Variable-Temperature Atomic Force Microscopy

2006 ◽  
Vol 8 (2) ◽  
pp. 21-22
Author(s):  
Dimitri A. Ivanov
2002 ◽  
Vol 01 (05n06) ◽  
pp. 725-730 ◽  
Author(s):  
M. S. XU ◽  
J. B. XU ◽  
J. AN

Variable temperature tapping mode atomic force microscopy is exploited to in situ visualize the morphological evolution of N, N'-di(naphthalene-1-yl)-N, N'-diphthalbenzidine (NPB) thin film. The apparent glass transition of the NPB thin film initially occurred at 60°C, proceeded until 95°C, and crystallization from the glassy state quickly appeared at 135°C. The NPB thin film gradually melted and disappeared when the temperature was above 175°C, revealing the underlying layer. These observations are technically helpful and significant to gauge the temperature dependent lifetime and luminance of organic light-emitting diodes.


2000 ◽  
Vol 39 (Part 1, No. 6B) ◽  
pp. 3830-3833 ◽  
Author(s):  
Takeshi Fukuma ◽  
Kei Kobayashi ◽  
Toshihisa Horiuchi ◽  
Hirofumi Yamada ◽  
Kazumi Matsushige

2016 ◽  
Author(s):  
Marco Natali ◽  
Daniele Passeri ◽  
Melania Reggente ◽  
Emanuela Tamburri ◽  
Maria Letizia Terranova ◽  
...  

MRS Advances ◽  
2018 ◽  
Vol 3 (44) ◽  
pp. 2705-2712
Author(s):  
Sergei Magonov ◽  
Shijie Wu

AbstractFast imaging in Atomic Force Microscopy enhances the capability of studying phase transitions and surface properties of materials at variable temperatures. This is demonstrated by measurements of several polymers [poly(diethylsiloxane), low-density polyethylene and ethylene-octene copolymer] and bitumen at low (down to -20°C) and high (up to +150°C) temperatures. Monitoring of structural transitions was performed at small and large (up to 40 μm) areas with 1-5°C/min cooling/heating rates. Novel data about dynamics and structural transitions of mesomorphic transitions and crystallization were obtained.


2001 ◽  
Vol 74 (5) ◽  
pp. 847-870 ◽  
Author(s):  
F. Clément ◽  
L. Bokobza ◽  
L. Monnerie

Abstract Silica-filled polydimethylsiloxane networks are submitted to successive stretching cycles, in order to get the stabilized stretching curve, at variable temperature. This study explains the peculiar temperature dependence of the first stretching curve of filled rubbers, and highlights the molecular origin of the stress-softening phenomenon, known as Mullins effect. Thanks to the comparison between the strain dependence of stress and the molecular orientation, this effect is attributed to the detachment from the filler surface or slippage on the filler surface, of chains having reached their limit of extensibility. Moreover, by taking advantage of Atomic Force Microscopy observations on stretched samples, the Mullins effect is shown to take place mainly in regions of high local concentration of silica. The experimental results are also compared to Bueche's model for the Mullins effect.


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