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                  Parylene HT
                  is a good insulator 
                  with low dissipation factor (D = 0.0002 at 60 Hz and D = 0.002 
                  at 1 kHz), with a surface energy of about 31 mN/m + 1 mN/m, 
                  and has a low polar surface energy component (< 
                  2 mN/m). 
                  
				  Parylene HT
                  films presenting a thickness d comprised between 
                  about 0.5 μm and about 10 μm, have a relative dielectric 
                  constant εr ranging from about 2.2 to about 2.4  
                  Parylene HT 
                  
                  is a transparent polymer in visible wavelength, 
                  and may advantageously be used also as hydrophobic layer 
                  coated on the window of an optical electrowetting device, 
                  especially an optical lens driven by electrowetting. 
                  Considering optical properties of Parylene HT, one important 
                  point is that this fluorinated parylene is very stable under 
                  UV wavelength light, compare to classical parylenes (such as 
                  Parylene N, C and D) which are very sensible to UV wavelength 
                  light. Moreover, Parylene HT
                  , show high reliable dielectric 
                  properties in time and at high temperature (85°C) 
                  in contact with both the conductive and non conductive fluids. 
                  
				  
				  Parylene HT
                  is also a very low polar polymer with a very low 
                  water (moisture) absorption (less to about < 0.01%, after 24h 
                  in contact with water at 23°C, 
                  according to ASTM D570) and is therefore most advantageously 
                  used for applications as dielectric layer in contact with 
                  water. 
                  Additionally, Parylene HT
                  films have shown high resistance to 
                  most chemicals, especially to most non conductive fluids (like 
                  chlorinated aromatic alkanes and alkenes or more general 
                  halogenated aromatic alkanes that can be used in liquid 
                  formulation for electrowetting applications). If need be, the 
                  adhesion of Parylene HT
                  on the lower plate, or on the 
                  substrate, of the electrowetting device may be controlled by 
                  an adhesion promoter between the lower plate (or the 
                  substrate) and the Parylene HT
                  layer. The adhesion promoter 
                  can be a fluorinated silane or a non fluorinated silane. 
                   
                  The use of Parylene HT 
                  
                  allows the formation of a layer having 
                  the required dielectric and hydrophobic properties in the same 
                  material, for example in a one CVD (chemical vapour 
                  deposition) coating step process. 
                  An optical electrowetting device comprising a conductive fluid 
                  and a non-conductive fluid, said fluids being non miscible, 
                  and an insulating substrate on which both fluids are in 
                  contact and form a triple interface, wherein insulating 
                  substrate comprises Parylene HT
                  polymer is new and forms 
                  another object of the present invention. 
                   
                  In particular, Parylene HT
                  has shown to be a very good 
                  solution for low voltage application. 
                  Indeed, in the field of electrowetting devices and especially 
                  in the field of optical liquid lens controlled by 
                  electrowetting phenomena, one important issue is to obtain a 
                  device working at the lowest voltage possible. 
                  
                  
                  
                  
                   
                  
                  
				  
                  The stability of an electrowetting system is dependent upon 
                  the choice of liquids, the dielectric material and the 
                  operating voltage.Substantial progress is reported herein on 
                  use of 300 nm thick poly-tetrafluoro-para-xylylene) (Parylene 
                  HT) films for almost 100° of reliable electrowetting 
                  modulation at only 15 V. Not only does 
                  
                  
				  
                  Parylene HT 
                  
                  exhibit 
                  improved resistance to dielectric failure as compared to 
                  poly(2-chloro-para-xylylene) (Parylene C), but 
				  Parylene HT
                  is 
                  shown to sustain continuous DC electrowetting to  
                  
                  <70° for 
                  >
                  6 hours. Furthermore, 
                  Parylene HT
                  has a surface energy such 
                  that when electrowetting in an alkane oil ambient, a Young’s 
                  angle of about 170° can beachieved without the traditional 
                  fluoropolymer top-coat. Also presented is a new and simple 
                  model for calculating electric field enhancement when 
                  electrowetting in an oil bath. It is shown that 
				  Parylene HT
                  is 
                  a promising candidate for low-voltage and large-area electrowetting devices such as displays and lab-on-chip 
                  
                  
                  Parylene HT
                  is deposited by vapor-phase-deposition and 
                  polymerization of tetrafluoro-p-xylylene. HT films have a 
                  dielectric constant of 2.24 at 1 MHz and show less than 2% 
                  weight loss in 2 hours at 450°C 
                  by isothermal thermal gravimetric analysis. While developing 
                  the deposition process of HT films it was found that the film 
                  surface morphology showed a dependence on deposition 
                  conditions. A systematic study of the surface roughness, 
                  refractive index, weight and thickness loss and FTIR of films 
                  deposited using different deposition conditions was done to 
                  determine the cause of the surface morphology variation 
                   
                  
                                                        
                                                         
                                                         
                   
                      
                  
                                    
                                    
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