Evaluation of the Instrument Resolution Effect for Various Neutron Reflectivity Measurement Methods

2013 ◽  
Vol 63 (7) ◽  
pp. 783-793
Author(s):  
Jeong Soo LEE*

2019 ◽  
Vol 91 (11) ◽  
pp. 1821-1835 ◽  
Author(s):  
Yoshifumi Sakaguchi ◽  
Hidehito Asaoka ◽  
Maria Mitkova

Abstract Silver photodiffusion is one of the attractive photo-induced changes observed in amorphous chalcogenides. In this research, we focus on amorphous S-rich germanium sulphide and study the kinetics of the silver photodiffusion by neutron reflectivity, as well as optical reflectivity. It was found from the neutron reflectivity profiles with 30 s time resolution that silver dissolved into the germanium sulphide layer, forming a metastable reaction layer between the Ag and the germanium sulphide layers, within 2 min of light exposure. Subsequently, silver slowly diffused from the metastable reaction layer to the germanium sulphide host layer until the Ag concentration in both layers became identical, effectively forming one uniform layer; this took approximately 20 min. Optical reflectivity reveals the electronic band structure of the sample, complementary to neutron reflectivity. It was found from the optical reflectivity measurement that the metastable reaction layer was a metallic product. The product could be Ag8GeS6-like form, which is regarded as the combination of GeS2 and Ag2S, and whose backbone is composed of the GeS4 tetrahedral units and the S atoms. We attribute the first quick diffusion to the capture of Ag ions by the latter S atoms, which is realised by the S–S bond in amorphous S-rich germanium sulphide, while we attribute the second slow diffusion to the formation of the Ag–Ge–S network, in which Ag ions are captured by the former GeS4 tetrahedral units.



hamon ◽  
2009 ◽  
Vol 19 (4) ◽  
pp. 234-237
Author(s):  
Emiko Mouri ◽  
Hideki Matsuoka




hamon ◽  
2009 ◽  
Vol 19 (1) ◽  
pp. 34-40
Author(s):  
Dai Yamazaki ◽  
Masahiro Hino


1991 ◽  
Vol 30 (3) ◽  
pp. 344 ◽  
Author(s):  
Michel Billardon ◽  
Marie Emmanuelle Couprie ◽  
Jean Michel Ortega ◽  
Michel Velghe


2017 ◽  
Vol 1499 ◽  
pp. 118-131 ◽  
Author(s):  
Alice R. Mazzer ◽  
Luke A. Clifton ◽  
Tatiana Perevozchikova ◽  
Paul D. Butler ◽  
Christopher J. Roberts ◽  
...  


Author(s):  
L. E. Thomas ◽  
J. S. Lally ◽  
R. M. Fisher

In addition to improved penetration at high voltage, the characteristics of HVEM images of crystalline materials are changed markedly as a result of many-beam excitation effects. This leads to changes in optimum imaging conditions for dislocations, planar faults, precipitates and other features.Resolution - Because of longer focal lengths and correspondingly larger aberrations, the usual instrument resolution parameter, CS174 λ 374 changes by only a factor of 2 from 100 kV to 1 MV. Since 90% of this change occurs below 500 kV any improvement in “classical” resolution in the MVEM is insignificant. However, as is widely recognized, an improvement in resolution for “thick” specimens (i.e. more than 1000 Å) due to reduced chromatic aberration is very large.



Author(s):  
Michael T. Postek

The term ultimate resolution or resolving power is the very best performance that can be obtained from a scanning electron microscope (SEM) given the optimum instrumental conditions and sample. However, as it relates to SEM users, the conventional definitions of this figure are ambiguous. The numbers quoted for the resolution of an instrument are not only theoretically derived, but are also verified through the direct measurement of images on micrographs. However, the samples commonly used for this purpose are specifically optimized for the measurement of instrument resolution and are most often not typical of the sample used in practical applications.SEM RESOLUTION. Some instruments resolve better than others either due to engineering design or other reasons. There is no definitively accurate definition of how to quantify instrument resolution and its measurement in the SEM.



2018 ◽  
Vol 11 (4) ◽  
pp. 249-266 ◽  
Author(s):  
Judith Znanewitz ◽  
Lisa Braun ◽  
David Hensel ◽  
Claudia Fantapié Altobelli ◽  
Fabian Hattke


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