4.7 Article

Fabrication of mesoporous Er doped ZnMnO3 nanoflake via sol gel approach for energy storage application

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CERAMICS INTERNATIONAL
卷 49, 期 9, 页码 13298-13309

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ELSEVIER SCI LTD
DOI: 10.1016/j.ceramint.2022.11.328

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In this study, perovskite materials doped with 15% erbium were fabricated using the solgel technique and analyzed for their performance as energy conversion systems. The shape, elemental composition, and crystalline phases were determined using SEM, EDX, and XRD. The Er-doped ZnMnO3 perovskite exhibited a specific capacitance of 1558.41 F g-1 with an energy density of 54.18 Wh kg-1 and power density of 250.18 W kg-1, surpassing the performance of pristine and other doped samples. Moreover, the 15% Er-doped ZnMnO3 maintained 98.39% of its initial capacitance during 2500 charge-discharge cycles at a current density of 5.0 A g-1, indicating its potential for long-term charge retention.
In the present study, perovskites have lately garnered considerable interest as potential electrochemical energy storage components. The fabricated ZnMnO3, and doped material (where, Er = 5, 10 and 15%) perovskite materials were fabricated with solgel technique and analyzed as an energy conversion system. Using scanning electron microscopy (SEM), energy dispersive X-rays spectroscopy (EDX) and X-ray diffraction (XRD), the shape, elemental and crystalline phases were determined. Using impedance spectroscopy and electrochemical capacitance analysis, the electrical capacity and impedance were determined. The Er doped ZnMnO3 perovskite resulted in 15% Er doped ZnMnO3 responses the specific capacitance of 1558.41 F g- 1 with an energy density of 54.18 Wh kg-1, and power density of 250.18 W kg-1 at a current density of 1.0 A g- 1 which was a considerable improvement over pristine and other doped samples. In addition, 15% Er doped ZnMnO3 preserved 98.39% of its initial capacitance during 2500 charge-discharge cycles at the highest current density of 5.0 A g-115% Er doped ZnMnO3 may maintain a significant amount of charge due to strong electrode-electrolyte contacts and anion-intercalated redox reactions.

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