N-Oxyl Radicals Trapped on Zeolite Surface Accelerate Photocatalysis

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 (FeO x /zeolite) under photoirradiati...

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Veröffentlicht in:ACS catalysis 2019-11, Vol.9 (11), p.10448-10453
Hauptverfasser: Ma, Runyuan, Chen, Wei, Wang, Liang, Yi, Xianfeng, Xiao, Yao, Gao, Xinhua, Zhang, Jian, Tang, Xiaomin, Yang, Chengguang, Meng, Xiangju, Zheng, Anmin, Xiao, Feng-Shou
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container_end_page 10453
container_issue 11
container_start_page 10448
container_title ACS catalysis
container_volume 9
creator Ma, Runyuan
Chen, Wei
Wang, Liang
Yi, Xianfeng
Xiao, Yao
Gao, Xinhua
Zhang, Jian
Tang, Xiaomin
Yang, Chengguang
Meng, Xiangju
Zheng, Anmin
Xiao, Feng-Shou
description 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 (FeO x /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·) formation. The formed radicals could activate the carbon–hydrogen bonds for accelerating the hydrocarbon oxidation into the corresponding ketones/carboxylic acids.
doi_str_mv 10.1021/acscatal.9b03737
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