4.7 Article

Improved hydrogen storage properties of Ti2CrV alloy by Mo substitutional doping

期刊

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 47, 期 23, 页码 11929-11937

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2022.01.212

关键词

Hydrogen storage materials; Ti-Cr-V alloy; Mo substitution; Microstructure; Cyclic property

资金

  1. Innovation Academy for Green Manufacture, Chinese Academy of Sciences [IAGM2020DB08]
  2. National Key Projects for Fundamental Research and Development of China [2021YFF0306103]
  3. Key R&D Program of Henan Province [202102210184]
  4. Key Research Program of the Chinese Academy of Sciences [ZDRW-CN-2021-3]
  5. Selfdeployed Projects of Ganjiang Innovation Academy, Chinese Academy of Sciences [E055B003, E055ZA01]

向作者/读者索取更多资源

An advancement in hydrogen storage property of the Ti2CrV alloy is achieved by Mo partial substitution for Ti, leading to improved hydrogen capacity and cycling performance.
Controllable hydrogen release is of great importance to the practical application of hydrogen storage materials. Ti2CrV alloy possesses the maximum hydrogen absorption capacity in the Ti-Cr-V series alloys, however, can hardly meet the reversible storage capacity of practical applications due to its stable dihydride. Here we report an advancement in hydrogen storage property of the Ti2CrV alloy by Mo partial substitution for Ti. Although the hydrogen absorption kinetics slightly decreased with the increase of Mo content, the Mo substitution alloy achieves an effective hydrogen capacity of 2.23 wt% cutting-off at 0.1 MPa, much higher than Ti2CrV alloy (0.8 wt%). It is ascribed that Mo partial substitution for Ti significantly decreased the dihydride stability as well as the enthalpy change value. The cyclic property of Ti2CrV alloy drastically decreased, while Mo substitution alloy with smaller FWHM value can maintain 90% storage capacity after 20 cycles. Because lattice strain and distortion of the Ti2CrV alloy were decreased by Mo doping.(c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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