Affiliation:
1. INM – Leibniz Institute for New Materials Campus D2 2 66123 Saarbrücken Germany
2. Saarland University Campus D2 2 66123 Saarbrücken Germany
3. Institute for Technical Chemistry and Environmental Chemistry Friedrich‐Schiller‐University Jena Philosophenweg 7a 07743 Jena Germany
4. Center for Energy and Environmental Chemistry Jena (CEEC Jena) Philosophenweg 7a 07743 Jena Germany
5. saarene – Saarland Center for Energy Materials and Sustainability Campus C4 2 66123 Saarbrücken Germany
Abstract
Supercapacitors are efficient and versatile energy storage devices, offering remarkable power density, fast charge/discharge rates, and exceptional cycle life. As research continues to push the boundaries of their performance, electrode fabrication techniques are critical aspects influencing the overall capabilities of supercapacitors. Herein, we aim to shed light on the advantages offered by dry electrode processing for advanced supercapacitors. Notably, our study explores the performance of these electrodes in three different types of electrolytes: organic, ionic liquids, and quasi‐solid states. By examining the impact of dry electrode processing on various electrode and electrolyte systems, we show valuable insights into the versatility and efficacy of this technique. The supercapacitors employing dry electrodes demonstrated significant improvements compared with conventional wet electrodes, with a lifespan extension of +45% in organic, +192% in ionic liquids, and +84% in quasi‐solid electrolytes. Moreover, the increased electrode densities achievable through the dry approach directly translate to improved volumetric outputs, enhancing energy storage capacities within compact form factors. Notably, dry electrode‐prepared supercapacitors outperformed their wet electrode counterparts, exhibiting a higher energy density of 6.1 Wh cm−3 compared with 4.7 Wh cm−3 at a high power density of 195 W cm−3, marking a substantial 28% energy improvement in the quasi‐solid electrolyte.
Funder
Alexander von Humboldt-Stiftung
Deutsche Forschungsgemeinschaft