光催化
石墨氮化碳
材料科学
降级(电信)
静电纺丝
多孔性
辐照
化学工程
纳米纤维
氮化碳
碳纤维
碳纳米纤维
纳米技术
复合材料
碳纳米管
化学
催化作用
复合数
聚合物
有机化学
工程类
核物理学
物理
电信
计算机科学
作者
Surya Prasad Adhikari,Ganesh Prasad Awasthi,Han Joo Kim,Chan Hee Park,Cheol Sang Kim
出处
期刊:Langmuir
[American Chemical Society]
日期:2016-06-02
卷期号:32 (24): 6163-6175
被引量:72
标识
DOI:10.1021/acs.langmuir.6b01085
摘要
We report a direct approach to the fabrication of a composite made of porous TiO2 nanofibers (NFs) and graphitic carbon nitride (g-C3N4) sheets, by means of an angled two-nozzle electrospinning combined with calcination process. Different wt % amounts of g-C3N4 particles in a polymer solution from one nozzle and TiO2 precursors containing the same polymer solution from another nozzle were electrospun and deposited on the collector. Structural characterizations confirm a well-defined morphology of the TiO2/g-C3N4 composite in which the TiO2 NFs are uniformly attached on the g-C3N4 sheet. This proper attachment of TiO2 NFs on the g-C3N4 sheets occurred during calcination. The prepared composites showed the enhanced photocatalytic activity over the photodegradation of rhodamine B and reactive black 5 under natural sunlight. Here, the synergistic effect between the g-C3N4 sheets and the TiO2 NFs having anisotropic properties enhanced the photogenerated electron-hole pair separation and migration, which was confirmed by the measurement of photoluminescence spectra, cyclic voltammograms, and electrochemical impedance spectra. The direct synthesis approach that is established here for such kinds of sheetlike structure and porous NFs composites could provide new insights for the design of high-performance energy conversion catalysts.
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