TY - JOUR
T1 - Plasmon-Enhanced Multiphoton Polymer Crosslinking for Selective Modification of Plasmonic Hotspots
AU - Morozov, Yevhenii M.
AU - Quilis, Nestor Gisbert
AU - Fossati, Stefan
AU - De Laporte, Laura
AU - Gusenbauer, Claudia
AU - Weber, Andreas
AU - Toca-Herrera, Jose Luis
AU - Wiesner, Fiona
AU - Jonas, Ulrich
AU - Dostalek, Jakub
N1 - © 2024 The Authors. Published by American Chemical Society.
PY - 2024/10/22
Y1 - 2024/10/22
N2 - 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.
AB - 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.
KW - plasmonic nanostructures
KW - plasmonic hotspot
KW - poly(N-isopropylacrylamide)
KW - thermoresponsive hydrogels
KW - multiphoton chemistry
KW - plasmonic enhancement
KW - selective modification
KW - addressable hotspots
KW - Binding
KW - Nanostructures
KW - Sensitivity
KW - Microfabrication
KW - Resonance
KW - Sensors
KW - Biosensors
UR - https://doi.org/10.1021/acs.jpcc.4c05936
UR - https://www.mendeley.com/catalogue/1d181be2-76cf-33b7-90b6-6929d90243bc/
U2 - 10.1021/acs.jpcc.4c05936
DO - 10.1021/acs.jpcc.4c05936
M3 - Article
C2 - 39502799
SN - 1932-7447
VL - 128
SP - 18641
EP - 18650
JO - The Journal of Physical Chemistry C
JF - The Journal of Physical Chemistry C
IS - 43
ER -