Electrorheology (ER) denotes the control of a material's flow properties (rheology) through an electric field. We have fabricated electrorheological suspensions of coated nanoparticles that show electrically controllable liquid-solid transitions. The solid state can reach a yield strength of 130 kPa, breaking the theoretical upper bound on conventional ER static yield stress that is derived on the general assumption that the dielectric and conductive responses of the component materials are linear. In this giant electrorheological (GER) effect, the static yield stress displays near-linear dependence on the electric field, in contrast to the quadratic variation usually observed. Our GER suspensions show low current density over a wide temperature range of 10-120 degrees C, with a reversible response time of <10 ms. Finite-element simulations, based on the model of saturation surface polarization in the contact regions of neighbouring particles, yield predictions in excellent agreement with experiment.

No abstract

Electrorheological fluids constitute a type of colloids that can vary their rheological characteristics upon the application of an electric field. The recently discovered giant electrorheological (GER) effect breaks the upper bound of the traditional ER effect, but a microscopic explanation is still lacking. By using molecular dynamics to simulate the urea-silicone oil mixture trapped in a nanocontact between two polarizable particles, we demonstrate that the electric field can induce the formation of aligned (urea) dipolar filaments that bridge the two boundaries of the nanoscale confinement. This phenomenon is explainable on the basis of a 3D to 1D crossover in urea molecules' microgeometry, realized through the confinement effect provided by the oil chains. The resulting electrical energy density yields an excellent account of the observed GER yield stress variation as a function of the electric field. Electrorheological (ER) fluids [1][2][3][4][5][6][7][8][9][10][11][12][13][14][15] are a type of colloidal dispersions which can vary their rheological characteristics through the application of an external electric field. The traditional ER mechanism is based on induced polarizations arising from the dielectric constant contrast between the solid particles and the fluid [6,12]. The recent discovery of the giant electrorheological (GER) effect [7][8][9][10][11][12], in urea-coated barium titanyl-oxalate nanoparticles ½NH 2 CONH 2 @BaTiOðC 2 O 4 Þ 2 , or BTRU for short, dispersed in silicone oil, has shown that the theoretical upper bound of the ER effect is no longer applicable to this new type of materials. Instead, a phenomenological model of the GER mechanism, based on aligned urea molecular dipoles in the small contact regions of the nanoparticles, yielded an adequate account of the observed effect [7,9,12]. However, a microscopic picture of how this can occur has so far eluded persistent efforts. Moreover, as the GER effect is highly sensitive to whether the dispersing oil can wet the solid particles [10,11], in contrast to the traditional ER fluids, a natural question is how this observation can be integrated into a coherent GER mechanism. In view of the fact that the GER effect has now been reproduced in many different material systems and therefore is becoming a much more general effect [14,15], answers to the above questions would not only be timely, but may also shed light on how to devise general strategies for harnessing and controlling the large electric energy stored in molecular dipoles.In this work we use molecular dynamics (MD) simulations to show that in a mixture of urea molecules with silicone oil chains confined between two bounding surfaces (denoted as substrates below) of a nanoscale contact, aligned urea molecular dipoles can form filaments snaking through the pores of the oil film to bridge the substrates. The required electric field for aligning the urea dipoles is found to be lowered by a factor of 2 to 3 in the presence of the oil chains, compared to that without the oil chains. More...