Catalytic bimetallic Janus particles swim by a bipolar electrochemical propulsion mechanism that results from electroosmotic fluid slip around the particle surface. The flow is driven by electrical body forces which are generated from a coupling of a reaction-induced electric field and net charge in the diffuse layer surrounding the particle. This paper presents simulations, scaling, and physical descriptions of the experimentally observed trend that the swimming speed decays rapidly with increasing solution conductivity. The simulations solve the full Poisson-Nernst-Planck-Stokes equations with multiple ionic species, a cylindrical particle in an infinite fluid, and nonlinear Butler-Volmer boundary conditions to represent the electrochemical surface reactions. The speed of bimetallic particles is reduced in high-conductivity solutions because of reductions in the induced electric field in the diffuse layer near the rod, the total reaction rate, and the magnitude of the rod zeta potential. This work suggests that the auto-electrophoretic mechanism is inherently susceptible to speed reductions in higher ionic strength solutions.
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April 2014
Research Article|
April 01 2014
Role of solution conductivity in reaction induced charge auto-electrophoresis
Jeffrey L. Moran;
Jeffrey L. Moran
a)
Department of Mechanical Engineering,
University of Washington
, Seattle, Washington 98195-2600, USA
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Jonathan D. Posner
Jonathan D. Posner
b)
Department of Mechanical Engineering,
University of Washington
, Seattle, Washington 98195-2600, USA
Search for other works by this author on:
a)
Present address: Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
b)
Author to whom correspondence should be addressed. Electronic mail: jposner@uw.edu
Physics of Fluids 26, 042001 (2014)
Article history
Received:
September 05 2013
Accepted:
February 07 2014
Citation
Jeffrey L. Moran, Jonathan D. Posner; Role of solution conductivity in reaction induced charge auto-electrophoresis. Physics of Fluids 1 April 2014; 26 (4): 042001. https://doi.org/10.1063/1.4869328
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