Uniform, Assembled 4 nm Mn3O4 Nanoparticles as Efficient Water Oxidation Electrocatalysts at Neutral pH

Electrochemical water splitting is one of the ways to produce environmentally‐friendly hydrogen energy. Transition‐metal (TM)‐based catalysts have been attracting attention due to their low cost and abundance, but their insufficient activity still remains a challenge. Here, 4 nm Mn3O4 nanoparticles...

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Veröffentlicht in:Advanced functional materials 2020-03, Vol.30 (10), p.n/a
Hauptverfasser: Cho, Kang Hee, Seo, Hongmin, Park, Sunghak, Lee, Yoon Ho, Lee, Moo Young, Cho, Nam Heon, Nam, Ki Tae
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Sprache:eng
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Zusammenfassung:Electrochemical water splitting is one of the ways to produce environmentally‐friendly hydrogen energy. Transition‐metal (TM)‐based catalysts have been attracting attention due to their low cost and abundance, but their insufficient activity still remains a challenge. Here, 4 nm Mn3O4 nanoparticles (NPs) are successfully synthesized and their electrochemical behavior is investigated. Using electrokinetic analyses, an identical water oxidizing mechanism is demonstrated between the 4 and 8 nm Mn3O4 NPs. In addition, it is confirmed that the overall increase in the active surface area is strongly correlated with the superb catalytic activity of the 4 nm Mn3O4 NPs. To further enhance the oxygen evolution reaction (OER) performance, Ni foam substrate is introduced to maximize the entire number of the NPs participating in OER. The 4 nm Mn3O4/Ni foam electrode exhibits outstanding electrocatalytic activity for OER with overpotential of 395 mV at a current density of 10 mA cm−2 under neutral conditions (0.5 m PBS, pH 7). Uniform 4 nm Mn3O4 nanoparticles (NPs) are synthesized and their electrokinetic behaviors are investigated under neutral conditions. The 4 nm Mn3O4 NPs exhibit outstanding electrocatalytic activity for OER, with an overpotential of 395 mV at a current density of 10 mA cm−2 under neutral conditions. Also, various electrochemical analyses verify that the increased surface area contributes to the high catalytic activity.
ISSN:1616-301X
1616-3028
DOI:10.1002/adfm.201910424