Pan Bin, Valappil Manila Ozhukil, Rateick Richard, Clarkson Christopher R, Tong Xia, Debuhr Chris, Ghanizadeh Amin, Birss Viola I
School of Civil and Resource Engineering, University of Science and Technology Beijing Beijing 10083 China.
Department of Chemical and Petroleum Engineering, University of Calgary Calgary T2N 1N4 AB Canada.
Chem Sci. 2022 Dec 23;14(6):1372-1385. doi: 10.1039/d2sc05705k. eCollection 2023 Feb 8.
An engineered nanoporous carbon scaffold (NCS) consisting of a 3-D interconnected 85 nm nanopore network was used here as a model material to investigate the nanoscale transport of liquids as a function of the polarity and magnitude of an applied potential ('electro-imbibition'), all in 1 M KCl solution. A camera was used to track both meniscus formation and meniscus jump, front motion dynamics, and droplet expulsion, while also quantifying the electrocapillary imbibition height () as a function of the applied potential of the NCS material. Although no imbibition was seen over a wide range of potentials, at positive potentials (+1.2 V the potential of zero charge (pzc)), imbibition was correlated with carbon surface electro-oxidation, as confirmed by both electrochemistry and post-imbibition surface analysis, with gas evolution (O, CO) seen visually only after imbibition was well underway. At negative potentials, vigorous hydrogen evolution reaction was observed at the NCS/KCl solution interface, well before imbibition began at -0.5 V, proposed to be nucleated by an electrical double layer charging-driven meniscus jump, followed by processes such as Marangoni flow, adsorption induced deformation, and hydrogen pressure driven flow. This study improves the understanding of electrocapillary imbibition at the nanoscale, being highly relevant in a wide range of multidisciplinary practical applications, including in energy storage and conversion devices, energy-efficient desalination, and electrical-integrated nanofluidics design.
本文使用了一种由三维互连的85纳米纳米孔网络组成的工程化纳米多孔碳支架(NCS)作为模型材料,在1 M KCl溶液中研究液体的纳米级传输与外加电势的极性和大小的关系(“电渗吸”)。使用相机跟踪弯月面的形成和跳跃、前沿运动动力学以及液滴排出,同时还量化了电毛细管渗吸高度()与NCS材料外加电势的函数关系。尽管在很宽的电势范围内都未观察到渗吸现象,但在正电势(+1.2 V 零电荷电势(pzc))下,渗吸与碳表面的电氧化相关,这通过电化学和渗吸后表面分析得到证实,只有在渗吸进行得很好之后才能肉眼观察到气体逸出(O、CO)。在负电势下,在NCS/KCl溶液界面观察到剧烈的析氢反应,早在渗吸在 -0.5 V开始之前就已出现,推测这是由双电层充电驱动的弯月面跳跃引发的,随后是诸如马兰戈尼流、吸附诱导变形和氢气压力驱动流等过程。这项研究增进了对纳米级电毛细管渗吸的理解,在包括能量存储和转换装置、节能海水淡化以及电集成纳米流体设计等广泛的多学科实际应用中具有高度相关性。