TY - JOUR
T1 - Two-Dimensional Plasmonic Super lattice Based on Au Nanoparticles Self-Assembling onto a Functionalized Substrate
AU - Corricelli, Michela
AU - Depalo, Nicoletta
AU - Fanizza, Elisabetta
AU - Altamura, Davide
AU - Giannini, Cinzia
AU - Siliqi, Dritan
AU - Di Mundo, Rosa
AU - Palumbo, Fabio
AU - Kravets, Vasily G
AU - Grigorenko, Alexander N
AU - Agostiano, Angela
AU - Striccoli, Marinella
AU - Curri, M Lucia
N1 - Times Cited: 2
PY - 2014
Y1 - 2014
N2 - Au nanoparticles (NPs) self-assembled by means of a simple solvent evaporation strategy in a two-dimensional (2D) superlattice with a highly controlled geometry and extending over micrometers squared when drop cast onto a suitably functionalized silicon substrate. The assembly procedure was defined by carefully monitoring experimental parameters, namely, dispersing solvent, deposition temperature, Au NP concentration, and chemistry of supporting substrate. The investigated parameters were demonstrated to play a significant role on the delicate energetic balance of the mutual NPs as well as NP-substrate interactions, ultimately directing the NP assembly. Remarkably, substrate surface chemistry revealed to be decisive to control the extent of the organization. Scanning electron microscopy demonstrated that the 2D superlattice extends uniformly over hundreds of square micrometers. Grazing-incidence small-angle X-ray scattering investigation validated the Au NP organization in crystalline domains and confirmed the role played by the surface chemistry of the substrate onto the 2D lattice assembly. Finally, preliminary spectroscopic ellipsometry investigation allowed extraction of optical constants of NP assemblies. The localized surface plasmon resonance modes of the NP assemblies were studied through a combined analysis of reflection, transmission, and ellipsometric data that demonstrated that the plasmonic properties of the Au NP assemblies strongly depend on the substrate, which was found to influence NP ordering and near-field interactions between NPs.
AB - Au nanoparticles (NPs) self-assembled by means of a simple solvent evaporation strategy in a two-dimensional (2D) superlattice with a highly controlled geometry and extending over micrometers squared when drop cast onto a suitably functionalized silicon substrate. The assembly procedure was defined by carefully monitoring experimental parameters, namely, dispersing solvent, deposition temperature, Au NP concentration, and chemistry of supporting substrate. The investigated parameters were demonstrated to play a significant role on the delicate energetic balance of the mutual NPs as well as NP-substrate interactions, ultimately directing the NP assembly. Remarkably, substrate surface chemistry revealed to be decisive to control the extent of the organization. Scanning electron microscopy demonstrated that the 2D superlattice extends uniformly over hundreds of square micrometers. Grazing-incidence small-angle X-ray scattering investigation validated the Au NP organization in crystalline domains and confirmed the role played by the surface chemistry of the substrate onto the 2D lattice assembly. Finally, preliminary spectroscopic ellipsometry investigation allowed extraction of optical constants of NP assemblies. The localized surface plasmon resonance modes of the NP assemblies were studied through a combined analysis of reflection, transmission, and ellipsometric data that demonstrated that the plasmonic properties of the Au NP assemblies strongly depend on the substrate, which was found to influence NP ordering and near-field interactions between NPs.
U2 - 10.1021/jp4126792
DO - 10.1021/jp4126792
M3 - Article
SN - 1932-7455
VL - 118
SP - 7579
EP - 7590
JO - Journal of Physical Chemistry C
JF - Journal of Physical Chemistry C
IS - 14
ER -