Organically modified silicate thin film and bulk samples were prepared using [3-(2-aminoethylamino)propyl] trimethoxysilane (AEAP-TMOS) as precursor with the addition of different amounts of AEAP-TMOS functionalized C-dots, prepared by reaction of AEAP-TMOS and citric acid at high temperature. The synthesis of surface functionalized C-dots was followed by Fourier Transform Infrared (FTIR) spectroscopy, and the C-dots optical properties were characterized by optical absorption and UV–vis fluorescence. Thin xerogel films and bulk samples were studied by FTIR, Raman and fluorescence spectroscopy. Intense blue-green emission was observed by UV excitation of functionalized C-dots. Carbon quantum dot (CQD) luminescence was preserved also in the xerogel matrices, and the energy transfer from the matrix to CQDs, which is a key characteristic for scintillation detectors, was investigated in the two systems.
Highly fluorescent xerogels with entrapped carbon dots for organic scintillators
GIAROLA, Marco;Daldosso, Nicola;MARIOTTO, Gino
2014-01-01
Abstract
Organically modified silicate thin film and bulk samples were prepared using [3-(2-aminoethylamino)propyl] trimethoxysilane (AEAP-TMOS) as precursor with the addition of different amounts of AEAP-TMOS functionalized C-dots, prepared by reaction of AEAP-TMOS and citric acid at high temperature. The synthesis of surface functionalized C-dots was followed by Fourier Transform Infrared (FTIR) spectroscopy, and the C-dots optical properties were characterized by optical absorption and UV–vis fluorescence. Thin xerogel films and bulk samples were studied by FTIR, Raman and fluorescence spectroscopy. Intense blue-green emission was observed by UV excitation of functionalized C-dots. Carbon quantum dot (CQD) luminescence was preserved also in the xerogel matrices, and the energy transfer from the matrix to CQDs, which is a key characteristic for scintillation detectors, was investigated in the two systems.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.