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               <dc:title>Predictive model for scanned probe oxidation kinetics</dc:title>
               <dc:creator>Dagata, J. A.</dc:creator>
               <dc:creator>Pérez Murano, Francesc</dc:creator>
               <dc:creator>Abadal Berini, Gabriel</dc:creator>
               <dc:creator>Morimoto, K.</dc:creator>
               <dc:creator>Inoue, T.</dc:creator>
               <dc:creator>Itoh, J.</dc:creator>
               <dc:creator>Yokoyama, H.</dc:creator>
               <dc:creator>American Physical Society</dc:creator>
               <dc:subject>Oxidation</dc:subject>
               <dc:subject>Process monitoring and control</dc:subject>
               <dc:subject>Spatial analysis</dc:subject>
               <dc:description>Previous descriptions of scanned probe oxidation kinetics involved implicit assumptions that one-dimensional, steady-state models apply for arbitrary values of applied voltage and pulse duration. These assumptions have led to inconsistent interpretations regarding the fundamental processes that contribute to control of oxide growth rate. We propose a model that includes a temporal crossover of the system from transient to steady-state growth and a spatial crossover from predominantly vertical to coupled lateral growth. The model provides an excellent fit of available experimental data.</dc:description>
               <dc:date>2000</dc:date>
               <dc:type>Article</dc:type>
               <dc:relation>Applied physics letters ; Vol. 76, Issue 19 (March 2000), p. 2710-2712</dc:relation>
               <dc:rights>open access</dc:rights>
               <dc:rights>Aquest material està protegit per drets d'autor i/o drets afins. Podeu utilitzar aquest material en funció del que permet la legislació de drets d'autor i drets afins d'aplicació al vostre cas. Per a d'altres usos heu d'obtenir permís del(s) titular(s) de drets.</dc:rights>
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