Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/2791
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dc.contributor.authorSowri Babu, K-
dc.contributor.authorRamachandra Reddy, A-
dc.contributor.authorSujatha, Ch-
dc.contributor.authorVenugopal Reddy, K.-
dc.contributor.authorMallika, A.N-
dc.date.accessioned2025-01-18T07:03:19Z-
dc.date.available2025-01-18T07:03:19Z-
dc.date.issued2013-
dc.identifier.citation10.1007/s40145-013-0069-6en_US
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/2791-
dc.descriptionNITWen_US
dc.description.abstractIn this paper, a simple and cheap method to prepare porous ZnO by using zinc nitrate, ethanol and triethanolamine (TEA) is reported. The as-prepared sample consisted of nano and micro pores. The sample was calcined at 300 °C, 400 °C and 500 °C with different heating rates. At 500 °C, the nano pores disappeared but the sample maintained its micro porosity. Field emission scanning electron microscopy (FE-SEM) pictures confirmed that the size and growth of ZnO nanoparticles depended on the heating conditions. The infrared (IR) absorption peak of Zn-O stretching vibration positioned at 457 cm−1 was split into two peaks centered at 518 cm−1 and 682 cm−1 with the change of morphology. These results confirmed that Fourier transform infrared (FT-IR) spectrum was sensitive to variations in particle size, shape and morphology. The photoluminescence (PL) spectrum of porous ZnO contained five emission peaks at 397 nm, 437 nm, 466 nm, 492 nm and 527 nm. Emission intensity enhanced monotonously with increase of temperature and the change was rapid between temperatures of 300 °C and 500 °C. This was due to the elimination of organic species and improvement in the crystallanity of the sample at 500 °C.en_US
dc.language.isoenen_US
dc.publisherJournal of Advanced Ceramicsen_US
dc.subjectSemiconductors;en_US
dc.subjectPorous ZnOen_US
dc.titleSynthesis and optical characterization of porous ZnOen_US
dc.typeArticleen_US
Appears in Collections:Physics

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