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Ph.d.-verja: Høgni Carlsson Kamban

týsdagur 31.05.2022, kl. 12:00, Aalborg Universitet

Týsdagin 31. mai 2022 verjir Høgni Carlsson Kamban ph.d.-ritgerð sína við Institut for Materialer og Produktion, Aalborg Universitet.

Heiti á ritgerðini: Field-induced Dissociation of Excitons in Mono- and Bilayer Structures.

Høvuðsvegleiðari er Thomas Garm Pedersen, professari á Institut for Materialer og Produktion, Aalborg Universitet.

Í metingarnendin eru:

Kjeld Pedersen, professari á Aalborg Universitet, súm fer at leiða verjuna

Kirill Bolotin, professari á Freie Universität Berlin

Nikolaj T. Zinner, professari á Aarhus Universitet

Abstract

The focus of this thesis is to study electric-field-induced dissociation of excitons in material structures based on both monolayer materials and bilayer heterostructures. Excitons are quasi-particles found in semiconductors and insulators. When an electron is excited from the valence band, typically by absorbing a photon, it leaves behind a vacancy in this band. This vacancy behaves like a positively charged particle and is referred to as a hole.

The excited electron and hole are attracted to one another via the Coulomb force due to their opposite electric charge. They may therefore form a bound state, and it is this bound state that is known as an exciton. Excitons in bulk semiconductors are usually weakly bound, and thermal agitation is sufficient to dissociate them into free electrons and holes. This is not the case for mono- and bilayer structures, however. As the number of layers composing the material structure reduces, the screening of the interaction between electrons and holes also reduces. This leads to a stronger interaction between electron-hole pairs, and exciton binding energies therefore become larger. Such strongly bound excitons are thermally stable, and it is therefore interesting to see if one may assist the dissociation process by applying in-plane electric fields to the excitons.

A recent experiment showed that the photoresponse rate of a WSe2 monolayer increases as a static electric field is applied to the excitons. The field-induced increase in photoresponse rate at weak fields was well described by a Wannier exciton dissociation model. However, it proved difficult to obtain theoretical predictions of exciton dissociation rates when the electric fields were sufficiently weak. One of the goals of the present thesis was to find a numerical method capable of efficiently computing these weak field dissociation rates. This method has subsequently been used to compute exciton dissociation rates in monolayer transition metal dichalcogenides (TMDs), phosphorene, and bilayer TMD heterostructures. The results indicate an exponential dependence on field strength, particularly in weak electric fields. The exciton binding energy is, furthermore, found to be the dominating parameter determining exciton dissociation rates, but reduced masses and substrate screening also have an impact. This is made clear by deriving an analytical weak field approximation in which all of these parameters are included.

Dissociation induced by THz pulses is also considered for excitons in monolayer TMDs. The results are obtained using a fully time-dependent Wannier model and indicate that realistic THz pulses are able to dissociate a substantial amount of excitons in realistic semiconductors.

Samband: Høgni Carlsson Kamban