Synergistic effect in liquid metal heartbeat with high-efficiency energy conversion

IF 9.1 Droplet Pub Date : 2025-01-06 DOI:10.1002/dro2.161
Shutong Wang, Sicheng Wang, Binbin Zhou, Dongmei Ren, Zhenwei Yu
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Abstract

The phenomenon of liquid metal “heartbeat” oscillation presents intriguing applications in microfluidic devices, drug delivery, and miniature robotics. However, achieving high vibrational kinetic energy outputs in these systems remains challenging. In this study, we developed a graphite ring electrode with V-shaped inner wall that enables wide-ranging control over the oscillation performance based on droplet size and the height of the V-shape. The mechanism driving the heartbeat is defined as a dynamic process involving the transformation of the oxide layer. Through electrochemical analysis, we confirmed three distinct states of the heartbeat and introduced a novel model to elucidate the role of the V-shaped structure in initiating and halting the oscillations. A comprehensive series of experiments explored how various factors, such as droplet volume, voltage, tilt angle, and V-shape height, affect heartbeat performance, achieving a significant conversion from surface energy to vibrational kinetic energy as high as 4732 J m−2 s−1. The increase in energy output is attributed to the synergistic effect of the V-shape height and droplet size on the oscillations. These results not only advance our understanding of liquid metal droplet manipulation but also pave the way for designing high-speed microfluidic pumping systems.

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具有高效能量转换的液态金属心跳协同效应
液态金属“心跳”振荡现象在微流体装置、药物输送和微型机器人中有着有趣的应用。然而,在这些系统中实现高振动动能输出仍然具有挑战性。在这项研究中,我们开发了一种v形内壁的石墨环电极,可以根据液滴大小和v形高度对振荡性能进行广泛控制。驱动心跳的机制被定义为涉及氧化层转化的动态过程。通过电化学分析,我们确认了心跳的三种不同状态,并引入了一个新的模型来阐明v形结构在启动和停止振荡中的作用。一系列综合实验探索了液滴体积、电压、倾斜角度和v形高度等各种因素如何影响心跳性能,实现了从表面能到振动动能的显著转换,最高可达4732 J m−2 s−1。能量输出的增加归因于v形高度和液滴尺寸对振荡的协同作用。这些结果不仅促进了我们对液态金属液滴操纵的理解,而且为设计高速微流体泵送系统铺平了道路。
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Issue Information Front Cover, Volume 5, Number 1, January 2026 Inside Front Cover, Volume 5, Number 1, January 2026 Back Cover, Volume 5, Number 1, January 2026 Inside Back Cover, Volume 5, Number 1, January 2026
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