Enhanced hydrogen storage performance of magnesium hydride catalyzed by medium-entropy alloy CrCoNi nanosheets

氢气储存 氢化镁 脱氢 催化作用 合金 氢化物 化学工程 活化能 动力学 材料科学 无机化学 化学 冶金 物理化学 有机化学 物理 量子力学 工程类
作者
Shuai Li,Fuying Wu,Yan Zhang,Ren Zhou,Zichuan Lu,Yiqun Jiang,Ting Bian,Danhong Shang,Liuting Zhang
出处
期刊:International Journal of Hydrogen Energy [Elsevier BV]
卷期号:50: 1015-1024 被引量:6
标识
DOI:10.1016/j.ijhydene.2023.08.308
摘要

The sluggish de/hydrogenation kinetics and stable thermodynamics of magnesium hydride (MgH2) are unfavorable for its large-scale application. Herein, the medium-entropy alloy CrCoNi nanosheets were synthesized and remarkably enhanced the low-temperature hydrogen storage performance of MgH2. Surprisingly, the initial dehydrogenation temperature of 9 wt% CrCoNi modified MgH2 was greatly reduced from 325 °C to 195 °C, a drop of 130 °C compared to non-additive MgH2. Also, the MgH2–CrCoNi composite released 4.84 wt% hydrogen at 300 °C even in 5 min and absorbed 3.19 wt% hydrogen at 100 °C within 30 min (3.2 MPa). The calculated de/rehydrogenation activation energy were reduced by 45 and 55 kJ mol−1, respectively. Further cyclic kinetics investigation indicates that the 9 wt%-CrCoNi doped MgH2 still presented good stability after 20 cycles, losing only 0.36 wt% hydrogen capacity. The XRD pattern validated that CrCoNi remained stable during the cyclic reaction process. Besides, the uniformly distributed CrCoNi nanosheets were in tight contact with the MgH2 surface, providing abundant catalytic active sites and low-energy barrier diffusion channels. Under synergistic catalysis, the H atoms are rapidly absorbed and released across the Mg/MgH2 interface, resulting in excellent kinetic properties. Briefly, this paper provides new references and inspirations to design efficient polymetallic catalysts for hydrogen storage materials.

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