Development of Ti-V-Cr-Mn-Mo-Ce high-entropy alloys for high-density hydrogen storage in water bath environments

被引:15
作者
Hu, Hua-Zhou [1 ]
Xiao, Hou-Qun [1 ]
He, Xin-Cong [1 ]
Zhou, Wen-Hao [1 ]
Zhang, Xiao-Xuan [1 ]
Tang, Rui-Zhu [1 ]
Li, Jie [1 ]
Ma, Chuan-Ming [1 ]
Chen, Qing-Jun [1 ]
机构
[1] Chinese Acad Sci, Jiangxi Inst Rare Earths, Ganjiang Innovat Acad, Key Lab Rare Earths, Ganzhou 341000, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Hydrogen storage alloys; High-entropy alloys; BCC structure; Heat treatment; Ce doping; ELECTROCHEMICAL PROPERTIES; MICROSTRUCTURE; PERFORMANCES;
D O I
10.1007/s12598-024-02618-8
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The V-based body-centered cubic (BCC)-type hydrogen storage alloys have attracted significant attention due to their high theoretical hydrogen storage capacity of 3.80 wt%. However, their practical application faces challenges related to low dehydriding capacity and poor activation performance. To overcome these challenges, a BCC-type Ti-V-Cr-Mn-Mo-Ce high-entropy alloy (HEA) with an effectively dehydriding capacity of 2.5 wt% above 0.1 MPa was prepared. By introduction of Mo and conducting heat treatment, the precipitation of Ti-rich phase in HEA was successfully suppressed, resulting in improved compositional uniformity and dehydriding capacity. Consequently, the effective dehydriding capacity increased significantly from 0.60 wt% to 2.50 wt% at 65 degrees C, surpassing that of other types of hydrogen storage alloys under the same conditions. Moreover, the addition of 1 wt% Ce enabled initial hydrogen absorption at 25 degrees C without the need for activation at 400 degrees C. Furthermore, Ce doping reduced the dehydriding activation energy of the Ti-V-Cr-Mn-Mo-Ce HEA from 52.71 to 42.82 kJ.mol(-1). Additionally, the enthalpy value of dehydrogenation decreased from 46.89 to 17.96 kJ.mol(-1), attributed to a decrease in the hysteresis factor from 0.68 to 0.52. These findings provide valuable insights for optimizing the hydrogen storage property of HEA.
引用
收藏
页码:5229 / 5241
页数:13
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