Activation Energy Of Reaction Research Articles

Hydrogen storage properties of MgH2 + Mg2NiH4–Co/C ternary nanocomposite

The application of ternary nanocomposite synergetic catalysis has proven to be an effective modification strategy for enhancing MgH2 hydrogen storage performance. The ternary magnesium-based hydrogen storage alloy, composed of MgH2+Mg2NiH4–Co/C, is successfully prepared and characterized. Through the optimized preparation process and the optimal ratio, it is observed that the catalyst Mg2NiH4–Co/C significantly reduces the reaction activation energy, resulting in a the initial hydrogen desorption temperature is approximately 60 °C lower than that of pure MgH2. The enhanced hydrogen storage properties are attributed to the synergistic catalytic effect of carbon (C) combined with the formation of Mg2Ni and Mg2Co facilitated by Ni and Co elements. Furthermore, the reversible phase transitions of Mg2Co/Mg2CoH5 and Mg2Ni/Mg2NiH4 serve as "hydrogen pumps" further aiding in hydrogen storage. This study extends the investigation of the synergistic catalytic effect of ternary nanocomposites to enhance the hydrogen storage performance of alloys.

Thermodynamic, chemical, and electrochemical studies of Aloe ferox Mill extract as a naturally developing copper corrosion inhibitor in HCl solution

Copper can be susceptible to corrosion in acidic cleaning solutions for desalination system, especially if the solution is highly concentrated or if the cleaning process involves extended exposure to the acid. In the current work, Aloe ferox Mill (AFM extract) can be used as a natural origin corrosion inhibitor for copper in 1.0 M HCl solution. The corrosion mitigation qualities of AFM extract were assessed by means of electrochemical, gravimetric, and surface examinations. AFM extract is a mixed-type inhibitor, based on polarization research findings. The inhibitory effectiveness of AFM extract rises with concentration, reaching its maximum level (93.3%) at 250 mg L–1. The inclusion of AFM extract raises the activation energy for the corrosion reaction from 7.15 kJ mol–1 (blank solution) to 28.6 kJ mol–1 (at 250 mg L–1 AFM extract).

Time-resolved surface reaction kinetics in the pressure gap.

We extend the use of our recently developed Near-Ambient Pressure Velocity Map Imaging (NAP-VMI) technique to study the kinetics and dynamics of catalytic reactions in the pressure gap. As an example, we show that NAP-VMI combined with molecular beam surface scattering allows the direct measurement of time- and velocity-resolved kinetics of the scattering and oxidation of CO on the Pd(110) surface with oxygen pressures at the surface up to 1 × 10-5 mbar, where different metastable surface structures form. Our results show that the c(2 × 4) oxide structure formed at low O2 pressure is highly active for CO oxidation. The velocity distribution of the CO2 products shows the presence of two reaction channels, which we attribute to reactions starting from two distinct but rapidly interconverting CO binding sites. The effective CO oxidation reaction activation energy is Er = (1.0 ± 0.13) eV. The CO2 production is suppressed at higher O2 pressure due to the number of antiphase domain boundaries increasing, and the missing row sites are filled by O-atoms at O2 pressures approaching 1 × 10-6 mbar. Filling of these sites by O-atoms reduces the CO surface lifetime, meaning the surface oxide is inactive for CO oxidation. We briefly outline further developments planned for the NAP-VMI and its application to other types of experiments.

Catalytic cyanate resin with polysulfide cation catalyst and its ultra‐high molecular weight polyethylene fiber composites for radome

AbstractCyanate (CE) resin and ultrahigh‐molecular‐weight polyethylene (UHMWPE) fiber are respectively important matrix and reinforcing material for lightweight and high wave‐transparent composites. However, the preparation and application of the composites is limited by the mismatch of molding temperature between CE resin and UHMWPE fiber. The best method to solve this problem is to catalyze the CE resin curing reaction and reduce its molding temperature from 270 to 135°C, which is the upper heat‐resistance temperature of UHMWPE fiber. In this study, the polysulfide catalyst (PSC) was used to catalyze CE resin curing reaction, reduce the curing reaction activation energy and the molding temperature. The apparent activation energy of the CE‐PSC resin decreases from 107.2 to 60.7 kJ mol−1, and the glass transition temperature of the CE‐PSC resin is 257.2°C, flexural strength and tensile strength are 120.2 and 60.8 MPa, respectively. As a result, the CE‐PSC/UHMWPE fiber composites, which are molded at the matching temperature of 135°C, have low density of 1.05 g cm−3, low dielectric constant of 2.4, low dielectric loss of 0.006, and high wave transmittance of 92.2%. Therefore, the CE‐PSC/UHMWPE fiber composites have wide application prospect in the field of light weight and high wave‐transparent composites.Highlights A novel catalytic CE resin can be cured at 135°C with low dielectric properties. The processing temperature mismatch between CE and UHMWPE fiber was solved. Catalytic CE/UHMWPE composites have lightweight and high wave‐transparent properties.

Direct Synthesis of Calcium Lactate through the Reaction of Glycerol with Calcium Hydroxide Catalyzed by Bimetallic AuCu/SiO2 Nanocatalysts

Bimetallic AuCu/SiO2 nanosized catalysts were prepared using the wet chemical reduction technique. From among Au0.1–1.5Cu10/SiO2 catalysts, the Au0.5Cu10/SiO2 catalyst gave the highest yield of calcium lactate of 87% at a glycerol conversion of 96% when the reaction of glycerol with calcium hydroxide at a mole ratio of calcium hydroxide to glycerol of 0.8:1 was conducted under an anaerobic atmosphere at 200 °C for 2 h. The interactions between metallic Au0 and Cu0 nanoparticles facilitate calcium lactate formation. The simulation of glycerol consumption rate with an empirical power-function reaction kinetics equation yielded a reaction activation energy of 44.3 kJ∙mol−1, revealing that the catalytic reaction of glycerol with calcium hydroxide to calcium lactate can be conducted by overcoming a mild energy barrier. The synthesis of calcium lactate through the catalytic reaction of glycerol with calcium hydroxide on a bimetallic AuCu/SiO2 nanosized catalyst under a safe anaerobic atmosphere is an alternative to the conventional calcium lactate production technique through the reaction of expensive lactic acid with calcium hydroxide.

A continuous melt extrusion approach toward polyethylene‐based vitrimers with improved crosslinking and performance

AbstractReported herein is a continuous one‐step melt extrusion approach for high‐density polyethylene (HDPE) vitrimers. A grafting agent and a coagent were used to produce high‐performing vitrimers. Maleic anhydride (MA) served as a reactive agent to facilitate crosslinking, while dimethyl maleate (DM) acted as a grafting enhancer by reducing the surface energy of HDPE grafted with MA. For comparison, MA alone was also tested as a grafting agent. The vitrimers obtained displayed superior mechanical properties compared with HDPE. The storage modulus, as well as crystallinity, were determined for the HDPE vitrimers. These vitrimers are reprocessable, thus supporting recycling efforts despite their crosslinked nature, owing to very fast relaxation due to low activation energy for the transesterification reaction. Consequently, these vitrimers are not only recyclable but also exhibit enhanced thermal and mechanical properties compared with conventional HDPE.

Preparation and Properties of Epoxy Adhesives with Fast Curing at Room Temperature and Low-Temperature Resistance.

Developing a highly efficient multifunctional epoxy adhesive is still an enormous challenge, which can rapidly cure at room temperature and has excellent low-temperature resistance performance and is crucial for the epoxy adhesive and electrical sealing fields during severe cold seasons. Herein, diglycidyl phthalate (DP) was synthesized with phthalic anhydride (PA) and epichlorohydrin (ECH) to enhance the curing rate and low-temperature resistance of bisphenol A diglycidyl ether (DGEBA) adhesive. The modified DP/DGEBA adhesives were systematically analyzed by gel time, mechanical properties, and aging resistance (time, temperature, and dry/wet treatment). The results showed that DP with highly active ester groups significantly accelerates the curing speed of DP/DGEBA. DP's rigid aromatic ring-benzene ring and flexible group-ester group gave the adhesive better low-temperature resistance. When the addition of DP was 10 wt % (based on the mass of DGEBA), the gel time of DP/DGEBA epoxy adhesives was reduced by 58 min compared to unmodified DGEBA epoxy adhesive, and after aging at low temperature (-20 °C) for 7 days, the tensile shear strengths of polyvinyl chloride (PVC) and aluminum plate increased by 76.2 and 80.6%, respectively. The results of non-isothermal curing kinetics and dynamic mechanical analysis suggested that when the amount of DP was 10 wt %, the reaction activation energy of DP/DGEBA epoxy adhesive decreased by 4.0%, and the cross-linking density increased by 8.9%. Moreover, the toughness of the modified adhesive was also improved. This study opens up a feasible way for the development of a low temperature-resistant epoxy adhesive cured rapidly at room temperature in practical application.

Construction of [P4442]2[IDA]/Zirconium Metal‐Organic Framework (UiO‐66) for Curing with Epoxy Resin

Curing agents for epoxy resin (EP) are one of the most important branches in the polymer materials field due to their enormous potential in many fields, but constructing them in a well‐controlled curing temperature remains challenging. Herein, a novel curing agent is constructed by the zirconium metal‐organic framework (UiO‐66) and [P4442]2[IDA] through an impregnation method. [P4442]2[IDA]@UiO‐66 is utilized as a functional nanofiller and curing agent to construct the [P4442]2[IDA]@UiO‐66/EP nanocomposites. The chemical structures of [P4442]2[IDA]@UiO‐66 were investigated by XRD, SEM, DSC, and TG characterizations. The various [P4442]2[IDA]@UiO‐66 with different loading amounts of [P4442]2[IDA] were used to investigate the curing behaviors of the EP‐51. The DSC results confirm that the curing temperature of the [P4442]2[IDA]@UiO‐66/EP is higher than that of [P4442]2[IDA]/EP. In addition, the kinetic parameters and the activation energy of the curing reaction were acquired according to the fitting of Kissinger equation and Ozawa equation. The drying time of [P4442]2[IDA]@UiO‐66/EP system at 40 °C was enhanced 17 times compare to that of [P4442]2[IDA]/EP system. This study opens new avenues for the rational design of EP nanocomposites by employing ionic liquids@MOFs composite materials as curing agent for wide engineering applications.

New design of eco-friendly Catalytic Electro - Photo Desulfurization process for real diesel fuel

Recently, due to the refineries processes considerations and environmental issues major limitations have been imposed on the sulfur compounds presented in petroleum distillates. Therefore, to reduce the sulfur compounds to minimum levels and to meet the global legislations, many of techniques were used, among them electro chemical photo desulfurization technique was used here. In this study, DBT was removed using electro chemical photo desulfurization over electrodes of titanium and stainless steel using Fe2O3/TiO2 as a catalyst under different temperatures (45, 60, 75 ℃), current density (10, 15, 20 A/m2), electrolyte concentration (25, 35, 45 wt%). The catalyst was characterized by different advanced surface techniques such as N2- adsorption-desorption, SEM-EDX, FTIR, and XRD. The reaction kinetic parameters (reaction order and activation energy) were estimated based on the experimental runs. According to the results obtained, this technique was revealed an efficient method with highest removal of 93.79% achieved using Fe2O3/TiO2 under the best of experimental operating conditions at 75 ℃, 20 A/m2 and 35 wt% of temperature, current density and electrolyte concentration respectively. It can be concluded that the electro chemical photo oxidative desulfurization reaction followed was pseudo 1st order and 41.67 kJ/mole activation energy over titanium dioxides catalyst.

Synthesis of Cu-MOF-derived complex copper–chromium oxides and their catalytic study on the thermal decomposition of ammonium perchlorate

In this work, a series of complex copper-chromium oxides were prepared by adjusting the molar ratio of Cr3+/Cu2+ using MOF-199 as a template. X-ray diffraction (XRD), scanning electron microscopy (SEM), Transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS) were used to characterize the structure, microscopic morphology and valence information of the samples. The specific surface area of the sample was estimated by the Brunauer-Emmett-Teller method (BET), and the pore size parameters of the sample were obtained by using the Barrett-Joyner-Halenda (BJH) model. The effect of the samples on the thermal decomposition process of ammonium perchlorate (AP) was investigated by differential scanning calorimetry-thermogravimetric analysis. The results show that the copper and chromium oxides in the complex exhibit good catalytic effects. Among them, CuCr(0.8) had the best catalytic effect, reducing the peak pyrolysis temperature of AP by 95.7 °C, increasing the heat release by 817 J/g, and reducing the reaction activation energy by 62.4 kJ/mol. Real-time FTIR was used to characterize the gas products during the thermal decomposition of AP, and the gas products of AP with CuCr(0.8) catalyst were different from those of pure AP, which may also be the reason for the increase of AP heat release after adding CuCr(0.8) catalyst.

Preparation of W-Ni-Cu Alloy Powder by Hydrogen Reduction of Metal Oxides

The effect of powder processing on the microstructure and sinterability of the heavy alloy W-Ni-Cu was investigated. The heavy alloy powders were prepared by the ball milling and hydrogen reduction of metal oxide powders. As the milling time increased, the size of the powder mixture decreased and at 5 h of milling was found to be about 2.5 μm. Microstructural analysis revealed that the powder mixture was changed to W and NiCu alloys with an average particle size of about 200 nm after hydrogen reduction at 800°C for 2 h. The reduction kinetics of the oxide powder mixture was evaluated by the amount of peak shift with heating rates using TGA in a N<sub>2</sub>-10% H<sub>2</sub> atmosphere. The activation energy of the reduction reaction, calculated from the slope of the Kissinger plot, was measured to be 42.8 kJ/mol for CuO, 57.9 kJ/mol for NiO, and 50.1~112.6 for kJ/mol WO<sub>3</sub>. The relative densities of the heavy alloy sintered at 1100oC and 1200oC using oxide powder were 81.4% and 96.0%, while the specimen using metal powder as a raw material showed a relatively low value of 67% and an inhomogeneous microstructure. It was explained that the changes in sintered microstructure with different powder synthesis methods are mainly due to the powder characteristics, such as the size of the particles of the initial mixed powder.

Thermal and calorimetric investigations of some vegetative fuels

AbstractBushfires pose a significant threat to numerous countries, often causing vast property damages and loss of lives. Efforts to combat and manage these fires heavily rely on predicting the fires' rate of spread and intensity. A significant component of these predictions involves understanding the thermophysical characteristics of vegetative fuels. The accuracy of predictive models (especially physical models) also depends on obtaining precise thermophysical and combustion parameters. This research aims to provide a comprehensive set of thermal degradation and combustion parameters for surface and near‐surface fuel samples collected during prescribed fire experiment conducted in April 2022 in Little Desert National Park, Victoria, Australia. Firstly, fuel properties like fuel height, moisture content, bulk density, fuel load and heat of combustion were meticulously characterized for both surface and near‐surface samples. Then activation energies for degradation reactions were determined using the Flynn–Wall–Ozawa method and for the determination of pre‐exponential factors, in most cases these reactions closely aligned with a Second order model. This was followed by determination of other parameters such as heat of reaction, specific heat and conductivity. It was found that the density, activation energy and heat of combustion did not vary significantly across the six samples under question. The comprehensive set of obtained parameters will likely help to facilitate better predictions in fire propagation modelling.

Analysis of Kinetic and Ohmic Resistances in PEM Water Electrolysis through Reference Electrode Measurements

We investigated a three electrode setup utilized in a temperature variation study to extract the activation energy for the half-cell reactions in PEM water electrolysis and the contributions of electronic resistances to ohmic resistance. The reference electrode configuration used in this investigation is an improved version of a setup previously introduced by our group. Enhancements have been made to minimize the influence of the reference electrode and improve the accuracy of electrochemical impedance spectroscopy.

Construction of Au quantum dots/nitrogen-defect-enriched graphite carbon nitride heterostructure via photo-deposition towards enhanced nitric oxide photooxidation

The challenge of mitigating pollution stemming from industrial exhaust emissions is a pressing issue in both academia and industry. This study presents the successful synthesis of nitrogen-defect-enriched graphite carbon nitride (g-C3N4) using a two-step calcination technique. Furthermore, a g-C3N4-Au heterostructure was fabricated through the photo-deposited Au quantum dots (QDs). When subjected to visible light irradiation, this heterostructure exhibited robust nitric oxide (NO) photooxidation activity and stability. With its fluffy, porous structure and large surface area, the nitrogen-defect-enriched g-C3N4 provides more active sites for photooxidation processes. The ability of g-C3N4 to absorb visible light is enhanced by the local surface plasmon resonance (LSPR) effect of Au QDs. Additionally, the lifetime of photogenerated charge carriers is extended by the presence of N defects and Au, which effectively prevent photogenerated electron-hole pairs from recombining during the photooxidation process. Moreover, the oxidation pathway of NO was analyzed through In-situ Fourier transform infrared (FT-IR) spectroscopy and Density Functional Theory (DFT) calculation. Computational findings revealed that the introduction of Au QDs decreases the activation energy of the oxidation reaction, thereby facilitating its occurrence while diminishing the formation of intermediate products. As a result, NO is predominantly converted to nitrate (NO3−). This work unveils a novel approach to constructing semiconductor-cocatalyst heterostructures and elucidates their role in NO photooxidation.

Kinetic investigation of Sulfur corrosion: first principles calculations

The expressions of two important kinetic parameters (chemical activation energy of electrode reaction and absolute potential of equilibrium state) that determine the reaction rate during the anodic dissolution reaction are derived from the thermodynamic and kinetic relationships of the anodic dissolution reaction, the relationship between absolute potential and current density in the anode dissolution process is constructed. Under the framework of first principles, the calculation model of the electrochemical corrosion anodic dissolution reaction is proposed. Density functional theory study of the process of dissolving Fe atoms from the surface of Fe(111) alloy models in vacuum and explicit water molecules. The addition of water molecules and sulfur atoms promotes charge transfer during dissolution and increases the corrosion rate, while water molecules reduce the work function, while S goes increases the work function. Through the corrosion current density model of activation energy, the role of alloy dissolution kinetics with different alloys added was explored. The analysis shows that the addition of Mn and Cr can greatly reduce the anodic corrosion rate and increase the corrosion resistance of Fe.

Regulation of Lewis acid sites on ZnO/SiW11Co for tunable photocatalytic activity toward water remediation

The function of surface acidity in catalytic reactions has been well studied in the field of conventional catalysis, nevertheless, regulating surface acidic sites and unveiling its roles during heterogeneous photocatalysis has been less frequently reported. To address this issue, we constructed a novel heterojunction photocatalyst of ZnO/SiW11Co with abundant Lewis acid sites for wastewater treatment. Under visible light irradiation, the optimal ZnO/SiW11Co was found to have the highest photocatalytic activity, achieving a degradation efficiency of 97.7% for Rhodamine B (RhB), 96.1% for tetracycline (TC), and 91.4% for methyl orange (MO). The RhB removal rate remained at 91.3% even after five cycles, indicating excellent stability and practicality of ZnO/SiW11Co. By compositing with SiW11Co, a typical polyoxometalates with unique super acid properties, ZnO/SiW11Co formed plentiful surface Lewis acid sites, as confirmed by the pyridine adsorption FT-IR and NH3-TPD. The as-formed Lewis acid sites could provide more active sites, making it easier for reactants to coordinate to the photocatalyst surface, which reduced the activation energy of photocatalytic reactions and accelerate RhB removal. Density functional theory (DFT) calculations unveiled the redistribution of electron-hole pairs, optimizing the light absorption and charge separation efficiency, which obeyed a Z-scheme mechanism. Combined active species capture experiments and electron spin resonance, •O2−, h+, and •OH were the main active substances for the photocatalytic degradation of RhB. Besides, the possible degradation pathways for RhB were analyzed using liquid chromatography-mass spectrometry (LC-MS). The work provided useful strategy for the design of high-performance photocatalysts via regulating surface Lewis acid sites toward water remediation.

Efficient degradation of vulcanized natural rubber into liquid rubber by catalytic oxidation

Waste tire rubber based on natural rubber (NR) represents an abundant feedstock for the production of valuable products. This study investigated an efficient approach to convert NR vulcanizates into liquid rubber with the number-average molar masses of 1.3 × 104 g/mol. Compared to the anaerobic liquefaction at 300°C for 3 min, NR vulcanizates were liquefied efficiently at 210°C for 3 min by thermo-oxidative degradation catalyzed by manganese (II) stearate. The apparent activation energy of the NR degradation reaction decreased from 470.8 kJ/mol to 208.2 kJ/mol with catalysis, which was attributed to the formation of a coordination complex between catalysts and peroxides via the single-electron transfer redox reaction, leading to the catalytic oxidative degradation of NR vulcanizates. The main chain scission and crosslink scission occurred simultaneously during the degradation process, and the main chain scission was the primary catalytic oxidation reaction according to the Horikx theory. In addition, the obtained liquid rubber contained carbonyls, ether linkages, and sulfoxide groups, as proved by FTIR and 13C-NMR. The catalytic oxidative degradation mechanism of NR vulcanizates was proposed based on the chemical structure of products and simulation results. The efficient method was proposed to highly facilitate the recycling and valorization of NR-based waste tire rubber.

Isothermal Reduction and Comparative Analysis of Reaction Kinetics of Sponge Iron Produced from Heamatite-Charcoal Reaction Using Non-contact Direct Reduction Method

The challenge of making sponge iron, or direct reduced iron (DRI), is hard to overstate. These are a key feed for metallurgical operations while iron extraction sets these limits, which include scarcity of metallurgical coke, poor environmental impact, and high production cost. Thus, the non-contact direct reduction process of DRIs has the potential to significantly reduce carbon deposition and CO2 emission from the ironmaking process. This work produced sponge iron from commercially acquired hematite ore using an alternative reducing agent (i.e. charcoal) under specified isothermal conditions. Comparative analysis of reaction kinetics models including Ginstein−Brounshtein and Shrinking core models was also performed to ascertain the resistances that control the reaction rate for reduction degree up to 98.1%. The reduction kinetics were found to be described by reaction control time and activation energies based on a shrinking core model as the reduction time lasted for 120minutes at temperatures 843~1273K. At temperatures above 973~1073K, the rate-limiting step was found to be solely an interfacial chemical reaction process, with an apparent activation energy of 196.1kJ/mol. In addition, a slowing trend was observed for iron ore sample sizes 10-20mm as a result of ash layer infiltration around the inner-core structure of the DRI metal matrix. The DRI morphological characteristics were performed using Scanning Electron Microscopy (SEM) and Electron Dispersive Spectrometry (EDS) to ascertain the mineralogical and morphological properties of the DRI samples. The XRF analysis confirms that the raw iron ore sample is hematite. Its iron content is 70.04% metallic iron (TFe) which has 83.59% Fe2O3 The SEM/EDS image also revealed the presence of micropores on the DRI morphology. This indicates that the reduction ratio and swelling extent rise with the temperature and time. This happens for all DRI sizes. However, the EDS result confirms the presence of gangue elements within the DRI metal matrix and mineralogical structure. The DRI contains very high silicon content up to 33.90%. So, a fluxing experiment is needed using limestone (CaCO3) or quicklime (CaO) quicklime to remove gangue (silicate, aluminate) from the DRI matrix. At the set reduction temperatures, the largest metallization degree of 93.05% at 1273K for a reduction time of 120mins was achieved. This showed that the overall reduction process still follows the expected chronological order since the NDR process uses CO gas from preheated charcoal. This makes DRI be produced from raw hematite under non-contact reduction bases. Therefore, the NDR technique offers a viable option for sponge iron production in modern-day iron and steelmaking processes.

Amorphous RhOx decorated black indium oxide for rapid and flexible NO2 detection at room temperature

This paper focuses on the preparation and characterization of a composite material made from rhodium oxide amorphous-decorated black indium oxide (RhOx/B-In2O3) for use in MEMS gas sensors. The sensors were utilized for the detection of NO2 gas at room temperature, and the results demonstrate that the RhOx/B-In2O3 sensor exhibits excellent gas selectivity, high response, and extremely short response/recovery times (8s/17s) to 5 ppm NO2 gas at room temperature. Additionally, a flexible NO2 gas sensor based on the optimized RhOx/B-In2O3 composite was fabricated to expand its application. One of the unique aspects of the RhOx/B-In2O3 material is the existence of defects, which allows for greater adsorption of NO2 gas. This feature contributes to the increased gas selectivity seen in the B-In2O3 material as compared with common In2O3. The chemical sensitization and electron-rich properties of amorphous RhOx further enhance the gas-sensing performance of the material by reducing the reaction activation energy and increasing surface-adsorbed oxygen. Overall, the results demonstrate the potential of the RhOx/B-In2O3 composite material for use in advanced gas-sensing technologies.

Core-shell structured α-AlH3/Fe2O3 thermite with improved heat-release and combustion performance

Thermites are widely used in propellants, explosives and ignition materials because of their high heat release rate and good combustion efficiency. Structural control over thermites to achieve improved performance leads to a promising research area. Among these, core-shell structured composites have attracted wide attention due to their excellent properties and close contact among components. Herein, core-shell structured α-AlH3/Fe2O3 thermites were prepared, which exhibit high heat-release and excellent combustion performance. At an equivalence ratio of 2.0, the core-shell structured α-AlH3/Fe2O3 has the most heat release (1213.8 J/g) and the lowest reaction activation energy (147.5 kJ/mol). The ignited combustion performance of α-AlH3/Fe2O3 was notably strengthened by the shorter ignition delay period (11 ms). Interestingly, the core-shell structured α-AlH3/Fe2O3 was less sensitive to electrostatic discharge, which suggests that the core-shell structured α-AlH3/Fe2O3 reaches the goal of high energy release and electrostatic safety. The core-shell thermite system with α-AlH3 as metal fuel could provide an efficient alternative to hunt for thermites with high reactivity.