High Hydrogen Research Articles

Sedimentary factors controlling the organic matter enrichment in oil shale, Seyitömer Lacustrine Basin, Western Anatolia: New implications from organic and inorganic geochemistry

AbstractWestern Anatolia, an important segment of the Alp‐Himalayan Belt, hosts numerous Neogene lacustrine basins with potential oil shale reserves surpassing 1.6 billion tonnes. Among these basins, the Seyitömer Basin (Kütahya) stands out, containing oil shales that are intercalated with claystone, marl, limestone and coal layers. This study presents a comprehensive dataset of organic and inorganic chemistry to gain insight into the palaeoclimate and palaeoenvironmental factors that control the enrichment of organic matter. The studied samples exhibit high total organic carbon contents, averaging 12.85% (ranging from 2.22 to 36.21%), high hydrogen indices (486–812 mgHC/g rock) and low oxygen indices (33–70 mgCO2/g total organic carbon), indicating their substantial hydrocarbon‐source potential. These characteristics indicate predominantly ‘excellent’ to occasionally ‘very good’ source rock qualities and very high oil potential. Their pyrolysis, gas chromatography and gas chromatography–mass spectrometer parameters indicate an immature‐early mature characteristic for Seyitömer oil shale samples. They comprise dominantly Type‐I kerogen with minor Type‐II kerogen and lacustrine algal organic matter. Their sedimentological characteristics, along with various geochemical values, such as total organic carbon versus S, B versus Ga and dibenzothiophene/phenanthrene, reveal a moderately deep fresh/brackish to saline lacustrine environment. The Ga/Rb, K/Al and Sr/Cu ratios suggest dominantly humid and warm climate conditions, occasionally interrupted by periods of less humidity. The prevalence of warm and humid climate conditions leads to intense chemical weathering processes, supported by high Chemical Index of Alteration and low Rb/Sr ratios in the associated oil shale samples. Intense chemical weathering and high runoff resulted in dissolved nutrient enrichment, promoting ecological dynamics favourable to increased productivity. Their low Pr/Ph and Mo/total organic carbon ratios, high Ni/Co ratio and, relatively low MoEF/UEF ratio, along with well‐developed lamination of the oil shales, indicate the presence of anoxic conditions in the bottom water. These anoxic conditions would have facilitated the preservation potential of organic matter in the samples. Thus, the palaeoclimate conditions integrated with sedimentary factors have an important role in the ecological dynamic and physical–chemical environmental conditions, ultimately contributing to the organic matter enrichment of the studied samples. This work provides a case study to better understand the sedimentary factors controlling organic matter enrichment in the lacustrine basins of the Alp‐orogenic belt.

CoCe composite catalyst for CO2 hydrogenation: Effect of pore structure

In order to realize the dual carbon goals of “carbon peaking” and “carbon neutrality”, the design and development CO2 hydrogenation catalyst with high performances is of great significance. In this study, the CoCe composite catalysts were prepared by different methods and used to CO2 catalytic hydrogenation. The physicochemical properties of the prepared catalysts were characterized by XRD, BET, TEM/HRTEM, and H2-TPD. The characterization results indicated that the studied CoCe composite catalytsts with different pore structure can be prepared by different preparation methods. The suitable preparation method can promote Co species to be dissolved into the CeO2 lattice to form Ce-O-Co solid solution, which can promote the corresponding Co species to be reduced by H2 to form active Co0 species. The large specific surface area and developed ordered mesoporous structure of the CoCe-HT catalyst precursor, which was prepared by hard-template method, are conducive to the formation of active Co0 species and activation of H2 to produce reactive H species. The CO2 hydrogenation activity of the studied CoCe composite catalysts follows the following order: CoCe-HT > CoCe-CP > CoCe-CA > CoCe-HY. The CoCe-HT catalyst showed high CO2 hydrogenation conversion of 53.9 % and good using stability at 360 °C for 600 min. However, the CoCe-CA prepared by complex method has a poor use stability.

In Situ Synthesis of Honeycomb Nanorods Ni3S2@NiCo-Layered-Double Hydroxide/Nickel Foam Electrocatalysts with High Performance Electrocatalytic Hydrogen Production

In Situ Synthesis of Honeycomb Nanorods Ni₃S₂@NiCo-Layered-Double Hydroxide/Nickel Foam Electrocatalysts with High Performance Electrocatalytic Hydrogen Production

Modification of gel properties of Meretrix meretrix (clam) with polysaccharides: physical characterization and interaction mechanism.

This study investigated the contribution of 11 polysaccharides (2%, w/w), including pectin (PC), κ-carrageenan (KC), ι-carrageenan (IC), gellan gum (GG), guar gum (GM), sodium alginate (SA), konjac gum (KG), gum arabic (GA), fucoidan (FC), locust bean gum (LBG), and curdlan (CD), to the gel and microstructural properties of Meretrix meretrix clam gel (MMG). The hardness, springiness and chewiness of MMG with KC, IC, GG, SA and FC addition increased by ~10%-250%, while PC, GM, KG and LBG groups decreased by ~0.6% to 69%. KC, IC, SA, GG and FC decreased the cooking loss rate (CLR) by 69.4% to 88.7% and correspondingly enhanced the water holding capacity (WHC) by 10.2% to 21.4%, which was accompanied by an increased bound water and immobilized water area and high hydrogen proton density. The addition of KC transformed the MMG microstructure from a loose network with large pores to a compact, dense network, reducing lacunarity by 57.9%. The primary intermolecular forces in MMG with the incorporation of KC, IC, GG, SA and FC were hydrophobic interactions and disulfide bonds, which increased by 32.8%-105.3% and 45.6%-114.5% than MMG alone, respectively. Collectively, KC, IC, GG, SA and FC could improve the gel properties of MMG and the strongest synergistic combination was found in the MMG/KC system. This study suggests that the incorporation of polysaccharides is a strategy with potential for modifying the gel properties of shellfish surimi products. © 2024 Society of Chemical Industry.

Ultrafine Pd nanoparticles confined in naphthalene-based covalent triazine frameworks for efficient and stable hydrogen production from formic acid

Formic acid (FA) is considered as a kind of promising hydrogen storage materials due to its economic feasibility, safety, stability and high hydrogen density. Nevertheless, it is a challenge to design a high-performance catalyst with high activity, selectivity and stability for the dehydrogenation of FA to generate hydrogen (H2). Herein, a range of covalent triazine frameworks (CTFs including 1,8-CTF, 1,5-CTF and 2,3-CTF) with abundant nitrogen atoms are developed to support palladium nanoparticles for efficiently catalyzing FA dehydrogenation. Ultrasmall palladium nanoparticles with a size of 1.2 ± 0.3 nm showed near 100 % H2 selectivity and high catalytic activity in FA dehydrogenation supported by 1,8-CTF. The activation energy of FA dehydrogenation catalyzed by Pd/1,8-CTF reaches 26.17 kJ·mol−1. In addition, Pd/1,8-CTF exhibits high stability and easy recyclability, and the catalytic activity is maintained even after 6 cycles. This work gives a feasible strategy to develop high-efficiency and selective nanocatalysts for H2 production from FA dehydrogenation.

Hydrogen and vacancy concentrations in [formula omitted]-iron under high hydrogen gas pressure and external stress: A first-principles neural network simulation study

The metal-hydrogen-vacancy interaction in α-iron is crucial for understanding hydrogen embrittlement behavior and developing reliable materials for green gaseous hydrogen applications; however, it remains underexplored, particularly in contexts involving external stress and high hydrogen gas pressure. In this study, we performed quantitative analyses of metal-vacancy–hydrogen interactions in α-iron, measured by hydrogen solubility and the thermodynamics of vacancy–hydrogen complexes, under such challenging conditions using a reliable first-principles neural network potential. High hydrogen gas pressures reaching up to 2 GPa were investigated. As the atomic concentration surpasses approximately 0.01, hydrogen solubility is dominated by hydrogen-induced lattice distortion (primarily volumetric expansion) and the interactions between hydrogen atoms within the metal matrix, resulting in significant deviations from Sieverts’ law. Our results reveal a significant effect of shear stress on hydrogen solubility, deviating from previously used equations. Moreover, the influence of external stress on the thermodynamics of the vacancy–hydrogen complex, particularly vacancy formation free energy, is uniquely characterized by hydrogen solubility, regardless of the external stress magnitude. It thereby offers a rapid method to estimate the vacancy properties under external stress based on readily accessible external-stress-free data.

Emission of high rovibrational hydrogen molecules under detached plasma by recycling on tungsten wall

Emission of high rovibrational hydrogen molecules under detached plasma by recycling on tungsten wall

Sustainable Rubber Nanocomposites for Hydrogen Sealings: Impact of Carbon Nano-Onions and Bio-Based Plasticizer

Additives play a crucial role in modifying and enhancing the properties of rubbers, improving mechanical strength, thermal stability, and chemical resistance to make them more suitable for various applications. The rubber industry faces challenges related to high resource consumption and toxic emissions, which are further impacted by the use of performance-enhancing additives. In hydrogen storage systems, tailored additives are required for rubbers to withstand elevated temperatures and high pressures, preventing hydrogen-induced swelling, a major cause of sealing failure. Herein, a novel form of carbonaceous material, carbon nano-onions (CNOs), and the bio-based plasticizer additive epoxidized soybean oil (ESO) are utilized in conventional silica-filled nitrile butadiene rubber (NBR) nanocomposites to develop low-carbon manufacturing high pressure hydrogen resistant O-rings for sealing applications. The results reveal that the incorporation of CNOs increases the crosslinking density (vc), assisted by ESO, in silica-filled NBR nanocomposites. While the conventional adipate-based plasticizer and ESO were found to be susceptible to high pressure hydrogen exposures, ESO demonstrated sustained compressive sealing properties with increase in von-Mises stress and in elevated thermo-oxidative conditions over time. The results of the life cycle assessment (LCA) recommend ESO for low-carbon manufacturing in rubber processing over conventional plasticizers.

The regulation of dislocation and precipitated phase improving hydrogen embrittlement resistance of pipeline steel in high pressure hydrogen environment

In this study, the hydrogen embrittlement behavior of quenched pipeline steel tempered at 550 °C to 650 °C in a high-pressure hydrogen environment was analyzed. Hydrogen permeation tests and microstructural analyses indicated that the dislocation density of the steel decreases with increasing tempering temperature, while precipitates gradually nucleate and grow. These hydrogen traps interact with hydrogen atoms, resulting in significantly higher diffusible hydrogen content in steel tempered at 550 °C compared to that tempered at 600 °C and 650 °C. Fatigue crack growth (FCG) test results show that steel tempered at 600 °C and 650 °C exhibits significantly better hydrogen embrittlement resistance than steel tempered at 550 °C. This is primarily due to the combined effect of the high hydrogen concentration, high dislocation density and low nano carbide content in the steel tempered at 550 °C, which inhibits dislocation slip and emission, leading to high crack tip stress and rapid crack propagation. In contrast, the low dislocation density and and dispersed nano carbides in steel tempered at 600 °C and 650 °C facilitate some dislocation slip and emission, result in crack tip stress relaxation and reduced crack propagation rate. Properly controlling the initial dislocation density and increasing the density of irreversible hydrogen traps can enhance the strength of materials while improving their resistance to hydrogen embrittlement.

P-tuned FeN2 binuclear sites for boosted CO2 electro-reduction

The recycling of CO2 through electrochemical processes offers a promising solution for alleviating the greenhouse effect; however, the activation of CO2 and desorption of *CO in electrocatalytic CO2 reduction (ECR) frequently encounter high energy barriers and competitive hydrogen evolution reactions (HERs), which are urgent problems that need to be addressed. In this study, a catalyst (P100–Fe–N/C) with homogeneous P–tuned FeN2 binuclear sites (N2PFe-FePN2) was successfully synthesised, demonstrating satisfactory performance in the ECR to CO. P100–Fe–N/C attains a peak FECO of 98.01% and a normalized TOF of 664.7 h-1 at −0.7 VRHE, surpassing the performance of the Fe binuclear catalyst without P and single-atoms catalysts. In the MEA cell, a FECO exceeding 90% can still be achieved. Density functional theory analysis indicates that the asymmetric coordination configuration induced by the incorporation of P facilitates a reduction in the system’s energy. The modulation of P results in the d-band centre of the catalyst being positioned closer to the Fermi level, which facilitates the interaction of the catalyst with CO2, allowing more electrons to be injected into the CO2 molecule at the Fe binuclear sites and inhibiting the HER. The P–tuned FeN2 binuclear sites effectively lower the *CO desorption barrier.

Exploring Phytochemical Compounds Against Pseudomonas Aeruginosa Using QSAR, Molecular Dynamics, and Free Energy Landscape

AbstractPseudomonas aeruginosa is a versatile opportunistic bacterium that presents a considerable risk in medical environments because of its strong adaptability and resistance to multiple medications. Targeting the LasR quorum sensing system, which plays a crucial role in controlling virulence factors and biofilm formation, is a key intervention point. In this study, in silico molecular docking, machine learning‐based Quantitative Structure‐Activity Relationship (QSAR) techniques along with molecular dynamics simulation were employed to screen phytochemical compounds for their ability to inhibit the LasR QS system, a key regulator of virulence in Pseudomonas aeruginosa. This study screened 1652 phytochemicals using the ML‐based QSAR model to identify 52 phytochemicals that had better activity than the control (N‐{[3,5‐dibromo‐2‐(methoxymethoxy)phenyl]methyl}‐2‐nitrobenzamide). The in silico molecular docking approach that targeted LasR identified compounds 5281647, 57331045, and 5281672 with high binding affinity and hydrogen bonds that were comparable to the control (docking score=−10.3 kcal/mol and hydrogen bonds=4). In the 200 ns post‐molecular dynamics simulation, 5281647 exhibited a stable RMSD of 0.25 nm, which was comparable to the control. The maximum number of hydrogen bonds was exhibited by 57331045, while 5281647 and 5281672 consistently exhibited four hydrogen bonds. Overall, the Principal component analysis (PCA) and Free Energy Landscape (FEL) analyses of the complexes demonstrated that these three compounds were in stable states. In comparison to the control (ΔGTOTAL=−39.58 kcal/mol), the cumulative binding free energy (ΔGTOTAL) for 5281647 and 57331045 was −39.95 kcal/mol and −39.25 kcal/mol, respectively. This further confirms the superior binding affinity of the two compounds. Both 5281647 and 57331045 were identified as potent inhibitors of the LasR transcription factor, which is essential for the quorum sensing of Pseudomonas aeruginosa, in the present investigation. These findings underscore the importance of further exploration and optimization of phytochemicals for combating bacterial infections, offering promising avenues for future drug discovery efforts targeting this resilient pathogen.

Pore coarsening mechanism during hot rolling induced by hydrogen gathering in Al-Mg alloy

A novel mechanism for pore coarsening during hot rolling was proposed that the hydrogen in the ingot, driven by non-uniform hydrostatic pressure, accumulates into the tortuous shrinkage cavities at the thickness center of the slab. High pressure hydrogen gas gradually changes the stomatal curvature and finally leads to pore coarsening.

Investigation in improving the Cs-free negative hydrogen ion production with short-pulse low power in the afterglow of pulse-power-modulated plasma sources

Abstract Pulse plasma ion sources have been shown to be capable of achieving high negative hydrogen ion densities ( n H − ) or currents. The fast cooling of the electrons and reduction in the electron density (n e) provide favorable plasma conditions to improve the H− production, with a high density ratio of negative hydrogen ions to electrons during the pulse-off period. The purpose of this research is to further improve the performance of volume-produced H− ion sources based on the pulse power modulation. In this study, a time-modulated negative hydrogen plasma sustained by 10 kHz pulse power at the typical gas pressure of 0.3 Pa was numerically investigated using a global model. The model is compared with measurements obtained in a pulsed radio frequency ion source and shows a reasonable agreement. A steplike low-high power strategy in the active glow period and a short-pulse low power in part of the afterglow period are employed to mitigate overshoot of the electron temperature (T e) in the initial stage of the pulse period and to optimize H− production in the afterglow, respectively. The model predicts that a small-magnitude, short-duration low power operation in the afterglow increases n H − and decreases n e from the onset of the low power until the beginning of the next high power pulse, due to a modest temporary increase in the T e (less than 2 eV). It facilitates dissociative electron attachments and thus H− formation. The reduction in the n e indicates that positive ions lost to the walls cannot be compensated by weak ionization. H− production with a low number of co-extracted electrons can be optimized by adjusting the magnitude and duration of the low power in the afterglow.

Hydrogen Separation Membranes: A Material Perspective

The global energy market is shifting toward renewable, sustainable, and low-carbon hydrogen energy due to global environmental issues, such as rising carbon dioxide emissions, climate change, and global warming. Currently, a majority of hydrogen demands are achieved by steam methane reforming and other conventional processes, which, again, are very carbon-intensive methods, and the hydrogen produced by them needs to be purified prior to their application. Hence, researchers are continuously endeavoring to develop sustainable and efficient methods for hydrogen generation and purification. Membrane-based gas-separation technologies were proven to be more efficient than conventional technologies. This review explores the transition from conventional separation techniques, such as pressure swing adsorption and cryogenic distillation, to advanced membrane-based technologies with high selectivity and efficiency for hydrogen purification. Major emphasis is placed on various membrane materials and their corresponding membrane performance. First, we discuss various metal membranes, including dense, alloyed, and amorphous metal membranes, which exhibit high hydrogen solubility and selectivity. Further, various inorganic membranes, such as zeolites, silica, and CMSMs, are also discussed. Major emphasis is placed on the development of polymeric materials and membranes for the selective separation of hydrogen from CH4, CO2, and N2. In addition, cutting-edge mixed-matrix membranes are also delineated, which involve the incorporation of inorganic fillers to improve performance. This review provides a comprehensive overview of advancements in gas-separation membranes and membrane materials in terms of hydrogen selectivity, permeability, and durability in practical applications. By analyzing various conventional and advanced technologies, this review provides a comprehensive material perspective on hydrogen separation membranes, thereby endorsing hydrogen energy for a sustainable future.

The fracture and perforation failure analysis of downhole tubes

：The downhole tubes were fractured and perforated after 5 years of shut-in due to high water cuts. This study employs a comprehensive array of analytical techniques to investigate the mechanisms behind fractures and perforations. Utilizing non-destructive testing (NDT), direct reading spectrometer, tensile strength testing machine, impact testing machine, optical microscope (OM), macroscopic fracture morphology observation, scanning electron microscope (SEM) and energy spectrum analysis (EDS), and sulfide stress corrosion cracking (SSCC) was studied. The reason for the fracture of the tubing is that under the condition of low pH value, high hydrogen sulfide environment, the tubing is fractured due to stress concentration caused by cracks in the outer thread relief groove. The perforation of the inner tube wall was caused by gradual wall thickness reduction under the influence of H2S, CO2, and Cl−, resulting in fouling and eventual perforation. To prevent tube corrosion during long-term shut-in, it is recommended to inject crude oil or diesel into the well.

Hydrothermal liquefaction of southern yellow pine with downstream processing for improved fuel grade chemicals production

The hydrothermal liquefaction (HTL) technique for liquefying lignocellulose biomass feedstock is often associated with low biocrude yield and poor fuel properties. This study examined the HTL of southern yellow pine sawdust and the hydrotreatment (HYD) of produced biocrudes in an effort to address these challenges. Pine HTL treatment was performed within water and water–ethanol mixed reaction medium at 250, 300, and 350℃ temperatures using metallic iron (Fe) as a catalyst. The rising reaction temperature in a water medium and increasing ethanol content in a mixed reaction medium were found to be effective in enhancing the biocrude yield from the non-catalytic pine HTL process. Maximum non-catalytic biocrude yield of 18 wt.% was produced in water at 350℃, whereas the ethanol and water (1:1 on mass basis) mixture generated the highest biocrude yield of 34 wt.% at 300℃ without any catalyst. The iron catalyst facilitated a maximum of 29 wt.% of biocrude yield as opposed to 18 wt.% without the catalyst at 350℃ in water. The use of an iron catalyst also raised the calorific value of produced biocrudes by 2.5–14 % within 250-350℃ in both water and water–ethanol media. The catalytic and non-catalytic biocrude products were chosen to undergo HYD treatment at 400 °C under high hydrogen pressure (initial 1000 psi) using an alumina-supported cobalt-molybdenum catalyst. The HYD treatment reduced the oxygen content of upgraded oils by 36–60 % compared to the parent HTL biocrudes with 35–37 MJ/kg calorific values. The simulated distillation detected the maximum gasoline range compounds in upgraded oil from catalyst and water–ethanol conditions, whereas the GC–MS analysis revealed the production of increased aromatic hydrocarbons in all upgraded HYD oils. This work has demonstrated the potential of ethanol and inexpensive iron catalyst in enhancing the biocrude production from pine, which could be upgraded to better fuel using the HYD process.

Orientation engineering of magnesium alloy: A review

Mg and its alloys have garnered significant attention due to their exceptional properties, including low density, good damping capacity, biocompatibility, recyclability, and high hydrogen storage capacity. These attributes position them as promising materials for applications in aerospace, transportation, electronics, and biomedical. The wrought Mg alloys, particularly in sheet form, are important materials for manufacturing lightweight structural components. However, their application is often constrained by relatively low room temperature formability. Preferred orientation, also known as texture, plays a crucial role in determining the plasticity and formability of Mg alloys. In this paper, we propose the concept of “orientation engineering”, which involves controlling the crystallographic orientation, thereby enhancing the plasticity and formability of Mg alloys. This review addresses two main aspects: firstly, it systematically explores how preferred orientation influences the plasticity and formability of Mg alloys, providing a foundation for orientation engineering. Secondly, it comprehensively introduces the development of methods to control grain orientation distribution, including alloying, pre-deformation, and asymmetric processing. This review might enhance the scientific understanding of orientation modification in Mg alloys and offer valuable guidance for future research on high-formability Mg alloys.

Simulated hydrogen diffusion in diamond grain boundaries

To evaluate hydrogen diffusion within diamond, a series of molecular dynamics simulations have been carried out in which diffusion coefficients and activation energies were determined. Diamond grown via chemical vapour deposition (CVD) contains a high hydrogen concentration within grain boundaries, because of this, common tilt grain boundaries were recreated from transmission electron microscopy images taken from literature. Diffusion coefficients of hydrogen placed within the grain boundary were estimated and compared to the bulk diffusion. Unlike many crystalline structures, some grain boundaries presented limited diffusion when compared to the bulk. Diffusion characteristics of grain boundaries are thought to be a result of channelling effects combined with the formation of sp3C-H bonds with sp2 carbon present within some grain boundaries - increasing and decreasing diffusion rates respectively. Potential wells were observed across some but not all the grain boundaries resulting in hydrogen trapping and anisotropic diffusion.

Design and test of a module of a breathable Electrostatic Shield for the MITICA 1 MV negative ion Beam Source

The electrical insulation of the MITICA Beam Source at 1 MV is a challenging issue, which has not been fully addressed so far on the basis of experimental results and of theoretical models available in literature. Being MITICA the full-size prototype of the Heating Neutral Beam Injector for the ITER fusion experiment, its electrical insulation is constituted just by vacuum gaps and alumina insulators, since other insulating materials such as SF6 gas or fibreglass-reinforced plastic (FRP) would be quickly degraded by the expected neutron flux produced by fusion reaction. Extrapolations based on HV tests on reduced-scale models have recently indicated the risk of electrical breakdowns in the vacuum gap between electrodes nominally operating at -1 MV and the vacuum vessel (at ground potential). The risk of electrical breakdown can be mitigated by introducing an intermediate Electrostatic Shield (ES), which essentially is an equipotential (metallic) enclosure surrounding the HV electrode, so as to divide the vacuum gap in two independent insulating gaps of 400 kV and 600 kV respectively. However, for optimal negative ion production, the ion source shall operate in H2 or D2 at a pressure of ∼ 0.3 Pa and unavoidably produces a flow of gas leaking out in the surrounding vacuum. Thus, the presence of an intermediate shield can substantially increase the background gas pressure in the vacuum gaps, and, due to the large gap length (0.6 m), exacerbate the risk of breakdown when the pressure approaches the conditions of Paschen-type discharges. In addition to this, RF-induced breakdowns were found on the rear side of the ion source during the operation of the prototype source SPIDER, which were somewhat correlated to a relatively high hydrogen pressure in that area. For these reasons, a structure capable of constituting a full equipotential barrier all around the BS and, at the same time, having sufficient gas conductivity (breathability) to allow efficient pumping of background gas, has been designed. In the first part of the paper, the requirements and design optimization of a breathable module of the intermediate ES are described. Then, an experimental campaign for the validation of the electrode implementation the test configurations and the experimental procedure is discussed.

Enhancing the dehydrogenation properties of LiAlH4 through the addition of ZrF4 for solid-state hydrogen storage

Hydrogen energy is emerging as an essential alternative to fossil fuels due to its clean energy profile, generating energy without greenhouse gas emissions. Solid-state hydrogen storage, particularly using complex hydrides like LiAlH4, holds promise due to high hydrogen capacities. However, practical applications of LiAlH4 face obstacles due to slow dehydrogenation kinetics and high decomposition temperatures. This study investigates the catalytic effect of ZrF4 on LiAlH4 to improve hydrogen storage properties. Incorporating 10wt.% ZrF4 has significantly lowered the onset desorption temperature from 160 °C to 80 °C. Desoption kinetic result showed that the addition of 10wt.% ZrF4 can enables the release of 5.6wt.% hydrogen in 120min at 100 °C, which is 50 times faster than in undoped samples. X-ray diffraction analysis indicated that ZrF4 facilitated the in-situ formation of Al3Zr and LiF phases during dehydrogenation, thereby enhancing catalytic efficiency. The desorption activation energies for first two reactions decreased significantly by ~ 16kJ/mol and ~24kJ/mol with ZrF4 doping. These findings suggest that ZrF4 effectively improves the hydrogen storage properties of LiAlH4, positioning it as a potential catalyst for solid-state hydrogen storage systems.