{"title":"3D-printed add-on allows using commercially available rotating disc electrodes in tilted position","authors":"Katharina Röhring, Falk Harnisch","doi":"10.1016/j.elecom.2024.107854","DOIUrl":null,"url":null,"abstract":"<div><div>Knowledge on reaction kinetics is essential for further understanding electrochemical reactions and the development of electrochemical processes. Different tools are available to study reaction kinetics of redox electrodes. One that is widely used is the rotating disk electrode (RDE). However, RDE has limitations when it comes to more complex electrochemical reactions, especially those involving gas evolution. Due to the facing downwards of the planar electrode surface evolving gas bubbles cannot escape by buoyance leading to temporarily and stochastically insultation. This limits using the RDE to low overpotentials or high rotation rates for these kind of reactions in order to prevent blockage of the electrode surface with gas bubbles. To overcome these limitations, we present a modification for commercially available RDE that is based on rapid prototyping using 3D-printing. This allows the RDE setup to be easily operated in a tilted position allowing the gas bubbles to escape from the electrode surface by buoyance. We validate the tilted RDE setup using the example of the well-studied redox pair ferro-/ferricyanide. This is achieved by calculating the diffusion coefficient for both redox species in straight and tilted position based on the Levich-equation. We show that the presented setup can be further used for more complex reactions.</div></div>","PeriodicalId":304,"journal":{"name":"Electrochemistry Communications","volume":"170 ","pages":"Article 107854"},"PeriodicalIF":4.7000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochemistry Communications","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1388248124001978","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
Knowledge on reaction kinetics is essential for further understanding electrochemical reactions and the development of electrochemical processes. Different tools are available to study reaction kinetics of redox electrodes. One that is widely used is the rotating disk electrode (RDE). However, RDE has limitations when it comes to more complex electrochemical reactions, especially those involving gas evolution. Due to the facing downwards of the planar electrode surface evolving gas bubbles cannot escape by buoyance leading to temporarily and stochastically insultation. This limits using the RDE to low overpotentials or high rotation rates for these kind of reactions in order to prevent blockage of the electrode surface with gas bubbles. To overcome these limitations, we present a modification for commercially available RDE that is based on rapid prototyping using 3D-printing. This allows the RDE setup to be easily operated in a tilted position allowing the gas bubbles to escape from the electrode surface by buoyance. We validate the tilted RDE setup using the example of the well-studied redox pair ferro-/ferricyanide. This is achieved by calculating the diffusion coefficient for both redox species in straight and tilted position based on the Levich-equation. We show that the presented setup can be further used for more complex reactions.
期刊介绍:
Electrochemistry Communications is an open access journal providing fast dissemination of short communications, full communications and mini reviews covering the whole field of electrochemistry which merit urgent publication. Short communications are limited to a maximum of 20,000 characters (including spaces) while full communications and mini reviews are limited to 25,000 characters (including spaces). Supplementary information is permitted for full communications and mini reviews but not for short communications. We aim to be the fastest journal in electrochemistry for these types of papers.