Wenfang Wang , Xi Zhang , Hang Ren , Yao Wang, Xueyi Wang, Yicheng Wang, Yumeng Li, Dong Liang, Taizhe Zhang, Shuai Wang, Yining Mu
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引用次数: 0
Abstract
In this work, we investigate the photoluminescence stability of CsPbBr3 perovskite quantum dot films under high-power excitation, focusing on the critical role of substrate morphology in modulating thermal dissipation and absorptance evolution. Conventional two-dimensional substrates induce severe thermal accumulation and spectral instability during continuous wave excitation, which compromises photoluminescence efficiency and color mixing accuracy in white-light communication. To overcome these challenges, we propose a novel three-dimensional microporous waveguide substrate combined with a method of ice-templated and spray-assisted deposition to fabricate stratified CsPbBr3/CsPbI2Br quantum dot films. This three-dimensional configuration enhances thermal dissipation, mitigates thermally induced degradation of perovskite quantum dots and stabilizes photoluminescence under optically modulated excitation. Experimental results show that the films based on the three-dimensional substrate exhibit a photostability threshold approximately 2.5 times higher than those based on planar substrates, demonstrating a significant enhancement in photoluminescence stability. Furthermore, the photoluminescence emission intensity is increased by approximately 4.35 times compared to the two-dimensional substrate. Notably, white-light mixing based on this structure is effectively localized in the CIE 1931 color space, with color mixing fluctuation reduced by approximately 81.68 % compared to the two-dimensional substrate. Our results demonstrate that the three-dimensional substrate, as a key determinant of photoluminescence performance, offers a promising path for the development of power-type perovskite devices.
期刊介绍:
The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid.
We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.