The
![](/i<font color=)
mages/gifchars/alpha.gif" BORDER=0>-,
![](/i<font color=)
mages/gifchars/beta2.gif" BORDER=0 ALIGN="middle">-,
![](/i<font color=)
mages/gifchars/gam
ma.gif" BORDER=0 >-, and
![](/i<font color=)
mages/gifchars/delta.gif" BORDER=0 >-MnO
2 nanorods were synthesized by the hydrother
mal method. Their catalytic propertiesfor CO oxidation were evaluated, and the effects of phase structures on the activities of the MnO
2 nanorodswere investigated. The activities of the catalysts decreased in the order of
![](/i<font color=)
mages/gifchars/alpha.gif" BORDER=0>-
![](/i<font color=)
mages/entities/ap.gif">
![](/i<font color=)
mages/gifchars/delta.gif" BORDER=0 >- >
![](/i<font color=)
mages/gifchars/gam
ma.gif" BORDER=0 >- >
![](/i<font color=)
mages/gifchars/beta2.gif" BORDER=0 ALIGN="middle">-MnO
2. Themechanism of CO oxidation over the MnO
2 nanorods was suggested as follows. The adsorbed CO was oxidizedby the lattice oxygen, and the MnO
2 nanorods were partly reduced to Mn
2O
3 and Mn
3O
4. Then, Mn
2O
3 andMn
3O
4 were oxidized to MnO
2 by gaseous oxygen. CO chemisorption, the Mn-O bond strength of the MnO
2,and the transfor
mation of intermediate oxides Mn
2O
3 and Mn
3O
4 into MnO
2 can significantly influence theactivity of the MnO
2 nanorods. The activity for CO oxidation was
mainly predominated by the crystal phaseand channel structure of the MnO
2 nanorods.