4.8 Article

N-Oxyl Radicals Trapped on Zeolite Surface Accelerate Photocatalysis

期刊

ACS CATALYSIS
卷 9, 期 11, 页码 10448-10453

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.9b03737

关键词

zeolite; supported catalysts; microporous structure; oxidation; photocatalysis

资金

  1. National Key Research andDevelopment Program of China [2018YFB0604801]
  2. National Natural Science Foundation of China [21822203, 91645105, 91634201]
  3. Natural Science Foundation of Zhejiang Province [LR18B030002]
  4. Foundation of State Key Laboratory of High -efficiency Utilization of Coal and Green Chemical Engineering [2017-K12]

向作者/读者索取更多资源

The zeolite materials have been industrially used in the thermal catalysis, but their function in photocatalysis has not been fully explored. Here we report that zeolites as supports could strengthen the radical formation after loading ferric oxide nanoparticles (FeOx/zeolite) under photoirradiation: Multiple theoretical and experimental studies demonstrate that the N-hydroxyphthalimide (NHPI) molecules could be trapped within the orifice of MFI zeolites via a sterically controllable adsorption, weakening the NO-H bonding to boost the phthalimide-N-oxyl radial (PINO center dot) formation. The formed radicals could activate the carbon-hydrogen bonds for accelerating the hydrocarbon oxidation into the corresponding ketones/carboxylic acids.

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