Nanowear on polymer films of different architecture

被引:48
作者
Berger, R.
Cheng, Y.
Foerch, R.
Gotsmann, B.
Gutmann, J. S.
Pakula, T.
Rietzler, U.
Schaertl, W.
Schmidt, M.
Strack, A.
Windeln, J.
Butt, H. -J.
机构
[1] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
[2] Johannes Gutenberg Univ Mainz, Inst Phys Chem, D-55099 Mainz, Germany
[3] IBM Res GmbH, Zurich Res Lab, CH-8803 Ruschlikon, Switzerland
关键词
D O I
10.1021/la0620399
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this paper, we describe atomic force microscope (AFM) friction experiments on different polymers. The aim was to analyze the influence of the physical architecture of the polymer on the degree and mode of wear and on the wear mode. Experiments were carried out with (1) linear polystyrene (PS) and cycloolefinic copolymers of ethylene and norbornene, which are stabilized by entanglements, (2) mechanically stretched PS, (3) polyisoprene-b-polystyrene diblock copolymers, with varying composition, (4) brush polymers consisting of a poly(methyl methacrylate) (PMMA) backbone and PS side chains, (5) PMMA and PS brushes grafted from a silicon wafer, (6) plasma-polymerized PS, and (7) chemically cross-linked polycarbonate. For linear polymers, wear depends critically on the orientation of the chains with respect to the scan direction. With increasing cross-link density, wear was reduced and ripple formation was suppressed. The cross-linking density was the dominating material parameter characterizing wear.
引用
收藏
页码:3150 / 3156
页数:7
相关论文
共 49 条
[1]   Comparison of macro- and nanotribological behavior with surface plastic deformation of polystyrene [J].
Aoike, T ;
Uehara, H ;
Yamanobe, T ;
Komoto, T .
LANGMUIR, 2001, 17 (07) :2153-2159
[2]  
BELL GI, 1978, SCIENCE, V200, P618, DOI 10.1126/science.347575
[3]  
BLOCHOWIAK M, 2006, IN PRESS MACROMOLECU
[4]  
Brandrup J., 1999, Polymer handbook, VII
[5]   Nano-indentation of polymeric surfaces [J].
Briscoe, BJ ;
Fiori, L ;
Pelillo, E .
JOURNAL OF PHYSICS D-APPLIED PHYSICS, 1998, 31 (19) :2395-2405
[6]   Synthesis and characterization of polymer brushes on micromechanical cantilevers [J].
Bumbu, GG ;
Kircher, G ;
Wolkenhauer, M ;
Berger, R ;
Gutmann, JS .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 2004, 205 (13) :1713-1720
[7]   Breaking polymer chains by dynamic plowing lithography [J].
Cappella, B ;
Sturm, H ;
Weidner, SM .
POLYMER, 2002, 43 (16) :4461-4466
[8]   Cantilevers with nano-heaters for thermomechanical storage application [J].
Drechsler, U ;
Bürer, N ;
Despont, M ;
Dürig, U ;
Gotsmann, B ;
Robin, F ;
Vettiger, P .
MICROELECTRONIC ENGINEERING, 2003, 67-8 :397-404
[9]   Influence of the molecular weight on the thermal and mechanical properties of ethylene/norbornene copolymers [J].
Ekizoglou, N ;
Thorshaug, K ;
Cerrada, ML ;
Benavente, R ;
Pérez, E ;
Pereña, JM .
JOURNAL OF APPLIED POLYMER SCIENCE, 2003, 89 (12) :3358-3363
[10]   Packing length influence in linear polymer melts on the entanglement, critical, and reptation molecular weights [J].
Fetters, LJ ;
Lohse, DJ ;
Milner, ST ;
Graessley, WW .
MACROMOLECULES, 1999, 32 (20) :6847-6851