催化作用
双金属片
苯
羟基化
苯酚
碳纤维
产量(工程)
石墨
化学
材料科学
化学工程
有机化学
冶金
复合数
工程类
复合材料
酶
作者
Lingdong Zeng,Hanying Liang,Ping An,Deng‐Guang Yu,Can Yang,Yidong Hou,Jinshui Zhang
标识
DOI:10.1016/j.apcata.2022.118499
摘要
Carbon encapsulated iron catalysts hold great potential for one-step hydroxylation of benzene to phenol due to their unique core-shell nanostructures. However, their catalytic performance is moderate, since the carbon shells have impeded their activity toward H2O2 activation. Herein, we demonstrate that alloying engineering of Fe cores with Co atoms is a promising strategy to address the issue about H2O2 activation. The incorporation of Co into Fe cores can generate strong synergetic effects to promote H2O2 activation, while still maintaining the structural benefits of carbon shells for benzene hydroxylation reaction. As a result, the phenol yield obtained on carbon encapsulated FeCo ([email protected]) reaches to 26.4 ± 0.7% with a selectivity of 96.2 ± 1.2%, much higher than that of [email protected] and [email protected] With the improved intrinsic catalytic behavior toward H2O2 activation and well-reserved carbon structure benefits, [email protected] should be a promising catalyst for a broad liquid-phase reactions using H2O2 as the oxidant.
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