Microfiber inclination, crystallinity, and water wettability of microfibrous thin-film substrates of Parylene C in relation to the direction of the monomer vapor during fabrication

2015 ◽  
Vol 345 ◽  
pp. 145-155 ◽  
Author(s):  
Chandraprakash Chindam ◽  
Nichole M. Wonderling ◽  
Akhlesh Lakhtakia ◽  
Osama O. Awadelkarim ◽  
Wasim Orfali
2004 ◽  
Vol 10 (5) ◽  
pp. 407-411 ◽  
Author(s):  
C.Y. Shih ◽  
T.A. Harder ◽  
Y.C. Tai
Keyword(s):  

Author(s):  
F.M. Sciammarella ◽  
C.A. Sciammarella ◽  
L. Lamberti ◽  
M. Styrcula ◽  
L. Wei ◽  
...  

Author(s):  
Amine Abdelkader Guermoudi ◽  
Pierre Yves Cresson ◽  
Amaria Ouldabbes ◽  
Ghizlane Boussatour ◽  
Tuami Lasri

1999 ◽  
Vol 558 ◽  
Author(s):  
C.D. Sheraw ◽  
D.J. Gundlach ◽  
T.N. Jackson

ABSTRACTWe have investigated the polymeric insulators benzocyclobutene (BCB), parylene C and polyimide for use as gate dielectrics in pentacene organic thin film transistors (TFTs). Atomic force microscopy (AFM) was used to examine the surface roughness of the polymeric dielectrics and the morphology of pentacene films deposited onto them. X-ray diffraction was used to examine the molecular ordering of pentacene films deposited onto the polymeric dielectrics. We find a correlation between the surface roughness of the gate dielectric and the grain size in deposited pentacene films, with smooth surfaces yielding larger, more dendritic grains. Despite significant changes in film morphology, pentacene TFTs using BCB, parylene C, or polyimide as the gate dielectric have performance comparable to devices using SiO2 as the gate dielectric. These results suggest that there is not a strong correlation between pentacene film grain size and field-effect mobility for these devices. Pentacene TFTs using BCB as the gate dielectric had field-effect mobility as high as 0.7 cm2/V-s, on/off ratio > 107, subthreshold slope less than 2 V/decade, and negative threshold voltage, making them an attractive candidate for use in organic-based large-area electronic applications on flexible substrates.


2013 ◽  
Vol 421 ◽  
pp. 337-341
Author(s):  
Chin Tun Chuang ◽  
Fa Ta Tsai ◽  
Ming Jun Kuo ◽  
Pei Chi Yu

This work aims to enhance the adhesion of Parylene-C (poly-chloro-p-xylylene C) thin film on PMMA, Glass and Aluminum substrates by chemical vapor deposition, surface improvement and treatment of substrate as well as analysis of film on Glass, PMMA, Aluminum and its surface adhesion by dipping under A-174 silane solution and conducting on plasma treatment (18 W). The results show that: (1) After oxygen-plasma pretreatment, the surface roughness of the 200nm-thickness film on glass substrate specimens decreases from 18nm to 7nm. (2) After dipped in prescription solution pretreatment, the residual stress reduces from 107MPa to 64MPa on glass substrate specimens. (3) The critical load of 600nm-thickness film increases from 14.1 to 18.5mN, showing the substrate after dipped in prescription solution pretreatment can improve the adhesion of the Parylene-C thin film on flat glass substrate specimens.


2012 ◽  
Vol 217-219 ◽  
pp. 1077-1082 ◽  
Author(s):  
Fa Ta Tsai ◽  
Chin Tun Chuang ◽  
Tsai Cheng Li ◽  
Pei Chi Yu

This work aims to enhance the surface wettability and adhesion of Parylene-C (poly-chloro-p-xylylene C) thin film on PMMA, glass and aluminum substrates by chemical vapor deposition. The results show that: (1) 0.56, 1, and 1.55g Parylene-C powders can deposit 200, 400, and 600nm films, respectively. (2) After oxygen-plasma pretreatment, the surface roughness of the 200nm-thickness film on glass substrate specimens decreases from 18nm to 7nm. (3) After dipped in prescription solution pretreatment, the residual stress reduces from 107MPa to 64MPa on glass substrate specimens. (4) In contact angle tests, the 600nm-thickness film on various flat substrates deposited process that has surface hydrophobic. (5) The critical load of 600nm-thickness film increases from 14.1 to 18.5mN, showing the substrate after dipped in prescription solution pretreatment can improve the adhesion of the Parylene-C thin film on flat glass substrate specimens.


1995 ◽  
Vol 390 ◽  
Author(s):  
David J. Monk ◽  
Mahesh Shah

ABSTRACTStresses in thin polymer films have been studied for some time by using wafer bowing, bending beams, microstructure release, and laser holographic techniques. An alternative technique for measuring stresses in thin films is discussed in the following paper. Piezoresistive anisotropically etched single crystal silicon pressure sensors are sensitive not only to applied pressure, but also to applied package stress. Deposited passivation materials, like silicone gels and polyimides, have been observed to change the sensitivity of the pressure sensor. In the current work, a thin, conformal polymeric coating (parylene C) is being developed for these pressure sensors. This thin film has been observed to reduce the sensitivity of the device as a function of the film thickness and modulus and the silicon thickness and modulus. The parylene C thin films exhibit a consistent change in film stress during annealing indicating a modification to polymer crystallinity and a corresponding change in material properties. Qualitatively, the electrical output on the pressure sensor compares favorably with measurements taken using wafer bowing. Experimental DMA and TMA work has been performed to determine the modulus (7.84 × 105 psi) and CTE (39 ppm/°C at 25 °C) of the material. However, literature values of modulus (4.1 × 105 psi) have been used with finite element analysis to model the stress effect more accurately for the thin conformal coating on the pressure sensor device. These results indicate that the sensitivity of the pressure sensor will be reduced approximately quadratically as a function of the polymer coating thickness. An empirical function has been derived to estimate sensitivity loss as a function of substrate (i.e., initial diaphragm material) modulus and thickness and coating modulus and thickness.


2018 ◽  
Vol 20 (3) ◽  
Author(s):  
Mats Forssell ◽  
Xiao Chuan Ong ◽  
Rakesh Khilwani ◽  
O. Burak Ozdoganlar ◽  
Gary K. Fedder

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