Structural and optical studies of Au doped titanium oxide films

NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION B-BEAM INTERACTIONS WITH MATERIALS AND ATOMS

卷:272

Article; Proceedings Paper

Alves, E.^1,2  Franco, N.^1,2  Barradas, N. P.^1,2  Nunes, B.¹  Lopes, J.³  Cavaleiro, A.⁴  Torrell, M.⁵  Cunha, L.⁵  Vaz, F.⁵ 

[1] Inst Tecnol & Nucl, P-2686953 Sacavem, Portugal

[2] Univ Lisbon, Ctr Fis Nucl, P-21649003 Lisbon, Portugal

[3] Inst Super Engn Lisboa, Lisbon, Portugal

[4] Univ Coimbra, SEC CEMUC, Dept Eng Mecan, P-3030788 Coimbra, Portugal

[5] Univ Minho, Ctr Fis, P-4800058 Guimaraes, Portugal

关键词: Ion Implantation;    TiO2 films;    Au nanoparticles;    Rutherford backscattering spectrometry;    Optical absorption;   

DOI  :  10.1016/j.nimb.2011.01.033

来源: Elsevier

【 摘 要 】

Thin films of TiO2 were doped with Au by ion implantation and in situ during the deposition. The films were grown by reactive magnetron sputtering and deposited in silicon and glass substrates at a temperature around 150 degrees C. The undoped films were implanted with Au fiuences in the range of 5 x 10(15) Au/cm(2)-1 x 10(17) Au/cm(2) with a energy of 150 keV. At a fluence of 5 x 10(16) Au/cm(2) the formation of Au nanoclusters in the films is observed during the implantation at room temperature. The clustering process starts to occur during the implantation where XRD estimates the presence of 3-5 nm precipitates. After annealing in a reducing atmosphere, the small precipitates coalesce into larger ones following an Ostwald ripening mechanism. In situ XRD studies reveal that Au atoms start to coalesce at 350 degrees C, reaching the precipitates dimensions larger than 40 nm at 600 degrees C. Annealing above 700 degrees C promotes drastic changes in the Au profile of in situ doped films with the formation of two Au rich regions at the interface and surface respectively. The optical properties reveal the presence of a broad band centered at 550 nm related to the plasmon resonance of gold particles visible in AFM maps. (C) 2011 Elsevier B.V. All rights reserved.

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