Abstract
Tuning the fine structure of carbon support is crucial for modifying the metal-support interface (MSI) in order to harvest a high-performance catalysis. Herein, a core–shell sp3@sp2 nanocarbon (nanodiamond@graphene, ND@G) and a pure sp2 carbon derivative (onion-like carbon, OLC) were applied to support Pd nanoparticles. We found that Pd/ND@G displayed a superior catalytic activity for CO oxidation reaction with a TOF of 2.9 times higher than that of Pd/OLC at 46 °C. Aberration-corrected high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) and ambient pressure X-ray photoelectron spectroscopy (AP-XPS) revealed that, different with the Pd/OLC system, a unique interface microstructure was formed in Pd/ND@G, which not only provides a high exposure of active sites, but also enhances the Pd surface reactivity toward oxygen species, thus leading to a superior catalytic activity of Pd/ND@G. Moreover, the temperature-programmed surface reaction (TPSR) results showed that CO oxidation on Pd/ND@G undergoes an unusual termolecular Eley–Rideal (TER) mechanism, which has a lower energy barrier as compared to the traditional Langmuir-Hinshelwood (LH) and ER mechanism.
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