Characterization of Atomic-Beam Deposited GeO1-xNx/HfO2 Stacks on Ge

2019 ◽  
Vol 1 (5) ◽  
pp. 9-16 ◽  
Author(s):  
M. Houssa ◽  
Thierry Conard ◽  
Jan Van Steenbergen ◽  
G. Mavrou ◽  
Y. Panayiotatos ◽  
...  
Keyword(s):  
2005 ◽  
Vol 35 (4a) ◽  
Author(s):  
A. Bebeachibuli ◽  
M. S. Santos ◽  
D. V. Magalhães ◽  
S. T. Müller ◽  
V.S. Bagnato

2001 ◽  
Vol 72 (1) ◽  
pp. 602-606 ◽  
Author(s):  
B. Brañas ◽  
D. Tafalla ◽  
F. L. Tabarés ◽  
P. Ortiz

2008 ◽  
Vol 80 (2) ◽  
pp. 217-252 ◽  
Author(s):  
Mushtaq Ahmed ◽  
Daniel V. Magalhães ◽  
Aida Bebeachibuli ◽  
Stella T. Müller ◽  
Renato F. Alves ◽  
...  

Cesium atomic beam clocks have been the workhorse for many demanding applications in science and technology for the past four decades. Tests of the fundamental laws of physics and the search for minute changes in fundamental constants, the synchronization of telecommunication networks, and realization of the satellite-based global positioning system would not be possible without atomic clocks. The adoption of optical cooling and trapping techniques, has produced a major advance in atomic clock precision. Cold-atom fountain and compact cold-atom clocks have also been developed. Measurement precision of a few parts in 10(15) has been demonstrated for a cold-atom fountain clock. We present here an overview of the time and frequency metrology program based on cesium atoms under development at USP São Carlos. This activity consists of construction and characterization of atomic-beam, and several variations of cold-atom clocks. We discuss the basic working principles, construction, evaluation, and important applications of atomic clocks in the Brazilian program.


Author(s):  
N.E. Lundblad ◽  
D. Aveline ◽  
R.J. Thompson ◽  
W.M. Klipstein ◽  
J.M. Kohel ◽  
...  
Keyword(s):  

Author(s):  
P. G. S. Dias ◽  
M. A. F. Biscassi ◽  
P. H. N. Magnani ◽  
R. F. Shiozaki ◽  
Ph. W. Courteille ◽  
...  
Keyword(s):  

Author(s):  
B. L. Soloff ◽  
T. A. Rado

Mycobacteriophage R1 was originally isolated from a lysogenic culture of M. butyricum. The virus was propagated on a leucine-requiring derivative of M. smegmatis, 607 leu−, isolated by nitrosoguanidine mutagenesis of typestrain ATCC 607. Growth was accomplished in a minimal medium containing glycerol and glucose as carbon source and enriched by the addition of 80 μg/ ml L-leucine. Bacteria in early logarithmic growth phase were infected with virus at a multiplicity of 5, and incubated with aeration for 8 hours. The partially lysed suspension was diluted 1:10 in growth medium and incubated for a further 8 hours. This permitted stationary phase cells to re-enter logarithmic growth and resulted in complete lysis of the culture.


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