Crystalline ZnO/Amorphous ZnO Core/Shell Nanorods: Self-Organized Growth, Structure, and Novel Luminescence
We have used pulsed-laser deposition, following a specific sequence of heating and cooling phases, to grow ZnO nanorods on ZnO buffer/Si(100) substrates, in a 600 mT oxygen ambient, without catalyst. In these conditions, the nanorods preferentially self-organize in the form of vertically aligned, co...
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Veröffentlicht in: | Journal of physical chemistry. C 2015-03, Vol.119 (9), p.4848-4855 |
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creator | Inguva, Saikumar Marka, Sandeep Kumar Vijayaraghavan, Rajani K McGlynn, Enda Srikanth, Vadali V. S. S Mosnier, J.-P |
description | We have used pulsed-laser deposition, following a specific sequence of heating and cooling phases, to grow ZnO nanorods on ZnO buffer/Si(100) substrates, in a 600 mT oxygen ambient, without catalyst. In these conditions, the nanorods preferentially self-organize in the form of vertically aligned, core/shell structures. X-ray diffraction analyses, obtained from 2θ–ω and pole figure scans, shows a crystalline (wurtzite) ZnO deposit with uniform c-axis orientation normal to the substrate. Field emission scanning electron microscopy, transmission electron microscopy (TEM), high resolution TEM, and selected area electron diffraction studies revealed that the nanorods have a crystalline core and an amorphous shell. The low-temperature (13 K) photoluminescence featured a strong I6 (3.36 eV) line emission, structured green band emission, and a hitherto unreported broad emission at 3.331 eV. Further studies on the 3.331 eV band showed the involvement of deeply bound excitonic constituents in a single electron–hole recombination. The body of structural data suggests that the 3.331 eV emission can be linked to the range of defects associated with the unique crystalline ZnO/amorphous ZnO core/shell structure of the nanorods. The relevance of the work is discussed in the context of the current production methods of core/shell nanorods and their domains of application. |
doi_str_mv | 10.1021/jp511783c |
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The low-temperature (13 K) photoluminescence featured a strong I6 (3.36 eV) line emission, structured green band emission, and a hitherto unreported broad emission at 3.331 eV. Further studies on the 3.331 eV band showed the involvement of deeply bound excitonic constituents in a single electron–hole recombination. The body of structural data suggests that the 3.331 eV emission can be linked to the range of defects associated with the unique crystalline ZnO/amorphous ZnO core/shell structure of the nanorods. The relevance of the work is discussed in the context of the current production methods of core/shell nanorods and their domains of application.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/jp511783c</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Journal of physical chemistry. 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Field emission scanning electron microscopy, transmission electron microscopy (TEM), high resolution TEM, and selected area electron diffraction studies revealed that the nanorods have a crystalline core and an amorphous shell. The low-temperature (13 K) photoluminescence featured a strong I6 (3.36 eV) line emission, structured green band emission, and a hitherto unreported broad emission at 3.331 eV. Further studies on the 3.331 eV band showed the involvement of deeply bound excitonic constituents in a single electron–hole recombination. The body of structural data suggests that the 3.331 eV emission can be linked to the range of defects associated with the unique crystalline ZnO/amorphous ZnO core/shell structure of the nanorods. 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C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Inguva, Saikumar</au><au>Marka, Sandeep Kumar</au><au>Vijayaraghavan, Rajani K</au><au>McGlynn, Enda</au><au>Srikanth, Vadali V. S. S</au><au>Mosnier, J.-P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Crystalline ZnO/Amorphous ZnO Core/Shell Nanorods: Self-Organized Growth, Structure, and Novel Luminescence</atitle><jtitle>Journal of physical chemistry. C</jtitle><addtitle>J. Phys. Chem. C</addtitle><date>2015-03-05</date><risdate>2015</risdate><volume>119</volume><issue>9</issue><spage>4848</spage><epage>4855</epage><pages>4848-4855</pages><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>We have used pulsed-laser deposition, following a specific sequence of heating and cooling phases, to grow ZnO nanorods on ZnO buffer/Si(100) substrates, in a 600 mT oxygen ambient, without catalyst. In these conditions, the nanorods preferentially self-organize in the form of vertically aligned, core/shell structures. X-ray diffraction analyses, obtained from 2θ–ω and pole figure scans, shows a crystalline (wurtzite) ZnO deposit with uniform c-axis orientation normal to the substrate. Field emission scanning electron microscopy, transmission electron microscopy (TEM), high resolution TEM, and selected area electron diffraction studies revealed that the nanorods have a crystalline core and an amorphous shell. The low-temperature (13 K) photoluminescence featured a strong I6 (3.36 eV) line emission, structured green band emission, and a hitherto unreported broad emission at 3.331 eV. Further studies on the 3.331 eV band showed the involvement of deeply bound excitonic constituents in a single electron–hole recombination. The body of structural data suggests that the 3.331 eV emission can be linked to the range of defects associated with the unique crystalline ZnO/amorphous ZnO core/shell structure of the nanorods. The relevance of the work is discussed in the context of the current production methods of core/shell nanorods and their domains of application.</abstract><pub>American Chemical Society</pub><doi>10.1021/jp511783c</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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title | Crystalline ZnO/Amorphous ZnO Core/Shell Nanorods: Self-Organized Growth, Structure, and Novel Luminescence |
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