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Environmental photochemistry by plasmonic semiconductor decorated GO nanocomposites: SERS detection and visible light driven degradation of aromatic dyes

机译:等离子体半导体修饰的GO纳米复合材料的环境光化学:SERS检测和可见光驱动的芳香族染料降解

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Environmental process such as toxic dye sensing and degradation can be stepped up through photochemical process such as surface enhanced Raman scattering (SERS) and Bight induced catalytic degradation. In this work, Titanium dioxide/silver/graphene oxide nanocomposites (TAG) were studied as ideal dual substrates for SEAS sensing and visible light driven degradation of Congo red (CR) and crystal violet (CV). Solvothermal route of synthesize used here resulted in a narrow size distribution (6-12 nm) of TAG. A shift towards the visible spectra observed in absorption spectroscopy along with the anatase phase titanium dioxide illustrated in the X-ray diffraction pattern and Raman spectra aided the activation of TAG under visible light irradiation. On addition of TAG, typical SEAS bands corresponding to the azo nature of CR were clearly exhibited by C-N symmetric bending modes and C-N stretching modes in the 1160 cm(-1)-1200 cm(-1) region. For CV, the aryl backbone represented by C-C bridge between two phenyl molecules at 1298 cm(-1) was recorded in the SEAS spectra. Visible light driven degradation of CV and CR in the presence of TAG resulted in high rate constants of 1.09 x 10(-2) /min and 1.26 x 10(-2) /min respectively. The reactive oxidative radical species in the photo-degradation reaction of dye was studied by using various scavengers. The observed augmented SEAS detection and photocatalytic degradation arises from the synergistic effects of plasmonic properties Ag NPs, anatase TiO2 and pi-pi stacking nature of GO. This study suggests that TAG can offer the right 00path way towards an ideal commercial pollutant detection and degradation system.
机译:可以通过光化学过程(例如表面增强拉曼散射(SERS)和Bight诱导的催化降解)来加快环境过程(例如有毒染料的感测和降解)的进程。在这项工作中,研究了二氧化钛/银/氧化石墨烯纳米复合材料(TAG)作为理想的双重基材,用于SEAS感测和可见光驱动的刚果红(CR)和结晶紫(CV)降解。此处使用的溶剂热合成路线导致TAG的尺寸分布狭窄(6-12 nm)。在X射线衍射图和拉曼光谱中说明,吸收光谱中观察到的可见光谱以及锐钛矿相二氧化钛和拉曼光谱的转变有助于TAG在可见光照射下的活化。在添加TAG之后,在1160 cm(-1)-1200 cm(-1)区域中,C-N对称弯曲模式和C-N拉伸模式清楚地显示了与CR的偶氮性质相对应的典型SEAS带。对于CV,在SEAS光谱中记录了在1298 cm(-1)处两个苯基分子之间的C-C桥所代表的芳基骨架。在TAG存在下,可见光驱动的CV和CR降解分别导致1.09 x 10(-2)/ min和1.26 x 10(-2)/ min的高速率常数。通过使用各种清除剂研究了染料的光降解反应中的反应性氧化自由基种类。观察到的增强的SEAS检测和光催化降解起因于等离子体等离子性质Ag NPs,锐钛矿TiO2和GO的pi-pi堆积性质的协同效应。这项研究表明,TAG可以为理想的商业污染物检测和降解系统提供正确的00途径。

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