Bacterial adhesion and inactivation on Ag decorated TiO2-nanotubes under visible light: Effect of the nanotubes geometry on the photocatalytic activity.

This study investigates the effect of the diameter of TiO2 nanotubes and silver decorated nanotubes on optical properties and photocatalytic inactivation of Escherichia coli under visible light. The TiO2 nanotubes (TiO2-NTs) were prepared using the electrochemical method varying the anodization potential starting from 20 V until 70 V. The Ag nanoparticles were carried out using the photoreduction process under the same experimental conditions. The diameter size was determined using the scanning electronic microscopy (SEM). TiO2-NTs diameter reached ∼100 nm at 70 V. Transmission electronic microscopy (TEM) imaging confirmed the TiO2-NTs surface decoration by silver nanoparticles. The Ag-NPs average size was found to be equal to 8 nm. The X-Ray diffraction (XRD) analysis confirm that all TiO2-NTs crystallize in the anatase phases regardless the used anodization potential. The decrease of the photoluminescence (PL) intensity of Ag NPs decorated TiO2-NTs indicates the decrease of the specific area when the nanotubes diameter increases. The UV-vis absorbance show that the absorption edges was bleu shifted with the increasing of nanotubes diameter, which can be explained by the increase of the crystallites average size. The bacterial adhesion and inactivation tests were carried in the dark and under light. Bacteria were seen to adhere on TiO2-NTs in the dark; however, under light the bacteria were killed before they establish a strong contact with the TiO2-NTs and Ag/TiO2-NTs surfaces. Bacterial inactivation kinetics were faster when the anodizing potential of the NTs-preparation increases. A total bacterial inactivation was obtained on ∼100 nm nanotubes diameter within 90 min. This result was attributed to the enhancement of the TNTs crystallinity leading to reduced surface defects. Redox catalysis was seen to occur under light on the TiO2-NTs and Ag/TiO2-NTs. the photo-induced antibacterial activity on the AgO/Ag2O decorated TiO2-NTs was attributed to the interfacial charge transfer mechanism (IFCT).

Optimizing the photochemical conversion of UV-vis light of silver-nanoparticles decorated TiO2 nanotubes based photoanodes.

Homogeneous decoration of TiO2 nanotubes (NTs) by Ag metallic nanoparticles (NPs) was carried out by a relatively simple photoreduction process. This Ag-NPs decoration was found to improve the photoconversion efficiency of the TiO2-NTs based photoanodes. The x-ray photoelectron spectroscopy and x-ray diffraction analyses confirmed that all the Ag-NPs are metallic and the underlying TiO2-NTs crystallize in the anatase phase after their annealing at 400 °C, respectively. Transmission electron microscopy observations have confirmed the effective decoration of the TiO2-NTs' surface by Ag-NPs, and allowed to measure the average Ag-NPs size, which was found to increase linearly from (4 ± 2) nm to (16 ± 4) nm when the photoreduction time is increased from 5 to 20 min. The diffuse reflectivity of the Ag-NPs decorated TiO2-NTs was found to decrease significantly as compared to the undecorated TiO2-NTs. Interestingly, the Ag-NPs decorated TiO2-NTs exhibited a significantly enhanced photochemical response, under visible radiation, with regards to the undecorated NTs. This enhancement was found to reach its maximum for the TiO2-NTs decorated with Ag-NPs having the optimal average diameter of ∼8.5 nm. The maximum photoconversion efficiency of Ag-NPs decorated TiO2-NTs was about two times greater than for the undecorated ones. This improved photo-electro-chemical response is believed to be associated with the additional absorption of visible light of Ag-NPs through the localized surface plasmon resonance phenomenon. This interpretation is supported by the fact that the photoluminescence intensity of the Ag-NPs decorated TiO2-NTs was found to decrease significantly as compared to undecorated NTs, due to charge carriers trapping in the Ag NPs. This demonstrates that Ag-NPs decoration promotes photogenerated charges separation in the TiO2-NTs, increasing thereby their capacity for current photogeneration. The surface decoration of TiO2 NTs by noble metals NPs is expected to impact positively the use of TiO2-NTs based photoanodes in some energetic applications such as hydrogen generation and photo-electrochemical solar cells.

Morphology and microstructure at different scales of porous silicon prepared by a nonconventional technique.

In this work we present first results concerning the detailed structure of porous silicon (PS) layers prepared by a new method using a vapour-etching (VE)-based technique. Studies of the photoluminescence properties of VE-based PS show that the visible emission occurs at high energies as compared with PS prepared by conventional techniques. To understand the VE-based PS features, we need to point out the PS microstructure throughout its general morphology. For this purpose a microscopy multiscale study was done. Scanning, conventional transmission, and high-resolution transmission electron microscopes were employed. The investigations were made on PS films prepared from moderately and heavily doped n- and p-type silicon. SEM images show that VE-based PS layers are essentially formed of clusters like interconnected structures. TEM studies show that these clusters are composed of nanocrystallites with different shapes. The effect of the doping type of the starting Si substrate on the characteristics of the PS layers was examined (thickness, porosity, behavior). Pore propagation was found to depend on doping type. The crystallinity of the PS layers was also locally studied in depth.