材料科学
光催化
纳米复合材料
扫描电子显微镜
傅里叶变换红外光谱
光谱学
可见光谱
煅烧
拉曼光谱
荧光光谱法
漫反射红外傅里叶变换
核化学
紫外可见光谱
透射电子显微镜
分析化学(期刊)
化学工程
纳米技术
复合材料
荧光
光学
化学
光电子学
有机化学
催化作用
物理
工程类
量子力学
作者
Petronela Pascariu,Corneliu Cojocaru,Petrișor Samoilă,Anton Airinei,Niculae Olaru,Aurelian Rotaru,Cosmin Romanițan,Lucian Barbu Tudoran,M. Suchea
标识
DOI:10.1016/j.surfin.2021.101644
摘要
This is the first-time report on the optimization of pure TiO2 and Cu/TiO2 nanocomposite photocatalytic fibrous materials fabricated by electrospinning followed by removal of the organic components by calcination at high temperature. Morphological investigations of the fabricated nanocomposites performed using scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were supported with spectroscopic investigations via X-ray diffraction (XRD), Energy-dispersive X-ray spectroscopy (EDS), Fourier-transform infrared spectroscopy (FT-IR), Raman spectroscopy, ultraviolet–visible spectroscopy (UV–Vis) and photoluminescence (PL) spectroscopy. These findings clearly indicate that the copper presence into TiO2 lattice triggers the sunlight-driven photocatalysis, as compared to pure TiO2 that use the ultraviolet light to achieve the photoactivation. As a result, remarkable photocatalytic activity on the degradation of Amaranth dye was obtained. The maximum color removal efficiency of 99.84% was observed for the degradation of Amaranth dye for an initial concentration of 25 mg/L, after 240 min of Vis-light irradiation. Excellent results were obtained for the case of 0.05%Cu/TiO2 nanocomposite (calcinated at 400 °C) that yielded to a maximum value for the constant rate (k = 2.089 × 10−2 min−1). As compared to the undoped material (TiO2/400 °C), the 0.05%Cu/TiO2 nanocomposite led an almost double reaction rate (the constant rate increasing from 1.015 × 10−2 to 2.089 × 10−2 min−1). In addition, the 0.05%Cu/TiO2 nanocomposite calcinated at 400 °C was tested for the degradation of Amaranth dye under visible-light irradiation. Thus, at catalyst doses of 0.4 to 0.8 g/L, the reaction rate constant attained the order of 10−2 min−1 under visible irradiation. These results are outstanding when compared with previously reported works.
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