氢气储存
氢
解吸
催化作用
结构精修
材料科学
化学工程
无机化学
化学
物理化学
晶体结构
结晶学
吸附
有机化学
工程类
作者
Zhichao Yu,Xin Liu,Yang Liu,Yuan Li,Zhuohan Zhang,Kangli Chen,Shumin Han
出处
期刊:Fuel
[Elsevier]
日期:2023-09-09
卷期号:357: 129726-129726
被引量:18
标识
DOI:10.1016/j.fuel.2023.129726
摘要
Multiple catalysts have exhibited high activity on improving the hydrogen storage performance of MgH2. Herein, the hydrogen ab/desorption kinetics of MgH2 is significantly improved by using Ni@C@CeO2 as the catalyst. The results show that 10 wt%-Ni@C@CeO2 doped MgH2 can absorb 4.51 wt% hydrogen within 60 min under low temperature 75 °C. Furthermore, the MgH2-Ni@C@CeO2 composites release approximately 4.88 wt% H2 within 10 min at 325 °C. Moreover, the composites show excellent cycling performance, with negligible decrease in hydrogen storage capacity, hydrogen uptake rate and hydrogen release rate after ten cycles at 350 °C. The Rietveld refinement of X-ray diffraction and transmittance electron microscopy measurements reveal that Mg2NiH4/Mg2Ni and CeH2.73 phases are in-situ formed. The mutual conversion of “Mg2Ni/Mg2NiH4” during hydrogen ab/desorption is a well-known “hydrogen pump” effect, which improvs the hydrogen storage performance of MgH2. The presence of CeH2.73 accelerate the conversion of Mg2Ni/Mg2NiH4, which we call ‘facilitated hydrogen pump’ effect. This attempt paves a potential way to achieve high performance Mg-based composites hydrogen storage materials via collaborative action between Ni and Ce species.
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