Buckminster fullerene (C60) based hybrid metal oxide materials are receiving considerable attention because of their excellent fundamental and applied aspects, like semiconducting, electron transfer, luminescent behaviors, etc. and this work briefly discusses the successful fabrication of C60 decorated ZnO tetrapod materials and their detailed structure-property relationships including device sensing applications. The electron microscopy investigations indicate that a quite dense surface coverage of ZnO tetrapods with C60 clusters is achieved. The spectroscopy studies confirmed the identification of the C60 vibrational modes and the C60 induced changes in the absorption and luminescence properties of the ZnO tetrapods. An increased C60 concentration on ZnO results in steeper ZnO bandgap absorption followed by well-defined free exciton and 3.31 eV line emissions. As expected, higher amounts of C60 increase the intensity of C60-related visible absorption bands. Pumping the samples with photons with an energy corresponding to these absorption band maxima leads to additional emission from ZnO showing an effective charge transfer phenomenon from C60 to the ZnO host. The density of states model obtained from DFT studies for pure and C60 coated ZnO surfaces confirms the experimental observations. The fabricated C60-ZnO hybrid tetrapod based micro- and nanodevices showed interesting ethanol gas sensing characteristics.

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Nanoparticles have been used for engineering composite materials to improve the intrinsic properties and/or add functionalities to pristine polymers. The majority of the studies have focused on the incorporation of spherical nanoparticles within the composite fibers. Herein, we incorporate anisotropic branched-shaped zinc oxide (ZnO) nanoparticles into fibrous scaffolds fabricated by electrospinning. The addition of the branched particles resulted in their protrusion from fibers, mimicking the architecture of a rose stem. We demonstrated that the encapsulation of different-shape particles significantly influences the physicochemical and biological activities of the resultant composite scaffolds. In particular, the branched nanoparticles induced heterogeneous crystallization of the polymeric matrix and enhance the ultimate mechanical strain and strength. Moreover, the three-dimensional (3D) nature of the branched ZnO nanoparticles enhanced adhesion properties of the composite scaffolds to the tissues. In addition, the rose stem-like constructs offered excellent antibacterial activity, while supporting the growth of eukaryote cells.

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A self-reporting polythiourethane/tetrapodal-ZnO (PTU/T-ZnO) composite is produced using spiropyran as an additive at a concentration as low as 0.5 wt %. Exposure to heat, UV light and mechanical force caused the spiropyran to undergo reversible isomerization indicated by a reversible color change. The studies have been conducted with a constant spiropyran concentration at 0.5 wt %, meanwhile varying the T-ZnO concentration from 0 to 7.5 wt %. The tetrapodal ZnO served as a prism: the light scattering effect of T-ZnO created a visual impression of uniform color distribution. The interconnected network of the tetrapodal of ZnO embedded in the PTU matrix enhanced the mechanical stability of the polymer leading to high impact resistance up to ∼232 kPa. PTU/spiropyran also emerged as a possible thermal sensing coating, due to its temperature sensitivity. Due to the broad green luminescence band (∼535 nm) in T-ZnO, the colored merocyanine form which absorbs in this region of the spectrum switches back to spiropyran at this wavelength. High concentrations of T-ZnO were shown to reduce the effect one of the switching triggers i.e., ultraviolet light. Using this property of T-ZnO it was possible to achieve a switchable system with the possibility of separating the stimuli.

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Failure indication can be life-saving and with little effort stress sensing glassfiber reinforced polythiourethane composite including 0.5 wt% mechanochrome can be produced which provides a clear indication of impact well before the material fails.

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