Functional nanocellulose films as fluorescent media

Fluorescent nanocellulose films fabricated via 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-mediated oxidation of cellulose nanofibers were prepared using two methods. In the first process, fluorescent particles were added halfway through the last vacuum filtration step of film fabrication. Three di...

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Main Authors: Indias, Johanna Mae M, Guerrero, Raphael A, Scarpa, Marina, Bettotti, Paolo
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Published: Archīum Ateneo 2018
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Online Access:https://archium.ateneo.edu/physics-faculty-pubs/7
https://ui.adsabs.harvard.edu/abs/2018SPIE10823E..11I/abstract
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Institution: Ateneo De Manila University
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spelling ph-ateneo-arc.physics-faculty-pubs-10062020-02-26T08:34:28Z Functional nanocellulose films as fluorescent media Indias, Johanna Mae M Guerrero, Raphael A Scarpa, Marina Bettotti, Paolo Fluorescent nanocellulose films fabricated via 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-mediated oxidation of cellulose nanofibers were prepared using two methods. In the first process, fluorescent particles were added halfway through the last vacuum filtration step of film fabrication. Three different particles were used: micro-pSi, micro-pSi with COOH, and Si-COOH nanocrystals. Several optical techniques were employed to characterize resulting films: UV-Vis spectrophotometry, fluorescence spectrophotometry, scanning electron microscopy (SEM), and Fourier transform infrared (FTIR) microscopy. All techniques revealed that particles retained their intrinsic properties after deposition on the film. Photoluminescence spectra of resulting films at λexcitation = 350 nm exhibited the following fluorescence peaks: λmicro-pSi = 600 nm, λmicro-pSi with COOH = 596 nm, λSi-COOH nanocrystals = 618 nm. A blue shift of at most 20 nm was observed when comparing particle fluorescence peak emission before and after deposition on the film. The peak shift was attributed to oxidation, as the particles remained in an aqueous solution during film fabrication. Continued observation of film fluorescence spectra showed that peak emission values are maintained for a month. A second method of fluorescent film fabrication involved the immersion of a dry, transparent nanocellulose film in a chlorophyll in acetone solution. Fluorescence spectra of the resulting hybrid film were taken using a UV laser as the excitation source (λexcitation = 355 nm). The fluorescence peak was found to be λchlorophyll = 683.21 nm. Both methods of film hybridization were effective in preparing nanocellulose films that show promise as stable fluorescent media. 2018-10-01T07:00:00Z text https://archium.ateneo.edu/physics-faculty-pubs/7 https://ui.adsabs.harvard.edu/abs/2018SPIE10823E..11I/abstract Physics Faculty Publications Archīum Ateneo Optics Physics
institution Ateneo De Manila University
building Ateneo De Manila University Library
country Philippines
collection archium.Ateneo Institutional Repository
topic Optics
Physics
spellingShingle Optics
Physics
Indias, Johanna Mae M
Guerrero, Raphael A
Scarpa, Marina
Bettotti, Paolo
Functional nanocellulose films as fluorescent media
description Fluorescent nanocellulose films fabricated via 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-mediated oxidation of cellulose nanofibers were prepared using two methods. In the first process, fluorescent particles were added halfway through the last vacuum filtration step of film fabrication. Three different particles were used: micro-pSi, micro-pSi with COOH, and Si-COOH nanocrystals. Several optical techniques were employed to characterize resulting films: UV-Vis spectrophotometry, fluorescence spectrophotometry, scanning electron microscopy (SEM), and Fourier transform infrared (FTIR) microscopy. All techniques revealed that particles retained their intrinsic properties after deposition on the film. Photoluminescence spectra of resulting films at λexcitation = 350 nm exhibited the following fluorescence peaks: λmicro-pSi = 600 nm, λmicro-pSi with COOH = 596 nm, λSi-COOH nanocrystals = 618 nm. A blue shift of at most 20 nm was observed when comparing particle fluorescence peak emission before and after deposition on the film. The peak shift was attributed to oxidation, as the particles remained in an aqueous solution during film fabrication. Continued observation of film fluorescence spectra showed that peak emission values are maintained for a month. A second method of fluorescent film fabrication involved the immersion of a dry, transparent nanocellulose film in a chlorophyll in acetone solution. Fluorescence spectra of the resulting hybrid film were taken using a UV laser as the excitation source (λexcitation = 355 nm). The fluorescence peak was found to be λchlorophyll = 683.21 nm. Both methods of film hybridization were effective in preparing nanocellulose films that show promise as stable fluorescent media.
format text
author Indias, Johanna Mae M
Guerrero, Raphael A
Scarpa, Marina
Bettotti, Paolo
author_facet Indias, Johanna Mae M
Guerrero, Raphael A
Scarpa, Marina
Bettotti, Paolo
author_sort Indias, Johanna Mae M
title Functional nanocellulose films as fluorescent media
title_short Functional nanocellulose films as fluorescent media
title_full Functional nanocellulose films as fluorescent media
title_fullStr Functional nanocellulose films as fluorescent media
title_full_unstemmed Functional nanocellulose films as fluorescent media
title_sort functional nanocellulose films as fluorescent media
publisher Archīum Ateneo
publishDate 2018
url https://archium.ateneo.edu/physics-faculty-pubs/7
https://ui.adsabs.harvard.edu/abs/2018SPIE10823E..11I/abstract
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