journal article·2010-10-12

Catalytic and Autocatalytic Mechanisms of Acid Amplifiers for Use in EUV Photoresists

Seth A. Kruger, Craig Higgins, Brian Cardineau, Todd R. Younkin, Robert L. Brainard

Chemistry of Materials· Volume 22· Issue 19
Publisher page

Abstract

Twelve fluorinated acid amplifiers (AAs) were synthesized and studied for use in photoresists exposed to 13.5 nm, extreme ultraviolet (EUV) light. Acid amplifiers are compounds that decompose in the presence of acid to generate more acid via catalytic or autocatalytic mechanisms. These AAs are composed of a body, trigger, and an acid precursor. Thermal decomposition rates of solutions of the AAs in C 6 D 6 / m -ethylphenol (50/50 wt %) at 100 °C were monitored by 19 F NMR with and without 1.2 equiv. of 2,4,6-tri- t -butylpyridine. All of the AAs in the presence of base decompose according to first-order kinetics with rate constants k Base . The rate constants, k Base, at various temperatures yielded the activation parameters Δ H ‡, Δ S ‡, and Δ G ‡ . The enthalpy of activation, Δ H, ‡, was in a narrow range of 16.6−19.1 (kcal/mol), whereas the entropy of activation, Δ S ‡, spanned from 0 to −12 (cal/(mol K)). When acid is allowed to build up in solution (in the absence of base), six of the AAs with tertiary triggers (Body-3) decompose autocatalytically, but the six with secondary triggers (Body-2) are unaffected. Although Body-2 AAs do not decompose autocatalytically, nonaflate acid does catalyze their decomposition. Lithographic evaluation showed that some AAs are capable of simultaneously improving the resolution, line-edge-roughness, and sensitivity of a control EUV photoresist. This simultaneous improvement was quantified using the Z -Parameter. The AAs investigated here were found to improve the Z -Parameter by as much as a factor of 3.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advancements in Photolithography Techniques · Electron and X-Ray Spectroscopy Techniques · Integrated Circuits and Semiconductor Failure Analysis

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

College of Nanoscale Science and Engineering, University at Albany, Albany, New York 12203

Intel Corporation, Hillsboro, Oregon 97124

References (24)

Show source-provided references
1. Ito H. · J. Photopolym. Sci. Technol. · 1994 · 7 · 43310.2494/photopolymer.7.433 ↗
2. Shumway M. D. · J. Vac. Sci. Technol., B · 2005 · 23 · 284410.1116/1.2134717 ↗
3. Gallatin G. M. · Proc. SPIE · 2008 · 6921 · 69211E/1
4. Brainard R. L. · Proc. SPIE · 2004 · 5374 · 7410.1117/12.536411 ↗
5. Ichimura K. · Chem. Rec. · 2002 · 2 · 4610.1002/tcr.10013 ↗
6. Gerdts C. J. · J. Am. Chem. Soc. · 2004 · 126 · 632710.1021/ja031689l ↗
7. Ichimura K. · Chem. Lett. · 1995 · 55110.1246/cl.1995.551 ↗
8. Arimitsu K. · J. Am. Chem. Soc. · 1998 · 120 · 3710.1021/ja972353c ↗
9. Kruger S. A. · J. Am. Chem. Soc. · 2009 · 131 · 986210.1021/ja901448d ↗
10. Noguchi S. · J. Photopolym. Sci. Technol. · 1997 · 10 · 31510.2494/photopolymer.10.315 ↗
11. Ohfuji T. · J. Photopolym. Sci Technol. · 1997 · 10 · 55110.2494/photopolymer.10.551 ↗
12. Arimitsu K. · Chem. Lett. · 1998 · 82310.1246/cl.1998.823 ↗
13. Kudo K. · Chem. Mater. · 1999 · 11 · 211910.1021/cm990054b ↗
14. Park S.-W. · J. Photopolym. Sci. Technol. · 1999 · 12 · 29310.2494/photopolymer.12.293 ↗
15. Naito T. · J. Photopolym. Sci. Technol. · 1999 · 12 · 50910.2494/photopolymer.12.509 ↗
16. Lee S. · J. Photopolym. Sci. Technol. · 2000 · 13 · 21510.2494/photopolymer.13.215 ↗
17. Ito H. · Macromol. Chem. Phys. · 2000 · 201 · 13210.1002/(SICI)1521-3935(20000101)201:1<132::AID-MACP132>3.0.CO;2-3 ↗
18. Huang W.-S. · Proc. SPIE · 2000 · 3999 · 59110.1117/12.388344 ↗
19. Wallow T. · Proc. SPIE · 2008 · 6921 · 1
20. Higgins C. · Proc. SPIE · 2009 · 7271 · 47
21. Gallatin G. M. · 2007
22. Brainard R. · J. Photopolym. Sci. Technol. · 2009 · 22 · 4310.2494/photopolymer.22.43 ↗
23. Capellos C. · 1972
24. Mack C. · 200710.1002/9780470723876 ↗