4.7 Article

Pd nanoparticles supported on CeO2 nanospheres as efficient catalysts for dehydrogenation from additive-free formic acid at low temperature

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FUEL
卷 302, 期 -, 页码 -

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ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2021.121142

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  1. Basic Science Center Program for Ordered Energy Conversion of the National Natural Science Foundation of China [51888103]

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Pd nanoparticles (NPs)-CeO2 based catalysts were successfully synthesized, with Pd NPs uniformly dispersed on CeO2 nanospheres showing excellent catalytic performance. Increasing Pd loading amount led to improved catalytic efficiency, with the 10 wt% Pd*CeO2 catalyst exhibiting the highest activity for dehydrogenation of formic acid. The superior performance of 10 wt% Pd*CeO2 can be attributed to the high dispersion of Pd NPs, more electron-rich Pd active sites, and the Strong Metal-Support Interactions (SMSI) between Pd and CeO2.
Pd nanoparticles (NPs)-based catalysts were synthesized, characterized, and used to efficiently catalyze hydrogen generation from formic acid (FA). A facile deposition-precipitation (DP) method was employed to synthesized Pd*CeO2 catalysts with the assistance of polyvinylpyrrolidone (PVP) as a surfactant. The Pd NPs were uniformly dispersed on the surface of CeO2 nanospheres to form x wt% Pd*CeO2 catalysts with various Pd loading amount (x = 0.5, 1, 3, 5, 10). The structural, morphological, surface properties were comprehensively investigated by various techniques including XRD, N2 adsorption-desorption, FE-SEM, HRTEM, XPS, Raman, H2-TPR and ICPMS. In particular, the Strong Metal-Support Interactions (SMSI) located at the interface between the active Pd NPs and the CeO2 support has been demonstrated through direct observations of hydrogen spillover phenomena and several advanced characterizations. With the increase of Pd loading, the catalytic efficiency of Pd*CeO2 catalysts was also improved. The prepared 10 wt% Pd*CeO2 catalyst exhibited the highest activity towards dehydrogenation of additive-free formic acid at 313 K, corresponding to an initial turn over frequency as high as 807.7 h-1. The superior performance of 10 wt% Pd*CeO2 could be attributed to the high dispersion of Pd NPs, more electron-rich Pd active sites and of course the SMSI between Pd and CeO2.

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