Enhanced hydrogen storage kinetics of MgH2 by the synergistic effect of Mn3O4/ZrO2 nanoparticles

被引:17
作者
Guemou, Samuel [1 ]
Gao, Dongqiang [1 ]
Wu, Fuying [1 ]
Zheng, Jiaguang [1 ]
Wei, Tao [1 ]
Yao, Zhendong [2 ]
Shang, Danhong [3 ]
Zhang, Liuting [1 ]
机构
[1] Jiangsu Univ Sci & Technol, Anal & Testing Ctr, Sch Energy & Power, Zhenjiang 212003, Peoples R China
[2] China Jiliang Univ, Sch Mat & Chem, Hangzhou 310018, Peoples R China
[3] Jiangsu Univ Sci & Technol, Sch Environm & Chem Engn, Zhenjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
THERMODYNAMICS; COMPOSITE; DEHYDROGENATION; MAGNESIUM; ALLOY;
D O I
10.1039/d2dt03769f
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
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 degrees C, which was 111 degrees C lower compared to the as-synthesized MgH2. At 250 degrees 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 degrees 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 degrees C under 3 MPa H-2 pressure, and 4.1 wt% hydrogen was taken up within 30 min at 100 degrees 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.
引用
收藏
页码:609 / 620
页数:12
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