Details
| Original language | English |
|---|---|
| Pages (from-to) | 400-408 |
| Number of pages | 9 |
| Journal | Journal of materials science |
| Volume | 46 |
| Publication status | Published - 3 Sept 2010 |
| Externally published | Yes |
Abstract
Recent interest in photolithographic processes employing single and two-photon absorption processes have afforded advanced opportunities to fabricate both planar and three-dimensional microstructures. The fabrication of such structures is dependent on the local polymerization of the organic moieties using photoinitiating molecules, and a key parameter to consider is the dependency of the photoreactivity of these initiators on the matrices in which they are dispersed. To our knowledge, there has been no comprehensive investigation reported on the photoreactivity dependency of commercially available photoinitiators inserted within hybrid sol-gel materials. The aim of this paper is to highlight and explain the influence of the composition of hybrid organic-inorganic sol-gel materials on the photoreactivity of UV-sensitive initiators. Of particular interest is the understanding of the interactions between photoinitiating molecules and the sol-gel matrix. It is shown that both the nature of the chelating agent as well as the degree of chelation of the inorganic part of the hybrid sol-gel material significantly influence the spectral absorption of the photoinitiator. It is demonstrated that metal-ligand charge transfer processes are the main phenomena responsible for the red shift of the absorption of the amino-functionalized photoinitiators, which is strongly dependent on the condensation of the materials.
ASJC Scopus subject areas
- Materials Science(all)
- General Materials Science
- Engineering(all)
- Mechanics of Materials
- Engineering(all)
- Mechanical Engineering
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In: Journal of materials science, Vol. 46, 03.09.2010, p. 400-408.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Influence of hybrid organic-inorganic sol-gel matrices on the photophysics of amino-functionalized UV-sensitizers
AU - Oubaha, M.
AU - Copperwhite, R.
AU - Boothman, C.
AU - Ovsianikov, A.
AU - Kiyan, R.
AU - Purlys, V.
AU - O'Sullivan, M.
AU - McDonagh, C.
AU - Chichkov, B.
AU - Gadonas, R.
AU - MacCraith, B. D.
N1 - Funding information: The authors wish to thank CIBA Specialty Chemicals Corporation for having generously provided the Irgacures photoinitiators employed in this study, and gratefully acknowledge the financial support of Enterprise Ireland under the ‘‘Commercialisation Fund Technology Development’’ project Multibiosense (TD/08/309). This study was also supported by the DFG Excellence Cluster ‘Rebirth’ and SFB Transregio 37, and ERASPOT. Authors would also like to thank the LaserLab initiative.
PY - 2010/9/3
Y1 - 2010/9/3
N2 - Recent interest in photolithographic processes employing single and two-photon absorption processes have afforded advanced opportunities to fabricate both planar and three-dimensional microstructures. The fabrication of such structures is dependent on the local polymerization of the organic moieties using photoinitiating molecules, and a key parameter to consider is the dependency of the photoreactivity of these initiators on the matrices in which they are dispersed. To our knowledge, there has been no comprehensive investigation reported on the photoreactivity dependency of commercially available photoinitiators inserted within hybrid sol-gel materials. The aim of this paper is to highlight and explain the influence of the composition of hybrid organic-inorganic sol-gel materials on the photoreactivity of UV-sensitive initiators. Of particular interest is the understanding of the interactions between photoinitiating molecules and the sol-gel matrix. It is shown that both the nature of the chelating agent as well as the degree of chelation of the inorganic part of the hybrid sol-gel material significantly influence the spectral absorption of the photoinitiator. It is demonstrated that metal-ligand charge transfer processes are the main phenomena responsible for the red shift of the absorption of the amino-functionalized photoinitiators, which is strongly dependent on the condensation of the materials.
AB - Recent interest in photolithographic processes employing single and two-photon absorption processes have afforded advanced opportunities to fabricate both planar and three-dimensional microstructures. The fabrication of such structures is dependent on the local polymerization of the organic moieties using photoinitiating molecules, and a key parameter to consider is the dependency of the photoreactivity of these initiators on the matrices in which they are dispersed. To our knowledge, there has been no comprehensive investigation reported on the photoreactivity dependency of commercially available photoinitiators inserted within hybrid sol-gel materials. The aim of this paper is to highlight and explain the influence of the composition of hybrid organic-inorganic sol-gel materials on the photoreactivity of UV-sensitive initiators. Of particular interest is the understanding of the interactions between photoinitiating molecules and the sol-gel matrix. It is shown that both the nature of the chelating agent as well as the degree of chelation of the inorganic part of the hybrid sol-gel material significantly influence the spectral absorption of the photoinitiator. It is demonstrated that metal-ligand charge transfer processes are the main phenomena responsible for the red shift of the absorption of the amino-functionalized photoinitiators, which is strongly dependent on the condensation of the materials.
UR - http://www.scopus.com/inward/record.url?scp=78650755471&partnerID=8YFLogxK
U2 - 10.1007/s10853-010-4853-1
DO - 10.1007/s10853-010-4853-1
M3 - Article
AN - SCOPUS:78650755471
VL - 46
SP - 400
EP - 408
JO - Journal of materials science
JF - Journal of materials science
SN - 0022-2461
ER -