Search Results (55)

Hydrogen is being extensively investigated as a carbon-free energy carrier, particularly for fuel-cell vehicles and long-term energy storage. Because H₂ can form explosive mixtures in air at concentrations as low as 4%, its safe use requires inexpensive, low-power sensors capable of reliable detection. Here, we investigated ribbon-like palladium–platinum nanostructures, referred to as PdPt nanoribbon/nanosheet hybrid structures (PdPt NR/NSs), for room-temperature chemiresistive H₂ sensing. Sensors were fabricated by drop-casting dispersions of the PdPt NR/NSs onto interdigitated electrodes. The sensor resistance increased upon exposure to H₂ because of hydrogen uptake by the PdPt NR/NSs and formation of a hydride phase with higher resistivity than the hydrogen-free alloy. The best-performing sensor, Pd₅Pt₈, was prepared using a 5:8 Pd:Pt precursor mass ratio, which yielded a measured Pd:Pt atomic ratio of approximately 1.3:1. This sensor showed a response time of 16 s and a response of 6.0% to 1 vol% H₂ in air. H₂ concentrations as low as 100 ppm were readily detected while maintaining a positive resistance response. These results demonstrate the potential of PdPt NR/NS architectures for low-power H₂ detection at ambient temperature. Full article

Ti-15V-3Al-3Cr-3Sn alloy (Ti-153) plates were subjected to a hydriding process to obtain Ti-153 powder which was further hot-press sintered (HPS) into porous electrodes to see their hydrogen storage and evolution capabilities. The effects of processing parameters on the hydrogenation behavior were characterized qualitatively and quantitatively utilizing X-ray diffractometry (XRD: D2 PHASER, BRUKER, USA, 30 kV-10 mA, Cu-Kα λ = 1.541838 Å), scanning electron microscopy (SEM: Hitachi 4800), and elemental analysis (EA: Heraeus vario III-NCSH). XRD and EA analyses demonstrate that the hydrogen absorption and evolution capabilities of the powdered electrodes are superior to those of the original bulk sheet specimens. The hydrogen uptake of the specimens was evaluated by cyclic electrolytic hydrogenation at 50 mA/cm² for various periods in a 1N H₂SO₄ aqueous solution containing 0.1 g/L As₂O₃, followed by solution treatment in a muffle furnace at 300 °C for 1 h. The subsequent dehydrogenation process was conducted at 300 °C and 4.67 Pa for 2 h. The optimal processing conditions in this study are as follows: (1) first, the Ti-153 sheets are treated in a hydrogen furnace at 300 °C under a hydrogen pressure of 50 atm for 15 h to obtain the raw powder; (2) subsequently, the raw powder is processed in a hot-pressing sintering furnace at 600 °C under 25 MPa for 2 h to yield the sintered electrodes. Full article

Vanadium oxides and alkali metal vanadates are promising electrode materials for electrochemical energy storage owing to their ability to access multiple oxidation states. In this study, mechanochemical reduction of V₂O₅ with alkali metal hydrides is explored as a facile route to obtain reduced vanadium oxide phases. Sodium hydride enables the rapid formation of mixed sodium vanadium oxide phases at room temperature, proceeding in a self-propagating manner after only a short milling period. To assess the generality of this approach, lithium hydride was evaluated as an alternative reducing agent and exhibited comparable reaction behavior and product distributions. Complementary theoretical calculations indicate that the corresponding reductions with elemental sodium and lithium are thermodynamically more favorable, displaying lower reaction enthalpies. This prediction is experimentally corroborated by the instantaneous ignition observed when elemental metals are used. Rietveld refinement reveals that all investigated reducing agents follow similar reaction pathways, yielding comparable mixtures of alkali metal vanadium oxides with consistent main phases. However, the use of highly ductile sodium metal results in significant mixing limitations, which can be mitigated only through cryogenic milling. These findings highlight mechanochemical reduction with alkali metal hydrides as a robust and practical strategy, particularly for systems in which metal ductility limits process efficiency, despite the associated risk of hydrogen evolution. Full article

The use of Mg-based alloys as anode materials in nickel–metal hydride (Ni–MH) batteries is significantly limited by rapid capacity loss during charge–discharge cycles. This study conducts a comprehensive examination of how variations in the concentrations of Mg and Pd impact the microstructural characteristics and electrochemical behavior of Mg–Pd–Ni ternary alloys, aiming to enhance cyclic durability and uncover the fundamental degradation mechanisms. This work demonstrates that increasing the Mg content tends to reduce the reversibility of electrochemical hydrogenation/dehydrogenation reactions and exacerbates the corrosion behavior of the milled Mg–Pd–Ni alloy electrodes, thus accelerating their capacity decay. On the contrary, raising the Pd content contributes to improving the reversibility of electrochemical hydrogenation/dehydrogenation reactions and the kinetic behavior of the alloys, yet it does not enhance corrosion resistance. Full article

Whether copper fundamentally alters Mo-centered redox thermodynamics or mainly tunes hydrogen adsorption in Ni–Mo electrocatalysts under alkaline hydrogen evolution reaction (HER) conditions remains unresolved. Density functional theory calculations combined with a field-corrected computational hydrogen electrode framework are used to evaluate the thermodynamic stability of H₃Mo, H₃MoOH, H₂Mo(OH)₂, and MoO(OH)₃ on Cu(111) and Ni(111) and to construct surface Pourbaix diagrams under electrochemical conditions. The results show that substrate identity reorganizes the redox stabilization hierarchy of these Mo intermediates. Across the examined conditions, at least one of H₃Mo, H₃MoOH, or MoO(OH)₃ is thermodynamically favored over H₂Mo(OH)₂ on both surfaces. However, only Cu(111) exhibits measurable pH-dependent free-energy shifts, reaching 0.25 eV on the reversible hydrogen electrode scale. The magnitude of this electrostatic modulation is comparable to the intrinsic substrate-dependent relative Gibbs free-energy differences, suggesting that Cu reshapes Mo redox thermodynamics rather than merely weakening hydrogen binding strength. Electronic structure and vibrational analyses further show that Cu(111) preferentially weakens Mo–O interactions, whereas Ni(111) more strongly perturbs Mo–H bonding in hydrogen-rich complexes. Overall, these results establish that substrate identity governs the electrostatic modulation of Mo redox thermodynamics under alkaline HER conditions and provide mechanistic insight into substrate effects relevant to Cu-containing Ni–Mo systems. Full article

Studies were conducted on the effect of the partial substitution of nickel in an LaNi₅ alloy with germanium (5% by weight) or magnesium (3.3% by weight), in addition to surface modification using phosphomolybdic heteropolyacid (MPA) on the course of corrosion and passivation processes of hydrogen electrodes in a highly alkaline environment. The investigations were carried out by means of electrochemical impedance spectroscopy (EIS) and the potentiodynamic methods to analyse changes in the electrochemical parameters as a function of exposure time. The surface topography of the electrodes and chemical composition were investigated utilising a KEYENCE VHX-7000 digital microscope (Osaka, Japan) and a scanning electron microscope (SEM) equipped with an energy-dispersive spectroscopy EDS X-ray microanalysis attachment. The novelty of this work lies in the systematic, time-dependent comparison of the effects of bulk and surface modifications on the evolution of corrosion-passivation mechanisms of electrodes based on the LaNi₅ alloy. It has been shown that the Mg and Ge additives improve corrosion resistance in the initial stage of exposure but lead to destabilisation of the passive layer during prolonged electrolyte interaction. A different effect was observed for the MPA-modified electrodes, in which a stable protective layer forms, limiting corrosion while maintaining favourable hydrogen desorption kinetics. The obtained results indicate the key role of exposure time (>140 h) in shaping the corrosion mechanisms and emphasise the need for simultaneous optimisation of the alloy composition and surface properties in the design of durable hydrogen electrodes. Full article

The main goal of this study was to develop and validate a laboratory-scale prototype of a rechargeable metal hydride (MH)–air battery integrating gas diffusion electrodes (GDEs) and MH electrodes with stable performance over extended operation (>500 h) and repeated charge–discharge cycling (>100 cycles). This work addresses the critical transition from optimized electrode materials to a functioning system by investigating its operation under deep-discharge conditions, a key but still insufficiently explored regime in the context of stationary renewable energy storage. In this respect, this study explicitly targets the practical applicability of the developed system rather than focusing solely on material-level performance. The most efficient electrode materials, previously optimized, were successfully integrated into a single-cell configuration and systematically evaluated under various operating conditions. By determining the limiting current density for stable GDE operation, an appropriate operating window was defined, enabling maximum capacity utilization without compromising electrode integrity. At a current density of 10 mA, the maximum depth of discharge was achieved at a cell voltage of 575 mV, ensuring operation in a regime that limits GDE degradation while maintaining high energy efficiency. In addition, the electrode retains its mechanical stability after operation is interrupted, indicating good structural robustness. Furthermore, the performance of two identical cells connected in series was investigated to assess system scalability. The cells were operated under near-limit conditions and exhibited stable behavior. Overall, the present results confirm that the developed MH–air battery system extends beyond laboratory-scale validation and shows strong potential for implementation in stationary energy storage applications. Full article

This study focuses on the structural and electrochemical behavior of the compound ZnLaFeO₄ as a negative electrode material for nickel–metal hydride (Ni-MH) batteries. The material was synthesized by a sol–gel hydrothermal method to assess the influence of lanthanum doping on the ZnFe₂O₄ spinel structure. X-ray diffraction revealed the formation of a dominant LaFeO₃ perovskite phase, with ZnFe₂O₄ and La₂O₃ as secondary phases. SEM analysis showed agglomerated grains with an irregular morphology. Electrochemical characterization at room temperature and a discharge rate of C/10 (full charge in 10 h) revealed a maximum discharge capacity of 106 mAhg⁻¹. Although La³⁺ doping modified the microstructure and slowed the activation process, the electrode exhibited stable cycling with moderate polarization behavior. The decrease in capacity during cycling is due mainly to higher internal resistance. These results highlight the potential and limitations of La-doped spinel ferrites as alternative negative electrodes for Ni-MH systems. Full article

In the present study, self-assembled hierarchical CoMn-LDH, CoMn@CuZnS, and CoMn@CuZnFeS heterostructured composites were synthesized for bifunctional applications. As an electrode for a supercapacitor, CoMn-LDH demonstrated superior areal and specific capacitance of 5.323 F cm⁻² (279.49 mAh/g) at 4 mA cm⁻², comparable to or even higher than other LDHs. The assembled AC//CoMn-LDH hybrid supercapacitor device further demonstrated better stability with 63% original capacitance over 20,000 cycles. Later, as a catalyst, CoMn-LDH, CoMn@CuZnS, and CoMn@CuZnFeS electrodes revealed better performance, with overpotentials of 340, 350, and 366 and −199, −215, and −222 mV to attain 10 mA cm⁻² of current density for the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER), respectively. Moreover, for CoMn-LDH, small Tafel slopes of 102 and 128 mV/dec were noticed for OER and HER with good stability compared to heterostructured electrodes. Full article

There is a high demand for nickel hydroxide as an engineering material used in the positive electrode of nickel metal hydride (Ni-MH) rechargeable batteries. These batteries are extensively used in various small instruments, disposable batteries, and electric vehicles. The structure of nickel hydroxide significantly influences the discharge capacity and energy density, key properties of Ni-MH batteries, and this structure is primarily determined by the synthesis method used. In this study, nickel hydroxide was synthesized using an electrochemical precipitation method, with current density acting as a parameter to control the desired phase of the product, whether α-nickel hydroxide, β-nickel hydroxide, or a combination of both. At a current density of 50 A/m², the synthesized nickel hydroxide demonstrated a smaller particle size and a superior discharge electrochemical property in comparison to that generated at 500 A/m². The effect of agitation in catholyte was also investigated to examine the change in discharge property of the precipitated material. The product synthesized at 500 A/m² from an agitated catholyte exhibited a tap density of 1.24 g/cc and an improved discharge capacity of 254 mAh per gram of Ni(OH)₂. Full article

The modular photoelectrochemical (PEC) reactor accommodating eight photoelectrodes with a total active area of up to 46 cm² has been designed and manufactured using the fused deposition modeling method. The device was equipped with an electrolyte flow system, a relay module for the photoelectrode connection, and a feedback-loop module for switching between counter electrodes. The performance and durability of the system were tested within three case study experiments. The water splitting process was successfully combined with an in situ hydrogen storage in the form of metal hydride phases (confirmed by powder X-ray diffraction) using Fe₂O₃- or WO₃-based photoanodes and LaNi₅-based cathodes. The PEC water oxidation at the anodes was realized either in a strongly alkaline electrolyte (pH > 13.5) or in acidified synthetic seawater (pH < 2) for Fe₂O₃ and WO₃ electrodes, respectively. In the latter case, the photoresponse of the anodes decreased the cell charging voltage by 1.7 V at the current density of 60 mA∙g⁻¹. When the seawater was used as an anolyte, the oxygen evolution reaction was accompanied by the chlorine evolution reaction. The manufactured PEC-metal hydride reactor revealed mechanical and chemical stability during a prolonged operation over 300 h and in the broad range of pH values. Full article

Metallic glasses (MGs) are a type of multicomponent non-crystalline metallic alloys obtained by rapid cooling, which possess several physical, mechanical, and chemical advantages against their crystalline counterparts. In this work, an Fe-based MG is explored as a hydrogen storage material, especially, due to the evidence in previous studies about the capability of some amorphous metals to store hydrogen. The evaluation of an Fe-based MG as a novel negative electrode material for nickel/metal hydride (Ni-MH) batteries was carried out through cyclic voltammetry and galvanostatic charge–discharge tests. A conventional LaNi₅ electrode was also evaluated for comparative purposes. The electrochemical results obtained by cyclic voltammetry showed the formation of three peaks, which are associated with the formation of Fe oxides/oxyhydroxides and hydroxides. Cycling charge/discharge tests revealed activation of the MG electrode. The highest discharge capacity value was 173.88 mAh/g, but a decay in its capacity was observed after 25 cycles, contrary to the LaNi₅, which presents an increment of the discharge capacity for all the current density values evaluated, reached its value maximum at 183 mAh/g. Characterization analyses performed by X-ray diffraction, Scanning Electron Microscopy and Raman Spectroscopy revealed the presence of corrosion products and porosity on the surface of the Fe-based MG electrodes. Overall, the Fe-based MG composition is potentially able to work as a negative electrode material, but degradation and little information about storage mechanisms means that it requires further investigation. Full article

Back-scattered electron imaging and X-ray elemental mapping were combined in a tabletop scanning electron microscope (SEM) to investigate cross-sections of three AA-type (mignon) nickel–metal hydride (NiMH) batteries from different manufacturers. All batteries underwent 500–800 charge/discharge cycles and reached their end of lifetime after several years as they could no longer hold any significant electric charge (less than 20% of nominal charge capacity), but none showed any short-circuiting. The types of degradation observed in this field study included electrode swelling, metallic nickel formation and carbon incorporation into pores in the positive electrodes and, in the negative electrodes, metal alloy segregation of different elements such as nickel, lanthanum and, in one case, sodium, as well as grain break-up and pore formation. All these phenomena could readily be observed at rather small magnifications. This will be important for the improvement of NiMH batteries, for which new generations with nominally slightly increased charge capacities are being marketed all the time. Full article

Whether it is fossil energy or renewable energy, the storage, efficient use, and multi-application of energy largely depend on the research and preparation of high-performance materials. The research and development of energy storage materials with a high capacity, long cycle life, high safety, and high cleanability will improve the properties of energy storage systems and promote their wide application. In recent years, Mg-based materials, from a comprehensive consideration of energy storage performance, raw material reserves, and prices, have demonstrated potential industrial applications as large-scale hydrogen storage materials. Nevertheless, Mg-based materials also have obvious disadvantages: as a hydrogen storage material, the hydrogen absorption/desorption rate is insufficient, as well as the high hydrogen absorption/desorption temperatures; as the electrode material of Ni-MH batteries, the reactions of Mg with alkaline electrolyte and corrosion are the main problems for applications. This article reviews different surface treatment methods and mechanisms for surface modifications of Mg-based materials for hydrogen storage and Ni-MH battery applications, as well as the performance of the materials after surface modifications. Multiple experimental studies have shown that the surface layer or state of Mg-based materials has a strong impact on their performance. Surface modification treatment can greatly improve the energy storage performance of magnesium-based materials for hydrogen storage and Ni-MH battery applications. Specifically, Mg-based materials can have a lower hydrogen absorption/desorption temperature and a faster hydrogen absorption/desorption rate when used as hydrogen storage materials and can improve the corrosion resistance, initial discharge capacity, and cycling stability in alkaline solutions when used as negative electrode materials for Ni-MH batteries. By offering an overview of the surface modification methods for Mg-based materials in two energy storage fields, this article can improve researchers’ understanding of the surface modification mechanism of Mg-based materials and contribute to improving material properties in a more targeted manner. While improving the material properties, the material’s preparation and surface modification treatment process are considered comprehensively to promote the development, production, and application of high-performance Mg-based materials. Full article

Functional liquid fluoroelastomers are in high demand in new energy fields. And these materials have potential applications in high-performance sealing materials and as electrode materials. In this study, a novel high-performance hydroxyl-terminated liquid fluoroelastomer (t-HTLF) with a high fluorine content, temperature resistance, and curing efficiency was synthesised from a terpolymer of vinylidene fluoride (VDF), tetrafluoroethylene (TFE), and hexafluoropylene (HFP). A carboxyl-terminated liquid fluoroelastomer (t-CTLF) with controllable molar mass and end-group content was first prepared from a poly(VDF-ter-TFE-ter-HFP) terpolymer using a unique oxidative degradation method. Subsequently, an efficient “one-step” reduction of the carboxyl groups (COOH) in t-CTLF into hydroxyl groups (OH) was achieved via the functional-group conversion method using lithium aluminium hydride (LiAlH₄) as the reductant. Thus, t-HTLF with a controllable molar mass and end-group content and highly active end groups was synthesised. Owing to the efficient curing reaction between OH and isocyanate groups (NCO), the cured t-HTLF exhibits good surface properties, thermal properties, and chemical stability. The thermal decomposition temperature (T_d) of the cured t-HTLF reaches 334 °C, and it exhibits hydrophobicity. The oxidative degradation, reduction, and curing reaction mechanisms were also determined. The effects of solvent dosage, reaction temperature, reaction time, and ratio of the reductant to the COOH content on the carboxyl conversion were also systematically investigated. An efficient reduction system comprising LiAlH₄ can not only achieve an efficient conversion of the COOH groups in t-CTLF to OH groups but also the in situ hydrogenation and addition reactions of residual double bonds (C=C) groups in the chain, such that the thermal stability and terminal activity of the product are improved while maintaining a high fluorine content. Full article