Oxygen Reduction Electrode Properties of Manganese Oxide Nanosheet-Based Materials
Two types of oxide nanosheet-based materials, H 3 O + -form regularly stacked manganese oxide nanosheets (H 3 O + -RG(Mn)) and H 3 O + -form randomly restacked manganese oxide nanosheets (H 3 O + -RE(Mn)) were synthesized by soft chemical methods, and their oxygen reduction reaction (ORR) activities...
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Veröffentlicht in: | Topics in catalysis 2009-06, Vol.52 (6-7), p.903-911 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Two types of oxide nanosheet-based materials, H
3
O
+
-form regularly stacked manganese oxide nanosheets (H
3
O
+
-RG(Mn)) and H
3
O
+
-form randomly restacked manganese oxide nanosheets (H
3
O
+
-RE(Mn)) were synthesized by soft chemical methods, and their oxygen reduction reaction (ORR) activities were examined by cyclic voltammetry (CV) and semi-steady-state voltammetry (SSV) with a rotating ring-disc electrode at 70 °C in 0.1 M KOH. Both samples showed high onset potentials (
E
on
) of the ORR current and high efficiencies (
Eff
4
) of the 4-electron reduction of oxygen, and
E
on
and
Eff
4
values were improved by electrochemical oxidation up to 1.2 V (vs. reversible hydrogen electrode) in the CV measurement prior to the SSV measurement. As a result, the nanosheet-based samples exhibited higher ORR activities than the starting materials, K
+
-form layered manganese oxide K
0.5
MnO
2
(K
+
-RG(Mn)) and Mn
2
O
3
, and a well-known ORR catalyst, MnO
2
. The H
3
O
+
-RE(Mn) sample electrochemically oxidized up to 1.2 V showed the highest ORR activity,
E
on
= 0.97 V and
Eff
4
= 99%, which were comparable to those of a conventional 20 mass% Pt/C catalyst. The comparison of their ORR activities, BET surface areas and X-ray photoelectron spectra suggests that the enhancement of the ORR activity is attributed to an increase in the numbers of the ORR active sites and a large amount of H
2
O in the interlayers and on the surface of the nanosheets because of rapid of H
2
O-supply enough for ORR in alkaline solution. |
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ISSN: | 1022-5528 1572-9028 |
DOI: | 10.1007/s11244-009-9224-2 |