Recently, one-dimensional nanostructures with different morphologies (such as nanowires, nanorods (NRs), and nanotubes) have become the focus of intensive research, because of their unique properties with potential applications. Among them, zinc oxide (ZnO) nanomaterials has been found to be highly attractive, because of the remarkable potential for applications in many different areas such as solar cells, sensors, piezoelectric devices, photodiode devices, sun screens, antireflection coatings, and photocatalysis. Here, we present an innovative approach to create a new modified textile by direct in situ growth of vertically aligned one-dimensional (1D) ZnO NRs onto textile surfaces, which can serve with potential for biosensing, photocatalysis, and antibacterial applications. ZnO NRs were grown by using a simple aqueous chemical growth method. Results from analyses such as X-ray diffraction (XRD) and scanning electron microscopy (SEM) revealed that the ZnO NRs were dispersed over the entire surface of the textile. We have demonstrated the following applications of these multifunctional textiles: (1) as a flexible working electrode for the detection of aldicarb (ALD) pesticide, (2) as a photocatalyst for the degradation of organic molecules (i.e., Methylene Blue and Congo Red), and (3) as antibacterial agents against Escherichia coli. The ZnO-based textile exhibited excellent photocatalytic and antibacterial activities, and it showed a promising sensing response. The combination of sensing, photocatalysis, and antibacterial properties provided by the ZnO NRs brings us closer to the concept of smart textiles for wearable sensing without a deodorant and antibacterial control. Perhaps the best known of the products that is available in markets for such purposes are textiles with silver nanoparticles. Our modified textile is thus providing acceptable antibacterial properties, compared to available commercial modified textiles.

ZnO nanoparticles were synthesized by co-precipitation with no capping agent followed by covering with ZnS using a solution-based chemical method at low temperature. By variation of the solution concentrations it was found that the fully-covering ZnS shell forms by a reaction of Na 2 S with ZnO NPs followed by the formation of ZnS nano-crystals by the reaction of Na 2 S with ZnCl 2. The mechanism that led to full coverage of the ZnO core is proposed to be the addition of ZnCl 2 at a later stage of the growth which guarantees a continuous supply of Zn ions to the core surface. Moreover, the ZnS nanocrystals that uniformly cover the ZnO NPs show no epitaxial relationship between the ZnO core and ZnS shell. The slow atomic mobility at the low reaction temperature is attributed to the non-epitaxial uniform ZnS shell growth. The rough surface of the ZnO grains provides initial nucleation positions for the growth of the ZnS shell nano-crystals. The low growth temperature also inhibits the abnormal growth of ZnS grains and results in the homogeneous coverage of ZnS nano-crystals on the ZnO core surface. The as-synthesized ZnO@ZnS core-shell nanoparticles were used as a photocatalyst to decompose Rose Bengal dye at three different pH values. ZnO@ZnS core-shell nanoparticles perform as a more active photocatalyst at a pH of 4, while pure ZnO nanoparticles are more efficient at a pH of 7.

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