School of Engineering, RMIT University, Swanston Street, Melbourne, Victoria 3001, Australia.
Institute of Chemical and Bioengineering, Department of Chemistry and Applied Biosciences, 8093 ETH Zürich, Switzerland.
Nat Commun. 2016 Aug 4;7:12402. doi: 10.1038/ncomms12402.
Components with self-propelling abilities are important building blocks of small autonomous systems and the characteristics of liquid metals are capable of fulfilling self-propulsion criteria. To date, there has been no exploration regarding the effect of electrolyte ionic content surrounding a liquid metal for symmetry breaking that generates motion. Here we show the controlled actuation of liquid metal droplets using only the ionic properties of the aqueous electrolyte. We demonstrate that pH or ionic concentration gradients across a liquid metal droplet induce both deformation and surface Marangoni flow. We show that the Lippmann dominated deformation results in maximum velocity for the self-propulsion of liquid metal droplets and illustrate several key applications, which take advantage of such electrolyte-induced motion. With this finding, it is possible to conceive the propulsion of small entities that are constructed and controlled entirely with fluids, progressing towards more advanced soft systems.
具有自推进能力的组件是小型自主系统的重要组成部分,而液态金属的特性能够满足自推进的标准。迄今为止,还没有人研究过周围电解质离子含量对打破对称并产生运动的液态金属的影响。在这里,我们仅使用水基电解质的离子特性来控制液态金属液滴的运动。我们证明了 pH 值或离子浓度梯度会在液态金属液滴上产生变形和表面马兰戈尼流。我们表明,利普曼主导的变形导致了液态金属液滴的最大速度,并且说明了一些利用这种电解质引起的运动的关键应用。有了这个发现,就有可能设想出完全由流体构建和控制的小型实体的推进,从而朝着更先进的软系统发展。