Alkaline Water Electrolysis Research Articles

Effect of Iron Doping in Ordered Nickel Oxide Thin Film Catalyst for the Oxygen Evolution Reaction.

Water splitting has emerged as a promising route for generating hydrogen as an alternative to conventional production methods. Finding affordable and scalable catalysts for the anodic half-reaction, the oxygen evolution reaction (OER), could help with its industrial widespread implementation. Iron-containing Ni-based catalysts have a competitive performance for the use in commercial alkaline electrolyzers. Due to the complexity of studying the catalysts at working conditions, the active phase and the role that iron exerts in conjunction with Ni are still a matter of investigation. Here, we study this topic with NiO(001) and Ni0.75Fe0.25O x (001) thin film model electrocatalysts employing surface-sensitive techniques. We show that iron constrains the growth of the oxyhydroxide phase formed on top of the Ni or NiFe oxide, which is considered the active phase for the OER. Besides, operando Raman and grazing incidence X-ray absorption spectroscopy experiments reveal that the presence of iron affects both, the disorder level of the active phase and the oxidative charge around Ni during OER. The observed compositional, structural, and electronic properties of each system have been correlated with their electrochemical performance.

Decoupling Electrolytic Water Splitting by an Oxygen-Mediating Process.

Decoupled water electrolysis systems, incorporating a reversible redox mediator that allows for the construction of membrane-free electrolyzers, have emerged as a promising approach to produce high-purity hydrogen with remarkable flexibility. The key factor crucial for practical applications lies in the development of mediator electrodes that possess suitable redox potential, high redox capacity, excellent cycling reversibility and stability. Herein, we introduce a novel concept of oxygen-mediating redox mediators (ORMs) employing Bi2O3 as an example material, which are capable of sequestering oxygen during the hydrogen evolution reaction and subsequently releasing it to generate oxygen gas under alkaline conditions. Thanks to its remarkable reversible redox activity and specific capacity, the Bi2O3 electrode boasts an impressive reversible specific capacity of 300.8 mA h g-1 and delivers outstanding cycling performance for >1000 cycles at a current density of 2.0 A g-1. Furthermore, the implementation of such a decoupled alkaline water electrolysis system can be integrated with a Bi2O3-Zn battery, enabling both power-to-fuel (hydrogen production) and chemical-to-power (rechargeable Bi2O3-Zn battery) conversion. With many oxygen-carrier materials readily available and the potential integration with rechargeable alkaline batteries, this study provides an alternative competitive route for membrane-free decoupled water splitting through the oxygen-mediating mechanism with combined energy transformation and storage.

Facile synthesis of spherical-shaped CeC2–TiO2 nanocomposite electrocatalyst with boosted alkaline OER

Developing noble metal-free multifunctional electrocatalysts to catalyze water oxidation is vital for future renewable energy systems. Herein, through several defect modifications, the CeC2–TiO2 nanocomposite on the strength of enriched oxygen vacancies was successfully fabricated by facile hydrothermal method on SS (stainless steel) substrate, attributed to the conductive ability for fast electron transportation. A well-defined phase growth, vibrational bonding of metal atoms, morphological determination, and elemental composition for synthesized heterostructured electrocatalysts were revealed by XRD, FTIR, TEM, and EDX, respectively. XPS has complied to understand the moderate binding energies of CeC2–TiO2 for OER intermediates, which signifies the strong interactions between electronic states of Ce, C, Ti, and O atoms. With the plentiful catalytic active sites, the resultant CeC2–TiO2 entails low overpotentials of only 169 mV and 108.8 mV/dec Tafel slope to afford 10 mA cm−2 for OER in 1.0 M KOH are tested through cyclic and linear sweep voltammogram measurements, thereby exhibit promising activity in alkaline water electrolysis. EIS measurements revealed a decreased polarization resistance for the composite dominated by the small semicircle diameter, corresponding to the adsorption of intermediates. Finally, observed results strongly recommended that the CeC2–TiO2 catalyst exhibited superior OER performance due to excellent electrical chemical coupling between CeC2 and TiO2.

Cost of Green Hydrogen

Acting in accordance with the requirements of the 2015 Paris Agreement, Poland, as well as other European Union countries, have committed to achieving climate neutrality by 2050. One of the solutions to reduce emissions of harmful substances into the environment is the implementation of large-scale hydrogen technologies. This article presents the cost of producing green hydrogen produced using an alkaline electrolyzer, with electricity supplied from a photovoltaic farm. The analysis was performed using the Monte Carlo method, and for baseline assumptions including an electricity price of 0.053 EUR/kWh, the cost of producing green hydrogen was 5.321 EUR/kgH2. In addition, this article presents a sensitivity analysis showing the impact of the electricity price before and after the energy crisis and other variables on the cost of green hydrogen production. The large change occurring in electricity prices (from 0.035 EUR/kWh to 0.24 EUR/kWh) significantly affected the levelized cost of green hydrogen (LCOH), which could change by up to 14 EUR/kgH2 in recent years. The results of the analysis showed that the parameters that successively have the greatest impact on the cost of green hydrogen production are the operating time of the plant and the unit capital expenditure. The development of green hydrogen production facilities, along with the scaling of technology in the future, can reduce the cost of its production.

Optimization of alkaline water electrolysis performance with binaphthyl-derived polybenzimidazole ion-solvating gel membrane

Polybenzimidazole-based ion-solvating membranes (ISMs) are regarded as a promising contender for alkaline water electrolysis separators due to their mechanical stability, excellent thermal stability, and gas tightness. However, the trade-off between hydroxide conductivity and alkaline stability restricts the application. In this paper, poly(2, 2'-(4, 4′-1, 1′-binaphthyl)-5, 5′-benzimidazole) (BN-PBI) was synthesized from a molecular design perspective, followed by the in-situ scrapping of a BN-PBI membrane and subsequent immersion in a KOH solution to yield a KOH-doped ion-solvating BN-PBI gel membrane. m-PBI and N-PBI gel membranes were also fabricated under the same conditions for comparison. The incorporation of the bulky and rigid binaphthyl groups increased the free volume of the polymer, which effectively regulated the absorption of alkali and water. Consequently, the BN-PBI gel membrane exhibited an impressive hydroxide conductivity of up to 274.48 mS cm−1 in a 6 M KOH solution at 80 °C. Moreover, the ionic conductivity retention was still above 62.43 % after a 3400 h ex-situ alkaline stability test. During the AWE test, the cell with the BN-PBI gel membrane achieved the highest current density of 750 mA cm−2 at a voltage of 2 V and 80 °C. Additionally, under a constant current density of 500 mA cm−2 in a 6 M KOH solution at 80 °C, the cell demonstrated stable performance over 180 h with a voltage fluctuation of only 39 μV. Therefore, this work proposes a new perspective on addressing the trade-off between hydroxide conductivity and alkaline stability, facilitating the development of new separator materials for alkaline water electrolysis.

A "Two-Pronged" Strategy to Boost Hydrogen Evolution Kinetics on NiFe-Based (Oxy)hydroxides via Oxygen Deficient Ni-Mo-Fe Coordinate Structures for Ultra-Stable Ampere-Level Alkaline Overall Water Splitting.

NiFe (oxy)hydroxides have been regarded as one of the state-of-the-art catalysts for oxygen evolution reaction (OER). Unfortunately, the sluggish hydrogen evolution reaction (HER) kinetics limit its application as bifunctional electrocatalyst for alkaline overall water splitting (OWS). Herein, a "two-pronged" strategy is proposed to construct highly active oxygen deficient Ni-Mo-Fe coordinate structures in NiFe (oxy)hydroxide (NFM-OVR/NF), which simultaneously reduces the energy barrier of Volmer and Heyrovsky steps during alkaline HER process and significantly accelerate the reaction kinetics. Consequently, NFM-OVR/NF delivers overpotentials as low as 25 and 234mV to achieve 10 and 1000mA cm-2 in 1.0M KOH, respectively. Furthermore, benefiting from excellent HER and OER activity, NFM-OVR/NF exhibits a remarkable OWS activity with cell voltages of 1.44V and 1.77V at 10 and 1000mA cm-2 in 1.0M KOH, and displays ultralong-term stability for 600h at 500mA cm-2, while remaining durable for 300h in an alkaline water electrolyzer in 30% KOH at 80°C. The calculated price per gallon of gasoline equivalent for the produced H2 is $ 0.92, which is much lower than 2026 U.S. Department of Energy target ($ 2.00), demonstrating feasibility and practicability of NFM-OVR/NF for industrial applications.

Effect of porous irregular ZrO2 nanoparticles on the performance of alkaline water electrolysis composite separator membranes under complex conditions

Developing composite separator membranes with low area resistance, high bubble point pressure, and long-term safety and stability is crucial for alkaline water electrolysis for hydrogen production as a key component of electrolyzer systems. In this study, PPS mesh fabric reinforced PSF@ZrO2 composite separator membranes were successfully prepared using the immersion-drawing phase inversion method, with PSF as the alkali-resistant polymer matrix and porous irregular ZrO2 nanoparticles as the hydrophilic additive. The experimental results showed that replacing commercial ZrO2 with porous irregular ZrO2 nanoparticles at an 85 wt% ZrO2 nanoparticle loading improved both bubble point pressure and current transmission efficiency, attributed to the change in the morphological structure of the ZrO2 nanoparticles. The P-Z85 composite separator membrane exhibited highly promising characteristics, with a high bubble point pressure of 3.76 bar and a low area resistance of 0.20 Ω cm2. Stability tests conducted in 30 wt% KOH electrolyte at 80 °C and a current density of 0.65 A cm−2 demonstrated excellent continuous electrolysis stability for the P-Z85 composite separator membrane. These results indicate that the PSF@ZrO2/PPS composite separator membrane prepared in this study exhibits excellent performance in 30 wt% KOH electrolyte, significantly extending its service life.

Arrayed metal phosphide heterostructure by Fe doping for robust overall water splitting

Transition metal phosphides (TMPs) show promise in water electrolysis due to their electronic structures, which activate hydrogen/oxygen reaction intermediates. However, TMPs face limitations in catalytic efficiency due to insufficient active sites, poor conductivity, and multiple intermediate steps in water electrolysis. Here, we synthesize a highly efficient bifunctional self-supported electrocatalyst, which consists of an N-doped carbon shell anchored on Fe-doped CoP/Co2P arrays on nickel foam (NC@Fe-CoxP/NF) using hydrothermal and phosphorization techniques. Experimental and theoretical results indicate that the modified morphology, with increased active site density and a tunable electronic structure induced by Fe doping in the CoP/Co2P heterostructure, leads to superior water electrolysis performance. The resulting NC@Fe0.1-CoP/Co2P/NF catalyst exhibits overpotentials of 122 mV for the hydrogen evolution reaction (HER) and 270 mV for the oxygen evolution reaction (OER) at 100 mA cm−2. Furthermore, using NC@Fe0.1-CoP/Co2P/NF as both the cathode and anode in an alkaline electrolyzer enables the cell system to achieve 100 mA cm−2 at a voltage of 1.70 V, while maintaining long-term catalytic durability. This work may pave the way for designing self-supported, highly efficient electrocatalysts for practical water electrolysis applications.

Vacancy-rich heterogeneous MnCo2O4.5@NiS electrocatalyst for highly efficient overall water splitting

Alkaline water electrolysis is regarded as a promising technology for sustainable energy conversion. Spinel oxides have attracted considerable attention as potential catalysts because of their diverse metal valence states. However, achieving the required current densities at low voltages is a challenge due to its limited active sites and suboptimal electron transport. In this study, we present a novel bifunctional catalyst composed of MnCo2O4.5 nanoneedles grown on NiS nanosheets for water electrolysis. Remarkably, MnCo2O4.5@NiS demonstrates exceptional catalytic activity, requiring 187 and 288 mV to achieve a current density of 100 mA cm−2 for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), respectively. The impressive performance of MnCo2O4.5@NiS is demonstrated by the lower value of voltage 1.44 V needed to deliver the current density of 10 mA cm−2, which outperformed the 1.66 V required for a commercial Pt/C||RuO2 system. Detailed structure analysis and density functional theory (DFT) calculations reveal that the MnCo2O4.5@NiS heterostructure enhances electron transfer at the interface, promotes the formation of oxygen vacancies and tunes the electronic structures of Mn and Co. These findings underscore the potential of MnCo2O4.5@NiS as an efficient and cost-effective electrocatalyst for hydrogen production.

Navigating Alkaline Hydrogen Evolution Reaction Descriptors for Electrocatalyst Design

The quest for efficient green hydrogen production through Alkaline Water Electrolysis (AWE) is a critical aspect of the clean energy transition. The hydrogen evolution reaction (HER) in alkaline media is central to this process, with the performance of electrocatalysts being a determining factor for overall efficiency. Theoretical studies using energy-based descriptors are essential for designing high-performance alkaline HER electrocatalysts. This review summarizes various descriptors, including water adsorption energy, water dissociation barrier, and Gibbs free energy changes of hydrogen and hydroxyl adsorption. Examples of how to apply these descriptors to identify the active site of materials and better design high-performance alkaline HER electrocatalysts are provided, highlighting the previously underappreciated role of hydroxyl adsorption-free energy changes. As research progresses, integrating these descriptors with experimental data will be paramount in advancing AWE technology for sustainable hydrogen production.

Technology for Green Hydrogen Production: Desk Analysis

The use of green hydrogen as a high-energy fuel of the future may be an opportunity to balance the unstable energy system, which still relies on renewable energy sources. This work is a comprehensive review of recent advancements in green hydrogen production. This review outlines the current energy consumption trends. It presents the tasks and challenges of the hydrogen economy towards green hydrogen, including production, purification, transportation, storage, and conversion into electricity. This work presents the main types of water electrolyzers: alkaline electrolyzers, proton exchange membrane electrolyzers, solid oxide electrolyzers, and anion exchange membrane electrolyzers. Despite the higher production costs of green hydrogen compared to grey hydrogen, this review suggests that as renewable energy technologies become cheaper and more efficient, the cost of green hydrogen is expected to decrease. The review highlights the need for cost-effective and efficient electrode materials for large-scale applications. It concludes by comparing the operating parameters and cost considerations of the different electrolyzer technologies. It sets targets for 2050 to improve the efficiency, durability, and scalability of electrolyzers. The review underscores the importance of ongoing research and development to address the limitations of current electrolyzer technology and to make green hydrogen production more competitive with fossil fuels.

Technical–Economic Analysis of Renewable Hydrogen Production from Solar Photovoltaic and Hydro Synergy in a Pilot Plant in Brazil

Renewable hydrogen obtained from renewable energy sources, especially when produced through water electrolysis, is gaining attention as a promising energy vector to deal with the challenges of climate change and the intermittent nature of renewable energy sources. In this context, this work analyzes a pilot plant that uses this technology, installed in the Itumbiara Hydropower Plant located between the states of Goiás and Minas Gerais, Brazil, from technical and economic perspectives. The plant utilizes an alkaline electrolyzer synergistically powered by solar photovoltaic and hydro sources. Cost data for 2019, when the equipment was purchased, and 2020–2023, when the plant began continuous operation, are considered. The economic analysis includes annualized capital, maintenance, and variable costs, which determines the levelized cost of hydrogen (LCOH). The results obtained for the pilot plant’s LCOH were USD 13.00 per kilogram of H2, with an efficiency loss of 2.65% for the two-year period. Sensitivity analysis identified the capacity factor (CF) as the main determinant of the LCOH. Even though the analysis specifically applies to the Itumbiara Hydropower Plant, the CF can be extrapolated to larger plants as it directly influences hydrogen production regardless of plant size or capacity.

Minimizing renewable hydrogen costs at producer's terminal gate with alkaline electrolyser, proton exchange membrane, and their co-installment: A regional case study in China

China leads in deploying large-scale alkaline (ALK) and proton exchange membrane (PEM) electrolysers for renewable hydrogen production. However, they are often overbuilt to handle intermittent renewable electricity (RE), leading to frequent system shutdowns, wasted capacity, or extensive investment. In this work, we propose a co-optimization solution in which ALK and PEM are collocated alongside hybrid RE supply from solar and wind energies. Implementing such a strategy could achieve the lowest hydrogen costs at producer's terminal gate, with production levelized costs of hydrogen (PLCOHs) down to 5.05, 4.13, 3.89, and 5.97 USD per kg respectively in south, north, west, and east regions of China. The co-optimization strategy, harnessing the combined strengths of ALK and PEM systems, efficiently minimizes hydrogen production costs while also presenting opportunities for the integration of advanced technologies into existing facilities.

PTFE as a Multifunctional Binder for High-Current-Density Oxygen Evolution.

Binder plays a crucial role in constructing high-performance electrodes for water electrolysis. While most research has been focused on advancing electrocatalysts, the application of binders in electrode design has yet to be fully explored. Herein, the in situ incorporation of polytetrafluoroethylene (PTFE) as a multifunctional binder, which increases electrochemical active sites, enhances mass transfer, and strengthens the mechanical and chemical robustness of oxygen evolution reaction (OER) electrodes, is reported. The NiFe-LDH@PTFE/NF electrode prepared by co-deposition of PTFE with NiFe-layered double hydroxide onto nickel foam demonstrates exceptional long-term stability with a minimal potential decay rate of 0.034mV h-1 at 500mA cm-2 for 1000 h. The alkaline water electrolyzer utilizing NiFe-LDH@PTFE/NF requires only 1.584V at 500mA cm-2 and sustains high energy efficiency over 1000 h under industrial operating conditions. This work opens a new path for stabilizing active sites to obtain durable electrodes for OER as well as other electrocatalytic systems.

Hydrogen production with a novel coaxial cylindrical electrolyser: A CFD study

This study introduces a unique coaxial cylindrical electrode design for Alkaline Water Electrolysers (AWEs) that is analyzed to show possible enhancements over the traditional stacked plate design. It investigates the performance of the proposed coaxial AWE for enhanced hydrogen production. Through comprehensive computational simulations, key performance indicators, such as current density and hydrogen volume fraction, are analyzed across various operating parameters. The results of this study indicate that the production rate of hydrogen achieves its highest level at a volume percentage of 3.4 %. This rate is significantly influenced by the concentration of the electrolyte, the distance between the cathode and anode rings, and, to a lesser degree, the porosity of the separator. Consequently, the optimized conditions demonstrate a promising increase in current densities, reaching 1000 mA/cm2 at an operating voltage of 2 V, showcasing the potential for developing more efficient and cost-effective AWE systems. This study further contributes valuable insights into the design and operational improvements needed for the advancement of large-scale hydrogen production technologies.

Substrate-Assisted Atomic Dispersion of Cobalt for Alkaline Water Electrolysis.

Atomically dispersed single-atom catalysts have recently attracted broad research interest due to their high atom efficiency and unique catalytic performance. In this study, atomic dispersion of cobalt is achieved using a chemical bath deposition method on a highly stable alkali titanate film (Ti/KTiO). These films were characterized using a variety of techniques, with atomic dispersion confirmed via grazing incidence X-ray absorption spectroscopy and ab initio modeling of single-atom systems. This modeling indicated that the alkali ion incorporated into the film facilitates atomic dispersion. Experimentally, the Ti/KTiO-supported Co(OH)2 catalysts exhibited remarkable electrochemical performance, with an overpotential of 163 mV to achieve a current density of 10 mA cm-2 with a catalyst loading of ∼0.1 mg cm-2 and high stability. These results show the potential of Ti/KTiO/Co(OH)2 catalysts for atomically efficient hydrogen production.

Hydrogen production from non-potable water resources: A techno-economic investment and operation planning approach

The production of hydrogen through water electrolysis facilitates large-scale energy storage, provides ancillary services, and supports the decarbonization of industries with hard-to-reduce emissions. As renewable energy adoption expands, the demand for these applications is increasing. However, water electrolysis currently faces challenges in cost competitiveness compared to other hydrogen production methods. Additionally, its reliance on potable water sources places additional strain on freshwater reserves. This study addresses these issues by exploring the economically optimal investment and operational strategy for hydrogen production using non-potable water sources. The goal is to maximize net profit through mathematical optimization, utilizing three advanced electrolysis technologies: alkaline electrolysis, proton exchange membrane electrolysis, and solid oxide electrolysis. The study examines three non-potable water sources: seawater, urban wastewater effluent, and rainwater. The model takes into account electricity market values from day-ahead and balancing markets, as well as the market values for hydrogen, oxygen, freshwater, and mixed solid salt. Two scenarios are analysed, reflecting varying levels of uncertainty in electricity price forecasts. Each scenario includes nine case studies, representing various combinations of water sources and electrolysis technologies. The results indicate that alkaline electrolysis and proton exchange membrane electrolysis are financially viable technologies, with potential annual net profits of up to 6.4 and 6.2 million euros, respectively. In contrast, solid oxide electrolysis incurs a negative net profit across all scenarios and is not economically viable under the given conditions. The main revenue sources are hydrogen sales and combined up-balancing and down-balancing services in electricity markets. Participation in the balancing market constitutes a significant portion (35 to 61%) of the total revenue in all cases with positive net profits, making it critical for economic viability. Rainwater is identified as the most cost-effective water source for hydrogen production. However, the costs associated with water treatment and brine management are minimal, contributing only 0.7 to 3.7% to the total cost of hydrogen production. Thus, differences in net profit are primarily attributed to the type of electrolysis technology used.

High stable poly (terphenyl-co-fluorene quinuclidinium) anion exchange membrane for alkaline water electrolysis

Developing anion exchange membranes (AEMs) is an effective way to reduce the cost of water electrolyser systems and fuel cell systems because of the no requirement of platinum-group-metal (PGM) catalysts. However, low conductivity and poor stability are the bottlenecks that constrain its development. In this work, we propose a series of performance enhanced poly (terphenyl-co-fluorene quinuclidinium) (TPFQ) AEMs. The hydroxide conductivity of TPFQ-10 reached 178.5 mS cm−1 at 80 °C. The rigid fluorene group gives the membrane better dimensional stability (swelling ratio: 7.7% in pure water and 1.2% in 10 M NaOH at 80 °C for TPFQ-10). In particular, the membranes exhibit extremely high alkaline stability, with almost no conductivity loss over more than 2000 h in a 10 M NaOH solution. The AEM water electrolysers (AEMWEs) with nickel-alloy foam electrodes shows an excellent current density of 2.32 A cm−2 at 2.0 V. The AEMWEs can work steadily at a current density of 0.5 A cm−2 in 5 M NaOH at 80 °C for more than 500 h, with a low voltage rising rate of 56 μV h−1.

Copper restructured transition metal/metal oxide heterostructure with a hierarchical nanostructure for accelerated water dissociation kinetics and alkaline hydrogen evolution

The slow kinetics of water dissociation on electrocatalysts lacking platinum hinders the advancement of cost-effective hydrogen production via alkaline water electrolysis. Herein, a hierarchically peach-flower-shaped electrocatalyst consisting of copper-restructured cobalt–nickel/cobalt–nickel oxide heterostructure anchored on copper nanowires (Cu-CoNiO/CoNi@Cu NWs) is developed for efficient hydrogen evolution reaction (HER). Benefiting from the optimized electronic configuration and geometric structure, this Cu-CoNiO/CoNi@Cu NWs catalyst performs an outstanding alkaline HER activity of 29 mV at 10 mA cm−2 and 98 mV at 100 mA cm−2, which is comparable with the state-of-the-art Pt/C catalyst (26 mV at 10 mA cm−2 and 117 mV at 100 mA cm−2). Our findings rank among the topmost catalytic efficiencies when compared to all previously reported non-noble metal catalysts and numerous noble metal catalysts. The combined experimental exploration and theoretical studies reveal that the incorporation of Cu dopant into CoNiO/CoNi heterostructure enhances electron transfer from metal atoms to O atom, leading to the formation of the polarized electric field to accelerate water dissociation and H evolution, eventually facilitating the overall alkaline HER process. The boosted electron exchange and mass transportation deriving from the introduction of Cu NWs and hierarchically peach-flower-shaped nanostructure further reinforce the HER activity of the Cu-CoNiO/CoNi catalyst.

Evaluation of anion exchange membrane water electrolysis performance using synthesised NiMoO4/Ni cathode via solution combustion synthesis in applied thermal reduction approach

The development of sustainable electrocatalysts is essential for the advancement of anion exchange membrane water electrolysis (AEMWE) technologies. Nickel molybdate-based catalysts may improve the efficiency of hydrogen evolution reaction (HER) during alkaline water electrolysis. This study investigated the influence of thermal reduction temperature on the synthesised NiMoO4-based catalyst via solution combustion synthesis (SCS) and its performance in HER and single-cell AEMWE. The optimal conditions for stable and active HER electrocatalysts were determined by investigating synthesised NiMoO4 catalysts at 450 °C, 550 °C and 750 °C. A NiMoO4 catalyst was characterised at different reduction temperatures through X-ray diffractometer (XRD), field emission scanning electron microscopy (FESEM), energy-dispersive spectroscopy (EDS) and Brunauer–Emmett–Teller (BET) analysis. Results revealed that the NiMoO4-450/Ni cathode became the highest performance 1 A/cm2 current density at 2.2 V and the NiMoO4-550/Ni cathode became the most stable performance among the catalysts, attaining. The average current density of NiMoO4-550/Ni fluctuated by only 22% from 24 h to 100 h.