Facile synthesis of TiO2/trititanate heterostructure with enhanced photoelectric efficiency for an improved photocatalysis
Facile synthesis of TiO2/trititanate heterostructure with enhanced photoelectric efficiency for an improved photocatalysis
复制标题
轻松合成 TiO2/三钛酸酯异质结构,提高光电效率,改善光催化性能
DOI:
10.1016/j.apsusc.2015.02.182
复制
发表时间:
2015-06
影响因子:
6.7
通讯作者:
Pengfei Fang
中科院分区:
文献类型:
--
作者:
Feitai Chen;Youji Li;Zhi Liu;Pengfei Fang
TiO2/trititanate photocatalyst was prepared by alkaline hydrothermal treatment of TiO2, and characterized by transmission electron microscopy, X-ray diffraction, and Raman etc. The photocatalytic activities of catalysts were evaluated by the photocatalytic degradation of rhodamine B (RhB). It is found that the heterostructure can be directly formed via the conversion of surface TiO2into trititanate. The coupled nanostructure possesses enhanced adsorption ability for RhB as compared with the raw TiO2, owing to the formation of an increased amount of hydroxyl groups on the prepared catalyst surface. Besides, the generated trititanate can successfully introduce a shallow energy level in the coupled composite, which results in the improvement of separation efficiency of photoinduced electron–hole pairs. In the degradation experiments, TiO2/trititanate exhibits much higher photocatalytic activity than the bare TiO2. These advantages of the coupled nanostructure in adsorption capacity and photoelectric efficiency may make it a wider application for the removal of organic pollutants.
登录
查看更多内容
影响因子:
11.4
作者:
Ou, Hsin-Hung;Liao, Ching-Hui;Lo, Shang-Lien
通讯作者:
Lo, Shang-Lien
影响因子:
22.1
作者:
M. Pelaez;F. Falaras;A. Kontos;A. A. Cruz-A.;K. O’Shea;P. Dunlop;J. Byrne;D. Dionysiou
通讯作者:
M. Pelaez;F. Falaras;A. Kontos;A. A. Cruz-A.;K. O’Shea;P. Dunlop;J. Byrne;D. Dionysiou
影响因子:
4.5
作者:
Shen, Xiaojun;Zhang, Jinlong;Tian, Baozhu
通讯作者:
Tian, Baozhu
影响因子:
15.1
作者:
Yanting Li;Lei Chen;Ya-nan Guo;Xiuguo Sun;Yu Wei
通讯作者:
Yanting Li;Lei Chen;Ya-nan Guo;Xiuguo Sun;Yu Wei
影响因子:
3.7
作者:
X. Xu;X. Ding;Qing Chen;Lianmao Peng
通讯作者:
X. Xu;X. Ding;Qing Chen;Lianmao Peng