Hydrogen storage properties of Mg0.10Ti0.30V0.25Zr0.10Nb0.25 lightweight high entropy alloy: A theoretical study

被引:16
作者
Deng, Yuhui [1 ]
Hu, Jutao [1 ]
Zhao, Siqin [1 ]
Wang, Weidu [2 ,3 ]
Xie, Lei [2 ]
Sun, Guangai [2 ]
Shen, Huahai [2 ]
Zu, Xiaotao [1 ]
Xiao, Haiyan [1 ]
机构
[1] Univ Elect Sci & Technol China, Sch Phys, Chengdu 611731, Peoples R China
[2] China Acad Engn Phys, Inst Nucl Phys & Chem, Mianyang 621900, Peoples R China
[3] Fudan Univ, Inst Modern Phys, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
First-principles calculation; Mg-based high entropy alloys; Phase transformation; Hydrogen storage; TOTAL-ENERGY CALCULATIONS; PHASE-STABILITY; BAND-STRUCTURE; DUAL FUEL; 1ST-PRINCIPLES; HYDRIDES; MICROSTRUCTURE; PERFORMANCE; ABSORPTION; SIMULATION;
D O I
10.1016/j.ijhydene.2023.07.075
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In the past several years, Mg-based high entropy alloys (HEAs) have attracted great attention in high gravimetric hydrogen storage capacity. In this work, the hydrogen storage properties of Mg0.10Ti0.30V0.25Zr0.10Nb0.25 HEA are investigated by first-principles calculations. With increasing hydrogen concentration, the structural stability of BCC and FCC hydrides decreases and increases, respectively. By comparing the lattice constants, number of hydrogenation-induced abnormal short hydrogen-hydrogen bonds and radial distribution functions of BCC and FCC hydrides, it is found that the hydrogen accommodation ability of BCC phase is weaker than that of FCC phase, and a BCC to FCC phase transformation occurs during hydrogenation process. Further total energy calculations suggest that the threshold hydrogen content of phase transformation for Mg0.10Ti0.30V0.25Zr0.10 Nb0.25 is around H/M = 1.16. By phonon spectra calculation, the maximum gravimetric hydrogen storage capacity of Mg0.10Ti0.30V0.25Zr0.10Nb0.25 is predicated to be as high as 3.16 wt%, demonstrating that Mg0.10Ti0.30V0.25Zr0.10Nb0.25 HEA is a potential hydrogen storage material. (c) 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:314 / 323
页数:10
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