arXiv subjects

Ulrike Diebold

Publications and source records attributed to Ulrike Diebold.

94 records · Page 6Linked to original sources

arXiv2013

Anisotropic two-dimensional electron gas at SrTiO3(110) protected by its native overlayer

Two dimensional electron gases (2DEGs) at a oxide heterostructures are attracting considerable attention, as these might substitute conventional semiconductors for novel electronic devices [1]. Here we present a minimal set-up for such a 2DEG -the SrTiO3(110)-(4 x 1) surface, natively terminated with one monolayer of chemically-inert titania. Oxygen vacancies induced by synchrotron radiation migrate under- neath this overlayer, this leads to a confining potential and electron doping such that a 2DEG develops. Our angular resolved photoemission spectroscopy (ARPES) and theoretical results show that confinement along (110) is strikingly different from a (001) crystal orientation. In particular the quantized subbands show a surprising "semi-heavy" band, in contrast to the analogue in the bulk, and a high electronic anisotropy. This anisotropy and even the effective mass of the (110) 2DEG is tunable by doping, offering a high flexibility to engineer the properties of this system.

cond-mat.mtrl-sci↗

arXiv2013

CO Induced Adatom Sintering in a Model Catalyst: Pd/Fe3O4

The coarsening of catalytically-active metal clusters is often accelerated by the presence of gases through the formation of mobile intermediates, though the exact mechanism through which this happens is often subject to debate. We use scanning tunneling microscopy (STM) to follow the CO induced coalescence of Pd adatoms supported on the Fe3O4(001) surface at room temperature. We show that highly-mobile Pd-carbonyl species, formed via the so-called skyhook effect, are temporarily trapped at other Pd adatoms. Once these reach a critical density, clusters nucleate; subsequent coarsening occurs through cluster diffusion and coalescence. While CO increases the mobility in the Pd/Fe3O4 system, surface hydroxyls have the opposite effect. Pd atoms transported to surface OH groups are no longer susceptible to the skyhook effect and remain isolated. Following the evolution from well-dispersed metal adatoms into clusters, atom-by-atom, allows identification of the key processes that underlie gas-induced mass transport.

cond-mat.mtrl-sci↗

arXiv2012

Ordered Array of Single Au Adatoms with Remarkable Thermal Stability: Au/Fe3O4(001)

We present a Scanning Tunneling Microscopy (STM) investigation of gold deposited at the magnetite Fe3O4(001) surface at room temperature. This surface forms a reconstruction with (\surd2\times\surd2)R45° symmetry, where pairs of Fe and neighboring O ions are slightly displaced laterally, forming undulating rows with 'narrow' and 'wide' adsorption sites. At fractional monolayer coverages, single Au adatoms adsorb exclusively at the narrow sites, with no significant sintering up to annealing temperatures of 400 °C. The strong preference for this site is possibly related to charge and orbital ordering within the first subsurface layer of the reconstructed Fe3O4(001) surface. Because of their high thermal stability, the ordered Au atoms at Fe3O4(001)- (\surd2\times\surd2)R45° could provide useful for probing the chemical reactivity of single atomic species.

cond-mat.mtrl-sci↗

arXiv2010

Observation and destruction of an elusive adsorbate with STM: O$_2$/TiO$_2$

When a slightly defective rutile TiO$_2$(110) surface is exposed to O$_2$ at elevated temperatures, the molecule dissociates at defects, filling O vacancies (\ov) and creating O adatoms (\oad) on {\tifc} rows. The adsorption of molecular O$_2$ at low temperatures has remained controversial. Low-Temperature Scanning Tunneling Microscopy (LT-STM) of O$_2$, dosed on TiO$_2$(110) at a sample temperature of $\approx$ 100 K and imaged at 17 K, shows a molecular precursor at \ov as a faint change in contrast. The adsorbed O$_2$ easily dissociates during the STM measurements, and formation of \oad's at both sides of the original \ov is observed.

cond-mat.mtrl-sci↗