Tunable stimulus-responsive friction mechanisms of polyelectrolyte films and tube forests†

نویسندگان

  • Lin Han
  • Jie Yin
  • Lifeng Wang
  • Khek-Khiang Chia
  • Robert E. Cohen
  • Michael F. Rubner
  • Christine Ortiz
  • Mary C. Boyce
چکیده

The pH-responsive frictional behavior of layer-by-layer assembled poly(allylamine hydrochloride) and poly(acrylic acid) multilayers is quantified in different geometric forms of a continuous planar film and anisotropic tube forests. A mechanistic change from surface adhesion dominated frictional behavior to visco/poroelasticity-governed shear occurs for the planar film upon pH-stimulus. This pH-dependent friction can be further controlled by the discrete anisotropic geometry of the tube forest, which introduces additional friction due to asymmetric deformation of the discrete bending of the tubes during lateral motion. This study provides important insights into the design of polyelectrolyte-based coatings with a wide range of controllable surface frictional properties, tuned via interactions between the inherent stimulus-responsive material behavior and the microgeometry of the anisotropic tube forest.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Geometrically controlled mechanically responsive polyelectrolyte tube arrays.

IO N Over the last two decades, there has been extensive work on stimulus-responsive materials and structures that undergo actuation, swelling, variable permeability and wettability, and aggregation in the presence of external environmental stimulus, e.g., pH, ionic strength, temperature, and pressure. [ 1–4 ] However, the design, fabrication, characterization, and fundamental understanding of ...

متن کامل

Tunable resistive m-dPEG acid patterns on polyelectrolyte multilayers at physiological conditions: template for directed deposition of biomacromolecules.

This paper describes a new class of salt-responsive poly(ethylene glycol) (PEG) self-assembled monolayers (SAMs) on top of polyelectrolyte multilayer (PEMs) films. PEM surfaces with poly(diallyldimethylammonium chloride) as the topmost layer are chemically patterned by microcontact printing (muCP) oligomeric PEG molecules with an activated carboxylic acid terminal group (m-dPEG acid). The resis...

متن کامل

Stimuli-responsive 2D polyelectrolyte photonic crystals for optically encoded pH sensing.

A versatile photonic crystal sensing motif based on a two-dimensional (2D) inverse opal monolayer of stimuli-responsive polyelectrolyte gel with tunable optical properties is reported. The photonic membrane shows prompt response to pH and can be readily read out from either its optical spectra or interference colours.

متن کامل

Reversible pH Stimulus-Response Material Based on Amphiphilic Block Polymer Self-Assembly and Its Electrochemical Application

Stimulus-responsive microporous solid thin films were successfully fabricated by simple molecular self-assembly via an amphiphilic block polymer, polystryene-b-polyacrylic acid (PS-b-PAA). The solid thin films exhibit different surface morphologies in response to external stimuli, such as environments with different pH values in aqueous solutions. The experiments have successfully applied atomi...

متن کامل

Tunable synthesis of Prussian Blue in exponentially growing polyelectrolyte multilayer films.

Polyelectrolyte multilayer (PEM) films have become very popular for surface functionalization and the design of functional architectures such as hollow polyelectrolyte capsules. It is known that properties such as permeability to small ionic solutes are strongly dependent on the buildup regime of the PEM films. This permeability can be modified by tuning the ionization degree of the polycations...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2012