Dual-Ionomer-Based Device: Acetylcholine Transport and Nonenzymatic Sensing.

The malfunctioning in the release of acetylcholine (ACh+), leading to consequential damages in the neural system, has become an impulsion for the development of numerous progressive transport and detection gadgets. However, several challenges, such as laterality and complexity of transport devices, low precision of amperometric detection systems, and sumptuous, multistaged enzymatic quantification methods, have not yet been overcome. Herein, ionomers, because of their selective ion transporting nature, are chosen as suitable candidates for being implemented into both targeted ACh+ delivery and sensing systems. Based on these two approaches, for the very first time in the literature, the disulfonated poly(arylene ether sulfone) membrane is concurrently (i) used in the mimicry of transduction of the electrical-to-ionic signal in a neural network as "Acetylcholine Pen" (ACh+ Pen) and (ii) operated as a highly sensitive, conductivity-based ACh+ quantifier. Our dual device, being able to operate under an actual action potential of 55 mVbias, shows a strong potential of future applicability in real-time ionic delivery-and-sensing systems.

Tailoring morphology to control defect structures in ZnO electrodes for high-performance supercapacitor devices.

Zinc oxide (ZnO) nanostructures were synthesized in the form of nanoparticles, nanoflowers and nanourchins. Structural, electronic and optical characterization of the samples was performed via standard techniques such as X-ray diffraction (XRD), scanning electron microscopy (SEM), photoluminescence, Raman and ultraviolet-visible (UV-Vis) spectroscopy. Point defect structures which are specific to each morphology have been investigated in terms of their concentration and location via state-of-the-art electron paramagnetic resonance (EPR) spectroscopy. According to the core-shell model, all the samples revealed core defects; however, the defects on the surface are smeared out. Finally, all three morphologies have been tested as electrode materials in a real supercapacitor device and the performance of the device, in particular, the specific capacitance and the storage mechanism, has been mediated by the point defects. Morphology-dependent defective ZnO electrodes enable the monitoring of the working principle of the supercapacitor device ranging from electric double-layer capacitors (EDLC) to pseudo-supercapacitors.

Investigation of Strain Effects on Photoelectrochemical Performance of Flexible ZnO Electrodes.

In this report, the growth of zinc oxide (ZnO) nanocrystals with various morphologies, nanoflower, nanosheet, and nanorod, on flexible stainless steel (SS) foils to be utilized as photoanodes in photoelectrochemical (PEC) solar cells has been presented. It has been aimed to provide flexibility and adaptability for the next generation systems with the incorporation of SS foils as electrode into PEC cells. Therefore, physical deformation tests have been applied to the prepared ZnO thin film photoanodes. These thin films have been thoroughly characterized before and after straining for better understanding the relationship between the morphology, straining effect and photoelectrochemical efficiency. We observed a notable increase in the maximum incident photon-to-current efficiency (IPCE) and durability of all ZnO photoelectrodes after straining process. The increase in IPCE values by 1.5 and 2.5 folds at 370 nm has been observed for nanoflower and nanorod morphologies, respectively after being strained. The maximum IPCE of 69% has been calculated for the ZnO nanorod structures after straining. Bending of the SS electrodes resulted in the more oriented nanorod arrays compared to its flat counterpart, which improved both the light absorption and also the photo-conversion efficiency drastically. The finite-difference time-domain simulations have also been carried out to examine the optical properties of flat and bent ZnO electrodes. Finally, it has been concluded that SS photoanodes bearing ZnO semiconducting material with nanoflower and nanorod morphologies are very promising candidates for the solar hydrogen generator systems in terms of efficiency, durability, flexibility, and lightness in weight.

Influence of Electrical and Ionic Conductivities of Organic Electronic Ion Pump on Acetylcholine Exchange Performance.

By using an easy and effective method of depositing conjugated polymers (PEDOT:PSS) on flexible substrates, a new design for organic bioelectronic devices has been developed. The purpose was to build up a system that mimics the motion of neurotransmitters in the synaptic cleft by obtaining an electrical to chemical signal transport. Fourier transform infrared (FTIR) spectroscopy and Raman measurements have demonstrated that electrochemical overoxidation region which separates the pristine PEDOT:PSS electrodes and allows ionic conduction has been achieved successfully. The influence of both electrical and ionic conductivities on organic electronic ion pump (OEIP) performances has been studied. The ultimate goal was to achieve the highest equilibrium current density at the lowest applied voltage via enhancing the electrical conductivity of PEDOT:PSS and ionic conductivity of electrochemically overoxidized region. The highest equilibrium current density, which corresponds to 4.81 × 1017 number of ions of acetylcholine was about 41 µA cm-2 observed for the OEIP with the electrical conductivities of 54 S cm-1. This was a threshold electrical conductivity beyond which the OEIP performances were not changed much. Once Nafion™ has been applied for enhancing the ionic conductivity, the equilibrium current density increased about ten times and reached up to 408 µA cm-2. Therefore, it has been demonstrated that the OEIP performance mainly scales with the ionic conductivity. A straightforward method of producing organic bioelectronics is proposed here may provide a clue for their effortless mass production in the near future.

Dealloyed Ruthenium Film Catalysts for Hydrogen Generation from Chemical Hydrides.

Thin-film ruthenium (Ru) and copper (Cu) binary alloys have been prepared on a Teflon™ backing layer by cosputtering of the precious and nonprecious metals, respectively. Alloys were then selectively dealloyed by sulfuric acid as an etchant, and their hydrogen generation catalysts performances were evaluated. Sputtering time and power of Cu atoms have been varied in order to tailor the hydrogen generation performances. Similarly, dealloying time and the sulfuric acid concentration have also been altered to tune the morphologies of the resulted films. A maximum hydrogen generation rate of 35 mL min-1 was achieved when Cu sputtering power and time were 200 W and 60 min and while acid concentration and dealloying time were 18 M and 90 min, respectively. It has also been demonstrated that the Ru content in the alloy after dealloying gradually increased with the increasing the sputtering power of Cu. After 90 min dealloying, the Ru to Cu ratio increased to about 190 times that of bare alloy. This is the key issue for observing higher catalytic activity. Interestingly, we have also presented template-free nanoforest-like structure formation within the context of one-step alloying and dealloying used in this study. Last but not least, the long-time hydrogen generation performances of the catalysts system have also been evaluated along 3600 min. During the first 600 min, the catalytic activity was quite stable, while about 24% of the catalytic activity decayed after 3000 min, which still makes these systems available for the development of robust catalyst systems in the area of hydrogen generation.