RESUMEN
Lanthanide-based metal-organic frameworks (MOFs) have great potential as magnetic refrigerants under cryogenic conditions and are comparable to conventional alloys and magnetic nanoparticles. In particular, MOFs with Gd3+ ions behave as excellent magnetic refrigerants because of their large spin ground states. However, the major drawback of Gd3+-based MOFs is that they are not affected by the ligand material owing to the excessively large spin-only magnetic moment; therefore, their application is limited to the cryogenic region in the magnetic cooling field. In this study, we report the magnetic properties and magnetocaloric effect (MCE) resulting from heterogenized MOFs obtained from the reaction of Gd3+ and Dy3+ ions and their varied molar composition with the formate ligand. For GdxDy1-x-(HCOO)3, where 0 ≤ x ≤ 1, the isothermal magnetic entropy change (ΔSm) increased with the increase in the fraction of Gd in the heterogenized MOFs. Meanwhile, with increasing Dy contents, the maximum peak temperature of ΔSm is shifted to a higher temperature while preserving a relatively high ΔSm value of 22.35 J·kg-1 K-1 at T = 7 K for an applied field change (ΔH) of 7 T despite the anisotropy and crystalline electric field effects. Furthermore, it was confirmed that the samples with a Dy content of 75% or more maintained the ΔSm operating temperature longer. Therefore, the current approach of including Dy3+ ions in lanthanide compounds provides the possibility of further extending the operating temperature of magnetic cooling materials from cryogenic temperatures.
RESUMEN
Nonmagnetic Pd exhibits ferromagnetism in the nanosize regime. Various stabilization agents, including surfactants, metal oxide supports, polymers, and porous materials (e.g., metal-organic frameworks (MOFs)), have been employed to prevent the agglomeration of metal nanoparticles. However, magnetic properties are greatly affected by the structural and electronic changes imposed by these stabilizing agents. In particular, metal-MOF hybrids (NPs@MOFs) have reduced magnetic properties, as reported by several authors. Herein, we report the enhancement in magnetic properties resulting from the combination of magnetic Pd NPs with UiO-66(Hf), which exhibits ferromagnetism, and the corresponding modifications in the hybridized structures. These hybridized structures are found to be strongly ferromagnetic, showing high magnetization and coercivity. We observed that the magnetic property is enhanced by 2 to 3 times upon including the Pd NPs on the surface of a UiO-66(Hf) shell support. For a fundamental understanding, the magnetization (M-H data) of the hybridized structure is analyzed with a modified Langevin function.
RESUMEN
Kinetic-quantum-sieving-assisted H2 :D2 separation in flexible porous materials is more effective than the currently used energy-intensive cryogenic distillation and girdle-sulfide processes for isotope separation. It is believed that material flexibility results in a pore-breathing phenomenon under the influence of external stimuli, which helps in adjusting the pore size and gives rise to the optimum quantum-sieving phenomenon at each stage of gas separation. However, only a few studies have investigated kinetic-quantum-sieving-assisted isotope separation using flexible porous materials. In addition, no reports are available on the microscopic observation of isotopic molecular transportation during the separation process under dynamic transition. Here, the experimental observation of a significantly faster diffusion of deuterium than hydrogen in a flexible pore structure, even at high temperatures, through quasi-elastic neutron scattering, is reported. Unlike rigid structures, the extracted diffusion dynamics of hydrogen isotopes within flexible frameworks show that the diffusion difference between the isotopes increases with an increase in temperature. Owing to this unique inverse trend, a new strategy is suggested for achieving higher operating temperatures for efficient isotope separation utilizing a flexible metal-organic framework system.
RESUMEN
Adsorptive separation using narrow-micropore adsorbents has demonstrated the potential to separate hydrogen isotopes. In this work, we employed an isotope-responsive separation using cobalt formate. A D2-responsive third sorption step was revealed, and consequently, a noticeable difference was observed in the uptakes of D2 and H2. This may have resulted from the additional space created for D2 due to its dense packing, as DFT calculations revealed that cobalt formate possesses 2.26 kJ/mol higher binding strength for D2 than for H2. The exploitation of this D2-responsive third sorption step renders a promising separation performance, with a D2/H2 selectivity of up to 44 at 25 K/1 bar. Lastly, cobalt formate was synthesized on a gram scale here, which makes it a prospect for commercialization.
RESUMEN
Nitrogen-enriched nanoporous polytriazines (NENPs) have been synthesized by ultrafast microwave-assisted condensation of melamine and cyanuric chloride. The experimental conditions have been optimized to tune the textural properties by synthesizing materials at different times, temperatures, microwave powers, and solvent contents. The maximum specific surface area (SABET) of 840 m2 g-1 was estimated in the sample (NENP-1) synthesized at 140 °C with a microwave power of 400 W and reaction time of 30 min. One of the major objectives of achieving a large nitrogen content as high as 52 wt % in the framework was realized. As predicted, the nitrogen amelioration has benefitted the application by capturing a very good amount of CO2 of 22.9 wt % at 273 K and 1 bar. Moreover, the CO2 storage capacity per unit specific surface area (per m2 g-1) is highest among the reported nanoporous organic frameworks. The interaction of the CO2 molecules with the polytriazine framework was theoretically investigated by using density functional theory. The experimental CO2 capture capacity was validated from the outcome of the theoretical calculations. The superior CO2 capture capability along with the theoretical investigation not only makes the nanoporous NENPs superior adsorbents for the energy and environmental applications but also provides a significant insight into the fundamental understanding of the interaction of CO2 molecules with the amine functionalities of the nanoporous frameworks.
RESUMEN
Cyclophosphazene-based inorganic-organic hybrid nanoporous materials (CHNMs) have been synthesized by a facile solvothermal method. The condensation of pyrrole with the reaction product of phosphonitrilic chloride trimer and 4-hydroxybenzaldehyde resulted in the formation of high-surface-area CHNMs. The maximum specific surface area (SABET) of 1328 m2 g-1 with hierarchical pore structures having micropores centered at 1.18 nm and mesopores in the range of 2.6-3.6 nm was estimated from the N2 sorption analysis. Observation of high SABET could be attributed to the synergy effect exerted by the cyclophosphazene moiety owing to its three-dimensional paddle wheel structure. The metal-free adsorbent exhibited a high and reversible CO2 uptake of 22.8 wt % at 273 K and 1 bar. The performance is on the higher side among the reported metal-free inorganic-organic hybrid nanoporous adsorbents. Moreover, the high H2 uptake of 2.02 wt % at 77 K and 1 bar is an added advantage. The superior performance of the adsorbents for the gas sorption applications could be attributed to the combined effect of high SABET and hierarchical pore structure, which has made CHNMs good candidates for energy and environmental applications.
RESUMEN
An iron(II)phthalocyanine (Fepc) modified mesoporous titania (Fepc-TiO2) nanocatalyst with a specific surface area of 215 m(2) g(-1) has been synthesized by a hydrothermal method. Fepc-TiO2 degrades one of the highly toxic chemical warfare agents, sulfur mustard (SM), photocatalytically under sunlight with an exposure time of as low as 70 min. Furthermore, the mesoporous Fepc-TiO2 also captured 2.1 mmol g(-1) of CO2 at 273 K and 1 atm.
