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Author Busby, Y. ♦ Pireaux, J. -J. ♦ Nau, S. ♦ Sax, S. ♦ List-Kratochvil, E. J. W. ♦ Novak, J. ♦ Banerjee, R. ♦ Schreiber, F.
Source United States Department of Energy Office of Scientific and Technical Information
Content type Text
Language English
Subject Keyword CLASSICAL AND QUANTUM MECHANICS, GENERAL PHYSICS ♦ MATERIALS SCIENCE ♦ ALUMINIUM COMPOUNDS ♦ ELECTRIC CURRENTS ♦ ELECTRIC POTENTIAL ♦ ELECTRODES ♦ EVAPORATION ♦ FILAMENTS ♦ IMAGES ♦ INACTIVATION ♦ LAYERS ♦ MASS SPECTROSCOPY ♦ MEMORY DEVICES ♦ MORPHOLOGY ♦ OXINE ♦ REFLECTIVITY ♦ SILVER ♦ TIME-OF-FLIGHT METHOD ♦ X RADIATION ♦ X-RAY PHOTOELECTRON SPECTROSCOPY
Abstract This work explores resistive switching mechanisms in non-volatile organic memory devices based on tris(8-hydroxyquinolie)aluminum (Alq{sub 3}). Advanced characterization tools are applied to investigate metal diffusion in ITO/Alq{sub 3}/Ag memory device stacks leading to conductive filament formation. The morphology of Alq{sub 3}/Ag layers as a function of the metal evaporation conditions is studied by X-ray reflectivity, while depth profile analysis with X-ray photoelectron spectroscopy and time-of-flight secondary ion mass spectrometry is applied to characterize operational memory elements displaying reliable bistable current-voltage characteristics. 3D images of the distribution of silver inside the organic layer clearly point towards the existence of conductive filaments and allow for the identification of the initial filament formation and inactivation mechanisms during switching of the device. Initial filament formation is suggested to be driven by field assisted diffusion of silver from abundant structures formed during the top electrode evaporation, whereas thermochemical effects lead to local filament inactivation.
ISSN 00218979
Educational Use Research
Learning Resource Type Article
Publisher Date 2015-08-21
Publisher Place United States
Journal Journal of Applied Physics
Volume Number 118
Issue Number 7


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