氢气储存
氢
氢化镁
脱氢
材料科学
动力学
双金属片
复合数
纳米颗粒
活化能
化学工程
无机化学
核化学
化学
催化作用
纳米技术
物理化学
金属
冶金
复合材料
有机化学
工程类
物理
量子力学
作者
Samuel Guemou,Dongqiang Gao,Fuying Wu,Jia-Guang Zheng,Tao Wei,Zhendong Yao,Danhong Shang,Liuting Zhang
出处
期刊:Dalton Transactions
[The Royal Society of Chemistry]
日期:2022-12-15
卷期号:52 (3): 609-620
被引量:20
摘要
As an ideal material for solid-state hydrogen storage, magnesium hydride (MgH2) has attracted enormous attention due to its cost-effectiveness, abundant resources, and outstanding reversibility. However, the high thermodynamics and poor kinetics of MgH2 still hinder its practical application. In this work, a simple stirring-hydrothermal method was used to successfully prepare bimetallic Mn3O4/ZrO2 nanoparticles, which were subsequently doped into MgH2 by mechanical ball milling to improve its hydrogen sorption performance. The MgH2 + 10 wt% Mn3O4/ZrO2 composite began discharging hydrogen at 219 °C, which was 111 °C lower compared to the as-synthesized MgH2. At 250 °C, the MgH2 + 10 wt% Mn3O4/ZrO2 composite released 6.4 wt% hydrogen within 10 min, whereas the as-synthesized MgH2 reluctantly released 1.4 wt% hydrogen even at 335 °C. Moreover, the dehydrogenated MgH2 + 10 wt% Mn3O4/ZrO2 sample started to charge hydrogen at room temperature. 6.0 wt% hydrogen was absorbed when heated to 250 °C under 3 MPa H2 pressure, and 4.1 wt% hydrogen was taken up within 30 min at 100 °C at the same hydrogen pressure. In addition, compared with the as-synthesized MgH2, the de/rehydrogenation activation energy values of the MgH2 + 10 wt% Mn3O4/ZrO2 composite were decreased to 64.52 ± 13.14 kJ mol-1 and 16.79 ± 4.57 kJ mol-1, respectively, which incredibly contributed to the enhanced hydrogen de/absorption properties of MgH2.
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