Enhanced fluorescence resonance energy transfer in CsPbBr3 quantum dot-rhodamine 640 molecule hybrid system: Toward high-efficiency and high-rate capability

IF 4.7 3区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Photochemistry and Photobiology A-chemistry Pub Date : 2025-06-01 Epub Date: 2025-01-21 DOI:10.1016/j.jphotochem.2025.116283
Bo Li , Yongfeng Wan , Caifeng Xiu , Yuliang Liu , Qi Li , Lixia Zhu , Hang Yin , Ying Shi
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Abstract

The fluorescence resonance energy transfer (FRET) process plays a crucial role in improving the efficiency of optoelectronic and photosynthetic devices. CsPbBr3 perovskite quantum dot (QD) serves as efficient photon absorbers and exciton generators, thus offering the potential to enhance FRET performance. However, a high-efficiency FRET process with high-rate capability has not been achieved in the CsPbBr3 perovskite QD-based system. Herein, we reported that the FRET process is improved in CsPbBr3 perovskite QD-rhodamine 640 molecule hybrid system in n-hexane solution. This phenomenon stems from an increased number of adsorbed acceptor and a decreased distance between donor and acceptor. When the adsorbed number reached 4.2, a near-unity FRET efficiency of 99.3 % was achieved. Meanwhile, femtosecond transient absorption spectroscopy reveals that the FRET process exhibits a high-rate capability of 0.57 ps−1. Consequently, this research will stimulate the development of high-performance light-emitting device of perovskite-based system.

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CsPbBr3量子点-罗丹明640分子杂化体系中增强的荧光共振能量转移:迈向高效率和高速率能力
荧光共振能量转移(FRET)过程对提高光电和光合器件的效率起着至关重要的作用。CsPbBr3钙钛矿量子点(QD)作为有效的光子吸收剂和激子发生器,从而提供了提高FRET性能的潜力。然而,在基于CsPbBr3钙钛矿qd的体系中,尚未实现具有高速率性能的高效FRET工艺。本文报道了在正己烷溶液中改进了CsPbBr3钙钛矿qd -罗丹明640分子杂化体系的FRET工艺。这种现象是由于吸附受体数量增加和供体与受体之间的距离减小所致。当吸附数达到4.2时,FRET效率达到99.3%。同时,飞秒瞬态吸收光谱显示FRET过程具有0.57 ps−1的高速率能力。因此,本研究将促进高性能钙钛矿基发光器件的发展。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
580
审稿时长
48 days
期刊介绍: JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds. All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor). The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.
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