Electro-Stretching and Electro-Coalescence of Sessile Drops of Conducting Polymer Solutions with and without Surfactant and Dielectric Particles.

IF 3.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Rafael Granda,Jevon Plog,Vitaliy R Yurkiv,Farzad Mashayek,Alexander L Yarin
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Abstract

The present study explores electrically driven stretching of individual conducting polymer drops and electro-coalescence of drop pairs on a dielectric surface under a strong electric field of 10 kV. Conducting PEDOT:PSS and PEDOT:PSS-PEO [poly(3,4-ethylenedioxythiophene):polystyrenesulfonate-poly(ethylene oxide)] drops were tested with and without a nonionic surfactant (Silwet L-77) and dispersed titanium dioxide (TiO2) particles. The surfactant dramatically reduced the solution's surface tension from ∼70 to ∼20 mN/m, and PEO doping increased viscosity and imparted shear-thinning behavior. Under the applied field, drops stretched between the electrodes and spread much wider than without voltage. This pronounced stretching is driven by electrostatic Maxwell stress overcoming capillarity (the electric capillary number CaE ∼ 0.9-2.3). The surfactant further enhanced deformation by lowering surface tension, and polarizable TiO2 particles introduced dielectrophoretic forces that also eased stretching. Furthermore, in surfactant-free cases, two initially separate drops underwent rapid electro-coalescence: upon field activation, finger-like protrusions formed within ∼2-5 ms from each drop to meet and create a narrow liquid bridge, which then expanded to merge the drops into one over a few seconds. However, drops containing surfactant (and TiO2) failed to coalesce, as strong Marangoni flow from surfactant-induced surface tension gradients dominated the Maxwell stress-driven attraction. Such surfactant-laden drops instead developed dendrite-like patterns at their trailing edges, with only a brief (∼millisecond) "handshake" contact and no full merging. These findings clarify how solution composition and interfacial and electrohydrodynamic mechanisms govern drop deformation and merging, providing insights for controlling drop behavior in coating processes. Moreover, the present experiments with drops of solutions of the conducting polymer with a surfactant (a superspreader SILWET L-77) and particles added reveal a novel phenomenon─a competition of the concentration-gradient Marangoni flow with electro-coalescence driven by the electric Maxwell stresses, which causes a noncoalescence even at a very high applied voltage.
有无表面活性剂和介电粒子的导电聚合物溶液中固定式液滴的电拉伸和电聚结。
本研究探讨了在10kv强电场作用下电介质表面单个导电聚合物液滴的电驱动拉伸和液滴对的电聚结。对PEDOT:PSS和PEDOT:PSS- peo[聚(3,4-乙烯二氧噻吩):聚苯乙烯磺酸-聚(环氧乙烷)]滴剂进行了导电测试,并对有无非离子表面活性剂(Silwet L-77)和分散的二氧化钛(TiO2)颗粒进行了测试。表面活性剂将溶液的表面张力从~ 70 mN/m显著降低到~ 20 mN/m, PEO掺杂增加了粘度并赋予剪切变薄行为。在外加电场下,液滴在电极之间伸展,比没有电压时扩散得更广。这种明显的拉伸是由静电麦克斯韦应力克服毛细作用(电毛细数CaE ~ 0.9-2.3)驱动的。表面活性剂通过降低表面张力进一步增强变形,而极化TiO2粒子引入介电泳力也减缓了拉伸。此外,在无表面活性剂的情况下,两个最初分离的液滴经历了快速的电聚:在场激活后,在距离每个液滴约2-5毫秒的时间内形成手指状突起,并形成一个狭窄的液体桥,然后在几秒钟内扩大并将液滴合并为一个。然而,含有表面活性剂(和TiO2)的液滴无法凝聚,因为表面活性剂诱导的表面张力梯度产生的强马兰戈尼流主导了麦克斯韦应力驱动的吸引力。这种含有表面活性剂的液滴在后缘形成了树突状的图案,只有短暂(约毫秒)的“握手”接触,没有完全融合。这些发现阐明了溶液组成、界面和电流体动力学机制如何控制液滴变形和合并,为控制涂层过程中的液滴行为提供了见解。此外,目前用表面活性剂(一种超扩散剂SILWET L-77)滴入导电聚合物溶液和添加粒子的实验揭示了一种新的现象──由麦克斯韦电应力驱动的浓度梯度马兰戈尼流与电聚结的竞争,即使在很高的施加电压下也会导致非聚结。
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来源期刊
Langmuir
Langmuir 化学-材料科学:综合
CiteScore
6.50
自引率
10.30%
发文量
1464
审稿时长
2.1 months
期刊介绍: Langmuir is an interdisciplinary journal publishing articles in the following subject categories: Colloids: surfactants and self-assembly, dispersions, emulsions, foams Interfaces: adsorption, reactions, films, forces Biological Interfaces: biocolloids, biomolecular and biomimetic materials Materials: nano- and mesostructured materials, polymers, gels, liquid crystals Electrochemistry: interfacial charge transfer, charge transport, electrocatalysis, electrokinetic phenomena, bioelectrochemistry Devices and Applications: sensors, fluidics, patterning, catalysis, photonic crystals However, when high-impact, original work is submitted that does not fit within the above categories, decisions to accept or decline such papers will be based on one criteria: What Would Irving Do? Langmuir ranks #2 in citations out of 136 journals in the category of Physical Chemistry with 113,157 total citations. The journal received an Impact Factor of 4.384*. This journal is also indexed in the categories of Materials Science (ranked #1) and Multidisciplinary Chemistry (ranked #5).
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