Guiding the Dewetting of Thin Polymer Films by Colloidal Imprinting

被引:6
|
作者
Ghezzi, Manuel [1 ]
Wang, Peng-Yuan [2 ,3 ]
Kingshott, Peter [2 ,3 ]
Neto, Chiara [1 ]
机构
[1] Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
[2] Swinburne Univ Technol, Ind Res Inst Swinburne, Hawthorn, Vic 3122, Australia
[3] Swinburne Univ Technol, Dept Chem & Biotechnol, Hawthorn, Vic 3122, Australia
来源
ADVANCED MATERIALS INTERFACES | 2015年 / 2卷 / 11期
基金
澳大利亚研究理事会;
关键词
LIQUID-FILMS; PATTERN-FORMATION; SURFACE; LITHOGRAPHY; INSTABILITY; FABRICATION; TRANSITION; DYNAMICS; INVERSION; CRYSTALS;
D O I
10.1002/admi.201500068
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Micropatterned surfaces are important in many biomedical and bioengineering applications, such as the development of biosensors. An approach for the creation of ordered surface patterns, fabricated combining colloidal crystals, consisting of ordered layers of micrometric particles, with dewetting of bilayers of thin polymer films is introduced. The produced patterns are both topographical and chemical in nature, consisting of ordered arrays of microscale holes imprinted in a polymer film, with tunable size. The spontaneous dewetting of the polymer film enables this tunability, with a maximum sevenfold increase in lateral size of the holes and sixfold increase in depth from imprinting to coalescence with neighboring holes. Polymer dewetting and layer inversion are seen to compete during the annealing of the polymer bilayers, and the optimal conditions for hole growth are identified. An in-depth investigation highlights the effects of UV-ozone treatment on the long-range ordering of the colloidal crystals and on preventing the dewetting of the imprinted bilayers. Ordered patterns of different size and depth are produced over large areas by tuning of the colloidal crystal assembly, UV surface treatment and dewetting conditions. Potential applications of the micropatterns produced in the present work include microarrays for single cell studies and biosensors.
引用
收藏
页数:10
相关论文
共 50 条
  • [1] Dewetting of thin polymer films
    T. Vilmin
    E. Raphaël
    [J]. The European Physical Journal E, 2006, 21 : 161 - 174
  • [2] Dewetting of thin polymer films
    Vilmin, T.
    Raphael, E.
    [J]. EUROPEAN PHYSICAL JOURNAL E, 2006, 21 (02): : 161 - 174
  • [3] Inhibition of dewetting of thin polymer films
    Xue, Longjian
    Han, Yanchun
    [J]. PROGRESS IN MATERIALS SCIENCE, 2012, 57 (06) : 947 - 979
  • [4] Nucleated dewetting of thin polymer films
    C. Lorenz-Haas
    P. Müller-Buschbaum
    J. Kraus
    D.G. Bucknall
    M. Stamm
    [J]. Applied Physics A, 2002, 74 : s383 - s385
  • [5] Nucleated dewetting of thin polymer films
    Lorenz-Haas, C
    Müller-Buschbaum, P
    Kraus, J
    Bucknall, DG
    Stamm, M
    [J]. APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING, 2002, 74 (Suppl 1): : S383 - S385
  • [6] Spinodal dewetting of thin polymer films
    Xie, R
    Karim, A
    Douglas, JF
    Han, CC
    Weiss, RA
    [J]. PHYSICAL REVIEW LETTERS, 1998, 81 (06) : 1251 - 1254
  • [7] Autophobicity and dewetting of thin polymer films
    Reiter, G
    [J]. ACTUALITE CHIMIQUE, 2003, (01): : 12 - 17
  • [8] DEWETTING OF THIN POLYMER-FILMS
    REITER, G
    [J]. PHYSICAL REVIEW LETTERS, 1992, 68 (01) : 75 - 78
  • [9] Dewetting of highly elastic thin polymer films
    Reiter, G
    [J]. PHYSICAL REVIEW LETTERS, 2001, 87 (18) : 186101 - 1
  • [10] Viscoelastic dewetting of constrained polymer thin films
    Gabriele, Sylvain
    Damman, Pascal
    Sclavons, Severine
    Desprez, Sylvain
    Coppee, Severine
    Reiter, Guenter
    Hamieh, Moustafa
    Al Akhrass, Samer
    Vilmin, Thomas
    Raphael, Elie
    [J]. JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2006, 44 (20) : 3022 - 3030