Ab initio and periodic DFT investigation of hydrogen storage on light metal-decorated MOF-5

The effect of light metal (M = Li, Be, Mg, and Al) decoration on the stability of metal organic framework MOF-5 and its hydrogen adsorption is investigated by ab initio and periodic density functional theory (DFT) calculations by employing models of the form BDC:M₂:nH₂ and MOF-5:M₂:nH₂, where BDC stands for the benzenedicarboxylate organic linker and MOF-5 represents the primitive unit cell. The suitability of the periodic DFT method employing the GGA-PBE functional is tested against MP2/6-311 + G* and MP2/cc-pVTZ molecular calculations. A correlation between the charge transfer and interaction energies is revealed. The metal-MOF-5 interactions are analyzed using the frontier molecular orbital approach. Difference charge density plots show that H₂ molecules get polarized due to the charge generated on the metal atom adsorbed over the BDC linker, resulting in electrostatic guest-host interactions.Our solid state results show that amongst the four metal atoms, Mg and Be decoration does not stabilize the MOF-5 to any significant extent. Li and Al decoration strengthened the H₂-MOF-5 interactions relative to the pure MOF-5 exhibited by the enhanced binding energies. The hydrogen binding energies for the Li- and Al-decorated MOF-5 were found to be sensible for allowing reversible hydrogen storage at ambient temperatures. A high hydrogen uptake of 4.3 wt.% and 3.9 wt.% is also predicted for the Li- and Al-decorated MOF-5, respectively.     

Computational exploration of magnesium-decorated carbon nitride (g-C3N4) monolayer as advanced energy storage materials

Density functional theory (DFT) computational studies were conducted to explore the hydrogen storage performance of a monolayer material that is built on the base of carbon nitride (g-C₃N₄, heptazine structure) with decoration by magnesium (Mg). We found that a 2 × 2 supercell can bind with four Mg atoms. The electronic charges of Mg atoms were transferred to the g-C₃N₄ monolayer, and thus a partial electropositivity on each adsorbed Mg atom was formed, indicating a potential improvement in conductivity. This subsequently causes the hydrogen molecules’ polarization, so that these hydrogen molecules can be efficiently adsorbed via both van der Waals and electrostatic interactions. To note, the configurations of the adsorbed hydrogen molecules were also elucidated, and we found that most adsorbed hydrogen molecules tend to be vertical to the sheet plane. Such a phenomenon is due to the electronic potential distribution. In average, each adsorbed Mg atom can adsorb 1–9 hydrogen molecules with adsorption energies that are ranged from ?0.25 eV to ?0.1 eV. Moreover, we realised that the nitrogen atom can also serve as an active site for hydrogen adsorption. The hydrogen storage capacity of this Mg-decorated g-C₃N₄ is close to 7.96 wt %, which is much higher than the target value of 5.5 wt % proposed by the U.S. department of energy (DOE) in 2020 [1]. The finding in this study indicates a promising carbon-based material for energy storage, and in the future, we hope to develop more advanced materials along this direction.     

A model study of effect of M = Li,Na, Be,Mg, and Al ion decoration on hydrogen adsorption of metal-organic framework-5

The effect of light metal ion decoration of the organic linker in metal-organic framework MOF-5 on its hydrogen adsorption with respect to its hydrogen binding energy (ΔB.E.) and gravimetric storage capacity is examined theoretically by employing models of the form MC₆H₆:nH₂ where M = Li⁺, Na⁺, Be²⁺, Mg²⁺, and Al³⁺. A systematic investigation of the suitability of DFT functionals for studying such systems is also carried out. Our results show that the interaction energy (ΔE) of the metal ion M with the benzene ring, ΔB.E., and charge transfer (Q_trans) from the metal to benzene ring exhibit the same increasing order: Na⁺ < Li⁺ < Mg²⁺ < Be²⁺ < Al³⁺. Organic linker decoration with the above metal ions strengthened H₂-MOF-5 interactions relative to its pure state. However, amongst these ions only Mg²⁺ ion resulted in ΔB.E. magnitudes that were optimal for allowing room temperature hydrogen storage applications of MOF-5. A much higher gravimetric storage capacity (6.15 wt.% H₂) is also predicted for Mg²⁺-decorated MOF-5 as compared to both pure MOF-5 and Li⁺-decorated MOF-5.     

Simulation of hydrogen storage tank packed with metal-organic framework

Hydrogen adsorption in high surface metal-organic framework (MOF) has generated significant interest over the past decade. We studied hydrogen storage processes of MOF-5 hydrogen storage systems with adsorbents of both the MOF-5 powder (0.13 g/cm³) and its compacted tablet (0.30 g/cm³). The charge–discharge cycles of the two MOF-5 adsorbents were simulated and compared with activated carbon. The physical model is based on mass, momentum and energy conservation equations of the adsorbent-adsorbate system composed of gaseous and adsorbed hydrogen, adsorbent bed and tank wall. The adsorption process was modeled using a modified Dubinin–Astakov (D–A) adsorption isotherm and its associated variational heat of adsorption. The model was implemented by means of finite element analysis software Comsol Multiphysics™, and the system simulation platform Matlab/Simulink™. The thermal average temperature from Comsol simulation is used to fill the gap between the system model and the multi-dimensional models. The heat and mass transfer feature of the model was validated by the experiments of activated carbon, the simulated pressure and temperatures are in good agreement with the experimental results. The model was further validated by the metal-organic framework of Cu-BTC and is being extended its application to MOF-5 in this study. The maximum pressure in the powder MOF-5 tank is much higher than that in the activated carbon tank due to the lower adsorbent density of MOF-5 and resulting lower hydrogen adsorption. The maximum pressure in the compacted MOF-5 tank is a little bit lower than that in the activated carbon tank due to the higher adsorbent density and resulting higher hydrogen adsorption. The temperature swings during the charge–discharge cycle of both MOF-5 tanks are higher than that of the activated carbon tank. These are caused mainly by pressure work in the powder MOF-5 tank and by adsorption heat in the compacted MOF-5 tank. For both MOF-5 hydrogen storage systems, the lumped parameter models implemented by Simulink agree well with experimental pressures and with pressures and thermal average temperatures from Comsol simulation.     

Effect of Zn/Co ratio in MOF-74 type materials containing exposed metal sites on their hydrogen adsorption behaviour and on their band gap energy

Simultaneous incorporation of Zn and Co ions into MOF-74 during the crystallization process has been studied, covering the whole Zn/Co concentration range (0-100% Co). The characterization techniques used, including X-ray diffraction, DR-UV-visible spectroscopy, N₂ adsorption isotherms and thermogravimetric analysis, strongly evidence the successful incorporation of both cations into the material framework, producing the crystallization of MOF-74 with 100% Co and MOF-74 with 100% Zn starting from Zn-free and Co-free initial mixtures, respectively, under the same conditions. H₂, CH₄ and CO₂ uptakes of MOF-74 type materials generally increase with framework Co content at any pressure, suggesting a relevant role of cobalt in the adsorption process. As expected, the comparison between the gas adsorption behavior of Co-substituted MOF-5 and Co-containing MOF-74 materials shows that exposed metal sites play a key role in MOF performance in adsorption. On the other hand, the good agreement between the evolution of the experimental band gap values as a function of the Co content and the computational-based predictions found in the literature further supports the coexistence of Zn²⁺ and Co²⁺ ions forming the MOF-74 metal clusters. Finally, we found that variations of both isosteric heat of hydrogen adsorption and band gap energy with the metal cluster composition show a parallel trend, although it is not systematic in the whole range of Zn/Co ratio. Indeed, a minimum band gap energy value and a maximum isosteric heat of H₂ adsorption value were found to appear simultaneously for Co-rich samples still having some Zn rather than for all-Co samples.     

Investigation of cryo-adsorption hydrogen storage capacity of rapidly synthesized MOF-5 by mechanochemical method

Comparisons were made between the samples mechanochemically (MOF-5(M)) and solvothermally (MOF-5(S)) prepared for the development of efficient hydrogen storage medium. Synthesized samples were undergone structural characterization as well as adsorption equilibrium measurements of hydrogen at temperature-pressure range 77 K–87 K and 0.1–10 MPa. Grand Canonical Monte Carlo (GCMC) simulations were further conducted to study the behaviors of hydrogen molecules adsorbed on MOF-5. It shows that, besides the advantage of large scale synthesis and a lower cost, mechanochemical method respectively brings about 207% and 90.5% increments in the specific surface area and the maximum excess adsorption capacity of hydrogen at 77 K within pressure range 0–10 MPa. Results also reveal that the crystal within MOF-5(M) is regular and distributing uniformly with a mean size only one tenth of that of the MOF-5(S); at 77 K within pressure range 0–10 MPa, Toth equation can predict the adsorption equilibrium data of hydrogen on two MOF-5 samples with a mean relative error less than 1.5%. It suggests that MOF-5(M) is more promising for hydrogen storage by adsorption for practical applications.     

Hydrogen permeation and diffusion in densified MOF-5 pellets

The metal-organic framework Zn₄O (BDC)₃ (BDC = 1,4-bezene dicarboxlate), also known as MOF-5, has demonstrated considerable adsorption of hydrogen, up to 7 excess wt.% at 77 K. Consequently, it has attracted significant attention for vehicular hydrogen storage applications. To improve the volumetric hydrogen density and thermal conductivity of MOF-5, prior studies have examined the hydrogen storage capacities of dense MOF-5 pellets and the impact of thermally conductive additives such as expanded natural graphite (ENG). However, the performance of a storage system based on densified MOF-5 powders will also hinge upon the rate of hydrogen mass transport through the storage medium. In this study, we further characterize MOF-5 compacts by measuring their hydrogen transport properties as a function of pellet density (ρ = 0.3–0.5 g cm⁻³) and the presence/absence of ENG additions. More specifically, the Darcy permeability and diffusivity of hydrogen in pellets of neat MOF-5, and composite pellets consisting of MOF-5 with 5 and 10 wt.% ENG additions, have been measured at ambient (296 K) and liquid nitrogen (77 K) temperatures. The experimental data suggest that the H₂ transport in densified MOF-5 is strongly related to the MOF-5 pellet density ρ.     

A theoretical study of the ability of 2D monolayer Au (111) to activate gas molecules

The adsorption and activation of gas molecules are investigated substantially in solid-gas heterogeneous catalysis. Here we investigated the interaction between gas molecules and unique two-dimensional monolayer Au (111) structure using density functional theory. It is found that CO₂, H₂O, N₂ and CH₄ molecules are weakly adsorbed on the surface with the adsorption energies between ?0.150 and ?0.250 eV due to van der Waals interaction. While CO, NO, NO₂, and NH₃ molecules are adsorbed more stably with the adsorption energies between ?0.300 and ?0.470 eV. Especially, the bond length of CO is stretched by 0.038 Å and the bond angle of NO₂ is obviously enlarged by 10.460°. The activation originates from the rearrangement of molecule orbitals and the orbitals hybridization between the partial orbitals of gas molecules and Au-5d orbitals. The fundamental analyses of adsorption mechanism and electronic properties may provide guidance for the applications of two-dimensional monolayer metal catalysis.PACSnumbers 73.22.-f, 73.61.-r     

Investigation of hydrogen storage on Sc/Ti-decorated novel B24N24

Inspired by the TM−N₄ coordination environment in single-atom catalysts, four novel TM-decorated B₂₄N₂₄ (TM = Sc, Ti) fullerenes with six TM−N₄ or TM−B₄ units are designed. Molecular dynamic simulations confirm that the four TM₆B₂₄N₂₄ fullerenes are thermodynamically stable. Their hydrogen storage properties were investigated using density functional theory calculations. Sc/Ti atoms bind to the N₄/B₄ cavities with an average interaction energy of 6.30–11.96 eV. Hence, the problem of clustering can be avoided. 36H₂ could be adsorbed with average hydrogen adsorption energies of 0.18–0.55 eV. The lowest hydrogen desorption temperatures at atmospheric pressure for Sc₆B₂₄N₂₄(N₄)–36H₂, Sc₆B₂₄N₂₄(B₄)–36H₂, Ti₆B₂₄N₂₄(N₄)–36H₂, and Ti₆B₂₄N₂₄(B₄)–36H₂ are 255 K, 318 K, 243 K, and 408 K, respectively. The maximum hydrogen gravimetric densities of the Sc₆B₂₄N₂₄ and Ti₆B₂₄N₂₄ systems are 7.74 wt% and 7.50 wt%, respectively. Therefore, the novel Sc₆B₂₄N₂₄ and Ti₆B₂₄N₂₄ could be suitable as potential hydrogen storage materials at ambient temperature.     

Multiscale study of the structure and hydrogen storage capacity of an aluminum metal-organic framework

First-principles calculations based on density functional theory and Grand Canonical Monte Carlo (GCMC) simulations are carried out to study the structure of a new Aluminum Metal-Organic Framework, MOF-519, and the possibility of storing molecular hydrogen therein. The optimized structure of the inorganic secondary building unit (SBU) of MOF-519 formed by eight octahedrally coordinated aluminum atoms is presented. The different storage sites of H₂ inside the SBU and the BTB ligand are explored. Our results reveal that the SBU exhibits two different favorable physisorption sites with adsorption energies of ?12.2 kJ/mol and ?1.2 kJ/mol per hydrogen molecule. We have also shown that each phenyl group of BTB has three stable H₂ adsorption sites with adsorption energies between ?6.7 kJ/mol and ?11.37 kJ/mol. Using GCMC simulations; we calculated the molecular hydrogen (H₂) gravimetric and volumetric uptake for the SBU and MOF-519. At 77 K and 100 bar pressure, the hydrogen uptake capacity of SBU is considerably enhanced, reaching 16 wt.%. MOF-519 has a high gravimetric uptake, 10 wt.% at 77 K and 4.9 wt.% at 233 K. It has also a high volumetric capacity of 65 g/L at 77 K and 20.3 g/L at 233 K, indicating the potential of this MOF for hydrogen storage applications.     

Charge transfer behaviors over MOF-5@g-C3N4 with NixMo1−xS2 modification

The composite photocatalyst Ni_xMo_1?xS₂/MOF-5@g-C₃N₄ was successfully synthesized by means of hydrothermal with two step methods and the effective photocatalytic activity improvement was obtained. With the introduction of Ni_xMo_1?xS₂, the H₂ production reached the maximum about 319 μmol under continuous visible light irradiation for 5 h, which was 30 times higher than that of pure g-C₃N₄ photocatalyst. A series of characterization results shown that the MOF-5@g-C₃N₄ on the surface of Ni_xMo_1?xS₂ provided the more active sites and improved the efficiency of photo-generated charge separation with SEM, XRD, TEM, EDX, XPS, UV–vis DRS, BET, FTIR, transient fluorescence and electro-chemistry etc. and the results of which were in good mutual corresponding with each other. Furthermore, the reaction mechanism over the compound catalyst Ni_x-Mo_1?xS₂/MOF-5@g-C₃N₄ was proposed.     

Enhanced hydrogen storage capacity of Pt-loaded CNT@MOF-5 hybrid composites

We report on an easy synthesis method for the preparation of a hybrid composite of Pt-loaded MWCNTs@MOF-5 [Zn₄O(benzene-1,4-dicarboxylate)₃] that greatly enhanced hydrogen storage capacity at room temperature. To prepare the composite, we first prepared Pt-loaded MWCNTs, which were then incorporated in-situ into the MOF-5 crystals. The obtained composite was characterized by various techniques such as powder X-ray diffractometry, optical microscopy, porosimetry by nitrogen adsorption, and hydrogen adsorption. The analyses confirmed that the product has a highly crystalline structure with a Langmuir specific surface area of over 2000 m²/g. The hybrid composite was shown to have a hydrogen storage capacity of 1.25 wt% at room temperature and 100 bar, and 1.89 wt% at cryogenic temperature and 1 bar. These H₂ storage capacities represent significant increases over those of virgin MOF-5s and Pt-loaded MWCNTs.     

Toward hydrogen storage material in fluorinated zirconium metal-organic framework (MOF-801): A periodic density functional theory (DFT) study of fluorination and adsorption

In this study, the structural properties and hydrogen adsorption energy of the fluorinated metal-organic framework (MOF)-801 were evaluated using density functional theory (DFT). We calculated the Zr–F bond distance to be approximately 0.225 nm, which is longer than the bond distance in zirconium fluoride compounds. Due to the electronegativity of F, this site was considered as an adsorption site for hydrogen. We determined the adsorption energy to be ?5 kcal/mol per hydrogen (H₂) molecule, which is higher than that of H₂ in pristine MOF. This value is also slightly lower than the adsorption energy in a metal-decorated MOF. The introduction of F atoms is determined to enhance the binding capacity of MOF-801.     

Hydrogen adsorption in metal- organic frameworks (MOFs): Effects of adsorbent architecture

In this work, the effect of metal-organic framework (MOF) structure of MOF-5 was investigated in hydrogen adsorption based on the degree of solvent exploitation and/or sample preparation procedures. In this regard, the characterization analyses of FT-IR, BET and PXRD pattern of MOF-5 samples were used to compare their architectures with different specific surface area and porosity in hydrogen adsorption. The results show that the pore size distribution of samples is related to the main peaks in the micropores, mesopores and macropores regions. One can found that the adsorption of hydrogen at room temperature (296 K) is controlled by diffusion of adsorbed hydrogen inside the pores of the crystals. Larger diffusivities at a given pressure are expected due to diffusion in macroporous. The values of heats of adsorption on prepared sample are calculated as 3.68 and 12.45 kJ mol^?1 for meso and macroporous regions, respectively. These results are suggesting that weak interactions between the adsorbed hydrogen molecules and MOF crystals is occur in mesoporous regions and the adsorption into macroprous which are filling in high temperature shows strong interaction.     

Synthesis and hydrogen-storage behavior of metal–organic framework MOF-5

Metal–organic framework MOF-5 (Zn₄O(BDC)₃), a microporous material with a high surface area and large pore volume, was synthesized by three approaches: direct mixing of triethylamine (TEA), slow diffusion of TEA, and solvothermal synthesis. The obtained materials were characterized by X-ray diffraction, scanning electron microscopy, thermogravimetric analysis, and nitrogen adsorption, and their hydrogen-storage capacities were measured. The different synthesis methods influenced the pore-structure parameters, morphologies and hydrogen-storage behavior of the obtained MOF-5. MOF-5 synthesized by the solvothermal approach showed a higher surface area and larger pore volume than the samples prepared by the other two approaches. Measurements of the hydrogen-storage behavior showed that the hydrogen-storage capacity was correlated with the specific surface area and pore volume of MOF-5.     

Enhancement of hydrogen storage properties of metal-organic framework-5 by substitution (Zn,Cd and Mg) and decoration (Li,Be and Na)

Two strategies of decoration by three elements Z = Li, Be and Na in cyclic site, and substitution of Zn by Mg and Cd in unit cell were used in the framework of functional density theory to tune the hydrogen storage properties of metal-organic framework-5 (MOF-5) based on Zn whose decomposition temperature and initial gravimetric capacity are 300 K and 1.57 wt% respectively.Based on the adsorption of hydrogen molecules in the crystal surface at three different adsorption sites with three orientations of H₂, we show that our system may reach a maximum gravimetric storage capacity of 4.09 wt% for multiple hydrogen molecules. Moreover, the functionalization of Z combined to the substitution, shows an exceptional improvement of hydrogen storage properties. For example, Mg-MOF-5 decorated with Li₂ has a capacity up to 5.41 wt% and 513 K as desorption temperature.     

Synthesis,characterization and hydrogen adsorption in mixed crystals of MOF-5 and MOF-177

Mixed MOF crystals with morphology similar to that of pure MOF-5 and pure MOF-177 were synthesized using two organic solvents: dimethylformamide (DMF) and diethylformamide (DEF). The mixed crystals were characterized with XRD, SEM and TGA for their physical properties and also evaluated for their hydrogen adsorption properties. The XRD and SEM results suggest that the mixed crystals are different from pure MOF-5 and pure MOF-177. The DMF-derived mixed MOF crystals have a slightly higher specific surface area, smaller pore diameter and greater pore volume than those of the DEF-derived crystals, and seem to be a better adsorbent than the DEF-derived crystals, which was confirmed by the higher hydrogen and nitrogen adsorption capacities on the DMF-derived crystals. The hydrogen adsorption capacities on the mixed MOF crystals are lower than those of pure MOF-5 and MOF-177. It was also observed that the hydrogen diffusion time constant increases with hydrogen pressure, and the heat of hydrogen adsorption decreases with adsorbed hydrogen amount on both mixed crystals.     

Influence of Pt decoration on the hydrogen storage performance of cup-stacked carbon nanotubes: A DFT study

The hydrogen adsorption behaviour of cup-stacked carbon nanotubes (CSCNTs) decorated with the platinum atom at four positions of the conical graphene layer (CGL) is investigated using density functional theory. The optimization shows that the inside lower edge position (IL) results have the best hydrogen adsorption parameters among the four positions. The Pt–H₂ distance is 1.54 Å, the H–H bond length (l_H-H) is 1.942 Å, and the hydrogen adsorption energy (E_ads) is 1.51 eV. The hydrogen adsorption of CSCNTs decorated by Pt at the IL position also has larger E_ads and l_H-H than the Pt-doped planar graphene, Pt-doped single-wall carbon nanotubes and Pt-doped carbon nanocones. The Pt atom at the IL position has a more significant polarization effect on the adsorbed H₂, it has trends to convert H₂ into two separate H atoms. While the hydrogen adsorption behaviour at other positions belongs to the Kubas coordination, the l_H-H and the E_ads increased not significantly.     

Sc and Ti-functionalized 4-tert-butylcalix[4]arene as reversible hydrogen storage material

Using the idea of metal functionalized material for H₂ storage, 4-tert-butylcalix[4]arene (CA) functionalized with Sc and Ti atoms are explored. The first principles density functional theory (DFT) with M06 functional and 6-311G(d,p) basis set is used to explore the hydrogen storage properties of metal functionalized CA. Sc and Ti strongly binds with CA by Dewar coordination with high binding energy. It is found that maximum four hydrogen molecules are adsorbed on each metal site in Sc and Ti functionalized CA. Hydrogen molecules are adsorbed on metals by Kubas and Niu-Rao-Jena mechanism. In Sc functionalized CA system all 4 hydrogen molecules on each Sc bind in molecular fashion while on each Ti in Ti functionalized CA, the first hydrogen molecule binds in dissociative fashion and remaining three hydrogen molecules bind in a molecular form. The stability of Sc and Ti functionalized CA is studied by computing conceptual DFT parameters, which obeys maximum hardness and minimum electrophilicity principle. Hirshfeld charge analysis and electrostatic potential map explore the charge transfer mechanism during the hydrogen adsorption. Born-Oppenheimer molecular dynamics simulations are performed at temperature range 200–473 K to study the stability of the system and the reversibility of adsorbed hydrogen from the system. The calculated H wt% is found to be 10.3 and 10.1, respectively for Sc and Ti functionalized CA systems on complete H₂ saturation. This study explores that Sc and Ti functionalized CA systems are efficient reversible hydrogen storage material.     

Remarkable improvement in hydrogen storage capacities of two-dimensional carbon nitride (g-C3N4) nanosheets under selected transition metal doping

We have performed DFT simulations to quest for an optimal material for onboard hydrogen (H₂) storage applications. Using first-principles calculations, we established that the selected transition metals (M: Sc, Ti, Ni, V) decorated two-dimensional (2D) g-C₃N₄ sheets as optimal materials with reversible and significantly high H₂ gravimetric densities. By effectively avoiding metal-metal (M-M) clustering effect in case of mono doping, up to four molecules of H₂ per dopant could be adsorbed with an average binding energy of around 0.30–0.6 eV/H₂, which is ideal for practical applications. Decorating the g-C₃N₄ sheet with (M-M) dimers, the systems are found to be even more efficient for H₂ binding than single dopant decoration. The stability of these M decorated g-C₃N₄ sheets have been confirmed with ab-initio molecular dynamics simulations. We have further calculated the H₂ desorption temperatures of metal decorated g-C₃N₄ sheets, which confirms the practical application of these metal decorated sheets at ambient working conditions.