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Enhanced plasmonic effects in AG decorated amorphous TiO2 nanotube arrays

机译:AG装饰无定形TiO2纳米管阵列的增强型等离子体效应

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In the present investigation SERS sensitivity and plasmonic-photonic interference coupling (P-PIC) in amorphous TiO2 nanotube (A[TNT]) and crystalline silver (Ag) nanoparticles was studied. TNT were synthesized by two step anodization on titanium (Ti) substrate. Using thermal evaporation, 20 nm Ag film overcoating on TNT structures was synthesized, which coalescence to form Ag nanoparticles, acting as a three dimensional (3D) surface enhanced raman spectroscopy (SERS) substrate for rhodamine 6G (R6G) molecule detection. The nanoarchitecture phase formation is confirmed by X-ray diffraction (XRD) analysis, Raman spectroscopy analysis. Surface morphology and the salient features are studied by scanning electron microscopy (SEM). Current decay time is also studied and compared for the samples respectively which show large current decay time for A[TNT]-Ag as compared to C[TNTAg]. UV-visible absorption studies shows larger red shift in the absorption band gap edge of A[TNT]-Ag samples as compared to C[TNT-Ag] samples. Moreover the TNT length variation in A[TNT]-Ag samples results into constructive or destructive interference, which in turn affect the P-PIC and R6G molecule detection as well as SERS intensity which was approximately three time higher than C[TNT-Ag].
机译:在非晶TiO 2纳米管(A [TNT])和结晶银(Ag)纳米颗粒在本调查SERS灵敏度和等离子体激元光子干扰耦合(P-PIC)进行了研究。 TNT通过对钛(Ti)基板两步阳极氧化来合成。使用热蒸发,20nm的Ag膜涂在TNT结构合成,其中聚结以形成银纳米颗粒,作为一个三维(3D)表面增强拉曼光谱(SERS)基材罗丹明6G(R6G)分子检测。所述纳米架构相形成是通过X射线衍射(XRD)分析,拉曼光谱分析证实。表面形态和显着特征是由扫描电子显微镜(SEM)研究。电流衰减时间进行了研究,并用于分别将样品相比,C [TNTAg]其示出大电流的衰减时间为A [TNT] -Ag比较。紫外 - 可见吸收研究显示较大的红移在A [TNT] -Ag样本的吸收的带隙边缘相比于C [TNT - 银]样品。此外在TNT长度变化A [TNT] -Ag样品的结果为长或相消干涉,这反过来又影响到P-PIC和R6G分子检测以及SERS强度这是比C大约三个时间更高[TNT - 银] 。

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