Sun Ze, Zhang Liuting, Yan Nianhua, Zheng Jiaguang, Bian Ting, Yang Zongming, Su Shichuan
College of Energy and Power, Jiangsu University of Science and Technology, Zhenjiang 212003, China.
Nanomaterials (Basel). 2020 Sep 3;10(9):1745. doi: 10.3390/nano10091745.
Magnesium hydride (MgH) has been considered as a potential material for storing hydrogen, but its practical application is still hindered by the kinetic and thermodynamic obstacles. Herein, Mn-based catalysts (MnCl and Mn) are adopted and doped into MgH to improve its hydrogen storage performance. The onset dehydrogenation temperatures of MnCl and submicron-Mn-doped MgH are reduced to 225 °C and 183 °C, while the un-doped MgH starts to release hydrogen at 315 °C. Further study reveals that 10 wt% of Mn is the better doping amount and the MgH + 10 wt% submicron-Mn composite can quickly release 6.6 wt% hydrogen in 8 min at 300 °C. For hydrogenation, the completely dehydrogenated composite starts to absorb hydrogen even at room temperature and almost 3.0 wt% H can be rehydrogenated in 30 min under 3 MPa hydrogen at 100 °C. Additionally, the activation energy of hydrogenation reaction for the modified MgH composite significantly decreases to 17.3 ± 0.4 kJ/mol, which is much lower than that of the primitive MgH. Furthermore, the submicron-Mn-doped sample presents favorable cycling stability in 20 cycles, providing a good reference for designing and constructing efficient solid-state hydrogen storage systems for future application.
氢化镁(MgH)被认为是一种潜在的储氢材料,但其实际应用仍受到动力学和热力学障碍的阻碍。在此,采用锰基催化剂(MnCl和Mn)并将其掺杂到MgH中以改善其储氢性能。MnCl和亚微米级Mn掺杂的MgH的起始脱氢温度分别降至225℃和183℃,而未掺杂的MgH在315℃开始释放氢气。进一步研究表明,10 wt%是较好的掺杂量,MgH + 10 wt%亚微米级Mn复合材料在300℃下8分钟内可快速释放6.6 wt%的氢气。对于氢化反应,完全脱氢的复合材料即使在室温下也开始吸收氢气,在100℃、3 MPa氢气压力下30分钟内几乎可再氢化3.0 wt%的氢。此外,改性MgH复合材料的氢化反应活化能显著降低至17.3±0.4 kJ/mol,远低于原始MgH的活化能。此外,亚微米级Mn掺杂样品在20次循环中表现出良好的循环稳定性,为未来设计和构建高效固态储氢系统提供了良好的参考。