Enhanced activity of alcohol oxidation on nitrogen-doped carbon by Fe-N interaction

被引:3
|
作者
Xu, Shurui [1 ]
Lin, Baoqiang [1 ]
Huang, Qihang [1 ]
Qiu, Wenting [1 ]
Yuan, Wenqian [1 ]
Xu, Weirui [1 ]
Xue, Xingfeng [1 ]
Zhong, Guoyu [1 ]
Liao, Wenbo [1 ]
Wang, Wenlong [1 ]
Fu, Xiaobo [1 ]
机构
[1] Dongguan Univ Technol, Sch Chem Engn & Energy Technol, Guangdong Prov Key Lab Distributed Energy Syst, Dongguan 523808, Peoples R China
基金
中国国家自然科学基金;
关键词
Porous carbon; Pyridinic N; Alcohol oxidation; CatalysisFe-N interaction; SELECTIVE AEROBIC OXIDATION; HIERARCHICAL POROUS CARBON; METAL-FREE CATALYSTS; BENZYL ALCOHOL; EFFICIENT CATALYST; OXIDE; 2,5-DIFORMYLFURAN; NANOTUBES; SYSTEM; ACID;
D O I
10.1016/j.diamond.2022.109635
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Oat-derived N-doped carbon with tunable N content (OA-NCs) were synthesized and applied in alcohol oxidation to selectively produce aldehyde. OA-NCs exhibited unexpectedly high performance in the oxidation of benzyl alcohol, cinnamyl alcohol and furfuryl alcohol. N species were characterized to interpret its promoting effect on their catalytic activity. Oxidation activity of pyridinic N in OA-NCs was sensitive to their structure while reac-tivity assessment disclosed it was more active to convert alcohols in presence of Fe3+, rather than pyrrolic-N or graphite-N. The superoxide radical was evidenced as the most reactive oxygen species in this reaction. The strong metal-support interaction (MSI) between pyridinic N and Fe3+, indicated by DFT calculation, was determined to be critical for the high activity of OA-CNs catalysts. The present work provides the insight into the positive effect of N-metal interaction in carbon materials on O2 activation and explores a green pathway for the selective production of aldehydes.
引用
收藏
页数:10
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