| Autor: |
Morozov, Yevhenii M., Gisbert Quilis, Nestor, Fossati, Stefan, De Laporte, Laura, Gusenbauer, Claudia, Weber, Andreas, Toca-Herrera, Jose Luis, Wiesner, Fiona, Jonas, Ulrich, Dostalek, Jakub |
| Zdroj: |
The Journal of Physical Chemistry - Part C; October 2024, Vol. 128 Issue: 43 p18641-18650, 10p |
| Abstrakt: |
A novel approach to selectively modify narrow subareas of metallic nanostructures adjacent to plasmonic hotspots, where strong electromagnetic field amplification occurs upon localized surface plasmon (LSP) excitation, is reported. In contrast to surface plasmon-triggered polymerization, it relies on plasmonically enhanced multiphoton crosslinking (MPC) of polymer chains carrying photoactive moieties. When they are contacted with metallic nanostructures and irradiated with a femtosecond near-infrared beam resonantly coupled with LSPs, the enhanced field intensity locally exceeds the threshold and initiates MPC only at plasmonic hotspots. This concept is demonstrated by using gold nanoparticle arrays coated with two specifically designed polymers. Local MPC of a poly(N,N-dimethylacrylamide)-based copolymer with an anthraquinone crosslinker is shown via atomic force microscopy. Additionally, MPC is tested with a thermoresponsive poly(N-isopropylacrylamide)-based terpolymer. The reversible thermally induced collapse and swelling of the MPC-formed hydrogel at specific nanoparticle locations are confirmed by polarization-resolved localized surface plasmon resonance (LSPR) spectroscopy. These hybrid metallic/hydrogel materials can be further postmodified, offering attractive characteristics for future spectroscopic/bioanalytical applications. |
| Databáze: |
Supplemental Index |
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