program

Natural Science Foundation of Shanghai

National Natural Science Foundation of China

Hangzhou Science and Technology Bureau of Zhejiang Province

Academ-ic/Technology Research Leader Program of Shanghai

Publisher

MDPI AG

Subject

Inorganic Chemistry

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