| Literature DB >> 33435502 |
Victor Shapovalov1, Alexander Guda1, Vera Butova1, Igor Shukaev2, Alexander Soldatov1.
Abstract
Electrochemical characterization of the novel sodium iron titanate Na0.9Fe0.45Ti1.55O4 was performed upon cycling in the Li-ion half-cell. The material exhibited stable cycling in the voltage range 2-4.5 V, and the number of alkali ions extracted per formula unit was approximately half of the Na stoichiometry value. Using laboratory X-ray absorption spectrometry, we measured operando Fe K-edge X-ray absorption spectra in the first 10 charge-discharge cycles and quantified the portion of charge associated with the transition metal redox reaction. Although 3d metals are commonly accepted redox-active centers in the intercalation process, we found that in all cycles the amount of oxidized and reduced Fe ions was almost 20% less than the total number of transferred electrons. Using density functional theory (DFT) simulations, we show that part of the reversible capacity is related to the redox reaction on oxygen ions.Entities:
Keywords: DFT calculations; Na-ion; X-ray absorption spectroscopy; cathode material; operando study; sodium iron titanate
Year: 2021 PMID: 33435502 DOI: 10.3390/nano11010156
Source DB: PubMed Journal: Nanomaterials (Basel) ISSN: 2079-4991 Impact factor: 5.076