Light-Regulated Electrostatic Interactions in Colloidal Suspensions

Kyle N. Plunkett,§ Ali Mohraz,# Richard T. Haasch, Jennifer A. Lewis,*# and Jeffrey S. Moore*§;
Departments of Chemistry and Materials Science & Engineering and the Materials Research Laboratory, University of Illinois at UrbanaChampaign, Urbana, Illinois 61801
J. Am. Chem. Soc., 2005, 127 (42), pp 14574–14575
DOI: 10.1021/ja054666a
Publication Date (Web): September 30, 2005
Copyright © 2005 American Chemical Society

Abstract

Abstract Image

The net charge of a colloidal particle was controlled using light and a new photocleavable self-assembled monolayer (SAM). The SAM contained a terminal ammonium group and a centrally located carboxylic acid group that was masked with an ortho-nitrobenzyl functionality. Once exposed to UV light, the 2-nitrobenzyl group was cleaved, therefore transforming the colloidal particle from a net positive (silica-SAM-NH3+) to a net negative (silica-SAM-COO-) charge. By varying the UV exposure time, their zeta potential could be tailored between +26 and −60 mV at neutral pH. To demonstrate a photoinduced gel-to-fluid phase transition, a binary colloidal suspension composed of silica-SAM-NH3+ and negatively charged, rhodamine-labeled silica particles was mixed to form a gel. Exposure to UV light rendered all of the particles negative and therefore converted the system into a colloidal fluid that settles to form a dense sediment.

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History

  • Published In Issue October 26, 2005
  • Received July 13, 2005

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