Active Modulation of Er3+ Emission Lifetime by VO2 Phase‐Change Thin Films

The active modulation of optical response of quantum emitters at the nanoscale is of paramount importance to realize tunable light sources for nanophotonic devices. Herein, a thin film of phase‐change material (VO2) is coupled to a 20 nm‐thick silica layer embedding Er3+ ions, and it is demonstrated...

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Published in:Advanced Photonics Research
Main Authors: Boris Kalinic, Tiziana Cesca, Alessandro Lovo, Carlo Scian, Roberto Macaluso, Fabio Bovino, Roberto Li Voti, Concita Sibilia, Giovanni Mattei
Format: Article
Language:English
Published: Wiley-VCH 2024-02-01
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Online Access:https://doi.org/10.1002/adpr.202300242
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author Boris Kalinic
Tiziana Cesca
Alessandro Lovo
Carlo Scian
Roberto Macaluso
Fabio Bovino
Roberto Li Voti
Concita Sibilia
Giovanni Mattei
author_facet Boris Kalinic
Tiziana Cesca
Alessandro Lovo
Carlo Scian
Roberto Macaluso
Fabio Bovino
Roberto Li Voti
Concita Sibilia
Giovanni Mattei
author_sort Boris Kalinic
collection DOAJ
container_title Advanced Photonics Research
description The active modulation of optical response of quantum emitters at the nanoscale is of paramount importance to realize tunable light sources for nanophotonic devices. Herein, a thin film of phase‐change material (VO2) is coupled to a 20 nm‐thick silica layer embedding Er3+ ions, and it is demonstrated how the active tuning of the local density of optical states near the erbium emitters provided by the thermally induced semiconductor‐to‐metal transition of VO2 can be used to dynamically control the Er3+ emission lifetime at telecom wavelength (1.54 μm). A decay rate contrast of a factor 2 is obtained between high temperature (90 °C), when VO2 is metallic, and room temperature, when VO2 is semiconductor, in agreement with calculations performed with the classical dipole oscillator analytical model. A hysteretic behavior is observed by measuring the Er3+ lifetime as a function of the temperature, whose parameters are consistent with those of grazing incidence X‐ray diffraction and optical transmittance measurements. The fractions of Er3+ ions that couple with VO2 in each phase at the different temperatures are determined by the analysis of the temporal decays. The results make the investigated system an optimal candidate for the development of tunable photon sources at telecom wavelength.
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spelling doaj-art-50d12f7dfd304ee5a239bcc3cbbe077f2025-08-20T00:49:06ZengWiley-VCHAdvanced Photonics Research2699-92932024-02-0152n/an/a10.1002/adpr.202300242Active Modulation of Er3+ Emission Lifetime by VO2 Phase‐Change Thin FilmsBoris Kalinic0Tiziana Cesca1Alessandro Lovo2Carlo Scian3Roberto Macaluso4Fabio Bovino5Roberto Li Voti6Concita Sibilia7Giovanni Mattei8Department of Physics and Astronomy NanoStructures Group University of Padova via Marzolo 8 I-35131 Padova ItalyDepartment of Physics and Astronomy NanoStructures Group University of Padova via Marzolo 8 I-35131 Padova ItalyDepartment of Physics and Astronomy NanoStructures Group University of Padova via Marzolo 8 I-35131 Padova ItalyDepartment of Physics and Astronomy NanoStructures Group University of Padova via Marzolo 8 I-35131 Padova ItalyDepartment of Engineering University of Palermo viale delle Scienze I-90128 Palermo ItalyDepartment SBAI Sapienza University of Roma via A. Scarpa 14 I-00161 Roma ItalyDepartment SBAI Sapienza University of Roma via A. Scarpa 14 I-00161 Roma ItalyDepartment SBAI Sapienza University of Roma via A. Scarpa 14 I-00161 Roma ItalyDepartment of Physics and Astronomy NanoStructures Group University of Padova via Marzolo 8 I-35131 Padova ItalyThe active modulation of optical response of quantum emitters at the nanoscale is of paramount importance to realize tunable light sources for nanophotonic devices. Herein, a thin film of phase‐change material (VO2) is coupled to a 20 nm‐thick silica layer embedding Er3+ ions, and it is demonstrated how the active tuning of the local density of optical states near the erbium emitters provided by the thermally induced semiconductor‐to‐metal transition of VO2 can be used to dynamically control the Er3+ emission lifetime at telecom wavelength (1.54 μm). A decay rate contrast of a factor 2 is obtained between high temperature (90 °C), when VO2 is metallic, and room temperature, when VO2 is semiconductor, in agreement with calculations performed with the classical dipole oscillator analytical model. A hysteretic behavior is observed by measuring the Er3+ lifetime as a function of the temperature, whose parameters are consistent with those of grazing incidence X‐ray diffraction and optical transmittance measurements. The fractions of Er3+ ions that couple with VO2 in each phase at the different temperatures are determined by the analysis of the temporal decays. The results make the investigated system an optimal candidate for the development of tunable photon sources at telecom wavelength.https://doi.org/10.1002/adpr.202300242decay rate controlerbium emissionphase-change materialssemiconductor-to-metal transitionvanadium dioxide
spellingShingle Boris Kalinic
Tiziana Cesca
Alessandro Lovo
Carlo Scian
Roberto Macaluso
Fabio Bovino
Roberto Li Voti
Concita Sibilia
Giovanni Mattei
Active Modulation of Er3+ Emission Lifetime by VO2 Phase‐Change Thin Films
decay rate control
erbium emission
phase-change materials
semiconductor-to-metal transition
vanadium dioxide
title Active Modulation of Er3+ Emission Lifetime by VO2 Phase‐Change Thin Films
title_full Active Modulation of Er3+ Emission Lifetime by VO2 Phase‐Change Thin Films
title_fullStr Active Modulation of Er3+ Emission Lifetime by VO2 Phase‐Change Thin Films
title_full_unstemmed Active Modulation of Er3+ Emission Lifetime by VO2 Phase‐Change Thin Films
title_short Active Modulation of Er3+ Emission Lifetime by VO2 Phase‐Change Thin Films
title_sort active modulation of er3 emission lifetime by vo2 phase change thin films
topic decay rate control
erbium emission
phase-change materials
semiconductor-to-metal transition
vanadium dioxide
url https://doi.org/10.1002/adpr.202300242
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