Preparation of superlong TiO2 nanotubes and reduced graphene oxide composite photocatalysts with enhanced photocatalytic performance under visible light irradiation

被引:14
|
作者
Lv, Sijia [1 ]
Wan, Junmin [1 ,2 ]
Shen, Yuewei [1 ]
Hu, Zhiwen [1 ]
机构
[1] Zhejiang Sci Tech Univ, Natl Engn Lab Text Fiber Mat & Proc Technol, Hangzhou 310018, Zhejiang, Peoples R China
[2] Zhejiang Sci Tech Univ, Engn Res Ctr Ecodyeing & Finishing Text, Minist Educ, Hangzhou 310018, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
CATALYTIC-ACTIVITY; DEGRADATION; WATER; PHOTODEGRADATION; PORPHYRIN; DYE;
D O I
10.1007/s10854-017-7346-z
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
A novel composite photocatalyst, reduced graphene oxide (rGO) modified superlong TiO2 nanotubes (LTNTs) with length of about 500 nm, has been successfully synthesized by improved hydrothermal process and heating reflux method. The prepared rGO-LTNT catalysts have been characterized and analyzed by transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) spectroscopy, Raman spectroscopy, powder X-ray diffraction (XRD), photoluminescence spectroscopy (PL) and electron paramagnetic resonance (EPR). The results from these investigations provided a deep insight into the physical structure and chemical composition of the rGO-LTNT nanocomposites and pure LTNT. Furthermore, the photocatalytic activity of rGO-LTNT nanocomposites for degradating methylene blue (MB) solution was evaluated under visible light irradiation. The obtained 1.5% rGO content of rGO-LTNT photocatalyst showed a purification of more than 50% MB in MB solution for an hour, which was about five times higher than that of the pure TNT. The results confirmed that the prepared rGO-LTNT nanocomposite photocatalysts showed excellent co-photocatalytic ability. That's because rGO played a critical role in utilizing solar light and increasing separation of the electron-hole pairs more efficiently, and which greatly accelerated the decomposition of organic pollutants in waste water or air.
引用
收藏
页码:14769 / 14776
页数:8
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