oxides with different crystalline structures (abbreviated as MnO2-I, MnO2-II, MnO2-III, and MnO2-IV) were synthesized by a uniform hydrothermal method. In the synthesis
of MnO2-I, 16 mmol KMnO4 (Sinopharm, China)
and 6 mmol MnSO4·H2O (Sinopharm, China)
were dissolved in 160 mL of deionized water under ultrasonic stirring
for 20 min, and the solution was kept at 140 °C for 12 h in a
200 mL Teflon-lined autoclave. The precipitation was further dried
at 110 °C for 12 h after thorough centrifugation and washing,
and then the obtained powder was annealed at 300 °C for 3 h in
air. The syntheses of MnO2-II, MnO2-III, and
MnO2-IV were similar to that of MnO2-I except
for the differences of precursors and hydrothermal conditions. Specifically,
MnO2-II was synthesized with (NH4)2S2O8 (Sinopharm, 10 mmol) and MnSO4·H2O (10 mmol). For MnO2-III, the solution
with (NH4)2S2O8 (16 mmol)
and MnSO4·H2O (16 mmol) was hydrothermally
reacted at 90 °C for 24 h. Further, MnO2-IV was synthesized
via the hydrothermal reaction of KMnO4 (36 mmol) and MnSO4·H2O (6 mmol) at 240 °C for 24 h. All
of the reagents were of analytical grade, and the catalysts were screened
with 40–60 mesh before the activity tests.