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Kinetics of photoinduced changes in Ag nanoparticles deposited on an indium tin oxide surface

Identifieur interne : 009A50 ( Main/Repository ); précédent : 009A49; suivant : 009A51

Kinetics of photoinduced changes in Ag nanoparticles deposited on an indium tin oxide surface

Auteurs : RBID : Pascal:06-0050942

Descripteurs français

Pascal (Inist)
- Cinétique, Spectre absorption, Spectre UV, Spectre visible, Conductivité superficielle, Densité optique, Champ local, Champ superficiel, Polariton surface, Plasmon, Etat excité, Phonon, Surstructure, Argent, Nanoparticule, Indium oxyde, Etain oxyde, Aluminium oxyde, Grenat aluminium yttrium, Yttrium oxyde, 6780.
Wicri :
- concept : Argent.

English descriptors

KwdEn :
- Absorption spectra, Aluminium oxides, Excited states, Indium oxides, Kinetics, Local field, Nanoparticles, Optical density, Phonons, Plasmons, Silver, Superstructure, Surface conductivity, Surface field, Surface polaritons, Tin oxides, Ultraviolet spectra, Visible spectra, YAG, Yttrium oxides.

Abstract

An enhancement of the UV-visible optical absorption spectra of Ag nanoparticles (NPs) deposited on indium tin oxide (ITO) surfaces of different resistance by a seed-mediated growth technique is presented. A bicolour coherent beam, obtained from a pulsed Nd:YAG laser providing a 1060-nm fundamental wavelength and a double-frequency one at 530 nm, was used. A significant change in the optical density is observed for Ag NPs on low-resistance ITO surfaces (4 Ω/square), while almost nothing occurs with high-resistance (50 Ω/square surfaces). The spectral position of the maximal absorption at 440 nm is almost preserved in both cases. This result is explained in terms at a local photoinduced static field and surface-plasmon polaritons interacting with photoexcited phonons. A grating effect, arising from the coherent bicolour light forming a superstructure as for quantum crystals, could be another contribution.

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Pascal:06-0050942

Le document en format XML

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<author><name sortKey="Kityk, I V" uniqKey="Kityk I">I. V. Kityk</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Institute of Physics, J. Dlugosz University of Czestochowa, Al. Armii Krajowej 13/15</s1>
<s2>42-217 Czestochowa</s2>
<s3>POL</s3>
<sZ>1 aut.</sZ>
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<country>Pologne</country>
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<author><name sortKey="Ebothe, J" uniqKey="Ebothe J">J. Ebothe</name>
<affiliation wicri:level="3"><inist:fA14 i1="02"><s1>Laboratoire de Microscopies and d'Etude de Nanostructures, Université de Reims, Equipe d'Accueil N3799 BP138, 21 rue Clément Ader</s1>
<s2>51685 Reims</s2>
<s3>FRA</s3>
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<country>France</country>
<placeName><region type="region" nuts="2">Champagne-Ardenne</region>
<settlement type="city">Reims</settlement>
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<author><name sortKey="Chang, G" uniqKey="Chang G">G. Chang</name>
<affiliation wicri:level="1"><inist:fA14 i1="03"><s1>International Innovation Center, Kyoto University</s1>
<s2>Sakyo-ku, Kyoto 606-8501</s2>
<s3>JPN</s3>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
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<country>Japon</country>
<wicri:noRegion>Sakyo-ku, Kyoto 606-8501</wicri:noRegion>
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<author><name sortKey="Oyama, M" uniqKey="Oyama M">M. Oyama</name>
<affiliation wicri:level="1"><inist:fA14 i1="03"><s1>International Innovation Center, Kyoto University</s1>
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<sZ>3 aut.</sZ>
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<country>Japon</country>
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<seriesStmt><idno type="ISSN">0950-0839</idno>
<title level="j" type="abbreviated">Philos. mag. lett.</title>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Absorption spectra</term>
<term>Aluminium oxides</term>
<term>Excited states</term>
<term>Indium oxides</term>
<term>Kinetics</term>
<term>Local field</term>
<term>Nanoparticles</term>
<term>Optical density</term>
<term>Phonons</term>
<term>Plasmons</term>
<term>Silver</term>
<term>Superstructure</term>
<term>Surface conductivity</term>
<term>Surface field</term>
<term>Surface polaritons</term>
<term>Tin oxides</term>
<term>Ultraviolet spectra</term>
<term>Visible spectra</term>
<term>YAG</term>
<term>Yttrium oxides</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Cinétique</term>
<term>Spectre absorption</term>
<term>Spectre UV</term>
<term>Spectre visible</term>
<term>Conductivité superficielle</term>
<term>Densité optique</term>
<term>Champ local</term>
<term>Champ superficiel</term>
<term>Polariton surface</term>
<term>Plasmon</term>
<term>Etat excité</term>
<term>Phonon</term>
<term>Surstructure</term>
<term>Argent</term>
<term>Nanoparticule</term>
<term>Indium oxyde</term>
<term>Etain oxyde</term>
<term>Aluminium oxyde</term>
<term>Grenat aluminium yttrium</term>
<term>Yttrium oxyde</term>
<term>6780</term>
</keywords>
<keywords scheme="Wicri" type="concept" xml:lang="fr"><term>Argent</term>
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<front><div type="abstract" xml:lang="en">An enhancement of the UV-visible optical absorption spectra of Ag nanoparticles (NPs) deposited on indium tin oxide (ITO) surfaces of different resistance by a seed-mediated growth technique is presented. A bicolour coherent beam, obtained from a pulsed Nd:YAG laser providing a 1060-nm fundamental wavelength and a double-frequency one at 530 nm, was used. A significant change in the optical density is observed for Ag NPs on low-resistance ITO surfaces (4 Ω/square), while almost nothing occurs with high-resistance (50 Ω/square surfaces). The spectral position of the maximal absorption at 440 nm is almost preserved in both cases. This result is explained in terms at a local photoinduced static field and surface-plasmon polaritons interacting with photoexcited phonons. A grating effect, arising from the coherent bicolour light forming a superstructure as for quantum crystals, could be another contribution.</div>
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<fA08 i1="01" i2="1" l="ENG"><s1>Kinetics of photoinduced changes in Ag nanoparticles deposited on an indium tin oxide surface</s1>
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<fA14 i1="01"><s1>Institute of Physics, J. Dlugosz University of Czestochowa, Al. Armii Krajowej 13/15</s1>
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<s3>POL</s3>
<sZ>1 aut.</sZ>
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<fA14 i1="02"><s1>Laboratoire de Microscopies and d'Etude de Nanostructures, Université de Reims, Equipe d'Accueil N3799 BP138, 21 rue Clément Ader</s1>
<s2>51685 Reims</s2>
<s3>FRA</s3>
<sZ>2 aut.</sZ>
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<fA14 i1="03"><s1>International Innovation Center, Kyoto University</s1>
<s2>Sakyo-ku, Kyoto 606-8501</s2>
<s3>JPN</s3>
<sZ>3 aut.</sZ>
<sZ>4 aut.</sZ>
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<fC01 i1="01" l="ENG"><s0>An enhancement of the UV-visible optical absorption spectra of Ag nanoparticles (NPs) deposited on indium tin oxide (ITO) surfaces of different resistance by a seed-mediated growth technique is presented. A bicolour coherent beam, obtained from a pulsed Nd:YAG laser providing a 1060-nm fundamental wavelength and a double-frequency one at 530 nm, was used. A significant change in the optical density is observed for Ag NPs on low-resistance ITO surfaces (4 Ω/square), while almost nothing occurs with high-resistance (50 Ω/square surfaces). The spectral position of the maximal absorption at 440 nm is almost preserved in both cases. This result is explained in terms at a local photoinduced static field and surface-plasmon polaritons interacting with photoexcited phonons. A grating effect, arising from the coherent bicolour light forming a superstructure as for quantum crystals, could be another contribution.</s0>
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<s5>08</s5>
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<s5>11</s5>
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<s5>11</s5>
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<s5>14</s5>
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<s5>18</s5>
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<s5>18</s5>
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<s2>NK</s2>
<s5>21</s5>
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<s2>NK</s2>
<s5>21</s5>
</fC03>
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Kinetics of photoinduced changes in Ag nanoparticles deposited on an indium tin oxide surface

Kinetics of photoinduced changes in Ag nanoparticles deposited on an indium tin oxide surface

Descripteurs français

English descriptors

Abstract

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri