Edson Laureto
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Edson Laureto has a total of 68 co-authors. Here are the top co-authors by number of shared publications:
- Ricardo Vignoto Fernandes
Universidade Estadual de Londrina
6 shared publications José Leonil Duarte
Univ Estadual Londrina, Ctr Ciencias Exatas, Dept Fis, BR-86051990 Londrina, PR, Brazil
3 shared publications- Alex Fabiano Cortez Campos
Laboratory for Environmental and Applied Nanoscience - LNAA, Faculdade UnB Planaltina, Universidade de Brasília, 73345-010, Brasília, DF, Brazil
2 shared publications - Amer Samir Safade2 shared publications
- Caio Matheus Ferreira2 shared publications
- Carolina Ferreira de Matos Jauris
Environmental Science and Technology Center, Campus Caçapava do Sul, Federal University of Pampa, Caçapava do Sul, RS, Brazil
2 shared publications
Latest Publications
- Open Access
- 12 June 2026
- Published by Elsevier in Materials Chemistry and Physics
- Vol. 363
Nano-confinement modulates the photo-oxidation of water-soluble rubrene in liquid and solid films
- 12 June 2026
- Published by Elsevier in Materials Chemistry and Physics
- Vol. 363
Open AccessNano-confinement modulates the photo-oxidation of water-soluble rubrene in liquid and solid films
- Open Access
- 9 May 2026
- Published by Elsevier in SSRN Electronic Journal
Nano-Confinement Modulates the Photo-Oxidation of Water-Soluble Rubrene in Liquid and Solid Films
Photo-oxidation remains a challenge for achieving long-term stability in organic electronic devices. Rubrene (Rub), a small-molecule semiconductor known for its exceptional optoelectronic properties, illustrates this problem as its highly sensitive to light and oxygen. In addition, its limited processability, requiring the use of halogen solvents or thermal evaporation for its deposition, further restricts its practical use in large-area processing . This works shows how both problems can be addressed by a colloidal approach where Rub is encapsulated through a miniemulsion method, producing stable, water-dispersible nanoemulsions (NPs). Their emission and absorption properties in the liquid, and solid films, show that nanoencapsulation preserves the intrinsic vibronic fingerprint of Rub, while inducing spectral shifts and emission narrowing, enhancing molecular ordering and stronger intermolecular coupling, quantified by calculating the Huang–Rhys factor. Systematic investigation of photo-oxidation kinetics reveals a modulation effect: in dispersion, Rub NPs oxidize faster than molecular Rub in chloroform, due to enhanced oxygen access from their large surface area, while maintaining colloidal stability. In contrast, NP-based Rub films exhibits significantly improved photostability, preserving over twice the residual absorbance of annealed neat Rub films under 11 W/m2 irradiation. Atomic Force Microscopy and Fourier Transform Infrared Spectroscopy confirm the synergistic role of excess surfactant and nanoencapsulation in Rub oxidation, while thermal annealing fine-tunes film morphology, improving stability and reducing oxygen diffusion pathways. This work establishes nanoemulsion-based confinement as an effective strategy to modulate photo-oxidation in highly reactive organic semiconductors, offering new design rules for environmentally processed, photostable optoelectronic materials and oxygen-sensing platforms.
- 9 May 2026
- Published by Elsevier in SSRN Electronic Journal
Open AccessNano-Confinement Modulates the Photo-Oxidation of Water-Soluble Rubrene in Liquid and Solid Films
Photo-oxidation remains a challenge for achieving long-term stability in organic electronic devices. Rubrene (Rub), a small-molecule semiconductor known for its exceptional optoelectronic properties, illustrates this problem as its highly sensitive to light and oxygen. In addition, its limited processability, requiring the use of halogen solvents or thermal evaporation for its deposition, further restricts its practical use in large-area processing . This works shows how both problems can be addressed by a colloidal approach where Rub is encapsulated through a miniemulsion method, producing stable, water-dispersible nanoemulsions (NPs). Their emission and absorption properties in the liquid, and solid films, show that nanoencapsulation preserves the intrinsic vibronic fingerprint of Rub, while inducing spectral shifts and emission narrowing, enhancing molecular ordering and stronger intermolecular coupling, quantified by calculating the Huang–Rhys factor. Systematic investigation of photo-oxidation kinetics reveals a modulation effect: in dispersion, Rub NPs oxidize faster than molecular Rub in chloroform, due to enhanced oxygen access from their large surface area, while maintaining colloidal stability. In contrast, NP-based Rub films exhibits significantly improved photostability, preserving over twice the residual absorbance of annealed neat Rub films under 11 W/m2 irradiation. Atomic Force Microscopy and Fourier Transform Infrared Spectroscopy confirm the synergistic role of excess surfactant and nanoencapsulation in Rub oxidation, while thermal annealing fine-tunes film morphology, improving stability and reducing oxygen diffusion pathways. This work establishes nanoemulsion-based confinement as an effective strategy to modulate photo-oxidation in highly reactive organic semiconductors, offering new design rules for environmentally processed, photostable optoelectronic materials and oxygen-sensing platforms.
- 21 February 2023
- Published by Springer Nature in Applied Physics A
- Vol. 129 (3) , 1-7
A synaptic device based on the optoelectronic properties of ZnO thin film transistors
- 21 February 2023
- Published by Springer Nature in Applied Physics A
- Vol. 129 (3) , 1-7
A synaptic device based on the optoelectronic properties of ZnO thin film transistors
- Open Access
- 16 May 2022
- Published by Universidade Estadual de Londrina in Semina: Ciências Exatas e Tecnológicas
- Vol. 43 (1) , 95-101
Analysis of the stability of organic photovoltaic devices through external quantum efficiency (EQE)
The use of solar panels for the purpose of converting solar energy into electrical energy has been increasingly common in the community, where the vast majority of these panels are produced from inorganic materials, especially silicon (Si). In recent decades, many researchers have been analyzing organic and hybrid materials in order to apply them to photovoltaic devices. The use of organic and hybrid materials in devices is advantageous due to some factors, such as: low production cost, variety of materials available, production of flexible devices. A fundamental analysis for any photovoltaic device is the external quantum efficiency measure (EQE). This technique correlates the number of incident photons with the number of electrons generated, making it possible to know in which region of the electromagnetic spectrum the photovoltaic device is more efficient. This work aims to apply the external quantum efficiency characterization technique for the evaluation of different types of photovoltaic devices in terms of their stability
- 16 May 2022
- Published by Universidade Estadual de Londrina in Semina: Ciências Exatas e Tecnológicas
- Vol. 43 (1) , 95-101
Open AccessAnalysis of the stability of organic photovoltaic devices through external quantum efficiency (EQE)
The use of solar panels for the purpose of converting solar energy into electrical energy has been increasingly common in the community, where the vast majority of these panels are produced from inorganic materials, especially silicon (Si). In recent decades, many researchers have been analyzing organic and hybrid materials in order to apply them to photovoltaic devices. The use of organic and hybrid materials in devices is advantageous due to some factors, such as: low production cost, variety of materials available, production of flexible devices. A fundamental analysis for any photovoltaic device is the external quantum efficiency measure (EQE). This technique correlates the number of incident photons with the number of electrons generated, making it possible to know in which region of the electromagnetic spectrum the photovoltaic device is more efficient. This work aims to apply the external quantum efficiency characterization technique for the evaluation of different types of photovoltaic devices in terms of their stability
- Open Access
- 19 December 2021
- Published by Journal of Experimental Techniques and Instrumentation in Journal of Experimental Techniques and Instrumentation
- Vol. 4 (04) , 1-12
Analysis of the polarization states of light through the experimental determination of the Stokes Parameters
Atualmente, fontes de luz polarizada encontram diversas aplicações em dispositivos optoeletrônicos, “displays”, em testes de tensões em peças mecânicas e até em estudos de mineralogia. Uma das principais necessidades é determinar o estado de polarização (linear, circular, elíptico, ou uma sobreposição destes) do feixe luminoso. Para este fim, aplicamos neste trabalho a técnica de Elipsometria de Emissão para investigar os estados de polarização de diferentes fontes de luz. Esta técnica está baseada na teoria de Stokes e os tipos de polarização estão correlacionados aos parâmetros de Stokes. Realizamos medidas em feixes de luz proveniente de um LASER polarizado, um LASER polarizado passando por um defasador quarto de onda a ± 45° (polarização circular), um LED despolarizado e, esse mesmo LED, com sua luz refletida sobre uma placa de vidro em diversos ângulos e inclusive no ângulo de Brewster. A montagem experimental é composta de um defasador quarto de onda, um polarizador linear e um detector de luz. Os resultados obtidos apresentaram um desvio de aproximadamente 1% em relação à polarização conhecida das fontes de luz. Desta maneira, foi possível constatar que a técnica de Elipsometria de Emissão pode ser aplicada para se determinar a polarização da luz proveniente de fontes luminosas em geral.
- 19 December 2021
- Published by Journal of Experimental Techniques and Instrumentation in Journal of Experimental Techniques and Instrumentation
- Vol. 4 (04) , 1-12
Open AccessAnalysis of the polarization states of light through the experimental determination of the Stokes Parameters
Atualmente, fontes de luz polarizada encontram diversas aplicações em dispositivos optoeletrônicos, “displays”, em testes de tensões em peças mecânicas e até em estudos de mineralogia. Uma das principais necessidades é determinar o estado de polarização (linear, circular, elíptico, ou uma sobreposição destes) do feixe luminoso. Para este fim, aplicamos neste trabalho a técnica de Elipsometria de Emissão para investigar os estados de polarização de diferentes fontes de luz. Esta técnica está baseada na teoria de Stokes e os tipos de polarização estão correlacionados aos parâmetros de Stokes. Realizamos medidas em feixes de luz proveniente de um LASER polarizado, um LASER polarizado passando por um defasador quarto de onda a ± 45° (polarização circular), um LED despolarizado e, esse mesmo LED, com sua luz refletida sobre uma placa de vidro em diversos ângulos e inclusive no ângulo de Brewster. A montagem experimental é composta de um defasador quarto de onda, um polarizador linear e um detector de luz. Os resultados obtidos apresentaram um desvio de aproximadamente 1% em relação à polarização conhecida das fontes de luz. Desta maneira, foi possível constatar que a técnica de Elipsometria de Emissão pode ser aplicada para se determinar a polarização da luz proveniente de fontes luminosas em geral.
- Open Access
- 29 January 2021
- Published by MDPI AG in Applied Sciences
- Vol. 11 (3) , 1234
Fast and Low-Cost Synthesis of MoS2 Nanostructures on Paper Substrates for Near-Infrared Photodetectors
Recent advances in the production and development of two-dimensional transition metal dichalcogenides (2D TMDs) allow applications of these materials, with a structure similar to that of graphene, in a series of devices as promising technologies for optoelectronic applications. In this work, molybdenum disulfide (MoS2) nanostructures were grown directly on paper substrates through a microwave-assisted hydrothermal synthesis. The synthesized samples were subjected to morphological, structural, and optical analysis, using techniques such as scanning electron microscopy (SEM), X-ray diffraction (XRD), and Raman. The variation of synthesis parameters, as temperature and synthesis time, allowed the manipulation of these nanostructures during the growth process, with alteration of the metallic (1T) and semiconductor (2H) phases. By using this synthesis method, two-dimensional MoS2 nanostructures were directly grown on paper substrates. The MoS2 nanostructures were used as the active layer, to produce low-cost near-infrared photodetectors. The set of results indicates that the interdigital MoS2 photodetector with the best characteristics (responsivity of 290 mA/W, detectivity of 1.8 × 109 Jones and external quantum efficiency of 37%) was obtained using photoactive MoS2 nanosheets synthesized at 200 °C for 120 min.
- 29 January 2021
- Published by MDPI AG in Applied Sciences
- Vol. 11 (3) , 1234
Open AccessFast and Low-Cost Synthesis of MoS2 Nanostructures on Paper Substrates for Near-Infrared Photodetectors
Recent advances in the production and development of two-dimensional transition metal dichalcogenides (2D TMDs) allow applications of these materials, with a structure similar to that of graphene, in a series of devices as promising technologies for optoelectronic applications. In this work, molybdenum disulfide (MoS2) nanostructures were grown directly on paper substrates through a microwave-assisted hydrothermal synthesis. The synthesized samples were subjected to morphological, structural, and optical analysis, using techniques such as scanning electron microscopy (SEM), X-ray diffraction (XRD), and Raman. The variation of synthesis parameters, as temperature and synthesis time, allowed the manipulation of these nanostructures during the growth process, with alteration of the metallic (1T) and semiconductor (2H) phases. By using this synthesis method, two-dimensional MoS2 nanostructures were directly grown on paper substrates. The MoS2 nanostructures were used as the active layer, to produce low-cost near-infrared photodetectors. The set of results indicates that the interdigital MoS2 photodetector with the best characteristics (responsivity of 290 mA/W, detectivity of 1.8 × 109 Jones and external quantum efficiency of 37%) was obtained using photoactive MoS2 nanosheets synthesized at 200 °C for 120 min.
- 16 July 2020
- Published by AIP Publishing in Journal of Applied Physics
- Vol. 128 (3) , 035502
Luminescent down-shifting film based on optimized mixture of organic dyes for improving the performance of P3HT:PC61BM photovoltaic devices
During the last few years, great interest has been given to research in organic solar cells. Apart from the low cost techniques needed for the production of the active layers, the plasticity of these types of materials offers an additional benefit compared to traditional silicon-based solar cells. However, the commercialization of organic photovoltaic technologies is limited by rapid degradation and low efficiency. Recently, the use of luminescent down-shifting (LDS) films has been explored as a tool for increasing the external quantum efficiency of organic-based devices. A previously observed superposition in the emission–absorption spectra of Kremer blue (Kb) and Coumarin 7 (C7) dyes suggests that an energy transfer process can take place among these molecules. Decay time photoluminescence measurements in samples were carried out to confirm a Föster resonance energy transfer process. An optimization process following the design of experiments methodology was carried out to adjust the optical properties of films for applications in the : organic photovoltaic device. An increment of 18.6% in the short circuit current density ( ) of : devices coated with a LDS film was observed. A degradation test shows a rapid drop in the electric current density of devices without the LDS film, which we attribute to the so-called burn-in, widely reported in the literature. For devices coated with the LDS film, no rapid drop in the electric current density was observed, suggesting that the use of the luminescent layer mitigates the photoinduced burn-in loss.- 16 July 2020
- Published by AIP Publishing in Journal of Applied Physics
- Vol. 128 (3) , 035502
Luminescent down-shifting film based on optimized mixture of organic dyes for improving the performance of P3HT:PC61BM photovoltaic devices
During the last few years, great interest has been given to research in organic solar cells. Apart from the low cost techniques needed for the production of the active layers, the plasticity of these types of materials offers an additional benefit compared to traditional silicon-based solar cells. However, the commercialization of organic photovoltaic technologies is limited by rapid degradation and low efficiency. Recently, the use of luminescent down-shifting (LDS) films has been explored as a tool for increasing the external quantum efficiency of organic-based devices. A previously observed superposition in the emission–absorption spectra of Kremer blue (Kb) and Coumarin 7 (C7) dyes suggests that an energy transfer process can take place among these molecules. Decay time photoluminescence measurements in samples were carried out to confirm a Föster resonance energy transfer process. An optimization process following the design of experiments methodology was carried out to adjust the optical properties of films for applications in the : organic photovoltaic device. An increment of 18.6% in the short circuit current density ( ) of : devices coated with a LDS film was observed. A degradation test shows a rapid drop in the electric current density of devices without the LDS film, which we attribute to the so-called burn-in, widely reported in the literature. For devices coated with the LDS film, no rapid drop in the electric current density was observed, suggesting that the use of the luminescent layer mitigates the photoinduced burn-in loss.- 22 January 2019
- Published by Wiley in Journal of Polymer Science Part B: Polymer Physics
- Vol. 57 (6) , 304-311
Magnetic properties of a polyfluorene derivative containing complexed neodymium ions
- 22 January 2019
- Published by Wiley in Journal of Polymer Science Part B: Polymer Physics
- Vol. 57 (6) , 304-311
Magnetic properties of a polyfluorene derivative containing complexed neodymium ions
- 1 July 2018
- Published by Elsevier in Journal of Luminescence
- Vol. 199, 348-351
Effect of pressure on the remixing process in CH3NH3Pb(I1-xBrx)3 perovskite thin films
- 1 July 2018
- Published by Elsevier in Journal of Luminescence
- Vol. 199, 348-351
Effect of pressure on the remixing process in CH3NH3Pb(I1-xBrx)3 perovskite thin films
- 30 November 2016
- Published by IOP Publishing in Journal of Physics D: Applied Physics
- Vol. 50 (2) , 025103
Development of multidye UV filters for OPVs using luminescent materials
Luminescence down-shifting (LDS) is used in several photovoltaic technologies aiming to improve the photon conversion efficiency (PCE) of the devices through the increase of the light harvesting in the regions of the electromagnetic spectrum where the EQE of the solar cells is poor. The aim of this work was to produce films of mixtures (blends) of two luminescent materials, dispersed in a poly-methyl methacrylate (PMMA) matrix, hoping to improve their properties both as LDS layer and as UV filter when applied on the clear, external surface of P3HT:PC 61 BM photovoltaic devices. The best results led to an increment of 7.4% in the PCE of the devices, and a six fold enhancement in their half-life ( T 50% ). This study indicates that multidye LDS layers with optimized optical properties can lead to an effective improvement in the performance and operational stability of OPVs.
- 30 November 2016
- Published by IOP Publishing in Journal of Physics D: Applied Physics
- Vol. 50 (2) , 025103
Development of multidye UV filters for OPVs using luminescent materials
Luminescence down-shifting (LDS) is used in several photovoltaic technologies aiming to improve the photon conversion efficiency (PCE) of the devices through the increase of the light harvesting in the regions of the electromagnetic spectrum where the EQE of the solar cells is poor. The aim of this work was to produce films of mixtures (blends) of two luminescent materials, dispersed in a poly-methyl methacrylate (PMMA) matrix, hoping to improve their properties both as LDS layer and as UV filter when applied on the clear, external surface of P3HT:PC 61 BM photovoltaic devices. The best results led to an increment of 7.4% in the PCE of the devices, and a six fold enhancement in their half-life ( T 50% ). This study indicates that multidye LDS layers with optimized optical properties can lead to an effective improvement in the performance and operational stability of OPVs.