dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorCamacho, Sabrina A.
dc.creatorAoki, Pedro H. B.
dc.creatorAssis, Francisco F. de
dc.creatorPires, Ana M.
dc.creatorOliveira, Kleber T. de
dc.creatorAroca, Ricardo F.
dc.creatorConstantino, Carlos J. L.
dc.date2015-12-07T15:34:18Z
dc.date2016-10-25T21:23:20Z
dc.date2015-12-07T15:34:18Z
dc.date2016-10-25T21:23:20Z
dc.date2015
dc.date.accessioned2017-04-06T09:29:42Z
dc.date.available2017-04-06T09:29:42Z
dc.identifierApplied Spectroscopy, v. 69, n. 4, p. 451-456, 2015.
dc.identifier1943-3530
dc.identifierhttp://hdl.handle.net/11449/131358
dc.identifierhttp://acervodigital.unesp.br/handle/11449/131358
dc.identifier10.1366/14-07625
dc.identifier25741784
dc.identifierhttp://dx.doi.org/10.1366/14-07625
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/941898
dc.descriptionThe synergistic effect produced by metallic nanoparticles when incorporated into different systems empowers a research field that is growing rapidly. In addition, organometallic materials are at the center of intensive research with diverse applications such as light-emitting devices, transistors, solar cells, and sensors. The Langmuir-Blodgett (LB) technique has proven to be suitable to address challenges inherent to organic devices, since the film properties can be tuned at the molecular level. Here we report a strategy to incorporate gold nanoparticles (AuNPs) into the LB film by co-deposition in order to achieve surface-enhanced Raman scattering (SERS) of the zinc(II)-protoporphyrin (IX) dimethyl ester (ZnPPIX-DME). Prior to the LB co-deposition, the properties of the Langmuir monolayer of ZnPPIX-DME at the air-water interface, containing AuNPs in the subphase, are studied through the surface-pressure versus mean molecular area (π-A) isotherms. The ZnPPIX-DME+AuNPs π-A isotherm presented a significant shift to higher molecular area, suggesting an interaction between both ZnPPIX-DME molecules and AuNPs. Those interactions are a key factor allowing the co-deposition of both AuNPs and ZnPPIX-DME molecules onto a solid substrate, thus forming the LB film. SERS of ZnPPIX-DME was successfully attained, ensuring the spatial distribution of the AuNPs. Higher enhancement factors were found at AuNP aggregates, as a result of the intense local electromagnetic field found in the metal nanoparticle aggregates. The main vibrational bands observed in the SERS spectra suggest a physical adsorption of the ZnPPIX-DME onto the surface of AuNPs. The latter is not only in agreement with the interactions pointed out by the π-A isotherms but also suggests that this interaction is kept upon LB film co-deposition.
dc.languageeng
dc.relationApplied Spectroscopy
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.titleCo-deposition of gold nanoparticles and metalloporphyrin using the langmuir-blodgett (LB) technique for Surface-Enhanced Raman Scattering (SERS)
dc.typeOtro


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