Andres Aldana, Andrew Houlton, Benjamin R Horrocks
{"title":"Structure and optical properties of ZnxCd1-xS and Cu:ZnxCd1-xS templated on DNA molecules","authors":"Andres Aldana, Andrew Houlton, Benjamin R Horrocks","doi":"10.1088/2632-959x/ad6f32","DOIUrl":null,"url":null,"abstract":"One-dimensional Zn<sub>x</sub>Cd<sub>1−x</sub>S and Cu: Zn<sub>\n<italic toggle=\"yes\">x</italic>\n</sub>Cd<sub>1−<italic toggle=\"yes\">x</italic>\n</sub>S nanostructures were prepared using DNA as a template to promote growth along the molecular axis. The formation of homogeneously alloyed nanocrystals with cubic zinc blende-type structures was verified using x-ray diffraction and Raman spectroscopy. X-ray photoemission spectra revealed the presence of Cu(I) in the doped Cu: Zn<sub>\n<italic toggle=\"yes\">x</italic>\n</sub>Cd<sub>1−<italic toggle=\"yes\">x</italic>\n</sub>S nanocrystals. The effectiveness of the DNA template to direct the semiconductor growth in one dimension was demonstrated by AFM and TEM. The nanostructures displayed a granular morphology comprising nanoparticles with an average diameter of 14 nm composed of assemblies of smaller crystallites of 2.0 nm in size. Rope-like assemblies with an average diameter of 48 nm and extending in length to several hundred micrometres were obtained by evaporation-induced self-assembly. UV-Vis absorption and emission spectra indicated that the optical bandgaps (2.89–4.00eV) and photoluminescence peaks (608–819 nm) of the DNA-templated nanocrystals could be precisely controlled by modifying the molar ratios of their Zn/Cd precursors. Doping with Cu(I) gave an increase in photoluminescence intensity and a composition-independent red-shift of 0.23 eV. The preparation of DNA-templated Zn<sub>\n<italic toggle=\"yes\">x</italic>\n</sub>Cd<sub>1−<italic toggle=\"yes\">x</italic>\n</sub>S and Cu: Zn<sub>\n<italic toggle=\"yes\">x</italic>\n</sub>Cd<sub>1−<italic toggle=\"yes\">x</italic>\n</sub>S provides a simple, low-temperature route to aqueous dispersions of inorganic materials with controlled optical gap.","PeriodicalId":501827,"journal":{"name":"Nano Express","volume":"43 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nano Express","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1088/2632-959x/ad6f32","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
One-dimensional ZnxCd1−xS and Cu: ZnxCd1−xS nanostructures were prepared using DNA as a template to promote growth along the molecular axis. The formation of homogeneously alloyed nanocrystals with cubic zinc blende-type structures was verified using x-ray diffraction and Raman spectroscopy. X-ray photoemission spectra revealed the presence of Cu(I) in the doped Cu: ZnxCd1−xS nanocrystals. The effectiveness of the DNA template to direct the semiconductor growth in one dimension was demonstrated by AFM and TEM. The nanostructures displayed a granular morphology comprising nanoparticles with an average diameter of 14 nm composed of assemblies of smaller crystallites of 2.0 nm in size. Rope-like assemblies with an average diameter of 48 nm and extending in length to several hundred micrometres were obtained by evaporation-induced self-assembly. UV-Vis absorption and emission spectra indicated that the optical bandgaps (2.89–4.00eV) and photoluminescence peaks (608–819 nm) of the DNA-templated nanocrystals could be precisely controlled by modifying the molar ratios of their Zn/Cd precursors. Doping with Cu(I) gave an increase in photoluminescence intensity and a composition-independent red-shift of 0.23 eV. The preparation of DNA-templated ZnxCd1−xS and Cu: ZnxCd1−xS provides a simple, low-temperature route to aqueous dispersions of inorganic materials with controlled optical gap.