اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدCollective excitations of hydrodynamically coupled driven colloidal particles
102
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
Two colloidal particles, driven around an optical vortex trap, have been recently shown to pair due to an interplay between hydrodynamic interactions and the curved path they are forced to follow. We demonstrate here, that this pairing interaction can be tuned experimentally, and study its effect on the collective excitations of many particles driven around such an optical trap. We find that even though the system is overdamped, hydrodynamic interactions due to driving give rise to non-decaying excitations with characteristic dispersion relations. The collective excitations of the colloidal ring reflect fluctuations of particle pairs rather than those of single particles.
قيم البحث
اقرأ أيضاً
We measure the energy exchanged between two hydrodynamically coupled micron-sized Brownian particles trapped in water by two optical tweezers. The system is driven out of equilibrium by random forcing the position of one of the two particles. The for
ced particle behaves as it has an effective temperature higher than that of the other bead. This driving modifies the equilibrium variances and cross-correlation functions of the bead positions: we measure an energy flow between the particles and an instantaneous cross-correlation, proportional to the effective temperature difference between the two particles. A model of the interaction which is based on classical hydrodynamic coupling tensors is proposed. The theoretical and experimental results are in excellent agreement.
We consider the unidirectional particle transport in a suspension of colloidal particles which interact with each other via a pair potential having a hard-core repulsion plus an attractive tail. The colloids are confined within a long narrow channel
and are driven along by a DC or an AC external potential. In addition, the walls of the channel interact with the particles via a ratchet-like periodic potential. We use dynamical density functional theory to compute the average particle current. In the case of DC drive, we show that as the attraction strength between the colloids is increased beyond a critical value, the stationary density distribution of the particles loses its stability leading to depinning and a time dependent density profile. Attraction induced symmetry breaking gives rise to the coexistence of stable stationary density profiles with different spatial periods and time-periodic density profiles, each characterized by different values for the particle current.
Thermally induced particle flow in a charged colloidal suspension is studied in a fluid-mechanical approach. The force density acting on the charged boundary layer is derived in detail. From Stokes equation with no-slip boundary conditions at the par
ticle surface, we obtain the particle drift velocity and the thermophoretic transport coefficients. The results are discussed in view of previous work and available experimental data.
We outline a basic strategy of how self-propulsion can be used to improve the yield of a typical colloidal self-assembly process. The success of this approach is predicated on the thoughtful design of the colloidal building block as well as how self-
propulsion is endowed to the particle. As long as a set of criteria are satisfied, it is possible to significantly increase the rate of self-assembly, and greatly expand the window in parameter space where self-assembly can occur. In addition, we show that by tuning the relative on/off time of the self-propelling force it is possible to modulate the effective speed of the colloids allowing for further optimization of the self-assembly process.
Weakly attractive interactions between the tips of rod-like colloidal particles affect their liquid-crystal phase behaviour due to a subtle interplay between enthalpy and entropy. Here, we employ molecular dynamics simulations on semi-flexible, repul
sive bead-spring chains of which one of the two end beads attract each other. We calculate the phase diagram as a function of both the volume fraction of the chains and the strength of the attractive potential. We identify a large number of phases that include isotropic, nematic, smectic A, smectic B and crystalline states. For tip attraction energies lower than the thermal energy, our results are qualitatively consistent with experimental findings: we find that an increase of the attraction strength shifts the nematic to smectic A phase transition to lower volume fractions, with only minor effect on the stability of the other phases. For sufficiently strong tip attraction, the nematic phase disappears completely, in addition leading to the destabilisation of the isotropic phase. In order to better understand the underlying physics of these phenomena, we also investigate the clustering of the particles at their attractive tips and the effective molecular field experienced by the particles in the smectic A phase. Based on these results, we argue that the clustering of the tips only affects the phase stability if lamellar structures (``micelles) are formed. We find that an increase of the attraction strength increases the degree of order in the layered phases.Interestingly, we also find evidence for the existence of an anti-ferroelectric smectic A phase transition induced by the interaction between the tips. A simple Maier-Saupe-McMillan model confirms our findings.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
