Laser ablation in liquid was utilized to prepare a TiO2 NP suspension in in deionized distilled water using Q-switch Nd: YAG laser at various laser energies and ablation times. The samples were characterized using UV–visible absorption spectra obtained with a UV–visible spectrophotometer (UV-Vis,) Fourier transform infrared (FTIR), X-ray diffraction (XRD), and transmission electron microscope (TEM). While, UV-Vis spectra showed the characteristic band-to-band absorption peak of TiO2 NPs in the UV range. FTIR analysis showed the existence of O-Ti-O bond. XRD patterns indicated the presence of (101) and (112) plane crystalline phases of TiO2. TEM images showed a spherical-like structure of TiO2 NPs with various size distributions depending on the ablation period. It was also found that there is a relationship between laser ablation time and TiO2 NP size distribution, where longer ablation times led to the smaller size distribution. The antibacterial activity of TiO2 NPs was evaluated with different species of bacteria such as Escherichia coli, Pseudomonas aeruginosa, Proteus vulgaris, and Staphylococcus aureus, using the liquid approach. The optimum activity of TiO2 NPs is found to be against E. coli at 1000 μg mL−1. Furthermore, adding, TiO2 NPs (1000 μg mL−1) in the presence of amoxicillin has a synergic effect on E. coli and S. aureus growth, as measured by the well diffusion method. However, both E. coli (11.6 ± 0.57mm) and S. aureus (13.3 ± 0.57mm) were inhibited by this process.

Narrow-band photoconductivity with a spectral width of 0.16 eV is obtained from solution-processed colloidal ZnO nanocrystals beneath the band-edge at 2.25 eV. A new model involving electron transfer from deep defects to discrete shallow donors is introduced to explain the narrow spectrum and the exponential form of the current rise and decay transients. The defects are tentatively assigned to neutral oxygen vacancies. The photocurrent responsivity can be enhanced by storage in air, and this correlates with the formation of carbonate surface species by capture of carbon dioxide during storage. This controllability is exploited to develop a low-cost and scalable photolithographic approach to pixelate photodetectors for applications such as object discrimination, sensing, etc. The spectral response can be spatially patterned so that dual (ultraviolet and green) and single (ultraviolet only) wavelength detecting ZnO pixels can be produced on the same substrate. This presents a new sensor mode with applications in security or full color imaging.

This work shows the enhancement of the visible photocatalytic activity of TiO2 NPs film using the localized surface plasmonic resonance of Au nanostructures.

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We report on the coupling of ZnO nanoparticles with plasmonic gold nanoislands in a solution-processed photodetector, which results in a clear enhancement in the optical absorption and the electrical responsivity of ZnO nanoparticles, to cover the visible and the near-IR (NIR) spectral range, well beyond its intrinsic optical absorption. This enhancement, which arises from the coupling between ZnO nanoparticles and the plasmonically mediated hot electron generation in the Au plasmonic nanoislands, results in a significant plasmonically driven photoresponse in the NIR of 2.5 × 10−5 A/W. The recorded photocurrent exhibits a persistent behavior, which is attributed to surface defect states in the ZnO nanoparticles. This study provides a route to the solution-processed, low-cost device fabrication schemes with important implications on low processing temperature optoelectronics technology to enhance the performance of photovoltaic devices over a wide solar spectrum. Additionally, this unusual behavior paves the way toward harnessing plasmonic resonances to probe and examine the surface defects of metal oxide semiconductors.

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