scholarly journals Order–disorder phase transition of the subsurface cation vacancy reconstruction on Fe3O4(001)

2020 ◽  
Vol 22 (16) ◽  
pp. 8336-8343 ◽  
Author(s):  
Björn Arndt ◽  
Barbara A. J. Lechner ◽  
Alexander Bourgund ◽  
Elin Grånäs ◽  
Marcus Creutzburg ◽  
...  
Keyword(s):  
Phase Transition ◽  
Scanning Tunneling Microscopy ◽  
Surface Defect ◽  
Cation Vacancy ◽  
Scanning Tunneling ◽  
X Ray Diffraction ◽  
Tunneling Microscopy ◽  
X Ray ◽  
Disorder Phase Transition

Magnetite surface defect dynamics followed by fast scanning tunneling microscopy and surface X-ray diffraction.

scholarly journals Interface morphology of a Cr(001)/Fe(001) superlattice determined by scanning tunneling microscopy and x-ray diffraction: A comparison

2001 ◽  
Vol 89 (1) ◽  
pp. 181-187 ◽  
Author(s):  
C. M. Schmidt ◽  
D. E. Bürgler ◽  
D. M. Schaller ◽  
F. Meisinger ◽  
H.-J. Güntherodt ◽  
...  
Keyword(s):  
Scanning Tunneling Microscopy ◽  
Scanning Tunneling ◽  
Interface Morphology ◽  
X Ray Diffraction ◽  
Tunneling Microscopy ◽  
X Ray

Scanning Tunneling Microscopy Imaging of Defects in Layered Compounds

1990 ◽  
Vol 209 ◽  
Author(s):  
G. P. E. M. Van Bakell ◽  
J. Th. M. De Hosson ◽  
T. Hibma
Keyword(s):  
Scanning Tunneling Microscopy ◽  
Structural Features ◽  
Layered Compounds ◽  
Scanning Tunneling ◽  
X Ray Diffraction ◽  
Tunneling Microscopy ◽  
Microscopy Imaging ◽  
X Ray ◽  
Sample Orientation ◽  
Stm Images

ABSTRACTStructural features of TiS2 were studied by scanning tunneling microscopy (STM) and single-crystal X-ray diffraction was applied as a complementary technique. STM images in air and at room temperature revealed, beside the trigonal symmetry of the lattice, several new features having this symmetry as well. We conclude that these features not only are to be described by structural defect phenomena which affect octahedral sites in the 1T-CdI2 structure but tetrahedral sites as well. Sample orientation determination by X-ray diffraction provides a unique relation between feature types and sites. A model is proposed in which displaced Ti atoms account for the observed features.

scholarly journals Structural examination of Au/Ge(001) by surface x-ray diffraction and scanning tunneling microscopy

2012 ◽  
Vol 85 (23) ◽  
Author(s):  
S. Meyer ◽  
T. E. Umbach ◽  
C. Blumenstein ◽  
J. Schäfer ◽  
R. Claessen ◽  
...  
Keyword(s):  
Scanning Tunneling Microscopy ◽  
Scanning Tunneling ◽  
X Ray Diffraction ◽  
Tunneling Microscopy ◽  
Structural Examination ◽  
X Ray

Structure analysis of thiouracil on Ag(111) and graphite (0001) by x-ray diffraction and scanning tunneling microscopy

1999 ◽  
Vol 214 (12) ◽  
Author(s):  
H. L. Meyerheim ◽  
F. Trixler ◽  
W. Stracke ◽  
W. M. Heckl
Keyword(s):  
Scanning Tunneling Microscopy ◽  
Bond Distance ◽  
Pyrimidine Ring ◽  
Unit Cell ◽  
Scanning Tunneling ◽  
X Ray Diffraction ◽  
Tunneling Microscopy ◽  
X Ray ◽  
Covalent Interaction ◽  
Inert Surface

AbstractThe geometric structures of ordered monolayers of large organic molecules (thiouracil) adsorbed to the surface of Ag(111) and graphite (0001) were analyzed using surface x-ray diffraction and scanning tunneling microscopy (STM), respectively. Although the substrates are different, in both cases the molecules are found to be arranged in parallel zig-zag rows. On graphite (0001) the molecules form a unit cell similar to the ([unk]1[unk])plane of the bulk crystal whereas on Ag(111) the detailed x-ray analysis gives evidence that, in contrast to the bulk structure, all but one of the intermolecular hydrogen bonds present in the bulk are broken. The intact pyrimidine rings are tilted by about 30° with respect to the Ag surface in comparison to flat lying molecules on graphite. An elongation of the C=S bond distance by 0.16(7) Å and an increase of the intra-pyrimidine-ring distances by about 0.11(10) Å relative to the bulk is observed which can be attributed to the covalent interaction of the molecule with the substrate. We conclude that for an inert surface like graphite, where the molecules merely interact by van der Waals forces, the molecules build a unit cell mainly determined by intermolecular hydrogen bridge bonds and therefore almost unchanged with respect to the bulk, whereas even in the case of a weakly interacting surface like Ag(111) the crystal structure can considerably be altered with respect to the bulk.

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