High-Field Scanning Probe Lithography in Hexadecane: Transitioning from Field Induced Oxidation to Solvent Decomposition through Surface Modification
High field scanning probe lithography in hexadecane leads to two different chemical reactions depending on surface hydrophilicity. On a hydrophilic surface, oxidation of the sample occurs; a hydrophobic surface, results in solvent decomposition and nanoscale deposition of etch resistant material. Th...
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Published in | Advanced materials (Weinheim) Vol. 19; no. 21; pp. 3570 - 3573 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag
05.11.2007
WILEY‐VCH Verlag |
Subjects | |
Online Access | Get full text |
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Summary: | High field scanning probe lithography in hexadecane leads to two different chemical reactions depending on surface hydrophilicity. On a hydrophilic surface, oxidation of the sample occurs; a hydrophobic surface, results in solvent decomposition and nanoscale deposition of etch resistant material. The features are characterized with photoelectron emission microscopy and are carbonaceous in nature with a highly cross‐linked bonding network. Tone reversal in a fluorinated etch is achieved. |
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Bibliography: | Department of Energy - No. DE-AC02-05CH11231; No. DE-AC03-76SF0098 ArticleID:ADMA200700716 SRC-DARPA Financial support of this research by NSF (SINAM and EEC-0425914), SRC-DARPA, and the Director, Office of Basic Energy Science, Office of Energy Research and Materials Sciences Division of the U.S. Department of Energy under Contract No.'s DE-AC02-05CH11231 and DE-AC03-76SF0098 is acknowledged with thanks. M.R. thanks INTEL for postdoctoral funding through the Materials Sciences Division, LBNL. The authors also thank Professor Calvin F. Quate for many helpful and stimulating discussions. NSF - No. SINAM and EEC-0425914 ark:/67375/WNG-CRRRWSML-4 istex:33C67E8C50B2A0E3CC36842CB1A7A85D9720B823 Financial support of this research by NSF (SINAM and EEC‐0425914), SRC‐DARPA, and the Director, Office of Basic Energy Science, Office of Energy Research and Materials Sciences Division of the U.S. Department of Energy under Contract No.'s DE‐AC02‐05CH11231 and DE‐AC03‐76SF0098 is acknowledged with thanks. M.R. thanks INTEL for postdoctoral funding through the Materials Sciences Division, LBNL. The authors also thank Professor Calvin F. Quate for many helpful and stimulating discussions. ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0935-9648 1521-4095 |
DOI: | 10.1002/adma.200700716 |