环己醇
化学
催化作用
选择性
分子
乙醚
功能群
吸附
二苯醚
水溶液
双水相体系
多相催化
有机化学
选择性吸附
反应机理
密度泛函理论
组合化学
反应性(心理学)
硅醚
表面改性
煅烧
相(物质)
作者
Zhongxi Jiang,Bin Hu,Xianmei Zhao,Hui Zhou,H. J. Yang,Yuangu Xia,Yanxia Shi,Yunpeng Zhao,Zhenghua Dai,Xiaowei Bai,Jian Li
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2026-03-12
卷期号:16 (7): 6295-6304
标识
DOI:10.1021/acscatal.5c07567
摘要
Constructing oxygen-containing functional groups and understanding their catalytic mechanism are crucial for the design of carbon-based catalysts. A Ni@C(O) catalyst rich in oxygen-containing functional groups was prepared by calcining oxygen-rich precursors in a nitrogen atmosphere. This catalyst exhibited a cyclohexanol selectivity of 96.5% in the aqueous phase catalytic conversion of diphenyl ether, which is significantly higher than that of traditional Ni/C catalysts, with selectivity typically below 50.0%. Mechanistic studies reveal that oxygen-containing functional groups promote the participation of water molecules in the reaction, which is key to achieving high selectivity. This effect occurs because oxygen-containing functional groups induce the adsorption of diphenyl ether molecules on the catalyst surface in a planar twisted configuration. The resulting adsorption geometry provides a favorable spatial environment for water molecules to attack the ether bond in diphenyl ether, thereby driving the selective formation of cyclohexanol. Furthermore, the Ni@C(O) catalyst maintained stable performance for 200 h in a fixed-bed continuous-flow experiment and exhibited broad applicability to a range of analogous substrates containing ether bonds.
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