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Dive into the research topics where William Brown Farnham is active.

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Featured researches published by William Brown Farnham.


Advances in Resist Technology and Processing XX | 2003

Single layer fluropolymer resists for 157-nm lithography

Michael Crawford; William Brown Farnham; Andrew E. Feiring; Jerald Feldman; Roger H. French; Kenneth Wayne Leffew; Viacheslav A. Petrov; Weiming Qiu; Frank Leonard Schadt; Hoang V. Tran; Robert Clayton Wheland; Fredrick Claus Zumsteg

We have developed a family of 157 nm resists that utilize fluorinated terpolymer resins composed of 1) tetrafluoroethylene (TFE), 2) a norbornene fluoroalcohol (NBFOH), and 3) t-butyl acrylate (t-BA). TFE incorporation reduces optical absorbance at 157 nm, while the presence of a norbornene functionalized with hexafluoroisopropanol groups contributes to aqueous base (developer) solubility and etch resistance. The t-butyl acrylate is the acid-catalyzed deprotection switch that provides the necessary contrast for high resolution 157 nm imaging. 157 nm optical absorbances of these resists depend strongly upon the amount of t-BA in the polymers, with the TFE/NBFOH dipolymers (which do not contain t-BA) exhibiting an absorbance lower than 0.6 μm-1. The presence of greater amounts of t-BA increases the absorbance, but also enhances the dissolution rate of the polymer after deprotection, yielding higher resist contrast. Formulated resists based upon these fluorinated terpolymer resins have been imaged at International Sematech, using the 157 nm Exitech microstepper with either 0.6 NA or 0.85 NA optics. We have carefully explored the relationship between imaging performance, resist contrast, optical absorbance, and t-BA content of these terpolymer resist resins, and describe those results in this contribution.


Proceedings of SPIE | 2013

High chi polymer development for DSA applications using RAFT technology

Michael Sheehan; William Brown Farnham; Hoang V. Tran; J. David Londono; Yefim Brun

Directed self-assembly (DSA) of block copolymers is proving to be an interesting and innovative method to make three-dimensional periodic, uniform patterns useful in a variety of microelectronics applications. Attributes critical to acceptable DSA performance of block copolymers include molecular weight uniformity, final purity, and reproducibility in all the steps involved in producing the polymers. Reversible Addition Fragmentation Chain Transfer (RAFT) polymerization technology enables the production of such materials provided that careful process monitoring and compositional homogeneity measurement systems are employed. It is uniquely suited to construction of multiblocks with components of widely divergent surface energies and functionality. We describe a high chi diblock system comprising partially fluorinated methacrylates and substituted styrenics. While special new polymer separation strategies involving controlled polymer particle assembly in liquid media are required for some monomer systems and molecular weight regimes, we have been able to demonstrate high yield and compositionally homogeneous diblocks of lamellar and cylindrical morphology with polydispersities < 1.1. During purification processes, these diblock materials undergo assembly processes in liquid media, and with appropriate controls, this allows for removal of soluble homopolymer contaminants. SAXS analyses of solid polymer samples provide estimates of lamellar d-spacing, and a good correlation with molecular weight is shown. This system will be described.


Journal of the American Chemical Society | 1983

Group-transfer polymerization. 1. A new concept for addition polymerization with organosilicon initiators

Owen W. Webster; Walter Raymond Hertler; Dotsevi Yao Sogah; William Brown Farnham; T. V. RajanBabu


Macromolecules | 1990

Oxyanions catalyze group-transfer polymerization to give living polymers

Ira B. Dicker; Gordon Mark Cohen; William Brown Farnham; Walter Raymond Hertler; Evan Dean Laganis; Dotsevi Y. Sogah


Archive | 1982

Process for preparing "living" polymers

William Brown Farnham; Dotsevi Yao Sogah


Journal of the American Chemical Society | 1990

Fluorinated macrocyclic ethers as fluoride ion hosts. Novel structures and dynamic properties

William Brown Farnham; D. Christopher Roe; David A. Dixon; Joseph C. Calabrese; Richard L. Harlow


Journal of the American Chemical Society | 1985

Crystal and molecular structure of tris(dimethylamino)sulfonium trifluoromethoxide. Evidence for negative fluorine hyperconjugation

William Brown Farnham; Bruce E. Smart; William J. Middleton; Joseph C. Calabrese; David A. Dixon


Archive | 1999

Fluorinated ionomers and their uses

Christopher Marc Doyle; William Brown Farnham; Andrew E. Feiring; Peter A. Morken; Mark Gerrit Roelofs


Journal of the American Chemical Society | 1986

Novel hypervalent (10-I-2) iodine structures

William Brown Farnham; Joseph C. Calabrese


Archive | 2000

Free radical polymerization method for fluorinated copolymers

Paul Gregory Bekiarian; William Brown Farnham

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