Spinel LiMn2O4 as a Capacitive Deionization Electrode Material with High Desalination Capacity: Experiment and Simulation
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College of Engineering, Chemical and Environmental Engineering Department, University of ArizonaIssue Date
2022-12-28
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Jiang, Y., Li, K., Alhassan, S. I., Cao, Y., Deng, H., Tan, S., ... & Chai, L. (2022). Spinel LiMn2O4 as a Capacitive Deionization Electrode Material with High Desalination Capacity: Experiment and Simulation. International Journal of Environmental Research and Public Health, 20(1), 517.Rights
© 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Capacitive deionization (CDI) is a newly developed desalination technology with low energy consumption and environmental friendliness. The surface area restricts the desalination capacities of traditional carbon-based CDI electrodes while battery materials emerge as CDI electrodes with high performances due to the larger electrochemical capacities, but suffer limited production of materials. LiMn2O4 is a massively-produced lithium-ion battery material with a stable spinel structure and a high theoretical specific capacity of 148 mAh·g−1, revealing a promising candidate for CDI electrode. Herein, we employed spinel LiMn2O4 as the cathode and activated carbon as the anode in the CDI cell with an anion exchange membrane to limit the movement of cations, thus, the lithium ions released from LiMn2O4 would attract the chloride ions and trigger the desalination process of the other side of the membrane. An ultrahigh deionization capacity of 159.49 mg·g−1 was obtained at 1.0 V with an initial salinity of 20 mM. The desalination capacity of the CDI cell at 1.0 V with 10 mM initial NaCl concentration was 91.04 mg·g−1, higher than that of the system with only carbon electrodes with and without the ion exchange membrane (39.88 mg·g−1 and 7.84 mg·g−1, respectively). In addition, the desalination results and mechanisms were further verified with the simulation of COMSOL Multiphysics. © 2022 by the authors.Note
Open access journalISSN
1661-7827PubMed ID
36612838Version
Final published versionae974a485f413a2113503eed53cd6c53
10.3390/ijerph20010517
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Except where otherwise noted, this item's license is described as © 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.
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