Femtosecond-laser processing of nitrobiphenylthiol self-assembled monolayers

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Anja Schröter
  • Steffen Franzka
  • Jürgen Koch
  • Boris N. Chichkov
  • Andreas Ostendorf
  • Nils Hartmann

Externe Organisationen

  • Universität Duisburg-Essen
  • Laser Zentrum Hannover e.V. (LZH)
  • Ruhr-Universität Bochum
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Seiten (von - bis)43-46
Seitenumfang4
FachzeitschriftApplied surface science
Jahrgang278
PublikationsstatusVeröffentlicht - 1 Feb. 2013
Extern publiziertJa

Abstract

Single-pulse femtosecond laser patterning of nitrobiphenylthiol monolayers on Au-coated Si substrates at λ = 800 nm, τ < 30 fs and ambient conditions has been investigated. After laser processing wet etching experiments are performed. Laser irradiation reduces the chemical resistance of the coating. In particular, the monolayer acts as a positive-tone resist. Burr-free pattern transfer is feasible at laser pulse fluences between 1 and 2.7 J/cm 2 . Minimum structure sizes at a 1/e laser spot diameter of about 1 μm are close to 300 nm, i.e. sub-wavelength processing is demonstrated. Noteworthy, however, no indications for negative-tone resist properties of processed monolayers are evident, that is, cross-linking of the biphenyl moieties, if at all, is marginal. Also, complementary labeling experiments provide no evidence for chemical transformation of the nitro end groups into amine functionalities. Perspectives of resonant fs-laser processing in exploiting the particular prospects of nitrobiphenylthiol monolayers as negative-tone resists and chemically patternable platforms are discussed.

ASJC Scopus Sachgebiete

Zitieren

Femtosecond-laser processing of nitrobiphenylthiol self-assembled monolayers. / Schröter, Anja; Franzka, Steffen; Koch, Jürgen et al.
in: Applied surface science, Jahrgang 278, 01.02.2013, S. 43-46.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Schröter, A, Franzka, S, Koch, J, Chichkov, BN, Ostendorf, A & Hartmann, N 2013, 'Femtosecond-laser processing of nitrobiphenylthiol self-assembled monolayers', Applied surface science, Jg. 278, S. 43-46. https://doi.org/10.1016/j.apsusc.2013.01.170
Schröter, A., Franzka, S., Koch, J., Chichkov, B. N., Ostendorf, A., & Hartmann, N. (2013). Femtosecond-laser processing of nitrobiphenylthiol self-assembled monolayers. Applied surface science, 278, 43-46. https://doi.org/10.1016/j.apsusc.2013.01.170
Schröter A, Franzka S, Koch J, Chichkov BN, Ostendorf A, Hartmann N. Femtosecond-laser processing of nitrobiphenylthiol self-assembled monolayers. Applied surface science. 2013 Feb 1;278:43-46. doi: 10.1016/j.apsusc.2013.01.170
Schröter, Anja ; Franzka, Steffen ; Koch, Jürgen et al. / Femtosecond-laser processing of nitrobiphenylthiol self-assembled monolayers. in: Applied surface science. 2013 ; Jahrgang 278. S. 43-46.
Download
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abstract = " Single-pulse femtosecond laser patterning of nitrobiphenylthiol monolayers on Au-coated Si substrates at λ = 800 nm, τ < 30 fs and ambient conditions has been investigated. After laser processing wet etching experiments are performed. Laser irradiation reduces the chemical resistance of the coating. In particular, the monolayer acts as a positive-tone resist. Burr-free pattern transfer is feasible at laser pulse fluences between 1 and 2.7 J/cm 2 . Minimum structure sizes at a 1/e laser spot diameter of about 1 μm are close to 300 nm, i.e. sub-wavelength processing is demonstrated. Noteworthy, however, no indications for negative-tone resist properties of processed monolayers are evident, that is, cross-linking of the biphenyl moieties, if at all, is marginal. Also, complementary labeling experiments provide no evidence for chemical transformation of the nitro end groups into amine functionalities. Perspectives of resonant fs-laser processing in exploiting the particular prospects of nitrobiphenylthiol monolayers as negative-tone resists and chemically patternable platforms are discussed.",
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AU - Schröter, Anja

AU - Franzka, Steffen

AU - Koch, Jürgen

AU - Chichkov, Boris N.

AU - Ostendorf, Andreas

AU - Hartmann, Nils

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N2 - Single-pulse femtosecond laser patterning of nitrobiphenylthiol monolayers on Au-coated Si substrates at λ = 800 nm, τ < 30 fs and ambient conditions has been investigated. After laser processing wet etching experiments are performed. Laser irradiation reduces the chemical resistance of the coating. In particular, the monolayer acts as a positive-tone resist. Burr-free pattern transfer is feasible at laser pulse fluences between 1 and 2.7 J/cm 2 . Minimum structure sizes at a 1/e laser spot diameter of about 1 μm are close to 300 nm, i.e. sub-wavelength processing is demonstrated. Noteworthy, however, no indications for negative-tone resist properties of processed monolayers are evident, that is, cross-linking of the biphenyl moieties, if at all, is marginal. Also, complementary labeling experiments provide no evidence for chemical transformation of the nitro end groups into amine functionalities. Perspectives of resonant fs-laser processing in exploiting the particular prospects of nitrobiphenylthiol monolayers as negative-tone resists and chemically patternable platforms are discussed.

AB - Single-pulse femtosecond laser patterning of nitrobiphenylthiol monolayers on Au-coated Si substrates at λ = 800 nm, τ < 30 fs and ambient conditions has been investigated. After laser processing wet etching experiments are performed. Laser irradiation reduces the chemical resistance of the coating. In particular, the monolayer acts as a positive-tone resist. Burr-free pattern transfer is feasible at laser pulse fluences between 1 and 2.7 J/cm 2 . Minimum structure sizes at a 1/e laser spot diameter of about 1 μm are close to 300 nm, i.e. sub-wavelength processing is demonstrated. Noteworthy, however, no indications for negative-tone resist properties of processed monolayers are evident, that is, cross-linking of the biphenyl moieties, if at all, is marginal. Also, complementary labeling experiments provide no evidence for chemical transformation of the nitro end groups into amine functionalities. Perspectives of resonant fs-laser processing in exploiting the particular prospects of nitrobiphenylthiol monolayers as negative-tone resists and chemically patternable platforms are discussed.

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