Colloquium

 

Dept of Physics & Astronomy

University of Maine, Orono, Maine

 

Presents

 

Robert W. Meulenberg

Materials Science and Technology Division

Lawrence Livermore National Laboratory

 

a candidate for the

Nanophysics position

in Physics & Astronomy

 

Electronic Structure of Semiconductor Nanocrystals:
Influence of the Surface

 

                For a thorough understanding of nanocrystalline material systems, knowledge of band gap widening and band alignment as a function of particle size, chemical doping, and surface termination is critical to rational design and utilization of these novel materials.  Tailoring the electronic properties of nanostructures is often achieved by confining electrons to dimensions comparable to their wavelength, which leads to quantum well states that modify the density of states. Until recently, the effect of the surface layer on the electronic and structural properties of the quantum dots has been neglected due to the inherent difficulty in both modeling and measuring this region.  In this presentation, I will discuss efforts into understating the impact the surface region of nanomaterials has on the overall properties of the crystal.

                Soft x-ray probes such as x-ray absorption spectroscopy, photoemission spectroscopy, and soft x-ray fluorescence experiments are used to determine the band edge shifts and doping effects on silicon, germanium, and cadmium selenide nanomaterials in order to better understand the electronic properties.  Clean Si and Ge nanocrystals films exhibit strong quantum confinement effects at the band edges with sub-monolayer coverages, but show a loss in band edge shifts at higher coverages.  This is due to the particle-particle interaction which can be controlled using an in situ surface passivation scheme.  Introduction of surface ligands to the Si and Ge systems induce strong changes in the observed band edge shifts.  For comparison, band edge shifts in CdSe nanocrystal films were investigated.  It was found that Cd s states located at the conduction band minimum (CBM) show drastic size dependencies while the Cd hybridized p levels located a few electron volts up from the CBM show more localized behavior.  Interestingly, changing the surface ligand has very little effect on the shift of the band edges, but does affect the local bonding significantly.  These changes manifest themselves in induced magnetism in the undoped CdSe nanocrystal system.  Lastly, the impact that chemical dopants have on the nanocrystal electronic structure is discussed.  In CdSe, the dopants can be used as a local probe for identifying changes in nanocrystal surface structure.  In addition, the chemical environment of Er in Si nanoparticles is probed and the band edge shifts as a function of both particle size and Er concentration are measured.  It is found that the 1.5 mm infrared luminescence can be achieved with proper passivation of the particles.  Overall, these experiments all show that the surface physics of nanostructured materials are complex and cannot be ignored for a complete understanding of the nanoparticle electronic structure.

Thursday, April 24, 2008
12:00 Noon
Arthur St. John Hill Auditorium