School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138.
Department of Physics, Harvard University, Cambridge, MA 02138.
Proc Natl Acad Sci U S A. 2019 Jan 22;116(4):1180-1184. doi: 10.1073/pnas.1813885116. Epub 2019 Jan 7.
We study the kinetics of crystal growth and melting of two types of colloidal crystals: body-centered cubic (BCC) crystals and face-centered cubic (FCC) crystals. A dielectrophoretic "electric bottle" confines colloids, enabling precise control of the motion of the interface. We track the particle motion, and by introducing a structural order parameter, we measure the jump frequencies of particles to and from the crystal and determine from these the free-energy difference between the phases and the interface mobility. We find that the interface is rough in both BCC and FCC cases. Moreover, the jump frequencies correspond to those expected from the random walk of the particles, which translates to collision-limited growth in metallic systems. The mobility of the BCC interface is greater than that of the FCC interface. In addition, contrary to the prediction of some early computer simulations, we show that there is no significant asymmetry between the mobilities for crystallization and melting.
体心立方(BCC)晶体和面心立方(FCC)晶体的生长和熔化动力学。介电泳“电瓶”限制胶体,能够精确控制界面的运动。我们跟踪颗粒的运动,并通过引入结构序参量,测量颗粒进出晶体的跳跃频率,并从这些频率确定相之间的自由能差和界面迁移率。我们发现,在 BCC 和 FCC 两种情况下,界面都是粗糙的。此外,跳跃频率与粒子随机行走所预期的频率相对应,这意味着在金属系统中,生长受到碰撞限制。BCC 界面的迁移率大于 FCC 界面的迁移率。此外,与一些早期计算机模拟的预测相反,我们表明,结晶和熔化的迁移率之间没有显著的不对称性。