Open this publication in new window or tab >>2020 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]
The research presented in this thesis has been focused on the study of thin Ag films, grown on metal-reconstructed Si(111) and Ge(111) surfaces.The films have been grown at room temperature, and the morphologiesand electronic structures of the films have been investigated using scanning tunneling microscopy and spectroscopy (STM/STS), low-energy electron diffraction (LEED) and angle-resolved photoelectron spectroscopy(ARPES).
On the Ga-, In-, and Sn/Si(111)-√3x√3 surfaces, the first layer of Ag forms a special interface which consists of short atomic rows, with slightly different appearances depending on the base surface. Starting from two monolayers (MLs), Ag grows as a thin film with bulk-like lattice parameters.
The electronic structures of the films reveal the behavior of the intrinsic quantum well states (QWSs). STS data show peaks in the filled states which move towards the Fermi level with increased thicknesses. These peaks have been compared with ARPES spectra and linked to the QWSs. The evolution of the QWSs with film thicknesses has been examined within, and extending upon, the established theoretical framework. The results point towards metal-reconstructed Si(111) surfaces using group III and IV elements as strong candidates for uniform film growth, and open up new avenues for studying electronic coupling effects between film/substrate.
On Sn/Si(111)-√3x√3, the Ag films grow in domains with two different lattice orientations, rotated 30° from each other. This is due to the interface consisting of two different structures, as revealed by the STM. One of the interfacial phases is a 3×3 honeycomb structure, and the other a line structure of short atomic rows with a three-fold symmetric 2√3×√3-R30° unit cell. Atomic models for the two interface phases have been proposed, based on two different spin configurations of the Sn/Si(111)-√3x√3 surface. The presence of two interfaces makes this system highly attractive for the study of interface related phenomena, and the difference in Ag filmson Sn/Ge(111) compared with Sn/Si(111) highlights the importance of electronic effects for the film growth.
Abstract [en]
From our everyday experiences, we are used to the world functioning in a certain way. As the size of things approach the nanometer scale, new physical phenomena and features arise that often contradict our intuition. One such phenomenon is the electron confinement. When the movement of electrons is restricted in space, the energy becomes quantized, so that only a few particular energy levels are allowed and all the energies between these levels are forbidden. This happens naturally in a metal thin film with a nanometer thickness. These allowed energy levels are called quantum well states. One way to create an artificial system is to grow thin metal films on semiconductor substrates.
This thesis presents research focused on Ag thin films on Si(111)- and Ge(111)-√3×√3 surfaces using Ga, In and Sn as adatoms. The morphologies and electronic structures of the interfaces and Ag films have been studied using a combination of scanning tunneling microscopy and photoelectron spectroscopy. The metal-reconstructed surfaces allow for Ag film formation to take place at room temperature. These surfaces also allow for layer-bylayer growth at very low coverages, which opens up the possibility to study coupling and interface related effects in the electronic structure of the films.
Place, publisher, year, edition, pages
Karlstad: Karlstads universitet, 2020. p. 48
Series
Karlstad University Studies, ISSN 1403-8099 ; 2020:23
Keywords
Quantum well states, thin films, semiconductor, STM, STS, ARPES
National Category
Condensed Matter Physics
Research subject
Physics
Identifiers
urn:nbn:se:kau:diva-79135 (URN)978-91-7867-131-1 (ISBN)978-91-7867-136-6 (ISBN)
Public defence
2020-09-11, 1B364, Frödingsalen, 10:15 (English)
Opponent
Supervisors
Note
Artikel 4 ingick som manuskript i avhandlingen, nu publicerad.
2020-09-112020-07-162020-10-05Bibliographically approved