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Electrical and Plasmonic Properties of Ligand‐Free Sn4+‐Doped In2O3 (ITO) Nanocrystals

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dc.contributor.author JAGADEESWARARAO, METIKOTI en_US
dc.contributor.author Pal, Somnath en_US
dc.contributor.author NAG, ANGSHUMAN en_US
dc.date.accessioned 2019-04-26T09:13:54Z
dc.date.available 2019-04-26T09:13:54Z
dc.date.issued 2016-03 en_US
dc.identifier.citation ChemPhysChem,17(5), 710-716. en_US
dc.identifier.issn 1439-4235 en_US
dc.identifier.issn 1439-7641 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2527
dc.identifier.uri https://doi.org/10.1002/cphc.201500973 en_US
dc.description.abstract Sn4+‐doped In2O3 (ITO) is a benchmark transparent conducting oxide material. We prepared ligand‐free but colloidal ITO (8 nm, 10 % Sn4+) nanocrystals (NCs) by using a post‐synthesis surface‐modification reaction. (CH3)3OBF4 removes the native oleylamine ligand from NC surfaces to give ligand‐free, positively charged NCs that form a colloidal dispersion in polar solvents. Both oleylamine‐capped and ligand‐free ITO NCs exhibit intense absorption peaks, due to localized surface plasmon resonance (LSPR) at around λ=1950 nm. Compared with oleylamine‐capped NCs, the electrical resistivity of ligand‐free ITO NCs is lower by an order of magnitude (≈35 mΩ cm−1). Resistivity over a wide range of temperatures can be consistently described as a composite of metallic ITO grains embedded in an insulating matrix by using a simple equivalent circuit, which provides an insight into the conduction mechanism in these systems. en_US
dc.language.iso en en_US
dc.publisher Wiley en_US
dc.subject Electrical and Plasmonic Properties en_US
dc.subject Doped In2O3 en_US
dc.subject ITO Nanocrystals en_US
dc.subject Doping transition metal en_US
dc.subject 2016 en_US
dc.title Electrical and Plasmonic Properties of Ligand‐Free Sn4+‐Doped In2O3 (ITO) Nanocrystals en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle ChemPhysChem en_US
dc.publication.originofpublisher Foreign en_US


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