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Polyphthalaldehyde resists

We are continuing to explore the limits of the PBOCST and polyphthalaldehyde resist systems, as well as other materials that incorporate chemical amplification. [Pg.20]

Films of polyphthalaldehyde, sensitized by cationic photoinitiators, have been imaged at 2-5-mJ/cm in the deep ultraviolet (DUV) (see Section 3.10), at 1 pC/cm (20 kV) electron beam radiation and at an unspecified dose of Al-A x-ray radiation. The ultimate utility of this "self-developing" resist system will depend upon its efficacy as an etch barrier. It seems clear that such materials would not serve as adequate etch masks for... [Pg.144]

Other three-component systems based on this chemistry have made use of the following acid-labile dissolution inhibitors polyphthalaldehyde (80), ketals of (J-ketoesters (81), and compounds containing C-O-Si bonds (82). Similar resists have also been used with other radiation sources these will be discussed in subsequent sections. [Pg.354]

Ito and Wilson (12) have extensively investigated another resist system of this type based on polyphthalaldehyde (Equation 24). [Pg.8]

In a typical experiment, polyphthalaldehyde was dissolved in bis-(2-methoxyethyl) ether or cyclohexanone, to which was added the onium salt at 10 wt% to the polymer. Films spin coated on Si wafers were baked at 100°C for 10 minutes and then image-wise exposed. Optical micrographs of the resist images generated upon UV, e-beam, and x-ray radiations are exhibited in Figures 7a, b, and c, respectively. [Pg.20]

The very first chemical amplification resist designed for use in bilayer lithography employed Si-containing polyphthalaldehyde as a top layer resin,... [Pg.184]


See other pages where Polyphthalaldehyde resists is mentioned: [Pg.92]    [Pg.92]    [Pg.144]    [Pg.168]    [Pg.19]    [Pg.19]    [Pg.20]    [Pg.140]    [Pg.141]    [Pg.607]    [Pg.196]    [Pg.673]    [Pg.244]    [Pg.971]    [Pg.972]    [Pg.607]    [Pg.61]   
See also in sourсe #XX -- [ Pg.194 ]




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Polyphthalaldehyde

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