热液循环
光催化
材料科学
可见光谱
兴奋剂
吸收边
锐钛矿
SN2反应
催化作用
结晶度
水热合成
锡
吸收(声学)
分解水
纳米技术
化学工程
光电子学
带隙
立体化学
化学
复合材料
有机化学
冶金
工程类
作者
Xiaohuan Jiang,Yingnan Duan,Yu Tian,Meng Chen,Maokun Li,Huanhuan Liu,Wanliang Yang,Mengkui Tian
出处
期刊:Rare Metals
[Springer Science+Business Media]
日期:2021-08-28
卷期号:41 (2): 406-414
被引量:28
标识
DOI:10.1007/s12598-021-01810-4
摘要
Abstract In this paper, a visible light‐responsive Sn 2+ and N co‐doped TiO 2 photocatalyst was prepared by facile one‐pot hydrothermal method. All as‐prepared samples were characterized in detail by a series of characterization approaches. The results showed that the Sn 2+ and N elements were co‐doped into TiO 2 , while the catalyst still maintains anatase crystal structure and gets irregular little nanocluster in diameter of 9–10 nm with higher specific surface area. The absorption edge of Sn 2+ and N co‐doped TiO 2 extends to the visible light region. Compared with Sn 2+ ‐doped TiO 2 and N‐TiO 2 , the absorption edges have obvious red‐shift of about 50 and 70 nm, respectively. The synergistic effect of O 2p‐N 2p and O 2p‐Sn 5s hybridization to form impurity levels is the main reason for the red‐shift. The hydrogen production performance of the Sn 2+ and N co‐doping TiO 2 ( n (N)/ n (Ti) = 1) catalyst reached the maximum value of 0.37 mmol·h −1 ·g −1 under visible light, which is higher than that of N‐doped TiO 2 and Sn 2+ ‐doped TiO 2 singly. This result is due to the wider visible light region‐responsive ability of Sn 2+ and N co‐doped into TiO 2 . Furthermore, mild hydrothermal methods will not make the Sn 2+ oxidized to Sn 4+ , which make the catalysts still maintain high photocatalytic performance. This work provides a simple and mild method for the preparation of dual‐element co‐doped TiO 2 with high crystallinity, excellent performance and broad application prospects.
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