Saiz Eduardo, Tomsia Antoni P
Ernest Orlando Lawrence Berkeley National Laboratory, Materials Sciences Division, University of California, Berkeley, California 94720, USA.
Nat Mater. 2004 Dec;3(12):903-9. doi: 10.1038/nmat1252. Epub 2004 Nov 14.
Despite its apparent simplicity, spreading of liquid metals at high temperatures has defied description and generalization. Wetting at high temperature is usually accompanied by interdiffusion and chemical reaction, but the forces that drive reactive spreading and the mechanisms that control its kinetics have been very poorly understood. The unsolved challenge has been to link macroscopic measurements such as the dynamic contact angle or the speed of a moving liquid front to phenomena occurring at the microscopic and even atomic level in the vicinity of the triple solid-liquid-vapour junction. We have taken a big step towards meeting this challenge. Our systematic analysis of the spreading of metal-metal systems with varying degrees of mutual solubility allows us to report on the fundamental differences between the mechanisms controlling spreading of organic liquids and liquid metals and on formation of Marangoni films driven by surface-tension gradients in high-temperature systems.
尽管液态金属在高温下的铺展看似简单,但其描述和概括却颇具难度。高温下的润湿通常伴随着相互扩散和化学反应,但驱动反应性铺展的力以及控制其动力学的机制却鲜为人知。尚未解决的挑战在于将宏观测量,如动态接触角或移动液面前沿的速度,与固 - 液 - 气三相交界处微观甚至原子层面发生的现象联系起来。我们在应对这一挑战方面迈出了重要一步。我们对具有不同互溶度的金属 - 金属体系铺展进行的系统分析,使我们能够报告控制有机液体和液态金属铺展机制之间的根本差异,以及高温体系中由表面张力梯度驱动的马兰戈尼膜的形成情况。