Josue R. Morales-Cifuentes
Josue R. Morales-Cifuentes
*This is an algorithmically generated author record based on publicly available information.
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Josue R. Morales-Cifuentes has a total of 2 co-authors. Here are the top co-authors by number of shared publications:
- Alberto Pimpinelli
Department of Physics, University of Maryland, College Park, Maryland 20742-4111, USA
1 shared publication - Theodore L. Einstein
Department of Physics and Condensed Matter Theory Center, University of Maryland, College Park, Maryland 20742-4111, USA
1 shared publication
Latest Publications
- 10 December 2014
- Published by American Physical Society (APS) in Physical Review Letters
- Vol. 113 (24) , 246101
How “Hot Precursors” Modify Island Nucleation: A Rate-Equation Model
We propose a novel island nucleation and growth model explicitly including transient (ballistic) mobility of the monomers deposited at rate , assumed to be in a hot precursor state before thermalizing. In limiting regimes, corresponding to fast (diffusive) and slow (ballistic) thermalization, the island density obeys scaling . In between is found a rich, complex behavior, with various distinctive scaling regimes, characterized by effective exponents and activation energies that we compute exactly. Application to of recent organic-molecule deposition experiments yields an excellent fit.- 10 December 2014
- Published by American Physical Society (APS) in Physical Review Letters
- Vol. 113 (24) , 246101
How “Hot Precursors” Modify Island Nucleation: A Rate-Equation Model
We propose a novel island nucleation and growth model explicitly including transient (ballistic) mobility of the monomers deposited at rate , assumed to be in a hot precursor state before thermalizing. In limiting regimes, corresponding to fast (diffusive) and slow (ballistic) thermalization, the island density obeys scaling . In between is found a rich, complex behavior, with various distinctive scaling regimes, characterized by effective exponents and activation energies that we compute exactly. Application to of recent organic-molecule deposition experiments yields an excellent fit.