Quantitative evaluation of the antibacterial factors of ZnO nanorod arrays under dark conditions: Physical and chemical effects on Escherichia coli inactivation.

Although zinc oxide nanorod (ZnO NR) arrays are a nanomaterial that offers efficient bactericidal activity, they have not been systematically evaluated to quantitatively investigate their disinfection mechanism under dark conditions. In this study, ZnO NR arrays of different lengths (0.5-4 µm) were uniformly grown via hydrothermal synthesis. The longer arrays exhibited higher Escherichia coli (E. coli) inactivation efficiency up to 94.2% even under darkness for 30 min. When the NR arrays were coated via Al2O3 atomic layer deposition, the inactivation efficiency was decreased to 56.4% because the generation of reactive oxygen species (ROS) and the leaching of Zn2+ ions were both hindered by the surficial coverage of defect sites. The morphological effect, i.e., the mechanical rupture of E. coli on the surface, contributed 56.4% of the bactericidal efficiency; chemical effects, i.e., ROS formation and zinc ion release, contributed the remaining 37.8% under dark conditions. The bactericidal effect of fabricated ZnO NR arrays was further validated in bottled and pond water spiked with E. coli, exhibiting 87.5% and 80.4% inactivation efficiencies, respectively, within 30 min. Understanding these antibacterial mechanisms is not only of significance for research in this and related fields but also beneficial for potential application in various fields, e.g., biomedical and antifouling areas.

Stretchable and colorless freestanding microwire arrays for transparent solar cells with flexibility.

Transparent solar cells (TSCs) are emerging devices that combine the advantages of visible transparency and light-to-electricity conversion. Currently, existing TSCs are based predominantly on organics, dyes, and perovskites; however, the rigidity and color-tinted transparent nature of those devices strongly limit the utility of the resulting TSCs for real-world applications. Here, we demonstrate a flexible, color-neutral, and high-efficiency TSC based on a freestanding form of n-silicon microwires (SiMWs). Flat-tip SiMWs with controllable spacing are fabricated via deep-reactive ion etching and embedded in a freestanding transparent polymer matrix. The light transmittance can be tuned from ~10 to 55% by adjusting the spacing between the microwires. For TSCs, a heterojunction is formed with a p-type polymer in the top portion of the n-type flat-tip SiMWs. Ohmic contact with an indium-doped ZnO film occurs at the bottom, and the side surface has an Al2O3 passivation layer. Furthermore, slanted-tip SiMWs are developed by a novel solvent-assisted wet etching method to manipulate light absorption. Finite-difference time-domain simulation revealed that the reflected light from slanted-tip SiMWs helps light-matter interactions in adjacent microwires. The TSC based on the slanted-tip SiMWs demonstrates 8% efficiency at a visible transparency of 10% with flexibility. This efficiency is the highest among Si-based TSCs and comparable with that of state-of-the-art neutral-color TSCs based on organic-inorganic hybrid perovskite and organics. Moreover, unlike others, the stretchable and transparent platform in this study is promising for future TSCs.

Morphology-Controlled Aluminum-Doped Zinc Oxide Nanofibers for Highly Sensitive NO2 Sensors with Full Recovery at Room Temperature.

Room-temperature (RT) gas sensitivity of morphology-controlled free-standing hollow aluminum-doped zinc oxide (AZO) nanofibers for NO2 gas sensors is presented. The free-standing hollow nanofibers are fabricated using a polyvinylpyrrolidone fiber template electrospun on a copper electrode frame followed by radio-frequency sputtering of an AZO thin overlayer and heat treatment at 400 °C to burn off the polymer template. The thickness of the AZO layer is controlled by the deposition time. The gas sensor based on the hollow nanofibers demonstrates fully recoverable n-type RT sensing of low concentrations of NO2 (0.5 ppm). A gas sensor fabricated with Al2O3-filled AZO nanofibers exhibits no gas sensitivity below 75 °C. The gas sensitivity of a sensor is determined by the density of molecules above the minimum energy for adsorption, collision frequency of gas molecules with the surface, and available adsorption sites. Based on finite-difference time-domain simulations, the RT sensitivity of hollow nanofiber sensors is ascribed to the ten times higher collision frequency of NO2 molecules confined inside the fiber compared to the outer surface, as well as twice the surface area of hollow nanofibers compared to the filled ones. This approach might lead to the realization of RT sensitive gas sensors with 1D nanostructures.

Enhanced piezoresponse of highly aligned electrospun poly(vinylidene fluoride) nanofibers.

Well-ordered nanostructure arrays with controlled densities can potentially improve material properties; however, their fabrication typically involves the use of complicated processing techniques. In this work, we demonstrate a uniaxial alignment procedure for fabricating poly(vinylidene fluoride) (PVDF) electrospun nanofibers (NFs) by introducing collectors with additional steps. The mechanism of the observed NF alignment, which occurs due to the concentration of lateral electric field lines around collector steps, has been elucidated via finite-difference time-domain simulations. The membranes composed of well-aligned PVDF NFs are characterized by a higher content of the PVDF ß-phase, as compared to those manufactured from randomly orientated fibers. The piezoelectric energy harvester, which was fabricated by transferring well-aligned PVDF NFs onto flexible substrates with Ag electrodes attached to both sides, exhibited a 2-fold increase in the output voltage and a 3-fold increase in the output current as compared to the corresponding values obtained for the device manufactured from randomly oriented NFs. The enhanced piezoresponse observed for the aligned PVDF NFs is due to their higher ß-phase content, denser structure, smaller effective radius of curvature during bending, greater applied strain, and higher fraction of contributing NFs.

Preparation, characterization, and application of TiO2-patterned polyimide film as a photocatalyst for oxidation of organic contaminants.

Photocatalytically active TiO2-patterned polyimide (PI) films (PI-TiO2) were fabricated using thermal transfer patterning (TTP). When subjected to hot pressing, the TiO2 nanoparticles electrosprayed on steel mesh templates were successfully transferred and formed checker plate patterns on PI film. FE-SEM studies confirmed that pressing at 350°C and 100MPa was optimum for obtaining patterns with uniform TiO2 coverage. When the quantity of TiO2 on the template increased, the amount of it immobilized on PI film also increased from 0.3245 to 1.2378mg per 25cm2. XPS studies confirmed the presence TiO2 on the patterns, and indicated the formation of carboxylic acid and amide groups on the PI surface during TTP. When tested under UVA irradiation, PI-TiO2 with 1.2378mg/25cm2 TiO2 loading exhibited the highest photocatalytic performance for methylene blue (10µM) degradation, with a rate constant of 0.0225min-1 and stable photocatalytic efficacy for 25 cycles of reuse. The PI-TiO2 was also successfully used to degrade amoxicillin, atrazine, and 4-chlorophenol. During photocatalysis, the toxicity of 4-chlorophenol against Vibrio fischeri and the antibiotic activity of amoxicillin against Escherichia coli were decreased. Overall, TTP was found to be a potentially scalable method for fabricating robust immobilized TiO2 photocatalyst.