Rational design of cobalt catalysts embedded in N-Doped carbon for the alcohol dehydrogenation to carboxylic acids

脱氢 催化作用 热解 结晶度 化学 碳纤维 有机化学 组合化学 材料科学 复合材料 结晶学 复合数
作者
Cheng Chen,Jing Hang,Zhiqin Wang,Zhong-Hui Zheng,Jun-Fei Gu,Wei Sang,Ye Yuan,Somboon Chaemchuen,Francis Verpoort
出处
期刊:Molecular Catalysis [Elsevier BV]
卷期号:535: 112891-112891 被引量:3
标识
DOI:10.1016/j.mcat.2022.112891
摘要

In this work, a series of Co catalysts (namely [email protected]) was designed and developed from the thermal treatment of ZIF-67. Through extensive screening of various parameters, [email protected]2/Ar exhibited the best catalytic performance in the acceptorless alcohol dehydrogenation to carboxylic acids. It was worth noting that [email protected]2/Ar enabled the efficient synthesis of various aromatic and aliphatic carboxylic acids in moderate to high yields. Besides, it was recyclable for 9 consecutive cycles without activity decay. Moreover, the effects of pyrolysis conditions on the catalytic performance of the resulting materials were thoroughly examined, and the rationale for the superiority of [email protected]2/Ar over the other prepared materials was also provided. Specifically, the pyrolysis atmosphere applying 95% of Ar gas and 5% of H2 gas (H2/Ar) resulted in the generation of ideal porosity and carbon nanotubes (CNTs), while utilizing 700 °C as the optimized pyrolysis temperature was ascribed to the comprehensive evaluation of materials crystallinity and defective structures. Furthermore, additional insights were gained by systematically exploring the oxidation states of Co in different catalysts. It was proposed that the Co–N species played a crucial role in this catalysis, while the contribution of other Co species, including Co0 and Co–O, could not be neglected. Finally, a plausible reaction mechanism was proposed based on the above observations and related literature reports.
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