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https://hdl.handle.net/10356/102957
Title: | Fluorine-doped Fe2O3 as high energy density electroactive material for hybrid supercapacitor applications | Authors: | Karthikeyan, Kaliyappan Amaresh, Samuthirapandian Lee, Sol Nip Aravindan, Vanchiappan Lee, Yun Sung |
Keywords: | DRNTU::Engineering::Nanotechnology | Issue Date: | 2014 | Source: | Karthikeyan, K., Amaresh, S., Lee, S. N., Aravindan, V., & Lee, Y. S. (2014). Fluorine-Doped Fe2O3 as High Energy Density Electroactive Material for Hybrid Supercapacitor Applications . Chemistry - An Asian Journal, 9(3), 852-857. | Series/Report no.: | Chemistry - An Asian Journal | Abstract: | Nanostructured α-Fe2O3 with and without fluorine substitution were successfully obtained by a green route, that is, microwave irradiation. The hematite phase materials were evaluated as a high-performance electrode material in a hybrid supercapacitor configuration along with activated carbon (AC). The presence of fluorine was confirmed through X-ray photoelectron spectroscopy and transmission electron microscopy. Fluorine-doped Fe2O3 (F-Fe2O3) exhibits an enhanced pseudocapacitive performance compared to that of the bare hematite phase. The F-Fe2O3/AC cell delivered a specific capacitance of 71 F g−1 at a current density of 2.25 A g−1 and retained approximately 90 % of its initial capacitance after 15 000 cycles. Furthermore, the F-Fe2O3/AC cell showed a very high energy density of about 28 W h kg−1 compared to bare hematite phase (∼9 W h kg−1). These data clearly reveal that the electrochemical performance of Fe2O3 can be improved by fluorine doping, thereby dramatically improving the energy density of the system. | URI: | https://hdl.handle.net/10356/102957 http://hdl.handle.net/10220/19153 |
ISSN: | 1861-4728 | DOI: | 10.1002/asia.201301289 | Research Centres: | Energy Research Institute @ NTU (ERI@N) | Rights: | © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. | Fulltext Permission: | none | Fulltext Availability: | No Fulltext |
Appears in Collections: | ERI@N Journal Articles |
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