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Efficient Selective Oxidation of Aromatic Alkanes by Double Cobalt Active Sites over Oxygen Vacancy-rich Mesoporous
Yali Liu1,2, Yuenan Zheng1,3, Danyang Feng4
1State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University, Changchun, Jilin, 130012, China.
Abstract:
The development of efficient catalyst for selective oxidation of hydrocarbon to functional compounds remains a challenge. Herein, mesoporous Co3 O4 (mCo3 O4 -350) showed excellent catalytic activity for selective oxidation of aromatic-alkanes, especially for oxidation of ethylbenzene with a conversion of 42 % and selectivity of 90 % for acetophenone at 120 °C. Notably, mCo3 O4 presented a unique catalytic path of direct oxidation of aromatic-alkanes to aromatic ketones rather than the conventional stepwise oxidation to alcohols and then to ketones. Density functional theory calculations revealed that oxygen vacancies in mCo3 O4 activate around Co atoms, causing electronic state change from Co3+ (Oh) →Co2+ (Oh) . Co2+ (Oh) has great attraction to ethylbenzene, and weak interaction with O2 , which provide insufficient O2 for gradual oxidation of phenylethanol to acetophenone. Combined with high energy barrier for forming phenylethanol, the direct oxidation path from ethylbenzene to acetophenone is kinetically favorable on mCo3 O4 , sharply contrasted to non-selective oxidation of ethylbenzene on commercial Co3 O4 .
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