Nating Yang, Shenglin Ni, Yuhan Sun, Yan Zhu
Index: 10.1016/j.mcat.2018.03.016
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Pd-based catalysts that prepared by traditional impregnation or co-precipitate method show remarkable activity for catalytic oxidation of hydrocarbon, unfortunately they tend to deactivate in the long-term reaction process or at high temperature by sintering and transformation of active species. We now report a facile strategy to synthesize Pd/Co3O4 with superior catalytic durability for the methane catalytic oxidation. In this method, Pd ions coordinate with −CoOCH2COOH that derived from Co precursor and form the Pd-Co precursor complex at first, this complex was further calcined into Pd/Co3O4 catalysts with strong interaction between Pd and cobalt oxide. Methane catalytic oxidation experiment demonstrated that such Pd-based catalyst possesses intrinsically enhanced catalytic activity and exhibits a high resistance toward deactivate in the harsh reaction condition, in sharp contrast to the conventional catalysts prepared via impregnation or deposition-precipitation routes. TEM, XPS, O2-TPO, and isotopic experiments further indicate that the Pd/Co3O4 could form stronger interaction between PdO and Co3O4 and produce more actives species during long-term reaction.
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