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Due to the poor activation performance and kinetics of Ti50V25Cr25 alloys, the element Zr was added to improve the phase structure of the alloy and achieve a high-performance hydrogen storage alloy. The Ti50−xV25Cr25Zrx (x = 0, 5, 7, and 9) system alloys were prepared by arc melting. The alloys were analyzed using an X-ray diffractometer (XRD), scanning electron microscope (SEM), and differential scanning calorimeter (DSC). The hydrogen storage capabilities of the alloys were also obtained by the Sievert volumetric method. The results indicated that the alloy with Zr added had a combination of the C15 Laves phase and the BCC phase, whereas the Zr-free alloy had a BCC single phase. The partial replacement of Zr with Ti resulted in an increase in the lattice parameters of the main phase. The hydrogen storage kinetic performance and activation of the alloys both significantly improved with an increasing Zr concentration. The time to reach 90% of the maximum hydrogen storage capacity decreased to 2946 s, 230 s, and 120 s, respectively, with the increases in Zr concentration. The initial hydrogen absorption content of the alloys increased and then decreased after the addition of the element Zr. The second phase expanded with an increasing Zr concentration, which in turn decreased the abundance of the BCC main phase. The Ti43V25Cr25Zr7 alloy showed good cycle stability and hydrogen-desorption performance, and it could absorb 90% of the maximum hydrogen storage capacity in around 230 s. The maximum hydrogen-absorption capacity of the alloy was 2.7 wt%. The diffusion activation energy of hydrogen desorption dropped from 102.67 kJ/mol to 92.62 kJ/mol. [ABSTRACT FROM AUTHOR]

The La 0.8- x Pr x Mg 0.2 Ni 3.8 (x = 0, 0.05, 0.1, 0.2, 0.3) alloy were synthesized useing the induction melting method. X-ray diffraction, scanning electron microscope, electron probe micro analyzer, and electrochemical tests were used to analyze the structure and electrochemical performance of the La 0.8- x Pr x Mg 0.2 Ni 3.8 (x = 0–0.3) alloy. It was studied how the Pr element affected the electrochemical characteristics and microstructure of the A 5 B 19 La-Mg-Ni based hydrogen storage alloy. The results show that the alloy consists of the CaCu 5 -LaNi 5 phase, 2 H-Pr 5 Co 19 phase, and 3R-Ce 5 Co 19 phase. The abundance of the A 5 B 19 phase increase with the increase of Pr content, while the abundance of the LaNi 5 phase decrease, and the addition of Pr promotes the formation of the 2 H-Pr 5 Co 19 phase. According to the results of the electrochemical test, every sample has good activation qualities, and the activation can be completed in 3–4 times. The activation properties are not significantly altered by the addition of Pr. The maximum discharge capacity increases at first, then decreases, reaching the highest 371.15 mAh g−1 at x = 0.2. The cyclic stability gradually improves with increasing content of Pr, and the maximum capacity retention rate reaches 85.80 % after 100 cycles. The primary factor influencing the alloy's high rate discharge ability is the exchange current density. With the increase of the exchange current density, the high rate discharge performance is gradually enhanced. • The La-Mg-Ni based hydrogen storage alloy A 5 B 19 has better performance than AB 3 and A 2 B 7. • The hydrogen storage alloy was partially substituted by Pr element with higher electronegativity. • The addition of Pr significantly improves the phase structure stability and cycle stability of the alloy. • The corrosion and oxidation of the alloy electrode during the cycle are improved. [ABSTRACT FROM AUTHOR]

Utilizing element substitution to enhance the hydrogen storage capabilities of Mg-based alloys represents a promising approach in the quest for efficient energy storage solutions. Thereby, in this paper, Ni is chosen to substitute a portion of Mg in a Ce–Mg-based alloy aimed at improving its hydriding and dehydriding performance. Mg 77+ x Ni 20- x Ce 3 (x = 0, 5, 10, 15) alloys are successfully prepared by the vacuum induction melting method. The structural characterizations of the alloys are performed using X-ray diffraction and scanning electron microscope. The alloys are composed of a primary phase of Mg 2 Ni, lamella eutectic composites of Mg + Mg 2 Ni, and some amount of CeMg 12 and Ce 2 Mg 17. In the as-cast Mg 87 Ni 10 Ce 3 alloy, the Mg 2 Ni phase disappears, transforming into a typical eutectic structure of hundreds of nanometers thick Mg–Mg 2 Ni lamellas. This structure significantly enhances the hydrogen storage kinetics, with a hydrogen absorption capacity of 5.66 wt% at 653 K and a desorption capacity of 5.45 wt% over 2 h at 683 K, outperforming other alloys. Moreover, its peak hydrogen release temperature is significantly lower than that of the Mg 92 Ni 5 Ce 3 alloy. The formation of the CeH 2.29 phase within the alloy acts as a catalyst, effectively improving the exothermic and endothermic kinetics of hydrogen absorption and desorption, resulting in a much lower hydrogen desorption activation energy compared to MgH 2. However, the variation in the activation energy of the alloy remains limited, ranging between 66.6 ∼71.1 kJ/mol. [Display omitted] • Mg 77+ x Ni 20- x Ce 3 (x = 0, 5, 10, 15) alloys were prepared in an induction furnace. • Ni substituting for Mg significantly lowers the peak temperature of hydrogen release. • Ni substituting for Mg reduces the desorption activation energy values. • The Mg 87 Ni 10 Ce 3 alloy can absorb more than 5.66 wt % H 2 within 120 min at 653K. [ABSTRACT FROM AUTHOR]