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Nanohybrid structured RuO2/Mn2O3/CNF as a catalyst for Na-O2 batteries

A 3D RuO2/Mn2O3/carbon nanofiber (CNF) composite has been prepared in this study by a facile two step microwave synthesis, as a bi-functional electrocatalyst towards oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). RuO2 nanoparticles with the mean size of 1.57 nm are uniformly di...

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Bibliographic Details
Published in:Nanotechnology 2018-11, Vol.29 (47), p.475401-475401
Main Authors: Tovini, Mohammad Fathi, Patil, Bhushan, Koz, Cevriye, Uyar, Tamer, Y lmaz, Eda
Format: Article
Language:English
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Summary:A 3D RuO2/Mn2O3/carbon nanofiber (CNF) composite has been prepared in this study by a facile two step microwave synthesis, as a bi-functional electrocatalyst towards oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). RuO2 nanoparticles with the mean size of 1.57 nm are uniformly distributed on Mn2O3 nano-rods grown on electrospun CNFs. The electrocatalytic activity of the composites are investigated towards ORR/OER under alkaline condition. The ternary RuO2/Mn2O3/CNF composite showed superior ORR activity in terms of onset potential (0.95 V versus RHE) and Tafel slope (121 mV dec−1) compared to its RuO2/CNF and Mn2O3/CNF counterparts. In the case of OER, the RuO2/Mn2O3/CNF exhibited 0.34 V over-potential value measured at 10 mA cm−2 and 52 mV dec−1 Tafel slope which are lower than those of the other synthesized samples and as compared to state of the art RuO2 and IrOx type materials. RuO2/Mn2O3/CNF also exhibited higher specific capacity (9352 mAh g carbon − 1 ) than CNF (1395 mAh g carbon − 1 ), Mn2O3/CNF (3108 mAh g carbon − 1 ) and RuO2/CNF (4859 mAh gcarbon−1) as the cathode material in Na-O2 battery, which indicates the validity of the results in non-aqueous medium. Taking the benefit of RuO2 and Mn2O3 synergistic effect, the decomposition of inevitable side products at the end of charge occurs at 3.838 V versus Na/Na+ by using RuO2/Mn2O3/CNF, which is 388 mV more cathodic compared with CNF.
ISSN:0957-4484
1361-6528
DOI:10.1088/1361-6528/aadfb7