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Resonant secondary light emission from plasmonic Au nanostructures at high electron temperatures created by pulsed-laser excitation.

ABSTRACT: Plasmonic nanostructures are of great current interest as chemical sensors, in vivo imaging agents, and for photothermal therapeutics. We study continuous-wave (cw) and pulsed-laser excitation of aqueous suspensions of Au nanorods as a model system for secondary light emission from plasmonic nanostructures. Resonant secondary emission contributes significantly to the background commonly observed in surface-enhanced Raman scattering and to the light emission generated by pulsed-laser excitation of metallic nanostructures that is often attributed to two-photon luminescence. Spectra collected using cw laser excitation at 488 nm show an enhancement of the broad spectrum of emission at the electromagnetic plasmon resonance of the nanorods. The intensity of anti-Stokes emission collected using cw laser excitation at 785 nm is described by a 300 K thermal distribution of excitations. Excitation by subpicosecond laser pulses at 785 nm broadens and increases the intensity of the anti-Stokes emission in a manner that is consistent with electronic Raman scattering by a high-temperature distribution of electronic excitations predicted by a two-temperature model. Broadening of the pulse duration using an etalon reduces the intensity of anti-Stokes emission in quantitative agreement with the model. Experiments using a pair of subpicosecond optical pulses separated by a variable delay show that the timescale of resonant secondary emission is comparable to the timescale for equilibration of electrons and phonons.

SUBMITTER: Huang J

PROVIDER: S-EPMC3903255 | biostudies-literature | 2014 Jan

REPOSITORIES: biostudies-literature

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Resonant secondary light emission from plasmonic Au nanostructures at high electron temperatures created by pulsed-laser excitation.

Huang Jingyu J Wang Wei W Murphy Catherine J CJ Cahill David G DG

Proceedings of the National Academy of Sciences of the United States of America 20140106 3

Plasmonic nanostructures are of great current interest as chemical sensors, in vivo imaging agents, and for photothermal therapeutics. We study continuous-wave (cw) and pulsed-laser excitation of aqueous suspensions of Au nanorods as a model system for secondary light emission from plasmonic nanostructures. Resonant secondary emission contributes significantly to the background commonly observed in surface-enhanced Raman scattering and to the light emission generated by pulsed-laser excitation o ...[more]

PMID: 24395798

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Project description:Integration of plasmonic nanoantennas with catalytically active reactors in deliberately designed hybrid supra-nanostructures creates a dual-functional materials platform, based upon which precise modulation of catalytic reaction kinetics becomes accomplishable through optical excitations of plasmon resonances. Here, we have developed a multistep synthetic approach that enables us to assemble colloidal Au@C/Pt core@shell/satellite supra-nanostructures, in which the Au core functions as a light-harvesting plasmonic nanoantenna, the Pt satellites act as catalytically active reactors, and the C shell serves as a nanoscale dielectric spacer separating the reactors from the antenna, respectively. By adjusting several synthetic parameters, the size of the Au core, the thickness of the C shell, and the surface coverage of Pt satellites can all be tuned independently. Choosing Pt-catalyzed cascade oxidation of 3,3',5,5'-tetramethylbenzidine in an aerobic aqueous environment as a model reaction, we have systematically studied the detailed kinetic features of the catalytic reactions both in the dark and under visible light illumination over a broad range of reaction conditions, which sheds light on the interplay between plasmonic and catalytic effects in these antenna-reactor nanohybrids. The plasmonic antenna effect can be effectively harnessed to kinetically modulate multiple crucial steps during the cascade reactions, benefiting from plasmon-enhanced interband electronic transitions in the Pt satellites and plasmon-enhanced intramolecular electronic excitations in chromogenic intermediate species. In addition to the plasmonic antenna effect, photothermal transduction derived from plasmonic excitations can also provide significant contributions to the kinetic enhancements under visible light illumination. The knowledge gained from this work serves as important guiding principles for rational design and structural optimization of plasmonic antenna-reactor hybrid nanomaterials, endowing us with enhanced capabilities to kinetically modulate targeted catalytic/photocatalytic molecule-transforming processes through light illumination.

Dataset Information

Resonant secondary light emission from plasmonic Au nanostructures at high electron temperatures created by pulsed-laser excitation.

Publications

Resonant secondary light emission from plasmonic Au nanostructures at high electron temperatures created by pulsed-laser excitation.

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