论文标题

主动物质的“等温”可压缩性

The "isothermal" compressibility of active matter

论文作者

Dulaney, Austin R., Mallory, Stewart A., Brady, John F.

论文摘要

我们证明了机械定义的“等温”可压缩性作为活性布朗颗粒悬浮液的热力学响应函数。正如机械稳定性标准所预期的那样,从主动压力计算出的可压缩性(碰撞和独特的游泳压力的组合)能够预测运动性诱导的相位分离的关键点。我们通过热力学可压缩性方程的主动形式将这种机械定义与静态结构因子联系起来,并发现两者是等效的,就像平衡系统一样。这种等效性表明,即使活动很大,压缩性也像热力学响应函数一样。最后,我们在定义主动化学电位时讨论相位界面的重要性。活跃化学电位的先前定义显示出在临界点上的准确性,但共存区域的崩溃。在机械可压缩性定义中包含游泳压力表明该界面对于确定相行为至关重要。

We demonstrate that the mechanically-defined "isothermal" compressibility behaves as a thermodynamic-like response function for suspensions of active Brownian particles. The compressibility computed from the active pressure - a combination of the collision and unique swim pressures - is capable of predicting the critical point for motility induced phase separation, as expected from the mechanical stability criterion. We relate this mechanical definition to the static structure factor via an active form of the thermodynamic compressibility equation and find the two to be equivalent, as would be the case for equilibrium systems. This equivalence indicates that compressibility behaves like a thermodynamic response function, even when activity is large. Finally, we discuss the importance of the phase interface when defining an active chemical potential. Previous definitions of the active chemical potential are shown to be accurate above the critical point but breakdown in the coexistence region. Inclusion of the swim pressure in the mechanical compressibility definition suggests that the interface is essential for determining phase behavior.

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