Calibration of chemically amplified resist models
Author(s) -
Jeff D. Byers,
John S. Petersen,
John L. Sturtevant
Publication year - 1996
Publication title -
proceedings of spie, the international society for optical engineering/proceedings of spie
Language(s) - English
Resource type - Conference proceedings
SCImago Journal Rank - 0.192
H-Index - 176
eISSN - 1996-756X
pISSN - 0277-786X
DOI - 10.1117/12.241875
Subject(s) - resist , calibration , stepper , lithography , biological system , computer science , photobleaching , materials science , photolithography , photoresist , optical proximity correction , nanotechnology , optics , optoelectronics , physics , layer (electronics) , quantum mechanics , fluorescence , biology
Chemically amplified (CA) resists are expected to provide the majority of the lithography capability for 0.25 micron feature sizes. The sensitivity of CA resists to processing conditions makes implementation of a resist system very dependent on the tool set (stepper, track etc.) used. Modeling of these systems can be useful in optimizing a process for a particular tool set. However, the modeling parameters are also sensitive to the target tool set. Variations in dose calibration between different steppers, the differing temperature ramps found in contact and proximity bakes, and batch to batch variations between resist materials are examples why resist model parameters require calibration to each tool set. An ideal calibration procedure would entail in-situ measurement techniques at each processing step. The techniques would analytically determine chemical, physical, and kinetic quantities relevant to the resist system and processing conditions. Methods previously used have included interferometric measurement of photobleaching, FTIR measurement of the deprotection extent1,2, in-situ DRM measurements3, etc. Unfortunately, few if any fabs are equipped with the necessary in -situ techniques for complete model calibration. Methodology:
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