One-pot synthesis of (anatase/bronze-type)-TiO2/carbon dot polymorphic structures and their photocatalytic activity for H2 generation

被引:13
作者
Khan, Sovann [1 ]
Kubota, Yuta [2 ]
Lei, Wenwei [1 ]
Suzuki, Norihiro [1 ,3 ]
Nakata, Kazuya [1 ,3 ,4 ]
Terashima, Chiaki [1 ,3 ]
Matsushita, Nobuhiro [2 ]
Fujishima, Akira [1 ]
Katsumata, Ken-ichi [1 ,3 ,5 ]
机构
[1] Tokyo Univ Sci, Photocatalysis Int Res Ctr, 2641 Yamazaki, Noda, Chiba 2788510, Japan
[2] Tokyo Inst Technol, Dept Mat Sci & Engn, Meguro Ku, 2-12-1 Ookayama, Tokyo 1528550, Japan
[3] Tokyo Univ Sci, Res Ctr Space Colony, 2641 Yamazaki, Noda, Chiba 2788510, Japan
[4] Tokyo Univ Agr & Technol, Grad Sch Bioapplicat & Syst Engn, 2-24-16 Nakacho, Koganei, Tokyo 1840012, Japan
[5] Tokyo Univ Sci, Fac Ind Sci & Technol, Dept Mat Sci & Technol, Katsushika Ku, 6-3-1 Niijuku, Tokyo 1258585, Japan
基金
日本学术振兴会;
关键词
Bronze-type-TiO2; Carbon dots; Heterostructure; Hydrogen evolution; CARBON DOTS; ANATASE; ENHANCEMENT; TIO2(B); RATIO;
D O I
10.1016/j.apsusc.2020.146650
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
We report the one-pot synthesis of anatase/bronze-type ((A/B)-TiO2) and carbon dots (CDs) via a simple solvothermal method using only TiCl4 and ethylene glycol. Control of the reaction temperature and duration enabled the compositions of pure (B) phase, (A/B)-TiO2/CDs, and (A)-TiO2/CDs to be tuned. A series of experiments on the synthesis conditions was carefully conducted at various temperatures (150-200 degrees C) for various reaction times (5-36 h). Pure phase (B)-TiO2 was obtained at 150 degrees C for all reaction times (5 to 36 h). The (B) phase was transformed to anatase at temperatures from 170 degrees C for reaction times longer than 12 h. At the same time, CDs were formed from the decomposition of ethylene glycol at temperatures greater than 160 degrees C and long reaction times (> 12 h). The photocatalytic activities of the composite catalysts were evaluated by H-2 generation from a water-ethylene glycol mixed solution under UV-visible light. H-2 generation rates were observed in this order: (A/B)-TiO2/CDs > (A)-TiO2/CDs > (B)-TiO2 > (A)-TiO2. This high photocatalytic activity for (A/B)TiO2/CDs is attributed to effective charge-separation and broad-light absorption. The developed method will be important for the facile synthesis of (A/B)-TiO2/CD materials and has more potential than conventional multi step methods.
引用
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页数:10
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