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Dual-function surface hydrogen bonds enable robust O2activation for deep photocatalytic toluene oxidation

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成果类型:
期刊论文
作者:
Li, Hao;Jiang, Fuze;Drdova, Sarka;Shang, Huan;Zhang, Lizhi;...
通讯作者:
Wang, Jing
作者机构:
[Drdova, Sarka; Li, Hao; Wang, Jing; Jiang, Fuze] Swiss Fed Inst Technol, Inst Environm Engn, CH-8093 Zurich, Switzerland.
[Drdova, Sarka; Li, Hao; Wang, Jing; Jiang, Fuze] Swiss Fed Labs Mat Sci & Technol, Empa, Lab Adv Analyt Technol, CH-8600 Dubendorf, Switzerland.
[Zhang, Lizhi; Shang, Huan] Cent China Normal Univ, Coll Chem, Inst Appl & Environm Chem, Key Lab Pesticide & Chem Biol,Minist Educ, Wuhan 430079, Peoples R China.
通讯机构:
[Wang, Jing] S
Swiss Fed Inst Technol, Inst Environm Engn, CH-8093 Zurich, Switzerland.
Swiss Fed Labs Mat Sci & Technol, Empa, Lab Adv Analyt Technol, CH-8600 Dubendorf, Switzerland.
语种:
英文
期刊:
Catalysis Science & Technology
ISSN:
2044-4753
年:
2021
卷:
11
期:
1
页码:
319-331
基金类别:
This work was partially supported by the Center for Filtration Research (CFR) at the University of Minnesota. We thank Dr. Artur Braun for providing GC system for part of our photocatalytic toluene removal experiments.
机构署名:
本校为其他机构
院系归属:
化学学院
摘要:
Solar-driven molecular oxygen activation by semiconductor photocatalysts is a prototypical reaction manifesting complex interactions among photons, charge carriers, and reactants. In this study, we demonstrate that energetic O2 activation towards volatile organic compound control can be realized via constructing a sophisticated surface hydrogen bond (HB) network having a dual-function. The extensive HBs established between the hydroxyl-rich BiOCl surface and phosphoric acid are first shown to significantly weaken surface Bi-O bonds, enabling fa...

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