ABSTRACT
Defects introduced to the surface of Bi(111) break the translational symmetry and modify the surface states locally. We present a theoretical and experimental study of the 2D defects on the surface of Bi(111) and the states that they induce. Bi crystals cleaved in ultrahigh vacuum (UHV) at low temperature (110 K) and the resulting ion-etched surface are investigated by low-energy electron diffraction (LEED), X-ray photoelectron spectroscopy, ultraviolet photoelectron spectroscopy (UPS), and scanning tunneling microscopy (STM) as well as spectroscopy (STS) techniques in combination with density functional theory (DFT) calculations. STS measurements of cleaved Bi(111) reveal that a commonly observed bilayer step edge has a lower density of states (DOS) around the Fermi level as compared to the atomic-flat terrace. Following ion bombardment, the Bi(111) surface reveals anomalous behavior at both 110 and 300 K: Surface periodicity is observed by LEED, and a significant increase in the number of bilayer step edges and energetically unfavorable monolayer steps is observed by STM. It is suggested that the newly exposed monolayer steps and the type A bilayer step edges result in an increase to the surface Fermi density as evidenced by UPS measurements and the Kohn-Sham DOS. These states appear to be thermodynamically stable under UHV conditions.
ABSTRACT
The main focus of this paper is the description of qualitatively new facilities for diagnostics of biological and medical objects and medical therapy obtained by applications of nanocrystalline scintillators. These facilities are based on abilities of nanoscintillators to selective conjugation with various biomolecular objects and noticeable variations of their atomic structures, X-ray diffraction (XRD) patterns, and light-emission characteristics induced by modifications of conditions on their external surfaces. Experimental results presented in this paper provide development of detection in vivo just inside a living organism of various viruses, cancer cells, and other pathological macromolecules by means of scanning X-ray diffractometry of nanoparticles introduced into the body. These data are produced by selective adsorption of pathological bioobjects by these nanoparticles and subsequent modifications of their XRD patterns. Application of narrow collimated X-ray beams and new types of X-ray detector matrices providing microscopic spatial resolution due to usage of nanoscintillators enables determination of the regions where these pathologies are localized with high accuracy. The procedure of detection of pathological organelles by this method improves possibilities for effective destruction of these pathologies by low-dose X-ray irradiation of the places of their localization. High effectiveness of this X-ray destruction is provided by concentrated absorption of X-ray quanta by the nanoscintillators and direct transfer of the absorbed energy to the pathological objects that are attached to the absorbing particles. Constructions of 3-D radiation detector matrices providing necessary microscopic spatial and angular resolutions of X-ray imaging are described on the basis of nanoscintillators, fiber light guides, and microcapillary matrices.
