4.7 Article

VO2 as a Highly Efficient Electrocatalyst for the Oxygen Evolution Reaction

Journal

NANOMATERIALS
Volume 12, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/nano12060939

Keywords

electrocatalysis; oxygen evolution reaction; water splitting; vanadium oxide; nanoparticles

Funding

  1. Technology development Program of the Korea government MSS [G21S318216201]
  2. National Research Foundation of Korea (NRF) grant of the Korea government MSIT [2019R1G1A1006231]
  3. National Research Foundation of Korea [2019R1G1A1006231] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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We report the high electrocatalytic activity of monoclinic VO2 (M1 phase) for the oxygen evolution reaction (OER) for the first time. The uniformly covering VO2 (M1) nanoparticles on the surface of carbon fibers show a low eta(10) and Tafel slope in a 1 M aqueous solution of KOH.
Herein, we report high electrocatalytic activity of monoclinic VO2 (M1 phase) for the oxygen evolution reaction (OER) for the first time. The single-phase VO2 (M1) nanoparticles are prepared in the form of uniformly covering the surface of individual carbon fibers constituting a carbon fiber paper (CFP). The VO2 nanoparticles reveal the metal-insulator phase transition at ca. 65 degrees C (heating) and 62 degrees C (cooling) with low thermal hysteresis, indicating a high concentration of structural defect which is considered a grain boundary among VO2 nanoparticles with some particle coalescence. Consequently, the VO2/CFP shows a high electrocatalytic OER activity with the lowest eta(10) (350 mV) and Tafel slope (46 mV/dec) values in a 1 M aqueous solution of KOH as compared to those of the vacuum annealed V2O5 and the hydrothermally grown VO2 (M1), alpha-V2O5, and gamma '-V2O5. The catalytically active site is considered V4+ components and V4+/5+ redox couples in VO2. The oxidation state of V4+ is revealed to be more favorable to the OER catalysis compared to that of V5+ in vanadium oxide through comparative studies. Furthermore, the amount of V5+ component is found to be increased on the surface of VO2 catalyst during the OER, giving rise to the performance degradation. This work suggests V4+ and its redox couple as a novel active component for the OER in metal-oxide electrocatalysts.

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