{"title":"(Keynote) Releasing the Bubbles: Efficient Phase Separation in (Photo-)Electrochemical Devices in Microgravity Environment","authors":"Katharina Brinkert, Álvaro Romero-Calvo, Oemer Akay, Shaumica Saravanabavan, Eniola Sokalu","doi":"10.1149/ma2023-01562715mtgabs","DOIUrl":null,"url":null,"abstract":"One of the major challenges human space exploration faces is the absence of buoyancy forces in orbit. Consequently, phase separation is severely hindered which impacts a large variety of space technologies including propellant management devices, heat transfer and life support systems e.g., during the production of oxygen and the recycling of carbon dioxide. Of particular interest are hereby (photo-)electrochemical (PEC) devices as they can produce essential chemicals such as oxygen and hydrogen in two set-ups: either, by coupling the electrochemical cell to external photovoltaic cells as currently utilized on the International Space Station or by direct utilization of sunlight in a monolithic device, where integrated semiconductor-electrocatalyst systems carry out the processes of light absorption, charge separation and catalysis in analogy to natural photosynthesis in one system. The latter device is particularly interesting for space applications due to present mass and volume constraints. Here, we discuss two combined approaches to overcome phase separation challenges in (photo-)electrolyzer systems in reduced gravitational environments: using the hydrogen evolution reaction (HER) as a model reaction, we combine nanostructured, hydrophilic electrocatalyst surfaces for efficient gas bubble desorption with magnetically-induced buoyancy to direct the produced hydrogen gas bubbles on specific trajectories away from the (photo-)electrode surface. (Photo-)current-voltage ( J-V ) profiles obtained in microgravity environments generated for 9.2 s at the Bremen Drop Tower show that our systems can operate with our two-fold approach near terrestrial efficiencies. Simulations of gas bubble trajectories accompany our experimental observations, allowing us to attribute the achieved phase separation in the PEC cells to the increased electrode wettability as well as the systematic use of diamagnetic and Lorentz forces.","PeriodicalId":11461,"journal":{"name":"ECS Meeting Abstracts","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ECS Meeting Abstracts","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1149/ma2023-01562715mtgabs","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
One of the major challenges human space exploration faces is the absence of buoyancy forces in orbit. Consequently, phase separation is severely hindered which impacts a large variety of space technologies including propellant management devices, heat transfer and life support systems e.g., during the production of oxygen and the recycling of carbon dioxide. Of particular interest are hereby (photo-)electrochemical (PEC) devices as they can produce essential chemicals such as oxygen and hydrogen in two set-ups: either, by coupling the electrochemical cell to external photovoltaic cells as currently utilized on the International Space Station or by direct utilization of sunlight in a monolithic device, where integrated semiconductor-electrocatalyst systems carry out the processes of light absorption, charge separation and catalysis in analogy to natural photosynthesis in one system. The latter device is particularly interesting for space applications due to present mass and volume constraints. Here, we discuss two combined approaches to overcome phase separation challenges in (photo-)electrolyzer systems in reduced gravitational environments: using the hydrogen evolution reaction (HER) as a model reaction, we combine nanostructured, hydrophilic electrocatalyst surfaces for efficient gas bubble desorption with magnetically-induced buoyancy to direct the produced hydrogen gas bubbles on specific trajectories away from the (photo-)electrode surface. (Photo-)current-voltage ( J-V ) profiles obtained in microgravity environments generated for 9.2 s at the Bremen Drop Tower show that our systems can operate with our two-fold approach near terrestrial efficiencies. Simulations of gas bubble trajectories accompany our experimental observations, allowing us to attribute the achieved phase separation in the PEC cells to the increased electrode wettability as well as the systematic use of diamagnetic and Lorentz forces.
人类太空探索面临的主要挑战之一是轨道上缺乏浮力。因此,相分离受到严重阻碍,影响到各种各样的空间技术,包括推进剂管理装置、传热和生命维持系统,例如在氧气生产和二氧化碳回收过程中。特别令人感兴趣的是(光电)电化学(PEC)装置,因为它们可以在两种设置中产生必需的化学物质,如氧和氢:要么是将电化学电池与外部光伏电池耦合,就像目前在国际空间站上使用的那样,要么是在一个单片装置中直接利用阳光,其中集成的半导体-电催化剂系统在一个系统中进行光吸收、电荷分离和催化过程,类似于自然光合作用。由于目前的质量和体积限制,后一种装置对于空间应用特别有趣。在这里,我们讨论了两种组合方法来克服在减少重力环境下(光)电解槽系统中相分离的挑战:使用析氢反应(HER)作为模型反应,我们结合了纳米结构,亲水电催化剂表面,用于有效的气泡解吸和磁诱导浮力,以指导产生的氢气气泡沿着特定的轨迹远离(光)电极表面。在不来梅落差塔(Bremen Drop Tower)获得的9.2 s微重力环境下的电流-电压(J-V)曲线表明,我们的系统可以以接近地面的双重效率运行。气泡轨迹的模拟伴随着我们的实验观察,使我们能够将PEC电池中实现的相分离归因于电极润湿性的增加以及抗磁性和洛伦兹力的系统使用。