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Chemical crosslinkable semiconductors

Positive-Tone Photoresists based on Dissolution Inhibition by Diazonaphthoquinones. The intrinsic limitations of bis-azide—cycHzed mbber resist systems led the semiconductor industry to shift to a class of imaging materials based on diazonaphthoquinone (DNQ) photosensitizers. Both the chemistry and the imaging mechanism of these resists (Fig. 10) differ in fundamental ways from those described thus far (23). The DNQ acts as a dissolution inhibitor for the matrix resin, a low molecular weight condensation product of formaldehyde and cresol isomers known as novolac (24). The phenoHc stmcture renders the novolac polymer weakly acidic, and readily soluble in aqueous alkaline solutions. In admixture with an appropriate DNQ the polymer s dissolution rate is sharply decreased. Photolysis causes the DNQ to undergo a multistep reaction sequence, ultimately forming a base-soluble carboxyHc acid which does not inhibit film dissolution. Immersion of a pattemwise-exposed film of the resist in an aqueous solution of hydroxide ion leads to rapid dissolution of the exposed areas and only very slow dissolution of unexposed regions. In contrast with crosslinking resists, the film solubiHty is controUed by chemical and polarity differences rather than molecular size. [Pg.118]


See other pages where Chemical crosslinkable semiconductors is mentioned: [Pg.296]    [Pg.325]    [Pg.132]    [Pg.354]    [Pg.303]    [Pg.315]    [Pg.431]    [Pg.49]    [Pg.172]    [Pg.274]    [Pg.159]    [Pg.160]    [Pg.29]    [Pg.764]    [Pg.100]    [Pg.420]    [Pg.164]   
See also in sourсe #XX -- [ Pg.299 ]




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