scholarly journals New method to analyze random telegraph signals in resistive random access memories

Author(s):  
Gerardo González-Cordero ◽  
Mireia B. González ◽  
Francisco Jiménez-Molinos ◽  
Francesca Campabadal ◽  
Juan Bautista Roldán
Author(s):  
Martin Versen ◽  
Achim Schramm ◽  
Jan Schnepp ◽  
Sascha Hoch ◽  
Tapan Vikas ◽  
...  

Abstract Soft defect localization (SDL) is a method of laser scanning microscopy that utilizes the changing pass/fail behavior of an integrated circuit under test and temperature influence. Historically the pass and fail states are evaluated by a tester that leads to long and impracticable measurement times for dynamic random access memories (DRAM). The new method using a high speed comparison device allows SDL image acquisition times of a few minutes and a localization of functional DRAM fails that are caused by defects in the DRAM periphery that has not been possible before. This new method speeds up significantly the turn-around time in the failure analysis (FA) process compared to knowledge based FA.


1992 ◽  
Vol 31 (Part 1, No. 12B) ◽  
pp. 4541-4544 ◽  
Author(s):  
Hirokazu Sayama ◽  
Shigenori Hara ◽  
Hiroshi Kimura ◽  
Yoshikazu Ohno ◽  
Shinichi Satoh ◽  
...  

2006 ◽  
Vol 45 (2B) ◽  
pp. 1253-1257 ◽  
Author(s):  
Jin-Young Choi ◽  
Jae-Sung Lee ◽  
Sang-Hoon Kim ◽  
Jang-Hyun Kim ◽  
Hyun Seok Yang ◽  
...  

Author(s):  
C. C. Clawson ◽  
L. W. Anderson ◽  
R. A. Good

Investigations which require electron microscope examination of a few specific areas of non-homogeneous tissues make random sampling of small blocks an inefficient and unrewarding procedure. Therefore, several investigators have devised methods which allow obtaining sample blocks for electron microscopy from region of tissue previously identified by light microscopy of present here techniques which make possible: 1) sampling tissue for electron microscopy from selected areas previously identified by light microscopy of relatively large pieces of tissue; 2) dehydration and embedding large numbers of individually identified blocks while keeping each one separate; 3) a new method of maintaining specific orientation of blocks during embedding; 4) special light microscopic staining or fluorescent procedures and electron microscopy on immediately adjacent small areas of tissue.


1960 ◽  
Vol 23 ◽  
pp. 227-232 ◽  
Author(s):  
P WEST ◽  
G LYLES
Keyword(s):  

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