Photocatalytic methane oxidation over a TiO2/SiNWs p-n junction catalyst at room temperature

被引:1
|
作者
Ta, Qui Thanh Hoai [1 ]
Nguyen, Luan Minh [1 ,2 ]
Nguyen, Ngoc Hoi [1 ,2 ]
Nguyen, Phan Khanh Thinh [3 ]
Nguyen, Dai Hai [1 ,2 ]
机构
[1] Vietnam Acad Sci & Technol, Inst Chem Technol, 1A TL29 St,Thanh Loc Ward,Dist 12, Ho Chi Minh City 700000, Vietnam
[2] Vietnam Acad Sci & Technol, Grad Univ Sci & Technol, 18 Hoang Quoc Viet St, Cau Giay Dist 100000, Hanoi, Vietnam
[3] Gachon Univ, Dept Chem & Biol Engn, 1342 Seongnamdaero, Seongnam Si 13120, Gyeonggi Do, South Korea
来源
关键词
photocatalysis; photocatalytic CH4 4 oxidation; p-n heterojunction; TiO2/SiNWs; 2; /SiNWs; ELECTRIC-FIELD; HETEROJUNCTION; CONVERSION; DESIGN; CH4;
D O I
10.3762/bjnano.15.92
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Rapid recombination of charge carriers in semiconductors is a main drawback for photocatalytic oxidative coupling of methane (OCM) reactions. Herein, we propose a novel catalyst by developing a p-n junction titania-silicon nanowires (TiO2/SiNWs) 2 /SiNWs) heterostructure. The structure is fabricated by atomic layer deposition of TiO2 2 on p-type SiNWs. The TiO2/SiNWs 2 /SiNWs heterostructure exhibited an outstanding OCM performance under simulated solar light irradiation compared to the single components. This enhanced efficiency was attributed to the intrinsic electrical field formed between n-type TiO2 2 and p-type SiNWs, which forces generated charge carriers to move in opposite directions and suppresses charge recombination. Besides, surface morphology and optical properties of the the p-n TiO2/SiNWs 2 /SiNWs catalyst are also beneficial for the photocatalytic activity. It is expected that the results of this study will provide massive guidance in synthesizing an efficient photocatalyst for CH4 4 conversion under mild conditions.
引用
收藏
页码:1132 / 1141
页数:10
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