The first one has been achieved by growing ZnO nanowires, nanorods, and nanobelts on the flexible polyethersulfone or polyethylene terephthalate (PET) substrate via a chemical solution method [6, 7]. The other one was an alternative way in which zig-zag-shaped or network electrodes (consisting of patterned

noble metals, carbon nanotubes, or graphene) were employed as a top electrode to efficiently bend the ZnO nanostructures for transmitting the external mechanical energy as well as possible [8, 9]. However, these kinds of top electrodes needed a somewhat sophisticated fabrication process for the preparation of patterned electrodes or synthesis of carbon-based nanomaterials. On the other hand, one-dimensional (1D) ZnO nanostructures including nanowires or nanorods provide an effective deformation (i.e., stretch and compression) under external Sotrastaurin clinical trial mechanical energy due to their high aspect ratio which generates the piezoelectric charges [10]. Additionally, they have been reliably synthesized and vertically integrated on various flexible substrates with ZnO seed coating by hydrothermal or electrochemical deposition (ED) method [11–14]. find more Particularly, the ED method has many advantages for growing 1D ZnO nanostructures because the electric

energy enables a short time process at low temperature [15]. In this work, we prepared ZnO nanorod

arrays (NRAs) on an indium tin oxide (ITO)-coated PET substrate (i.e., ITO/PET) using the ED method and fabricated ZnO NRA-based NGs with an efficient top electrode TSA HDAC molecular weight which was obtained by evaporating gold (Au) onto the surface of silica spheres. SPTLC1 Herein, the multilayer of silica spheres was facilely deposited on the PET substrate by rolling the colloidal solution of silica spheres. Methods Figure 1 shows the schematic diagram for the fabrication of the Au-coated silica sphere array as a top electrode of ZnO NRA-based NGs: (i) preparation of colloidal solution (i.e., dispersed by silica spheres) on the PET substrate, (ii) rolling and drying the colloidal solution, and (iii) e-beam evaporation of Au onto the silica sphere array. Silica spheres were synthesized using a modified Stober process [16]. After the mixture solution with 200 ml of ethanol, 40 ml of ammonia, and 40 ml of de-ionized (DI) water was kept at 60°C, 20 ml of tetraethyl orthosilicate (TEOS) was slowly dropped for 2 h using a burette. Here, all the chemicals were of analytical grade (Sigma-Aldrich, St. Louis, MO, USA). Then, the silica sphere powder was obtained by centrifugation and drying at 70°C. After that, the powder was mixed with ethanol at a concentration of 50 g/l. To increase the viscosity of the colloidal solution, 0.2% weight of poly-4-vinylphenol was added [17].