论文标题
活性胶体的强制微流变学
Forced microrheology of active colloids
论文作者
论文摘要
通过考虑维持浸湿的恒定恒定胶体胶体探针稳定运动所需的外力,研究了稀释活性(自propeld)胶体悬浮液的粒子跟踪微流变学。如果探针速度为零,则悬浮微结构是各向同性的,但由于其自我刺激而在接触时表现出活跃浴颗粒的边界积累。随着探针通过悬浮液的移动,微结构会从非平衡的各向同性状态变形,这使我们能够使用Stokes拖动定律为悬架定义微视率。对于缓慢的探针,我们表明主动悬浮液表现出游泳的行为,在游泳速度增加的情况下,其微持率逐渐从被动悬架逐渐降低。当探针速度快速时,悬浮活性会因探针的快速对流而掩盖,并且测得的微度粘度与被动悬浮液的区别没有区别。通常,对于有限活性,悬浮液表现出速度稀释的行为 - 虽然零速度高于被动悬浮液,但作为探针速度的函数。这些行为源于悬浮活性和硬球之间的相互作用,排除了探针和浴粒子之间的体积相互作用。
Particle-tracking microrheology of dilute active (self-propelled) colloidal suspensions is studied by considering the external force required to maintain the steady motion of an immersed constant-velocity colloidal probe. If the probe speed is zero, the suspension microstructure is isotropic but exhibits a boundary accumulation of active bath particles at contact due to their self-propulsion. As the probe moves through the suspension, the microstructure is distorted from the nonequilibrium isotropic state, which allows us to define a microviscosity for the suspension using the Stokes drag law. For a slow probe, we show that active suspensions exhibit a swim-thinning behavior in which their microviscosity is gradually lowered from that of passive suspensions as the swim speed increases. When the probe speed is fast, the suspension activity is obscured by the rapid advection of the probe and the measured microviscosity is indistinguishable from that of passive suspensions. Generally for finite activity, the suspension exhibits a velocity-thinning behavior -- though with a zero-velocity plateau lower than passive suspensions -- as a function of the probe speed. These behaviors originate from the interplay between the suspension activity and the hard-sphere excluded-volume interaction between the probe and a bath particle.