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Please use this identifier to cite or link to this item: https://dspace.ffh.bg.ac.rs/handle/123456789/2486
Title: Synthesis, Characterization and Electrochemical Properties of Iron Doped Phosphate Tungsten Heteropoly Acid (Fe-PWA) and it’s Bronze (Fe-PWB): Comparative Study
Authors: Acković, Jovana
Micić, Ružica
Nedić, Zoran
Petrović, Tamara 
Senćanski, Jelena
Pagnacco, Maja
Tančić, Pavle
Keywords: 12-tungstophosporic acid iron salt;Cyclic voltammetry;Heteropoly compound;Iron phosphate tungsten bronze;Keggin anion
Issue Date: 1-Jan-2024
Journal: Science of Sintering
Abstract: 
In this work, synthesized 12-tungstenphosphoric acid (H3PW12 O40 × nH2O; PWA) was further ionically exchanged with Fe3+ ions, which led to the formation of the 12-tungstophosporic acid iron salt, (FePW12O40 × nH2O; Fe-PWA). Fe-PWA was then subjected to thermal analysis (TGA/DTA), determining the phase transition temperature of 576°C from Fe-PWA to its corresponding phosphate tungsten bronze doped with iron, Fe-PWB. Using the X-ray powder diffraction (XRPD), Fourier-transform infrared spectroscopy (FTIR), and Scanning electron microscopy with an energy dispersive X-ray spectroscopy (SEM-EDS) method, the obtained Fe-PWA and Fe-PWB were additionally characterized, and compared. Due to channels and cavities in their structures, Fe-PWA and Fe-PWB were next examined as electrode materials for aqueous rechargeable batteries. Electrochemical measurements were done in aqueous solutions of 6 M LiNO3 by cyclic voltammetry. Fe-PWA and Fe-PWB exhibit different redox processes, which are discussed thoroughly in this work. Electrochemical results are showing that within the Fe-PWA structure, more Li+ ions can be intercalated in the first discharge cycle, but consecutive cycling leads to a fast capacity fade. While the Fe-PWB redox process was stable during cycling, its specific capacity is limited by the material's poor electrical conductivity. Improvements in Fe-PWB conductivity must be addressed in future studies in order to boost material’s electrochemical performance.
URI: https://dspace.ffh.bg.ac.rs/handle/123456789/2486
ISSN: 0350820X
DOI: 10.2298/SOS230812053A
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University of Belgrade
Faculty of Physical Chemistry
Studentski trg 12-16
11158 Belgrade 118
PAC 105305
SERBIA
University of Belgrade Faculty of Physical Chemistry