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Tailored TiO2(110) surfaces and their reactivity

C L Pang et al 2006 Nanotechnology 17 5397-5405   doi: 10.1088/0957-4484/17/21/019  Help

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C L Pang1,2, O Bikondoa3, D S Humphrey2, A C Papageorgiou2, G Cabailh2, R Ithnin4, Q Chen2, C A Muryn3, H Onishi1 and G Thornton2
1 Department of Chemistry, Faculty of Science, Kobe University, Kobe 657-8501, Japan
2 London Centre for Nanotechnology and Chemistry Department, University College London, London WC1H 0AJ, UK
3 School of Chemistry, University of Manchester, Manchester M13 9PL, UK
4 Pusat Asasi Sains, Universiti Malaya, 50603 Kuala Lumpur, Malaysia
E-mail: chi.pang@ucl.ac.uk

Abstract. Electron bombardment from a filament as well as voltage pulses from a scanning tunnelling microscope tip have been employed to modify the surface of TiO2(110). Individual H atoms are selectively desorbed with electrical pulses of +3 V from the scanning tunnelling microscope tip, whilst leaving the oxygen vacancies intact. This allows us to distinguish between oxygen vacancies and hydroxyl groups, which have a similar appearance in scanning tunnelling microscopy images. This then allows the oxygen vacancy-promoted dissociation of water and O2 to be followed with the microscope. Electrical pulses between +5 and +10 V induce local TiO2(110)1 × 2 reconstructions centred around the pulse. As for electron bombardment of the surface, relatively low fluxes increase the density of oxygen vacancies whilst higher fluxes lead to the 1 × 2 and other 1 × n reconstructions.

Print publication: Issue 21 (14 November 2006)
Received 12 July 2006, in final form 15 September 2006
Published 13 October 2006

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