Environmentally Friendly Graphene Inks for Touch Screen Sensors

Graphene-based materials have attracted significant attention in many technological fields, but scaling up graphene-based technologies still faces substantial challenges. High-throughput top-down methods generally require hazardous, toxic, and high-boiling-point solvents. Here, an efficient and inexpensive strategy is proposed to produce graphene dispersions by liquid-phase exfoliation (LPE) through a combination of shear-mixing (SM) and tip sonication (TS) techniques, yielding highly concentrated graphene inks compatible with spray coating. The quality of graphene flakes (e.g., lateral size and thickness) and their concentration in the dispersions are compared using different spectroscopic and microscopy techniques. Several approaches (individual SM and TS, and their combination) are tested in three solvents (N-methyl-2-pyrrolidone, dimethylformamide, and cyrene). Interestingly, the combination of SM and TS in cyrene yields high-quality graphene dispersions, overcoming the environmental issues linked to the other two solvents. Starting from the cyrene dispersion, a graphene-based ink is prepared to spray-coat flexible electrodes and assemble a touch screen prototype. The electrodes feature a low sheet resistance (290 Ω □⁻¹) and high optical transmittance (78%), which provide the prototype with a high signal-to-noise ratio (14 dB) and multi-touch functionality (up to four simultaneous touches). These results illustrate a potential pathway toward the integration of LPE-graphene in commercial flexible electronics.     

Poly(2,5-Dihydroxy-1,4-Benzoquinonyl Sulfide) As an Efficient Cathode for High-Performance Aqueous Zinc–Organic Batteries

Aqueous rechargeable zinc-ion batteries (ZIBs) have attracted considerable attention as a promising candidate for low-cost and high-safety electrochemical energy storage. However, the advancement of ZIBs is strongly hindered by the sluggish ionic diffusion and structural instability of inorganic metal oxide cathode materials during the Zn²⁺ insertion/extraction. To address these issues, a new organic host material, poly(2,5-dihydroxy-1,4-benzoquinonyl sulfide) (PDBS), has been designed and applied for zinc ion storage due to its elastic structural factors (tunable space and soft lattice). The aqueous Zn-organic batteries based on the PDBS cathode show outstanding cycling stability and rate capability. The coordination moieties (O and S) display the strong electron donor character during the discharging process and can act as the coordination arms to host Zn²⁺. Also, under the electrochemical environment, the malleable polymer structure of PDBS permits the rotation and bending of polymer chains to facilitate the insertion/extraction of Zn²⁺, manifesting the superiority and uniqueness of organic electrode materials in the polyvalent cation storage. Finally, quasi-solid-state batteries based on aqueous gel electrolyte demonstrate highly stable capacity under different bending conditions.     

Single chamber Solid Oxide Fuel Cells selective electrodes: A real chance with brownmillerite-based nanocomposites

In this contribution brownmillerite-based nanocomposite cathode for Single-Chamber Solid Oxide Fuel Cells is developed. These cells can be very attractive especially for small and cheap devices because of the absence of seals. The efficiency of SC-SOFCs is strictly connected to the selectivity of anode and cathode, the bottleneck for this technology. The development of a cathode inert in fuel oxidation is particularly challenging. Our strategy is to start from a catalytically un-active support (CFA = Ca₂FeAl_0.95Mg_0.05O₅) and induce the formation of iron oxide based nanoparticles, expected to activate oxygen. Symmetric (CFA + FeO_x/CGO/CFA + FeO_x) and complete cells (CFA + FeO_x/CGO/Ni-CGO) are studied in air and methane/oxygen 2:1 mixture. The Area Specific Resistance of CFA + FeO_x is less than 1/3 that of CFA. The high selectivity allows to reach an efficiency of 25%; power still needs to be increased but we demonstrated the possibility to develop selective low cost electrodes. The effect of air, methane/oxygen exposure and the heat treatments were carefully investigated.     

Discriminating between the effect of pulse width and duty cycle on the hydrogen generation performance of 3-D electrodes during pulsed water electrolysis

The present study investigates the effect of applying voltage and current pulses during alkaline water electrolysis using 3-D Ni-based electrodes. The pulses had a square shape and alternated hydrogen production and resting time. When voltage pulses were applied, it was observed that the current at on-time was systematically higher than the current during DC electrolysis. However, during off-time, a change in polarization was observed, which decreased the overall voltage pulse performance. For pulses with a 50% duty cycle and a pulse width of 1 ms, the current response was mainly capacitive and almost no hydrogen production occurred. Current pulses on the other hand were proven to be much more promising in improving the energetic process efficiency. In that case, a pulse period of 2 ms resulted in an overpotential reduction of 17% for a 50% duty cycle. This reduction further increased to 28% when decreasing the duty cycle to 20%. Finally, in all cases where faradaic processes were dominant, applying a forced electrolyte flow was shown to be beneficial.     

Comparative study of Ti-C-Ni-Al,Ti-C-Ni-Fe,and Ti-C-Ni-Al/Ti-C-Ni-Fe coatings produced by magnetron sputtering,electro-spark deposition,and a combined two-step process

Comparative study of Ti-C-Ni-Fe, Ti-C-Ni-Al, and Ti-C-Ni-Al/Ti-C-Ni-Fe coatings obtained by electro-spark deposition (ESD) using TiCNi electrode, magnetron sputtering (MS) of TiCNiAl target, and a combination of these methods (MS-ESD) was carried out. The coating microstructures and elemental compositions were studied by means of X-ray diffraction, scanning electron microscopy, energy-dispersive spectroscopy, and glow discharge optical emission spectroscopy. The materials were tested in terms of their hardness, elastic modulus, elastic recovery, crack resistance, friction coefficient, and wear resistance under sliding, impact and abrasive conditions, as well as corrosion- and oxidation resistance. The work demonstrated that the utilization of a combined two-step MS-ESD technology permits to obtain bilayers made of Ti-C-Ni-Al/Ti-C-Ni-Fe coatings with improved crack-, wear- and oxidation resistance compared with their single-layered Ti-C-Ni-Al counterparts deposited by MS, and with reduced friction coefficient and enhanced corrosion resistance compared with ESD Ti-C-Ni-Fe coatings.     

Flow control with electrode bank arrangements by electrohydrodynamics force for heat transfer enhancement in a porous medium

Active flow control with electrohydrodynamics (EHD) force in the channel flow has been numerically investigated for enhancing heat transfer. This study focuses on the effect of electrode bank arrangements and the number of electrodes on corona wind and fluid flow for heat transfer onto a porous medium. Aligned and staggered configurations of electrode banks are compared. The numerical results show that electric field intensity depends on electrical voltage and the number of electrodes. Shear flow is increased with larger numbers of electrodes and in the aligned configuration, resulting in the enhancement of vortex strength. The swirling flow from staggered configurations spread wider than that of aligned configurations, but the aligned configuration produced more turbulence. In addition, the temperature distribution in the channel flow is increased with increasing numbers of electrodes. With the effect of swirling flow, airflow above the porous sample surface is faster leads the heat to more transfer to the porous sample surface. This causes the temperature of porous medium to increase rapidly so the convective heat transfer coefficient on porous medium surface is increased. Finally, the modified case of the numerical results is validated against the experimental results. The experimental flow visualization is based on the incense smoke technique, in order to verify the accuracy of the swirling flow pattern subjected to the electric field. It is shown that the comparison results in both techniques are in good agreement.     

Conductive Hydrogel-Based Electrodes and Electrolytes for Stretchable and Self-Healable Supercapacitors

Stretchable self-healing supercapacitors (SCs) can operate under extreme deformation and restore their initial properties after damage with considerably improved durability and reliability, expanding their opportunities in numerous applications, including smart wearable electronics, bioinspired devices, human–machine interactions, etc. It is challenging, however, to achieve mechanical stretchability and self-healability in energy storage technologies, wherein the key issue lies in the exploitation of ideal electrode and electrolyte materials with exceptional mechanical stretchability and self-healing ability besides conductivity. Conductive hydrogels (CHs) possess unique hierarchical porous structure, high electrical/ionic conductivity, broadly tunable physical and chemical properties through molecular design and structure regulation, holding tremendous promise for stretchable self-healing SCs. Hence, this review is innovatively constructed with a focus on stretchable and self-healing CH based electrodes and electrolytes for SCs. First, the common synthetic approaches of CHs are introduced; then the stretching and self-healing strategies involved in CHs are systematically elaborated; followed by an explanation of the conductive mechanism of CHs; then focusing on CH-based electrodes and electrolytes for stretchable self-healing SCs; subsequently, application of stretchable and self-healing SCs in wearable electronics are discussed; finally, a conclusion is drawn along with views on the challenges and future research directions regarding the field of CHs for SCs.