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White-Light Emission of Amine-Functionalized Organic/Inorganic Hybrids: Emitting Centers and Recombination Mechanisms

Carlos, L. D., Sá Ferreira, R. A., Pereira, R. N., Assunção, M., de Zea Bermudez, V.·2004·The Journal of Physical Chemistry B

Abstract

This work discusses the recombination mechanisms and the chemical nature of the emitting centers subjacent to the white-light emission of sol−gel derived amine-functionalized hybrids lacking metal activator ions, such as those based on 3-aminopropyl)triethoxysilane (APTES), 3-glycidyloxypropyltrimethoxysilane (GPTES), and on urea and urethane precursors. The white-light photoluminescence (PL) results from a convolution of the emission originated in the NH (NH 2 ) groups of the urea or urethane bridges (APTES- and GPTES-based hybrids) with electron−hole recombinations occurring in the siloxane nanoclusters. These two components reveal a radiative recombination mechanism typical of donor−acceptor pairs, mediated by some localized centers. Photoinduced proton-transfer between defects such as NH 3 + and NH - (GPTES- and APTES-based hybrids) or NH 2 + and N - (di-ureasils and di-urethanesils) is proposed as the mechanism responsible for the NH-related component. Electron paramagnetic resonance data suggest that the specific PL mechanism subjacent to the component associated with the siliceous nanodomains involves oxygen-related defects.

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Metadata

Authors
Carlos, L. D., Sá Ferreira, R. A., Pereira, R. N., Assunção, M., & de Zea Bermudez, V.
Venue
The Journal of Physical Chemistry B
Published
2004-09-01
Volume
108
Issue
39
Pages
14924-14932
ISSN
  • 1520-5207 (ISSN-L)
  • 1520-6106
OpenAlex
W1971316651
Cited by
233
References
1
FWCI
11.46
Type
journal article
Language
en
Open access
closed

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