Exponential Growth of Lbl Films with Incorporated Inorganic Sheets

Thursday, November 20, 2008: 8:51 AM
Room 105-B (Pennsylvania Convention Center)

Paul Podsiadlo, Chemical Engineering, University of Michigan, Ann Arbor, MI
Marc Michel, Chemical Engineering, University of Michigan, Ann Arbor, MI
Jungwoo Lee, Biomedical Engineering, University of Michigan, Ann Arbor, MI
Eric Verploegen, Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, MA
Nadine Wong Shi Kam, Chemical Engineering, University of Michigan, Ann Arbor, MI
Jaebeom Lee, University of Michigan, Ann Arbor, MI
Vincent Ball, Institut National de la Santé et de la Recherche Médicale
Ying Qi, Electron Microbeam Analysis Laboratory, University of Michigan, Ann Arbor, MI
Anastasios J. Hart, Massachusetts Institute of Technology, Cambridge, MA
Paula T. Hammond, Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA
Nicholas Kotov, Chemical Engineering, University of Michigan, Ann Arbor, MI

The fastest growth pattern of layer-by-layer (LBL) assembled films is exponential LBL (e-LBL), which has both fundamental and practical importance. It is associated with “in-and-out” diffusion of flexible polymers, and thus was considered to be impossible for films containing clay sheets with strong barrier function, preventing diffusion. Here, we demonstrate that e-LBL for inorganic sheets is possible in a complex tri-component film of poly(ethyleneimine) (PEI), poly(acrylic acid) (PAA), and Na+-montmorillonite (MTM). This system displayed clear e-LBL patterns both in terms of initial accumulation of materials and unusually thick individual bilayers later in deposition process with film thicknesses reaching 200 ěm for films composed of 200 pairs of layers. Successful incorporation of MTM layers was observed by scanning electron microscopy and thermo-gravimetric analysis. Surprisingly, the growth rate was found to be nearly identical in films with and without clay layers, which suggests fast permeation/reptation of polyelectrolytes between the nanosheets during the “in-and-out” diffusion of polymer. Considering these findings, e-LBL growth property is expected for a wide array of available inorganic nanoscale components and have a potential to greatly expand the e-LBL field and LBL field altogether. The large thickness and rapid growth of the films affords fast preparation of nanostructured materials which is essential for multiple practical applications ranging from optical devices to ultrastrong composites.
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