Skip to main content
. 2017 Jun 28;56(31):8986–8991. doi: 10.1002/anie.201701115

Figure 1.

Figure 1

Atomically dispersed Pt on CeO2 (the as‐prepared catalyst) undergoes some reduction to form subnanometer Pt particles after reaction. Isolated Pt single atoms are circled. The monometallic catalyst does not show any selectivity to propylene despite its high activity (100 % conversion at 680 °C). a) XPS spectra of the fresh and spent Pt/CeO2 catalyst after propane dehydrogenation at 680 °C for 6 h. b) STEM images of the as‐prepared Pt/CeO2 catalyst (calcined 800 °C in air). c) STEM image of the spent Pt/CeO2 catalyst after 3 cycles of propane dehydrogenation at 680 °C for 6 h each, with an intermediate oxidation at 580 °C for 2 h after each cycle. Scale bar=5 nm.