Low-Temperature Nitrogen Doping in Ammonia Solution for Production of N-Doped TiO2-Hybridized Graphene as a Highly Efficient Photocatalyst for Water Treatment

被引:115
作者
Qian, Wen [1 ,2 ]
Greaney, P. Alex [3 ]
Fowler, Simon [1 ,2 ]
Chiu, Sheng-Kuei [4 ]
Goforth, Andrea M. [4 ]
Jiao, Jun [1 ,2 ]
机构
[1] Portland State Univ, Dept Phys, Portland, OR 97201 USA
[2] Portland State Univ, Dept Mech & Mat Engn, Portland, OR 97201 USA
[3] Oregon State Univ, Sch Mech Ind & Mfg Engn, Corvallis, OR 97331 USA
[4] Portland State Univ, Dept Chem, Portland, OR 97201 USA
来源
ACS SUSTAINABLE CHEMISTRY & ENGINEERING | 2014年 / 2卷 / 07期
基金
美国国家科学基金会;
关键词
Graphene; N-doped TiO2; Low temperature doping; Ammonia solution; Photocatalyst; Wastewater treatment; OPTICAL-PROPERTIES; TIO2-GRAPHENE NANOCOMPOSITES; TIO2; PHOTOCATALYSTS; RAMAN-SPECTROSCOPY; COMPOSITE; TITANIUM; OXIDE; PERFORMANCE; LAYER; PHOTODEGRADATION;
D O I
10.1021/sc5001176
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
To facilitate the potential application of TiO2 as an efficient photocatalyst, the modulation of its band gap and electrical structure is of great significance. Herein, we report a very simple nitrogen (N)-doping method to obtain N-doped TiO2, which is hybridized with graphene sheets at a temperature as low as 180 degrees C and using an ammonia solution as the N source and reaction medium. X-ray photoelectron spectroscopy analysis revealed that the atomic N level could reach 2.4 atomic percent when the reaction time was 14 h. Photoluminescence (PL) emission spectra indicated that N-doped TiO2/graphene composites have drastically suppressed TiO2 PL intensity when compared to undoped TiO2, confirming the lower recombination rate of electron hole pairs in the N-doped TiO2. Additionally, photodegradation data showed that the decomposition rate of methylene blue with our N-doped TiO2/graphene photocatalyst is twice as fast as a commercial Degussa P25 catalyst. Furthermore, density functional theory (DFT) calculations demonstrate that N doping creates empty states in the band gap of the TiO2 that are below the Fermi energy of graphene. Thus, when N-doped TiO2 is brought into contact with graphene, these states become filled by electrons from the graphene, shifting the TiO2 bands upward relative to the graphene. Such a shift in band alignment across the TiO2/graphene heterojunction makes transfer of the photoexcited electron more energetically favorable. This work provides a very convenient chemical route to the scalable production of N-doped TiO2/graphene photocatalyst for potential applications in wastewater treatment.
引用
收藏
页码:1802 / 1810
页数:9
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