The leaching of ionic PAGs from model resist films into a static water volume is shown to follow first order kinetics. From the saturation concentration and the leaching time constant, the leaching rate at time zero is obtained which is a highly relevant parameter for evaluating lens contamination potential. The levels of leaching seen in the model resists generally exceed both static and rate-based dynamic leaching specifications. The dependence of leaching on anion structure shows that more hydrophobic anions have lower saturation concentration; however, the time constant of leaching increases with anion chain length. Thus in our model system, the initial leaching rates of nonaflate and PFOS anions are identical. Investigation of a water pre-rinse process unexpectedly showed that some PAG can still be leached from the surface although the pre-rinse times greatly exceeded the times required for saturation of the leaching phenomenon, which are expected to correspond to complete depletion of leachable PAG from the surface. A model is proposed to explain this phenomenon through re-organization of the surface as the surface energy changes during the air/water/air contact sequence of the pre-rinse process. The efficiency of developer-soluble top barrier layers in reducing leching and their impact on lithography are described as well as the effect of PAG doping into the top layers. © 2005 TAPJ.
CITATION STYLE
Dammel, R. R., Pawlowski, G., Romano, A., Houlihan, F. M., Kim, W. K., Sakamuri, R., … McKenzie, D. (2005). Leaching phenomena and their suppresion in 193 nm immersion lithography. Journal of Photopolymer Science and Technology, 18(5), 593–602. https://doi.org/10.2494/photopolymer.18.593
Mendeley helps you to discover research relevant for your work.