scholarly journals Silicon etching in a pulsed HBr/O2 plasma. I. Ion flux and energy analysis

Author(s):  
Moritz Haass ◽  
Maxime Darnon ◽  
Gilles Cunge ◽  
Olivier Joubert ◽  
David Gahan
2007 ◽  
Vol 36 (5) ◽  
pp. 321-332 ◽  
Author(s):  
Yu. N. Grigoryev ◽  
A. G. Gorobchuk
Keyword(s):  

2020 ◽  
Vol 137 (3) ◽  
pp. 313-316
Author(s):  
R. Knizikevičius
Keyword(s):  

Vacuum ◽  
2012 ◽  
Vol 86 (12) ◽  
pp. 1964-1968 ◽  
Author(s):  
R. Knizikevičius
Keyword(s):  

Micromachines ◽  
2021 ◽  
Vol 12 (10) ◽  
pp. 1143
Author(s):  
Thomas Tillocher ◽  
Jack Nos ◽  
Gaëlle Antoun ◽  
Philippe Lefaucheux ◽  
Mohamed Boufnichel ◽  
...  

The cryogenic process is well known to etch high aspect ratio features in silicon with smooth sidewalls. A time-multiplexed cryogenic process, called STiGer, was developed in 2006 and patented. Like the Bosch process, it consists in repeating cycles composed of an isotropic etching step followed by a passivation step. If the etching step is similar for both processes, the passivation step is a SiF4/O2 plasma that efficiently deposits a SiOxFy layer on the sidewalls only if the substrate is cooled at cryogenic temperature. In this paper, it is shown that the STiGer process can achieve profiles and performances equivalent to the Bosch process. However, since sidewall passivation is achieved with polymer free plasma chemistry, less frequent chamber cleaning is necessary, which contributes to increase the throughput.


Author(s):  
J. R. Fields

The energy analysis of electrons scattered by a specimen in a scanning transmission electron microscope can improve contrast as well as aid in chemical identification. In so far as energy analysis is useful, one would like to be able to design a spectrometer which is tailored to his particular needs. In our own case, we require a spectrometer which will accept a parallel incident beam and which will focus the electrons in both the median and perpendicular planes. In addition, since we intend to follow the spectrometer by a detector array rather than a single energy selecting slit, we need as great a dispersion as possible. Therefore, we would like to follow our spectrometer by a magnifying lens. Consequently, the line along which electrons of varying energy are dispersed must be normal to the direction of the central ray at the spectrometer exit.


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