Search Results (7)

Among various H₂ production methods, splitting water using renewable electricity for H₂ production is regarded as a promising approach due to its high efficiency and zero carbon emissions. The oxygen evolution reaction (OER) is an important part of splitting water, but also the main bottleneck. The anodic oxygen evolution reaction (OER) for water electrolysis technology involves multi-electron/proton transfer and has sluggish reaction kinetics, which is the key obstacle to the overall efficiency of electrolyzing water. Therefore, it is necessary to develop highly efficient and cheap OER electrocatalysts to drive overall water splitting. Herein, a series of efficient RuO₂-Co₃O₄ composites were synthesized via a straightforward three-step process comprising solvothermal synthesis, ion exchange, and calcination. The results indicate that using 10 mg of RuCl₃·xH₂O and 15 mg of Co-MOF precursor in the second ion exchange step is the most effective way to acquire the Co₃O₄-RuO₂-10 (RCO-10) composite with the largest specific area and the best electrocatalytic performance after the calcination process. The optimal Co₃O₄-RuO₂-10 composite powder catalyst displays low overpotential (η₁₀ = 272 mV), a small Tafel slope (64.64 mV dec⁻¹), and good electrochemical stability in alkaline electrolyte; the overall performance of Co₃O₄-RuO₂-10 surpasses that of many related cobalt-based oxide catalysts. Furthermore, through integration with a carbon cloth substrate, Co₃O₄-RuO₂-10/CC can be directly used as a self-supporting electrode with high stability. This work presents a straightforward method to design Co₃O₄-RuO₂ composite array catalysts for high-performance electrocatalytic OER performance. Full article

In this research, a thin layer of multi-metallic non-precious catalyst is prepared by electroplating from an electrolyte bath containing Ni, Co, and Fe sulfates over pressed commercial nickel foam electrode. The composition of the deposited catalytic film and its morphology are characterized by scanning electron microscopy (SEM) with energy dispersion X-ray (EDX) techniques. The efficiency of the prepared binder-free electrodes for electrochemical water splitting is investigated in a self-designed short water electrolysis stack with zero-gap configuration of the integrated single cells and hybrid electrical connections. The separator used is a commercial Zirfon Perl 500 membrane, doped with 25% KOH. The performance of the catalyst, the single cells, and the developed electrolyzer stack are examined by steady state polarization curves and stationery galvanostatic stability tests in the temperature range 20 °C to 80 °C. The NiFeCoP multi-metallic alloy demonstrates superior catalytic efficiency compared to the pure nickel foam electrodes and reliable stability with time. The single cells in the stack show identical performance and the cumulative stack parameters strictly follow the theoretical considerations. The applied hybrid electrical connections enable scaling of both the stack voltage and the passing current, which in turn ensures flexibility with regard to the input power and the hydrogen production capacity. Full article

Hydrogen fuel is a clean and versatile energy carrier that can be used for various applications, including transportation, power generation, and industrial processes. Electrocatalytic water splitting could be the most beneficial and facile approach for producing hydrogen. In this work, transition metal selenide composites with carbon nanotubes (CNTs) have been investigated for electrocatalytic water splitting. The synthesis process involved the facile one-step hydrothermal growth of transition metal nanoparticles over the CNTs and acted as an efficient electrode toward electrochemical water splitting. Scanning electron microscopy and XRD patterns reveal that nanoparticles were firmly anchored on the CNTs, resulting in the formation of composites. The electrochemical measurements reveal that CNT composite with nickel–cobalt selenides (NiCo-Se/CNTs@NF) display remarkable oxygen evolution reaction (OER) activity in basic media, which is an important part of hydrogen production. It demonstrates the lowest overpotential (η_10mAcm⁻²) of 0.560 V vs. RHE, a reduced Tafel slope of 163 mV/dec, and lower charge transfer impedance for the OER process. The multi-metallic selenide composite with CNTs demonstrating unique nanostructure and synergistic effects offers a promising platform for enhancing electrocatalytic OER performance and opens up new avenues for efficient energy conversion and storage applications. Full article

Constructing a heterogeneous interface using different components is one of the effective measures to achieve the bifunctionality of nanocatalysts, while synergistic interactions between multiple interfaces can further optimize the performance of single-interface nanocatalysts. The non-precious metal nanocatalysts MoS₂/NiSe₂/reduced graphene oxide (rGO) bilayer sandwich-like nanostructure with multiple well-defined interfaces is prepared by a simple hydrothermal method. MoS₂ and rGO are layered nanostructures with clear boundaries, and the NiSe₂ nanoparticles with uniform size are sandwiched between both layered nanostructures. This multiple-interfaced sandwich-like nanostructure is prominent in catalytic water splitting with low overpotential for oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) and almost no degradation in performance after a 20 h long-term reaction. In order to simulate the actual overall water splitting process, the prepared nanostructures are assembled into MoS₂/NiSe₂/rGO||MoS₂/NiSe₂/rGO modified two-electrode system, whose overpotential is only 1.52 mV, even exceeded that of noble metal nanocatalyst (Pt/C||RuO₂~1.63 mV). This work provides a feasible idea for constructing multi-interface bifunctional electrocatalysts using nanoparticle-doped bilayer-like nanostructures. Full article

In this paper, the problem of optimizing the design of an inductive Magneto-Hydro-Dynamic (MHD) electric generator is formalized as a multi-objective optimization problem where the conflicting objectives consist of maximizing the output power while minimizing the hydraulic losses and the mass of the apparatus. In the proposal, the working fluid is ionized with periodical pulsed discharges and the resulting neutral plasma is unbalanced by means of an intense DC electrical field. The gas is thus split into two charged streams, which induce an electromotive force into a magnetically coupled coil. The resulting generator layout does not require the use of superconducting coils and allows you to manage the issues related to the conductivity of the gas and the corrosion of the electrodes, which are typical limits of the MHD generators. A tailored multi-objective optimization algorithm, based on the Tabu Search meta-heuristics, has been implemented, which returns a set of Pareto optimal solutions from which it is possible to choose the optimal solution according to further applicative or performance constraints. Full article

Low-hydrogen-containing amorphous silicon (a-Si) was deposited at a low temperature of 80 °C using a very high frequency (VHF at 162 MHz) plasma system with multi-split electrodes. Using the 162 MHz VHF plasma system, a high deposition rate of a-Si with a relatively high deposition uniformity of 6.7% could be obtained due to the formation of high-ion-density (>10¹¹ cm⁻³) plasma with SiH₄ and a lack of standing waves by using small multi-split electrodes. The increase in the radio frequency (RF) power decreased the hydrogen content in the deposited silicon film and, at a high RF power of 2000 W, a-Si with a low hydrogen content of 3.78% could be deposited without the need for a dehydrogenation process. The crystallization of the a-Si by ultraviolet (UV) irradiation showed that the a-Si can be crystallized with a crystallinity of 0.8 and a UV energy of 80 J without dehydrogenation. High-resolution transmission electron microscopy showed that the a-Si deposited by the VHF plasma was a very small nanocrystalline-like a-Si and the crystalline size significantly grew with the UV irradiation. We believe that the VHF (162 MHz) multi-split plasma system can be used for a low-cost low-temperature polysilicon (LTPS) process. Full article

The oxygen evolution reaction (OER) is a complex multi-step four-electron process showing sluggish kinetics. Layered double hydroxides (LDH) were reported as promising catalysts for the OER, but their low electrical conductivity restricts their widespread applications. To overcome this problem, a composite material containing Mn-Co LDH ultrathin nanosheet and highly conductive graphene was synthesized for the first time. Benefited from the high electrocatalytic activity and the superior charge transfer ability induced by these components, the new material shows superior OER activity. Used as the OER catalyst, a high current density of 461 mA cm⁻² at 2.0 V vs. RHE (reversible hydrogen electrode) was measured besides shows a low overpotential of 0.33 V at 10 mA cm⁻². Moreover, the new composite also shows a superior bifunctional water splitting performance as catalyst for the OER and HER (hydrogen evolution reaction) catalysts. Our results indicate that the presented material is a promising candidate for water splitting which is cheap and efficient. Full article