AVS 56th International Symposium & Exhibition | |
Thin Film | Thursday Sessions |
Session TF-ThP |
Session: | Aspects of Thin Films Poster Session |
Presenter: | H. Zhou, Stanford University |
Authors: | H. Zhou, Stanford University P.W. Loscutoff, Stanford University S.F. Bent, Stanford University |
Correspondent: | Click to Email |
Lithography at the sub-22 nm length scale will require resist films under 50nm thick with a high degree of homogeneity. Current resists that are in use for ultraviolet lithography may not be suitable for the projected transition to extreme ultraviolet (EUV) wavelengths, leading to active study of alternative materials solutions. One method for gaining sub-nanometer control over the thickness and composition of photoresist film is molecular layer deposition (MLD), which utilizes a series of self-limiting reactions of organic molecules. In this study, a variety of nanoscale organic films were deposited by MLD via urea coupling chemistry, which occurs by reaction of isocyanates and amines. Films were deposited on substrates that were first prepared by vapor deposition of 3-aminopropyltriethoxysilane on hydroxylated SiO2 surfaces to yield an amine-terminated surface, as confirmed by ellipsometry and XPS. Following amine termination, the diisocyanate and diamine precursors were dosed in a binary cycle, and this cycling was repeated to yield the desired thickness of organic film. Ellipsometry indicates a linear growth rate of 4.5 Å/cycle for the standard coupling of phenylene diisocyanate (PDIC) and ethylenediamine (ED). The urea coupling moiety is confirmed by infrared spectroscopy, and films are shown to have stoichiometric composition by XPS. Temperature dependent measurements show that the films have good thermal stability. To fabricate EUV resists, we have explored a variety of backbones contained within the amine and isocyanate linking groups to tune the functions of the organic films. By changing the backbone of the MLD precursors, we have incorporated ketal-based acid-labile groups into the film and have shown that after incorporation of photoacid generator (PAG), UV exposure, post-exposure bake and development, the films are cleaved, leading to potential use as photoresists. Results of applying the nanoscale oligourea films for advanced photoresist application will be presented.