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Physica status solidi. PSS-RRL. Rapid research letters, 2014-11, Vol.8 (11), p.917-923
2014

Details

Autor(en) / Beteiligte
Titel
Growth of SrTiO3 on Si(001) by hybrid molecular beam epitaxy
Ist Teil von
  • Physica status solidi. PSS-RRL. Rapid research letters, 2014-11, Vol.8 (11), p.917-923
Ort / Verlag
Berlin: WILEY-VCH Verlag Berlin GmbH
Erscheinungsjahr
2014
Link zum Volltext
Quelle
Wiley Online Library Journals Frontfile Complete
Beschreibungen/Notizen
  • We report the heteroepitaxial growth of SrTiO3 thin films on Si(001) by hybrid molecular beam epitaxy (hMBE). Here, elemental strontium and the metal‐organic precursor titanium tetraisopropoxide (TTIP) were co‐supplied in the absence of additional oxygen. The carbonization of pristine Si surfaces during native oxide removal was avoided by freshly evaporating Sr into the hMBE reactor prior to loading samples. Nucleation, growth and crystallization behavior as well a structural properties and film surfaces were characterized for a series of 46‐nm‐thick SrTiO3 films grown with varying Sr to TTIP fluxes to study the effect of non‐stoichiometric growth conditions on film lattice parameter and surface morphology. High quality SrTiO3 thin films with epitaxial relationship (001)SrTiO3 || (001)Si and [110]SrTiO3 || [100]Si were demonstrated with an amorphous layer of around 4 nm thickness formed at the SrTiO3/Si interface. The successful growth of high quality SrTiO3 thin films with atomically smooth surfaces using a thin film technique with scalable growth rates provides a promising route towards heterogeneous integration of functional oxides on Si. (© 2014 WILEY‐VCH Verlag GmbH &Co. KGaA, Weinheim) The authors report the successful heteroepitaxial growth of high quality SrTiO3 thin films on Si with atomically smooth surfaces and controllable stoichiometry using a combinatorial thin film growth technique. The inherent ability to scale up the growth rates provides a promising route towards heterogeneous integration of functional oxides on Si.
Sprache
Englisch
Identifikatoren
ISSN: 1862-6254
eISSN: 1862-6270
DOI: 10.1002/pssr.201409383
Titel-ID: cdi_proquest_journals_1624921008

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