Enhancing
the electrocatalytic activity of low-cost transition-metal
oxides for oxygen reduction reaction (ORR) is a crucial challenge
for extensive application of fuel cells. A promising approach demonstrated
previously is the formation of catalysts with mixed valent metal active
sites. Because catalysis happens primarily on the surface of the catalyst,
we hypothesize that creating such active sites only on the surface
will be an effective strategy for improving the catalytic activities.
Here, we present a partial oxidation approach that grows δ-MnO2 nanoflakes on the surface of octahedron Mn3O4 nanocrystals for increasing their ORR activity. The δ-MnO2/Mn3O4 nanocomposite exhibits significantly
improved ORR activity with a half-wave potential of 0.75 V versus
reversible hydrogen electrode, which is ∼110 and ∼90
mV lower than those of the Mn3O4 nanocrystal
and δ-MnO2 nanoflakes in their pure forms, respectively.
The electrochemical impedance spectroscopy reveals that the δ-MnO2/Mn3O4 nanocomposite possesses a lower
ORR charge transfer resistance than either component alone. We propose
that the reason for such significant improvement in catalytic activities
is due to the tuning of the position of δ-MnO2 nanoflake
d-band center by the Mn3O4 nanocrystal which
can effectively facilitate the electron transfer between the active
sites and adsorbed oxygen molecules. This work illustrates a facile
pathway to improve catalytic activity of mixed valence metal oxides