Abstract
The strong metal-support interaction (SMSI) for supported Ni/CeO2 catalysts with different CeO2 nanomorphologies was systematically explored. The degree of encapsulation of Ni particles originating from the SMSI effect was found to follow the trend of Ni/CeO2-(111) > Ni/CeO2-(100) > Ni/CeO2-(110 + 100), which parallels the CO2 hydrogenation activity. Quasi in situ XPS reveals the presence of Ce3+ sites in accordance with the formation of an amorphous surface CeOx layer encapsulating the Ni nanoparticles. In situ DRIFTS indicates the reaction pathway and rate-determining step are dependent on the degree of the SMSI effect, leading to distinct selectivities towards CH4, especially at a high weight hourly space velocity (WHSV). These findings present a fundamental strategy about tailoring catalytic performance through support facet dependent susceptibility of SMSI phenomena.
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