Photoluminescence Dynamics of CdSe QD/polymer Langmuir-Blodgett Thin Films: Morphology Effects

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Main Authors: Martín-García, Beatriz, Paulo, Pedro M. R., Costa, Sílvia M. B., Velázquez, M. Mercedes
Format: Preprint
Published: 2026
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author Martín-García, Beatriz
Paulo, Pedro M. R.
Costa, Sílvia M. B.
Velázquez, M. Mercedes
author_facet Martín-García, Beatriz
Paulo, Pedro M. R.
Costa, Sílvia M. B.
Velázquez, M. Mercedes
contents Thin films of colloidal semiconductor CdSe quantum-dots (QDs) and a styrene/maleic anhydride copolymer were prepared by the Langmuir-Blodgett technique and their photoluminescence was characterized by confocal fluorescence lifetime microscopy. In the films, the photoluminescence dynamics are strongly affected by excitation energy migration between close-packed quantum-dots and energy trapping by surface-defective QDs or small clusters of aggregated QDs. Polymer/QD films with more aggregated QD regions exhibit lower PL intensities and faster decays, which we attribute primarily to the increased ability of excitations to find trap sites among more close-packed QD regions. This was confirmed by comparing films from bilayer or co-spreading deposition, and varying the QD-to-polymer composition or the surface pressure at deposition. The more regular films, such as those obtained by bilayer deposition at high-pressure, display more surface emission intensity and decays with less accentuated curvature. Decay analysis was performed with a model that accounts for excitation energy migration and trapping in the films. In the framework of the model, the photoluminescence dynamics are related to film morphology through the density of energy traps. A lower amount of QD clustering in the films reflects on a lower density of energy traps and, thus, on more emissive QD films, as inferred here for bilayer films relatively to co-spreading films.
format Preprint
id arxiv_https___arxiv_org_abs_2601_14331
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Photoluminescence Dynamics of CdSe QD/polymer Langmuir-Blodgett Thin Films: Morphology Effects
Martín-García, Beatriz
Paulo, Pedro M. R.
Costa, Sílvia M. B.
Velázquez, M. Mercedes
Materials Science
Other Condensed Matter
Thin films of colloidal semiconductor CdSe quantum-dots (QDs) and a styrene/maleic anhydride copolymer were prepared by the Langmuir-Blodgett technique and their photoluminescence was characterized by confocal fluorescence lifetime microscopy. In the films, the photoluminescence dynamics are strongly affected by excitation energy migration between close-packed quantum-dots and energy trapping by surface-defective QDs or small clusters of aggregated QDs. Polymer/QD films with more aggregated QD regions exhibit lower PL intensities and faster decays, which we attribute primarily to the increased ability of excitations to find trap sites among more close-packed QD regions. This was confirmed by comparing films from bilayer or co-spreading deposition, and varying the QD-to-polymer composition or the surface pressure at deposition. The more regular films, such as those obtained by bilayer deposition at high-pressure, display more surface emission intensity and decays with less accentuated curvature. Decay analysis was performed with a model that accounts for excitation energy migration and trapping in the films. In the framework of the model, the photoluminescence dynamics are related to film morphology through the density of energy traps. A lower amount of QD clustering in the films reflects on a lower density of energy traps and, thus, on more emissive QD films, as inferred here for bilayer films relatively to co-spreading films.
title Photoluminescence Dynamics of CdSe QD/polymer Langmuir-Blodgett Thin Films: Morphology Effects
topic Materials Science
Other Condensed Matter
url https://arxiv.org/abs/2601.14331