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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 |
Appears in Collections: | Journal Article |
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