Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Ulrich Schaedeli is active.

Publication


Featured researches published by Ulrich Schaedeli.


Proceedings of SPIE, the International Society for Optical Engineering | 1996

Bilayer resist approach for 193-nm lithography

Ulrich Schaedeli; Eric Tinguely; Andrew J. Blakeney; Pasquale Alfred Falcigno; Roderick R. Kunz

Tremendous efforts to extend optical lithography beyond the quarter micrometer boundary, which is currently achievable with KrF-excimer laser lithography, are ongoing. One-hundred- ninety-three nm lithography, using ArF-excimer lasers, is believed to be the technology of choice to approach the ambitious sub-0.2 micrometer resolution target. Single layer, positive tone resist systems, which can be developed with aqueous base, would be preferred. However, it might well turn out that the targeted requirements can only be fulfilled by resist systems which involve some type of dry etch steps. This paper focuses on a positive tone bilayer resist system, which is based on novel silicon containing methacrylate polymers bearing acid labile side groups. Due to a unique combination of monomeric building blocks, polymers with high silicon concentrations and, at the same time, high thermal flow stability are obtained. Hardbaked novolac is used as the planarizing layer. Resists systems based on the new silicon containing polymers demonstrated 0.175 micrometer resolution capability, a thermal flow stability greater than 120 degrees Celsius, and an etch selectivity ratio greater than 20.


Advances in Resist Technology and Processing XI | 1994

Relationship between physical properties and lithographic behavior in a high-resolution positive-tone deep-UV resist

Ulrich Schaedeli; Norbert Muenzel; Heinz Holzwarth; Sydney G. Slater; Omkaram Nalamasu

A chemically amplified positive tone resist system, based on new maleimide polymers and a photoacid generator, has been developed, called MISTRAL (Maleimide-Styrene based Resist for Advanced Lithography). These polymers, which are insoluble in aqueous base, consist of two different types of monomers: blocked p- hydroxystyrenes and N-substituted maleimides. In the irradiated zones of the resist film, the phenols are regenerated by the presence of a photoacid, thereby making the resist soluble in an appropriate developer. The maleimides, on the other hand, are needed to introduce high thermal stability and good film properties. The maleimides can further be used to tailor the dissolution properties of the resist. A variety of different MISTRAL polymers have been prepared, starting from the corresponding monomers. Changes in the molecular weight, the types of monomers used and their ratio in the feed have been analyzed: a correlation study between the physical properties of the MISTRAL polymers and their lithographic behavior was systematically performed, revealing quarter micron resolution capabilities.


Advances in Resist Technology and Processing X | 1993

1,3-dioxolyl acetals as powerful crosslinkers of phenolic resin

Ulrich Schaedeli; Norbert Muenzel; Heinz Holzwarth

The principle of chemical amplification has proven to be successful for the design of highly sensitive, high resolution resist materials of both positive and negative tone, respectively. This paper discusses our new approach to a high resolution, aqueous base developable deep-UV negative tone resist. It is based on the acid catalyzed cleavage of acetal blocked aromatic aldehydes, which, if treated with strong Broensted acid, react with the surrounding phenolic resin in a Friedel-Crafts type reaction, thereby leading to matrix crosslinking. Resists based on this type of crosslinking chemistry show good deep-UV transparency, have high sensitivity, and can be developed with an aqueous base.


Archive | 1999

Radiation sensitive terpolymer, photoresist compositions thereof and 193 nm bilayer systems

Ulrich Schaedeli; Andrew J. Blakeney; Thomas Steinhausler; Daniela White; Allen H. Gabor


Archive | 1998

Terpolymers containing organosilicon side chains

Ulrich Schaedeli; Eric Tinguely; Manfred Hofmann; Pasquale Alfred Falcigno; Carl-Lorenz Mertesdorf


Archive | 1998

Radiation sensitive compositions of terpolymers containing organosilicon side chains

Ulrich Schaedeli; Eric Tinguely; Manfred Hofmann; Pasquale Alfred Falcigno; Carl-Lorenz Mertesdorf


Archive | 1998

Wet-chemical, developable, etch-stable photoresist for UV radiation with a wavelength below 200 nm

Ulrich Schaedeli; Manfred Hofmann; Norbert Muenzel; Arnold Grubenmann


Journal of Photopolymer Science and Technology | 1996

EVALUATION OF MATERIALS FOR 193-nm LITHOGRAPHY

Ulrich Schaedeli; Eric Tinguely; Katiuscia Cherubini; Beatrice Maire; Andrew J. Blakeney; Pasquale Alfred Falcigno; Roderick R. Kunz


Archive | 1996

Terpolymers containing organosilicon side chains and their use for the production of relief structures

Ulrich Schaedeli; Eric Tinguely; Manfred Hofmann; Pasquale Alfred Falcigno; Carl-Lorenz Mertesdorf


Archive | 1994

Method of making micropatterns.

Ulrich Schaedeli

Collaboration


Dive into the Ulrich Schaedeli's collaboration.

Top Co-Authors

Avatar

Roderick R. Kunz

Massachusetts Institute of Technology

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge