The surface structures of heterogeneous catalysts significantly impact catalytic performance,especially for structure-sensitive reactions.In this study,we employed surface techniques such as low-energy ion scattering ...The surface structures of heterogeneous catalysts significantly impact catalytic performance,especially for structure-sensitive reactions.In this study,we employed surface techniques such as low-energy ion scattering spectroscopy,X-ray photoelectron spectroscopy,and Fourier transform infrared spectroscopy with CO as a probe(CO-FTIR)to investigate the surface dynamics of Rh/Al_(2)O_(3)catalysts for propane dehydrogenation(PDH).We observed a notable induction process for PDH on Rh/Al_(2)O_(3)catalysts,marked by significant variations in propane conversion,methane,and propylene selectivities.These changes were attributed to substantial coke formation.Aberration-corrected high-angle annular dark-field scanning transmission electron microscopy)and CO-FTIR revealed the coexistence of Rh nanoparticles,clusters,and single atoms on the surface.Through various dynamic quasi in-situ characterizations,we found that coke preferentially covered Rh clusters,thereby inhibiting C-C bond breaking and methane formation.Meanwhile,Rh single atoms were less affected by coke coverage and remained exposed as active and selective sites for PDH,favoring propylene production.This work underscores the sensitivity of PDH to the sizes of Rh species,with isolated Rh single atoms promoting propylene formation.展开更多
文摘The surface structures of heterogeneous catalysts significantly impact catalytic performance,especially for structure-sensitive reactions.In this study,we employed surface techniques such as low-energy ion scattering spectroscopy,X-ray photoelectron spectroscopy,and Fourier transform infrared spectroscopy with CO as a probe(CO-FTIR)to investigate the surface dynamics of Rh/Al_(2)O_(3)catalysts for propane dehydrogenation(PDH).We observed a notable induction process for PDH on Rh/Al_(2)O_(3)catalysts,marked by significant variations in propane conversion,methane,and propylene selectivities.These changes were attributed to substantial coke formation.Aberration-corrected high-angle annular dark-field scanning transmission electron microscopy)and CO-FTIR revealed the coexistence of Rh nanoparticles,clusters,and single atoms on the surface.Through various dynamic quasi in-situ characterizations,we found that coke preferentially covered Rh clusters,thereby inhibiting C-C bond breaking and methane formation.Meanwhile,Rh single atoms were less affected by coke coverage and remained exposed as active and selective sites for PDH,favoring propylene production.This work underscores the sensitivity of PDH to the sizes of Rh species,with isolated Rh single atoms promoting propylene formation.
