Affiliation:
1. State Key Laboratory of Heavy Oil Processing College of Chemical Engineering China University of Petroleum (East China) Qingdao 266580 China
2. Center for Reliability Science and Technologies Center for Green Technology Chang Gung University Taoyuan 33302 Taiwan
3. Kidney Research Center Department of Nephrology Chang Gung Memorial Hospital Linkou Taoyuan 33305 Taiwan
Abstract
AbstractThis study adopts a facile and effective in situ encapsulation‐oxidation strategy for constructing a coupling catalyst composed of atomically dispersed Pt‐doped Co3O4 spinel nanoparticles (NPs) embedded in polyhedron frames (PFs) for robust propane total oxidation. Benefiting from the abundant oxygen vacancies and more highly valent active Co3+ species caused by the doping of Pt atoms as well as the confinement effect, the optimized 0.2Pt‐Co3O4 NPs/PFs catalyst exhibits excellent propane catalytic activity with low T90 (184 °C), superior apparent reaction rate (21.62×108 (mol gcat−1 s−1)), low apparent activation energy (Ea = 17.89 kJ mol−1), high turnover frequency ( 811×107 (mol gcat−1 s−1)) as well as good stability. In situ diffuse reflectance infrared Fourier transform spectroscopy and density functional theory calculations indicate that the doping of Pt atoms enhances the oxygen activation ability, and decreases the energy barrier required for CH bond breaking, thus improving the deep oxidation process of the intermediate species. This study opens up new ideas for constructing coupling catalysts from atomic scale with low cost to enhance the activation of oxygen molecules and the deep oxidation of linear short chain alkanes at low temperature.
Funder
Natural Science Foundation of Shandong Province
National Natural Science Foundation of China
Fundamental Research Funds for the Central Universities
Subject
General Materials Science,General Chemistry
Cited by
10 articles.
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