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Ultrafast low-energy electron diffraction at surfaces

Probing transitions and phase-ordering of charge-density waves

dc.contributor.advisorRopers, Claus Prof. Dr.
dc.contributor.authorVogelgesang, Simon
dc.date.accessioned2019-02-22T09:10:00Z
dc.date.available2019-02-22T09:10:00Z
dc.date.issued2019-02-22
dc.identifier.urihttp://hdl.handle.net/11858/00-1735-0000-002E-E5A1-F
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-7305
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-7305
dc.language.isoengde
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc530de
dc.titleUltrafast low-energy electron diffraction at surfacesde
dc.title.alternativeProbing transitions and phase-ordering of charge-density wavesde
dc.typedoctoralThesisde
dc.contributor.refereeRopers, Claus Prof. Dr.
dc.date.examination2018-12-05
dc.subject.gokPhysik (PPN621336750)de
dc.description.abstractengDue to their reduced dimensionality, surfaces and quasi two-dimensional materials exhibit numerous intriguing physical phenomena that drastically differ from the bulk. To resolve these effects and the associated dynamics at their intrinsic timescales requires experimental methodologies combining a high surface sensitivity with the essential temporal resolution. However, to date, there are still very few methods that facilitate investigation of the structural degrees of freedom of surfaces on the atomic scale along with a temporal resolution of femtoseconds or picoseconds. Addressing these challenges, this thesis covers the development and application of ultrafast low-energy electron diffraction in a backscattering geometry to study structural dynamics at surfaces. In this context, a central aspect is the development of a miniaturized and laser-driven electron source based on a nanometric needle photocathode. Using such a sharp metal tip, the photoemitted electron bunches offer a particularly high coherence and remarkably short pulse durations, which were also successfully implemented recently in ultrafast transmission electron microscopy, as well as in time-resolved transmission low-energy electron diffraction. Employing the capabilities of this novel technique, so-called transition metal dichalcogenides constitute an ideal prototype system. Specifically, in the present work, the transient structural disorder of charge-density waves at the surface of 1T-TaS2 has been examined. Following the optically induced transition between two temperature-dependent charge-density wave phases, this method enables the observation of a highly disordered transient state and the subsequent phase-ordering kinetics. More precisely, the temporal evolution of the growing charge-density correlation length is traced over several hundreds of picoseconds and found to obey a power-law scaling behavior. Due to the particular properties of the charge-density wave system at hand, the observed transient disorder can be explained by the ultrafast formation of topological defects and their subsequent annihilation. These results are complemented by a numerical modeling using a timedependent Ginzburg-Landau approach. Finally, two different excitation schemes demonstrating the possibility to study the relaxation of the investigated sample on the nanosecond and microsecond timescale are presented, as well as future prospects of ultrafast low-energy electron diffraction, including other promising surface sample systems.de
dc.contributor.coRefereeMathias, Stefan Prof. Dr.
dc.subject.engultrafast low-energy electron diffractionde
dc.subject.engULEEDde
dc.subject.engstructural dynamicsde
dc.subject.engsurface sciencede
dc.subject.englaser-driven electron sourcede
dc.subject.engnanoscale photoemitterde
dc.subject.engultrashort electron pulsesde
dc.subject.eng1T-TaS2de
dc.subject.engtransition metal dichalcogenidede
dc.subject.engcharge-density wavede
dc.subject.engCDWde
dc.subject.engphase transitionde
dc.subject.engphase ordering kineticsde
dc.subject.engtopological defectsde
dc.identifier.urnurn:nbn:de:gbv:7-11858/00-1735-0000-002E-E5A1-F-1
dc.affiliation.instituteFakultät für Physikde
dc.identifier.ppn105463758X


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