RESUMEN
In this study, the Ni/NiO catalyst was demonstrated to enhance the hydrogen storage performance of MgH2. The dehydrogenation of MgH2+10 wt% Ni/NiO started at approximately 180 °C, achieving 5.83 wt% of dehydrogenation within 10 min at 300 °C. Completely dehydrogenated, MgH2 began to rehydrogenate at about 50 °C, absorbing about 4.56 wt% of hydrogen in 10 min at 150 °C. In addition, the activation energies of dehydrogenation and rehydrogenation of MgH2+10 wt% Ni/NiO were 87.21 and 34.84 kJ/mol. During the dehydrogenation/rehydrogenation cycle, Mg2Ni/Mg2NiH4 could promote hydrogen diffusion, thus enhancing the hydrogen storage performance of Mg/MgH2.
RESUMEN
V-based solid solution materials hold a significant position in the realm of hydrogen storage materials because of its high hydrogen storage capacity. However, the current dehydrogenation temperature of V-based solid solution exceeds 350 °C, making it challenging to fulfill the appliance under moderate conditions. Here advancements in the hydrogen storage properties and related mechanisms of TiV1.1Cr0.3Mn0.6 + x LiAlH4 (x = 0, 5, 8, 10 wt.%) composites is presented. According to the first principle calculation analysis, the inclusion of Al and Li atoms will lower the binding energy of hydride, thus enhancing the hydrogen absorption reaction and significantly decreasing the activation difficulty. Furthermore, based on crystal orbital Hamilton population (COHP) analysis, the strength of the VâH and TiâH bonds after doping LiAlH4 are reduced, leading to a decrease of the hydrogen release activation energy (Ea) for the V-based solid solution material, thus the hydrogen release process is easier to carry out. Additionally, the structure of doped LiAlH4 exhibits an outstanding hydrogen release rate of 2.001 wt.% at 323 K and remarkable cycling stability.
RESUMEN
Due to its high hydrogen storage efficiency and safety, Mg/MgH2 stands out from many solid hydrogen storage materials and is considered as one of the most promising solid hydrogen storage materials. However, thermodynamic/kinetic deficiencies of the performance of Mg/MgH2 limit its practical applications for which a series of improvements have been carried out by scholars. This paper summarizes, analyzes and organizes the current research status of the hydrogen storage performance of Mg/MgH2 and its improvement measures, discusses in detail the hot studies on improving the hydrogen storage performance of Mg/MgH2 (improvement measures, such as alloying treatment, nano-treatment and catalyst doping), and focuses on the discussion and in-depth analysis of the catalytic effects and mechanisms of various metal-based catalysts on the kinetic and cyclic performance of Mg/MgH2. Finally, the challenges and opportunities faced by Mg/MgH2 are discussed, and strategies to improve its hydrogen storage performance are proposed to provide ideas and help for the next research in Mg/MgH2 and the whole field of hydrogen storage.
RESUMEN
Hydrogen is a potential green alternative to conventional energy carriers such as oil and coal. Compared with the storage of hydrogen in gaseous or liquid phases, the chemical storage of hydrogen in solid complex hydrides is safer and more effective. In this study, the complex hydride composite 2LiBH4-Li3AlH6 with different amounts of TiF3 was prepared by simple ball-milling and its hydrogen storage properties were investigated. Temperature programmed desorption and differential scanning calorimetry were used to characterize the de/rehydrogenation performance, and X-ray diffraction and scanning electron microscopy (SEM) were used to explore the phase structure and surface topography of the materials. The dehydrogenation temperature decreased by 48°C in 2LiBH4-Li3AlH6 with 15 wt% TiF3 composites compared to the composite without additives while the reaction kinetics was accelerated by 20%. In addition, the influence of hydrogen back pressure on the 2LiBH4-Li3AlH6 with 5 wt% TiF3 composite was also investigated. The results show that hydrogen back pressure between 2.5 and 3.5 bar can improve the reversible performance of the composite to some extent. With a back pressure of 3.5 bar, the second dehydrogenation capacity increased to 4.6 wt% from the 3.3 wt% in the 2LiBH4-Li3AlH6 composite without hydrogen back pressure. However, the dehydrogenation kinetics was hindered. About 150 h, which is 100 times the time required without back pressure, was needed to release 8.7 wt% of hydrogen at 3.5 bar hydrogen back pressure. The SEM results show that aluminum was aggregated after the second cycle of dehydrogenation at the hydrogen back pressure of 3 bar, resulting in the partial reversibility of the 5 wt% TiF3-added 2LiBH4-Li3AlH6 composite.
RESUMEN
Hydrogen-induced disproportionation (HID) during the cycles of absorption and desorption leads to a serious decline in the storage capacity of the ZrCo alloy, which has been recognized as the biggest obstacle to its application. Therefore, the prerequisite of a ZrCo application is to solve its anti-disproportionation problem in the field of rapid hydrogen isotope storage. Beyond surface modification and nanoball milling, this work systematically reviews the method of element substitution, which can obviously improve the anti-disproportionation. From a micro angle, as hydrogen atoms that occupy the 8e site in the ZrCoH3 lattice are instable and are considered to be the driving force of disproportionation, researchers believe that element substitution by changing the occupation of hydrogen atoms at the 8e site can improve the anti-disproportionation of the alloy. At present, Ti/Nb substitutions for the Zr terminal among substitute elements have an excellent anti-disproportionation performance. In this work, up-to-date research studies on anti-disproportionation and its disproportionation mechanism of the ZrCo alloy are introduced by combining experiments and simulations. Moreover, the optimization of the alloy based on the occupation mechanism of 8e sites is expected to improve the anti-disproportionation of the ZrCo alloy.
RESUMEN
Magnesium hydride (MgH2) is regarded as a promising solid-state hydrogen storage material, on account of its moderate price and high gravimetric capacity. However, MgH2's inferior kinetic of hydrogen release impedes its widespread application. In this work, we use core-shell Co@N-rich carbon (CoNC) additive as catalysts to ameliorate the performances of MgH2. The surface morphologic structures and hydrogen desorption kinetics of different MgH2-CoNC composites are systematically studied. We find that MgH2-5 wt% CoNC with carbon contents of 17% (CoNC0) composites exhibit better hydrogen desorption performance. At 325°C, the MgH2-5 wt% CoNC0 composites can release up to 6.58 wt% of H2 in 5 min, which is much higher than 0.3 wt% for pure MgH2. Our results demonstrate that importing the core-shell structured catalysts can effectively enhance the hydrogen release kinetics.