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Double layered, one-pot hydrothermal synthesis of M-TiO2 (M = Fe3+, Ni2+, Cu2+ and Co2+) and their application in photocatalysis
被引:17
作者:
Chen YingYing
[1
,2
,3
]
Xie YongBing
[1
,2
]
Yang Jun
[3
]
Cao HongBin
[1
,2
]
Liu Hui
[3
,4
]
Zhang Yi
[1
,2
]
机构:
[1] Natl Engn Lab Hydromet Cleaner Prod Technol, Beijing 100190, Peoples R China
[2] Chinese Acad Sci, Key Lab Green Proc & Engn, Inst Proc Engn, Beijing 100190, Peoples R China
[3] Chinese Acad Sci, State Key Lab Multiphase Complex Syst, Inst Proc Engn, Beijing 100190, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金:
中国国家自然科学基金;
关键词:
double layered;
hydrothermal synthesis;
metal ions doped TiO2;
photocatalysis;
DOPED TITANIA;
TIO2;
DEGRADATION;
PERFORMANCE;
POLLUTANTS;
CATALYSTS;
ANATASE;
IONS;
D O I:
10.1007/s11426-013-4938-1
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
A double layered, one-pot hydrothermal method was adopted in this work to prepare transition metal ions (Fe3+, Ni2+, Cu2+ and Co2+) doped TiO2. The morphology and chemical properties of TiO2 and the status of metal ions were characterized with XRD, TEM, BET, UV-Vis and XPS analysis. TEM images show that the obtained TiO2 was very uniform with an average particle size of 10.4 nm. XPS, TEM and XRD results show that transitional metals were doped onto TiO2 in the form of ions. Photocatalytic decomposition of oxalic acid under UV illumination and methylene blue degradation under visible light on these materials were conducted, respectively. The results reveal that Cu2+-TiO2 and Co2+-TiO2 showed a highest activity under UV and visible light illumination, respectively, and they were both more active than commercial P25 TiO2. With this special design of double layers, the hydrolysis of titanium precursor in the system with water can be easily controlled and metal ions are simply doped. This strategy can be further applied to synthesize metal ion doped TiO2 using various metal precursors with controllable amounts, and thus lead to better optimization of highly active photocatalyst.
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页码:1783 / 1789
页数:7
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