Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/140906
Title: Titanium carbide-decorated graphite felt as high performance negative electrode in vanadium redox flow batteries
Authors: Ghimire, Purna Chandra
Schweiss, Rüdiger
Scherer, Günther G.
Wai, Nyunt
Lim, Tuti Mariana
Bhattarai, Arjun
Nguyen, Tam Duy
Yan, Qingyu
Keywords: Engineering::Environmental engineering
Issue Date: 2018
Source: Ghimire, P. C., Schweiss, R., Scherer, G. G., Wai, N., Lim, T. M., Bhattarai, A., . . . Yan, Q. (2018). Titanium carbide-decorated graphite felt as high performance negative electrode in vanadium redox flow batteries. Journal of Materials Chemistry A, 6(15), 6625-6632. doi:10.1039/c8ta00464a
Journal: Journal of Materials Chemistry A
Abstract: This paper presents a novel method for preparing binder-free, uniformly distributed titanium carbide (TiC) nanoparticles on graphite felt (GF) surfaces for use as negative electrode in an all vanadium redox flow battery (VRFB). TiO2 particles were grown on the surface of the GF using hydrothermal synthesis and were subsequently converted to TiC by way of a carbothermal reaction. Cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and VRFB single cell tests unequivocally confirm the catalytic effect of TiC towards the negative redox couple V2+/V3+. A VRFB employing a TiC-decorated electrode in the negative half-cell exhibited a 13% gain in energy efficiency (EE) at a current density of 100 mA cm−2, compared to reference cells assembled solely with pristine graphite felts. Moreover, VRFB cells employing the modified electrode show excellent stability with high capacity retention over repetitive cycling. These results suggest that TiC nanoparticles supported on carbon fibres constitute a high performance negative electrode for VRFBs.
URI: https://hdl.handle.net/10356/140906
ISSN: 2050-7488
DOI: 10.1039/c8ta00464a
Rights: © 2018 The Royal Society of Chemistry. All rights reserved. This paper was published in Journal of Materials Chemistry A and is made available with permission of The Royal Society of Chemistry.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:IGS Journal Articles

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