7 research outputs found
Local structure of In_(0.5)Ga_(0.5)As from joint high-resolution and differential pair distribution function analysis
High resolution total and indium differential atomic pair distribution
functions (PDFs) for In_(0.5)Ga_(0.5)As alloys have been obtained by high
energy and anomalous x-ray diffraction experiments, respectively. The first
peak in the total PDF is resolved as a doublet due to the presence of two
distinct bond lengths, In-As and Ga-As. The In differential PDF, which involves
only atomic pairs containing In, yields chemical specific information and helps
ease the structure data interpretation. Both PDFs have been fit with structure
models and the way in that the underlying cubic zinc-blende lattice of
In_(0.5)Ga_(0.5)As semiconductor alloy distorts locally to accommodate the
distinct In-As and Ga-As bond lengths present has been quantified.Comment: 9 pages, 7 figur
Local structure study of In_xGa_(1-x)As semiconductor alloys using High Energy Synchrotron X-ray Diffraction
Nearest and higher neighbor distances as well as bond length distributions
(static and thermal) of the In_xGa_(1-x)As (0<x<1) semiconductor alloys have
been obtained from high real-space resolution atomic pair distribution
functions (PDFs). Using this structural information, we modeled the local
atomic displacements in In_xGa_(1-x)As alloys. From a supercell model based on
the Kirkwood potential, we obtained 3-D As and (In,Ga) ensemble averaged
probability distributions. This clearly shows that As atom displacements are
highly directional and can be represented as a combination of and
displacements. Examination of the Kirkwood model indicates that the standard
deviation (sigma) of the static disorder on the (In,Ga) sublattice is around
60% of the value on the As sublattice and the (In,Ga) atomic displacements are
much more isotropic than those on the As sublattice. The single crystal diffuse
scattering calculated from the Kirkwood model shows that atomic displacements
are most strongly correlated along directions.Comment: 10 pages, 12 figure
Rationale, design, implementation, and baseline characteristics of patients in the DIG trial: A large, simple, long-term trial to evaluate the effect of digitalis on mortality in heart failure
This article provides a detailed overview of the rationale for key aspects of the protocol of the Digitalis Investigation Group (DIG) trial. It also highlights unusual aspects of the study implementation and the baseline characteristics. The DIG trial is a large, simple, international placebo-controlled trial whose primary objective is to determine the effect of digoxin on all cause mortality in patients with clinical heart failure who are in sinus rhythm and whose ejection fraction is less than or equal to 0.45. An ancillary study examines the effect in those with an ejection fraction > 0.45. Key aspects of the trial include the simplicity of the design, broad eligibility criteria, essential data collection, and inclusion of various types of centers. A total of 302 centers in the United States and Canada enrolled 7788 patients between February 1991 and September 1993. Follow-up continued until December 1995 with the results available in Spring 1996