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dc.contributor.authorHailstone, Richarden_US
dc.contributor.authorErdtmann, Daviden_US
dc.date.accessioned2006-12-18T17:51:56Zen_US
dc.date.available2006-12-18T17:51:56Zen_US
dc.date.issued1994-10-01en_US
dc.identifier.citationJournal of Applied Physics 76N7 (1994) 4184-4191en_US
dc.identifier.issn0021-8979en_US
dc.identifier.urihttp://hdl.handle.net/1850/3133en_US
dc.description.abstractPrevious workers have explained photoconductivity decay in AgBr microcrystals by proposing a model involving lattice relaxation following shallow surface trapping of electrons. This model is investigated using Monte Carlo simulations in which the electron and hole undergo a random walk in the volume of the microcrystals and are shallowly trapped at the surface. The decay rate is controlled by the thermal barrier that must be overcome to achieve a lower-energy lattice configuration, as well as by the density and cross section of the shallow surface traps. The simulation results lend support to the lattice relaxation model, but also suggest a significant role of free-electron/trapped-hole recombination in the photoconductivity decay. The experimentally observed increase in decay time with increasing microcrystal size is also seen in the simulations. This size dependence is due to the effect of the surface-to-volume ratio on the distribution between free and shallowly trapped states for the electron.en_US
dc.format.extent68438 bytesen_US
dc.format.mimetypeapplication/pdfen_US
dc.language.isoen_USen_US
dc.publisherAmerican Institute of Physicsen_US
dc.relation.ispartofseriesvol. 76en_US
dc.relation.ispartofseriesno. 7en_US
dc.subjectComputerized simulationen_US
dc.subjectDecayen_US
dc.subjectFilmsen_US
dc.subjectGrain sizeen_US
dc.subjectLattice relaxationen_US
dc.subjectMonte Carlo methoden_US
dc.subjectPhotoconductivityen_US
dc.subjectPolycrystalsen_US
dc.subjectSilver bromidesen_US
dc.subjectTrapsen_US
dc.titleComputer simulation of photoconductivity decay in AgBr microcrystals: Relaxation modelen_US
dc.typeArticleen_US
dc.identifier.urlhttp://dx.doi.org/10.1063/1.357372


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