ABSTRACT
Active matter drives its constituent agents to move autonomously by harnessing free energy, leading to diverse emergent states with relevance to both biological processes and inanimate functionalities. Achieving maximum reconfigurability of active materials with minimal control remains a desirable yet challenging goal. Here, we employ large-scale, agent-resolved simulations to demonstrate that modulating the activity of a wet phoretic medium alone can govern its solid-liquid-gas phase transitions and, subsequently, laminar-turbulent transitions in fluid phases, thereby shaping its emergent pattern. These two progressively emerging transitions, hitherto unreported, bring us closer to perceiving the parallels between active matter and traditional matter. Our work reproduces and reconciles seemingly conflicting experimental observations on chemically active systems, presenting a unified landscape of phoretic collective dynamics. These findings enhance the understanding of long-range, many-body interactions among phoretic agents, offer new insights into their non-equilibrium collective behaviors, and provide potential guidelines for designing reconfigurable materials.
ABSTRACT
In recent years, manipulation of particles by inertial microfluidics has attracted significant attention. However, most studies focused on inertial focusing of particles suspended within liquid phase, in which the ratio of the density of the particle to that of the medium is O(1). The investigation on manipulation of aerosol particles in an inertial microfluidics is very limited. In this study, we numerically investigate the aerosol particle's motion in a 3D straight microchannel with rectangular cross section by fully resolved simulation of the particle-air flow. The air flow is modeled by the Navier-Stokes equations. The particle's motions, including translation and rotation, are governed, respectively, by the Newton's second law and the Euler equations without using any approximation models for the lift and drag forces. The coupled mathematical model is numerically solved by combining immersed boundary with lattice Boltzmann method (IB-LBM). We find that the Reynolds number (Re), the particle's initial position, particle's density and diameter are the influential parameters in this process. The equilibrium positions and their stabilities of aerosols are different from those suspended in liquid.
ABSTRACT
Polyacetylene (PA) was synthesized for the first time under mild conditions via polymerization of acetylene in n-octane with AlCl3 as a catalyst, whereby a series of PA-derived carbon materials were obtained. Their composition and structure were characterized and their electrochemical performance was evaluated systematically. It is found that acetylene gas at 1 MPa can polymerize explosively at room temperature under catalysis of AlCl3, forming acetylene black-like PA and a great amount of H2, while in the presence of n-octane solvent, acetylene polymerizes smoothly at higher temperature (30 to 300 °C), forming PA with a H(CH[double bond, length as m-dash]CH) n H structure. A series of PA-derived carbon materials are obtained by treating PA with KOH at 800 °C. The as-synthesizzed PA-100-KOH exhibits a high specific surface area (â¼2500 m2 g-1), high specific capacitance (241 F g-1 at a current density of 0.1 A g-1 and 143 F g-1 at 5 A g-1), low AC resistance, and good cycling stability with 91.7% maintenance of capacity after 2000 cycles at a current density of 2 A g-1. This paper provides a new method for the facile synthesis of PA and a novel carbon source for supercapacitor electrode materials with excellent electrochemical performance and practical application.
