Standing waves on Si(100) and Ge(100) surfaces observed by scanning tunneling microscopy

2005 ◽  
Vol 72 (23) ◽  
Author(s):  
Keisuke Sagisaka ◽  
Daisuke Fujita
1994 ◽  
Vol 50 (16) ◽  
pp. 12246-12249 ◽  
Author(s):  
J. C. Woicik ◽  
G. E. Franklin ◽  
Chien Liu ◽  
R. E. Martinez ◽  
I.-S. Hwong ◽  
...  

MRS Advances ◽  
2016 ◽  
Vol 1 (22) ◽  
pp. 1645-1650 ◽  
Author(s):  
Igor Altfeder ◽  
Sarah M. Eichfeld ◽  
Rachel D. Naguy ◽  
Joshua A. Robinson ◽  
Andrey A. Voevodin

ABSTRACTUsing scanning tunneling microscopy (STM) we observed atomic scale interference patterns on quasi-freestanding WSe2 islands grown on top of graphene. The bias-independent double atomic size periodicity of these patterns and the sharp Brillouin zone edge revealed by 2D STM Fourier analysis indicate formation of optical phonon standing waves due to scattering on intercalating defects supporting these islands. Standing wave patterns of both synchronized and non-synchronized optical phonons, corresponding to resonant and non-resonant phonon scattering regimes, were experimentally observed. We also found the symmetry breaking effect for individual phonon wave packets, one of the unique features distinguishing phonon standing waves. We show that vibrational and electronic anharmonicities are responsible for STM detection of these patterns. A significant contribution to the interference contrast arises from quantum zero-point oscillations.


Author(s):  
H.-J. Cantow ◽  
H. Hillebrecht ◽  
S. Magonov ◽  
H. W. Rotter ◽  
G. Thiele

From X-ray analysis, the conclusions are drawn from averaged molecular informations. Thus, limitations are caused when analyzing systems whose symmetry is reduced due to interatomic interactions. In contrast, scanning tunneling microscopy (STM) directly images atomic scale surface electron density distribution, with a resolution up to fractions of Angstrom units. The crucial point is the correlation between the electron density distribution and the localization of individual atoms, which is reasonable in many cases. Thus, the use of STM images for crystal structure determination may be permitted. We tried to apply RuCl3 - a layered material with semiconductive properties - for such STM studies. From the X-ray analysis it has been assumed that α-form of this compound crystallizes in the monoclinic space group C2/m (AICI3 type). The chlorine atoms form an almost undistorted cubic closed package while Ru occupies 2/3 of the octahedral holes in every second layer building up a plane hexagon net (graphite net). Idealizing the arrangement of the chlorines a hexagonal symmetry would be expected. X-ray structure determination of isotypic compounds e.g. IrBr3 leads only to averaged positions of the metal atoms as there exist extended stacking faults of the metal layers.


Author(s):  
I. H. Musselman ◽  
R.-T. Chen ◽  
P. E. Russell

Scanning tunneling microscopy (STM) has been used to characterize the surface roughness of nonlinear optical (NLO) polymers. A review of STM of polymer surfaces is included in this volume. The NLO polymers are instrumental in the development of electrooptical waveguide devices, the most fundamental of which is the modulator. The most common modulator design is the Mach Zehnder interferometer, in which the input light is split into two legs and then recombined into a common output within the two dimensional waveguide. A π phase retardation, resulting in total light extinction at the output of the interferometer, can be achieved by changing the refractive index of one leg with respect to the other using the electrooptic effect. For best device performance, it is essential that the NLO polymer exhibit minimal surface roughness in order to reduce light scattering. Scanning tunneling microscopy, with its high lateral and vertical resolution, is capable of quantifying the NLO polymer surface roughness induced by processing. Results are presented below in which STM was used to measure the surface roughness of films produced by spin-coating NLO-active polymers onto silicon substrates.


Sign in / Sign up

Export Citation Format

Share Document