As
director of the Scanned Probe Microscopy (SPM) lab, I manage
two state-of-the-art UHV SPM instruments: an Omicron
variable-temperature scanning tunneling microscope (VTSTM) and
a JEOL 4500A AFM/STM (variable-temperature) additionally
equipped with a field-emission SEM. I have had the opportunity
to apply my expertise in very productive collaborations with
students and post-doctoral researchers from the University of
Maryland and with external visitors. The following is a brief
description of current projects.
Graphene: Structure and Electronic
Properties
Since its discovery in 2004, graphene has emerged at the
forefront of condensed matter research due to its unique
combination of electrical, mechanical and chemical
properties. As a one-atom thick material system,
graphene is exquisitely sensitive to the presence of
impurities adsorbed on it, and is subject to a host of
extrinsic effects which govern its behavior in any
particular experimental realization. Surprisingly, the
apparently simple issue of graphene topography on
SiO2 remains controversial to the present
day, in spite of several published studies using UHV
STM. Much of the controversy derives from comparisons at
inequivalent resolution (graphene may be measured with
STM, whereas SiO2 must be measured by
AFM). Our recent measurements show that SiO2
is actually slightly rougher than graphene, which leads
to a natural, intuitive understanding of graphene
topography on SiO2 in terms of established
physics of membrane adhesion [1]. Exfoliated
graphene inherits the near-perfect atomic structure of
its parent material, and is observed to be essentially
free of point defects which produce intervalley
scattering. We showed that ion-irradiated graphene has
strong intervalley scattering with a minimum
conductivity below 4e2/πh and a diverging
resistivity at low temperature[2], using 4-probe
transport measurements in UHV. Forthcoming experiments
will probe the defect structure using scanned-probe
measurements in the AFM/STM/SEM facility.
Organic electronics
Current work in organic electronics is motivated by the need to
produce electronic devices that are inexpensive, flexible, and
suitable for mass production in large sheet-like quantities. Our
materials-based investigations of organic systems have been organized
along two main thrusts: (1) STM-based characterization of molecular
adlayers on single-crystal metallic substrates, which explores
self-assembly of multi-component systems; and (2) AFM characterization
(coupled with transport measurements) of molecular semiconductors
which determines the influence of structure on electronic transport
behavior.
Electromigration-Induced Mass
Transport Electromigration is the structural
rearrangement of material systems driven by high
electrical current density. Although studies of
electromigration are generally motivated by the need to
mitigate against long-term component failure in integrated
circuits, our work places it in a rather unique context
with respect to nanotechnology. By measuring the response
of nanostructures to a driving current, we can determine
the coupling of structural fluctuations to electrical
properties, for example the resistance noise which is
generated by structural fluctuations. Initial experiments
determined the effect of electromigration bias on the
fluctuation of atomic steps on a Ag(111)
surface[3,4]. More recent work provides a much more
dramatic observation of electromigration as manifested by
the directed motion of adatom and vacancy islands on
Ag(111), with unambiguous demonstration as a reversal of
velocity with applied current direction[5]. A common
feature of both experiments is the unexpectedly large
coupling of surface structural features to electrical
current, implying a substantial noise effect in nanoscale
systems due to structural fluctuations.
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