In-situ synthesis of heterojunction TiO2/MnO2 nanostructure with excellent performance in vacuum ultraviolet photocatalytic oxidation of toluene

被引:72
|
作者
Zhang, Yingguang [1 ]
Wu, Muyan [1 ]
Kwok, Y. H. [1 ]
Wang, Yifei [1 ]
Zhao, Wei [1 ]
Zhao, Xiaolong [1 ]
Huang, Haibao [2 ]
Leung, Dennis Y. C. [1 ]
机构
[1] Univ Hong Kong, Dept Mech Engn, Hong Kong, Peoples R China
[2] Sun Yat Sen Univ, Sch Environm Sci & Engn, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Heterojunction; VUV-PCO; Catalytic ozonation; Ozone decomposition; Photocatalytic mechanism; VOLATILE ORGANIC-COMPOUNDS; EXPOSED; 001; FACETS; GASEOUS FORMALDEHYDE OXIDATION; BIRNESSITE-TYPE MNO2; ANATASE TIO2; RISK-ASSESSMENT; GAS-PHASE; DEGRADATION; OZONE; REMOVAL;
D O I
10.1016/j.apcatb.2019.118034
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of TiO2/MnO2 heterojunction catalysts were fabricated through an in-situ hydrothermal method, and for the first time, catalysts with this heterojunction structure were used for VUV-PCO toluene degradation. After the MnO2 coating, the TiO2/MnO2 catalysts performed excellently for both VOCs degradation and residual ozone decomposition with removal efficiency reaching 96.0% and 99.9%, respectively. The enhanced photocatalytic activity towards toluene degradation could be attributed to the heterojunction structure of TiO2/MnO2, which provides excellent contact between MnO2 and TiO2, and suppresses the recombination of photogenerated electron-hole pairs. Moreover, benefiting from the MnO2, the ozone generated in the system could be efficiently utilized and eliminated during the VUV-PCO process. The photocatalytic mechanism of TiO2/MnO2 for the toluene degradation and ozone decomposition was proposed.
引用
收藏
页数:11
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