Stabilization of polystyrene thin films by introduction of a functional end group

Shinichiro Shimomura, Manabu Inutsuka, Koichiro Tajima, Masaaki Nabika, Satoru Moritomi, Hisao Matsuno, Keiji Tanaka

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

The thin film stabilities of ω-N-(3-(dimethylamino)propyl)propylamide-terminated polystyrene (PS-N) and its blends with conventional polystyrene (PS-H) supported on silicon wafers with a native oxide layer were examined. Whereas a 20-nm-thick film of PS-H with a number-average molecular weight of ∼50k decomposed at 423 K, a comparable PS-N film and blended films containing a PS-N fraction of >40 wt% were stable. Although the local conformation of chains at the substrate interface was not the same for PS with and without the functional end group, the glass transition temperature at the interface was identical for both PS-H and PS-N. The residual adsorbed layer on the substrate after washing the films with a good solvent was thicker for PS-N than for PS-H. This implies that end functionalization, rather than segmental dynamics, affects chain movement on a large scale.

Original languageEnglish
Pages (from-to)949-953
Number of pages5
JournalPolymer Journal
Volume48
Issue number9
DOIs
Publication statusPublished - Sep 1 2016

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Polystyrenes
Stabilization
Thin films
Substrates
Silicon wafers
Thick films
Washing
Oxides
Conformations
Molecular weight

All Science Journal Classification (ASJC) codes

  • Polymers and Plastics
  • Materials Chemistry

Cite this

Stabilization of polystyrene thin films by introduction of a functional end group. / Shimomura, Shinichiro; Inutsuka, Manabu; Tajima, Koichiro; Nabika, Masaaki; Moritomi, Satoru; Matsuno, Hisao; Tanaka, Keiji.

In: Polymer Journal, Vol. 48, No. 9, 01.09.2016, p. 949-953.

Research output: Contribution to journalArticle

Shimomura, Shinichiro ; Inutsuka, Manabu ; Tajima, Koichiro ; Nabika, Masaaki ; Moritomi, Satoru ; Matsuno, Hisao ; Tanaka, Keiji. / Stabilization of polystyrene thin films by introduction of a functional end group. In: Polymer Journal. 2016 ; Vol. 48, No. 9. pp. 949-953.
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