Recent progress of nanotechnology in enhancing hydrogen storage performance of magnesium-based materials: A review

被引:71
|
作者
Sui, Yongqi [1 ,3 ]
Yuan, Zeming [1 ,2 ,3 ,4 ]
Zhou, Dongsheng [1 ]
Zhai, Tingting [1 ,3 ]
Li, Xiaoming [1 ]
Feng, Dianchen [1 ,3 ]
Li, Yiming [1 ]
Zhang, Yanghuan [1 ,2 ]
机构
[1] Inner Mongolia Univ Sci & Technol, Instrumental Anal Ctr, Baotou 014010, Peoples R China
[2] Cent Iron & Steel Res Inst, Dept Funct Mat Res, Beijing 100081, Peoples R China
[3] Inner Mongolia Univ Sci & Technol, Collaborat Innovat Ctr Integrated Exploitat Bayan, Baotou 014010, Peoples R China
[4] Inner Mongolia Univ Sci & Technol, Instrumental Anal Ctr, 7 Aerding Rd, Baotou 014010, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogen energy; Mg; Hydrogen storage; Nano-catalysis; Nanosized; CARBON NANOTUBES; ELECTROCHEMICAL PROPERTIES; DEHYDROGENATION KINETICS; HIGH-PRESSURE; MG; NI; HYDRIDE; ALLOY; LA; NICKEL;
D O I
10.1016/j.ijhydene.2022.06.310
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
Hydrogen has attracted wide attention in the field of new energy, triggering a comprehensive study of hydrogen production, storage and application. This paper mainly studies the hydrogen storage capacity of magnesium-based materials with nanostructure. The reversible hydrogen capacity of Mg-based hydrogen storage materials can reach 7.6 wt%, but due to its poor kinetic and thermodynamic properties, its hydrogen storage performance is not as good as other hydrogen storage materials. In order to reduce the desorption temperature of materials, many studies have been carried out. Alloying, nanostructure and adding catalyst are feasible methods to improve the properties of Mg-based hydrogen storage alloys. By adding catalyst and alloy with other transition elements, the dehydrogenation temperature of magnesium-based materials has been reduced to less than 200 ?. The hydrogen storage of magnesium-based alloys has been practically applied.(c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:30546 / 30566
页数:21
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