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Gas sensor properties of Ag- and Pd-decorated SnO micro-disks to NO2, H-2 and CO: Catalyst enhanced sensor response and selectivity

dc.contributor.authorBarbosa, Martin S. [UNESP]
dc.contributor.authorSuman, Pedro H. [UNESP]
dc.contributor.authorKim, Jae J.
dc.contributor.authorTuller, Harry L.
dc.contributor.authorVarela, Jose A. [UNESP]
dc.contributor.authorOrlandi, Marcelo O. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionMIT
dc.date.accessioned2018-11-28T00:05:43Z
dc.date.available2018-11-28T00:05:43Z
dc.date.issued2017-02-01
dc.description.abstractThe gas sensor response of tin monoxide micro-disks, functionalized with noble metal nanoparticles (Pd and Ag), to NO2, H-2 and CO were studied by monitoring changes in their resistance upon exposure to the various gases. The tin monoxide, with unusually low Sn oxidation state, was synthetized by carbothermal reduction. Surface modification by Pd and Ag catalysts was achieved by coating the micro-disks by metallic nanoparticle dispersions, prepared by the polyol reduction process, followed by thermal treatment. SEM and TEM analysis showed nanoparticles to be well-dispersed over the SnO surfaces. The decorated SnO micro-disks exhibited high sensor response to reducing gases such as H-2 and CO. On the other hand, the catalytic particles tended to reduce the sensor response to oxidizing gases such as NO2. The catalytic activity of Pd nanoparticles was tied to chemical sensitization while that of Ag nanoparticles to electronic sensitization. Impedance spectroscopy enabled deconvolution of different contributions to the sensor response with only the Ag-decorated specimens exhibiting two RC time constants. Thus, in contrast to undecorated and Pd-decorated specimens, nearly 80% of Ag modified SnO's response to H-2 was controlled by changes in the interface between particles and disks. Sensor response to H-2 was optimal at higher temperatures (300 degrees C), NO2 at 200 degrees C while that for Pd-decorated materials; maximum sensor response to CO was observed at lower temperatures (under 150 degrees C), where CO absorption by metal nanoparticles is favored. (C) 2016 Elsevier B.V. All rights reserved.en
dc.description.affiliationSao Paulo State Univ, Dept Phys Chem, BR-14800900 Sao Paulo, Brazil
dc.description.affiliationMIT, Dept Mat Sci & Engn, Cambridge, MA 02139 USA
dc.description.affiliationUnespSao Paulo State Univ, Dept Phys Chem, BR-14800900 Sao Paulo, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipMRSEC Program of the National Science Foundation
dc.description.sponsorshipIdFAPESP: 2012/51195-3
dc.description.sponsorshipIdFAPESP: 2013/08734-3
dc.description.sponsorshipIdFAPESP: 2013/18511-1
dc.description.sponsorshipIdFAPESP: 2014/50725-4
dc.description.sponsorshipIdCNPq: 447760/2014-9
dc.description.sponsorshipIdMRSEC Program of the National Science Foundation: DMR - 141980
dc.format.extent253-261
dc.identifierhttp://dx.doi.org/10.1016/j.snb.2016.07.157
dc.identifier.citationSensors And Actuators B-chemical. Lausanne: Elsevier Science Sa, v. 239, p. 253-261, 2017.
dc.identifier.doi10.1016/j.snb.2016.07.157
dc.identifier.fileWOS000388951300030.pdf
dc.identifier.issn0925-4005
dc.identifier.urihttp://hdl.handle.net/11449/165387
dc.identifier.wosWOS:000388951300030
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofSensors And Actuators B-chemical
dc.relation.ispartofsjr1,406
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectGas sensors
dc.subjectSnO
dc.subjectCatalyst
dc.subjectImpedance spectroscopy
dc.subjectSensitization
dc.titleGas sensor properties of Ag- and Pd-decorated SnO micro-disks to NO2, H-2 and CO: Catalyst enhanced sensor response and selectivityen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentFísico-Química - IQARpt

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