Abstract
Understanding the metal-support interaction (MSI) is crucial to comprehend how the catalyst support affects performance and whether this interaction can be exploited in order to design new catalysts with enhanced properties. Spatially resolved soft X-ray absorption spectroscopy (XAS) in combination with Atomic Force Microscopy (AFM) and Scanning Helium Ion-Milling Microscopy (SHIM) has been applied to visualise and characterise the behaviour of individual cobalt nanoparticles (CoNPs) supported on two-dimensional substrates (SiO (x) Si(100) (x < 2) and rutile TiO(2)(110)) after undergoing reduction-oxidation-reduction (ROR). The behaviour of the Co species is observed to be strongly dependent on the type of support. For SiO (x) Si a weaker MSI between Co and the support allows a complete reduction of CoNPs although they migrate and agglomerate. In contrast, a stronger MSI of CoNPs on TiO(2) leads to only a partial reduction under H(2) at 773 K (as observed from Co L(3)-edge XAS data) due to enhanced TiO(2) binding of surface-exposed cobalt. SHIM data revealed that the interaction of the CoNPs is so strong on TiO(2), that they are seen to spread at and below the surface and even to migrate up to ∼40 nm away. These results allow us to better understand deactivation phenomena and additionally demonstrate a new understanding concerning the nature of the MSI for Co/TiO(2) and suggest that there is scope for careful control of the post-synthetic thermal treatment for the tuning of this interaction and ultimately the catalytic performance.