Please use this identifier to cite or link to this item: doi:10.22028/D291-28912
Volltext verfügbar? / Dokumentlieferung
Title: In Situ Tracking of Partial Sodium Desolvation of Materials with Capacitive, Pseudocapacitive, and Battery-like Charge/Discharge Behavior in Aqueous Electrolytes
Author(s): Srimuk, Pattarachai
Lee, Juhan
Budak, Öznil
Choi, Jaehoon
Chen, Ming
Feng, Guang
Prehal, Christian
Presser, Volker
Language: English
Title: Langmuir : the ACS journal of surfaces and colloids
Volume: 34
Issue: 44
Startpage: 13132
Endpage: 13143
Publisher/Platform: ACS
Year of Publication: 2018
Publikation type: Journal Article
Abstract: Aqueous electrolytes can be used for electrical double-layer capacitors, pseudocapacitors, and intercalation-type batteries. These technologies may employ different electrode materials, most importantly high-surface-area nanoporous carbon, two-dimensional materials, and metal oxides. All of these materials also find more and more applications in electrochemical desalination devices. During the electrochemical operation of such electrode materials, charge storage and ion immobilization are accomplished by non-Faradaic ion electrosorption, Faradaic ion intercalation at specific crystallographic sites, or ion insertion between layers of two-dimensional materials. These processes may or may not be associated with a (partial) loss of the aqueous solvation shell around the ions. Our work showcases the electrochemical quartz crystal microbalance as an excellent tool for quantifying the change in effective solvation. We chose sodium as an important cation for energy storage materials (sodium-based aqueous electrolytes) and electrochemical desalination (saline media). Our data show that a major amount of water uptake occurs during ion electrosorption in nanoporous carbon, while battery-like ion insertion between layers of titanium disulfide is associated with an 80% loss of the initially present solvation molecules. Sodiation of MXene is accomplished by a loss of 90% of the number of solvent molecules, but nanoconfined water in-between the MXene layers may compensate for this large degree of desolvation. In the case of sodium manganese oxide, we were able to demonstrate the full loss of the solvation shell.
DOI of the first publication: 10.1021/acs.langmuir.8b02485
URL of the first publication: https://pubs.acs.org/doi/abs/10.1021/acs.langmuir.8b02485
Link to this record: hdl:20.500.11880/27816
http://dx.doi.org/10.22028/D291-28912
ISSN: 1520-5827
0743-7463
Date of registration: 17-Sep-2019
Faculty: NT - Naturwissenschaftlich- Technische Fakultät
Department: NT - Materialwissenschaft und Werkstofftechnik
Professorship: NT - Prof. Dr. Volker Presser
Collections:UniBib – Die Universitätsbibliographie

Files for this record:
There are no files associated with this item.


Items in SciDok are protected by copyright, with all rights reserved, unless otherwise indicated.