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MgH2+20%(w)MgTiO3复合材料的吸/放氢性能
引用本文:王家盛,韩树民,李媛,沈娜,张伟.MgH2+20%(w)MgTiO3复合材料的吸/放氢性能[J].物理化学学报,2015,30(12):2323-2327.
作者姓名:王家盛  韩树民  李媛  沈娜  张伟
作者单位:1. 燕山大学环境与化学工程学院, 河北省应用化学重点实验室, 河北 秦皇岛 066004;
2. 燕山大学亚稳材料科学与技术国家重点实验室, 河北 秦皇岛 066004
基金项目:国家自然科学基金(50971112, 51001043)及河北省高等学校科学技术研究重点项目(ZD2014004)资助
摘    要:为了降低MgH2的吸放氢温度, 提高其吸放氢动力学性能, 本文通过球磨方法制备了MgH2+20%(w)MgTiO3复合储氢材料, 并研究了其储氢性能. X射线衍射(XRD)结果表明, MgTiO3在与MgH2球磨过程中生成Mg2TiO4和TiO2, 并且Mg2TiO4和TiO2在体系的吸放氢过程中保持稳定, 能够对MgH2的吸放氢过程产生催化作用. 程序升温脱附和吸/放氢动力学测试结果表明, 添加MgTiO3后MgH2的初始放氢温度从389 ℃降至249 ℃.150 ℃下的吸氢量从0.977%(w)提高到2.902%(w), 350 ℃下的放氢量从2.319%(w)提高到3.653%(w). 同时, MgH2放氢反应的活化能从116 kJ·mol-1降至95.7 kJ·mol-1. 与MgH2相比, MgH2+20%(w) MgTiO3复合材料的热力学与动力学性能均有显著提高, 这主要是由于球磨和放氢过程中原位生成的TiO2和Mg2TiO4具有良好的催化活性.

关 键 词:储氢性能  2''  '''')  MgH2" target="_blank">">MgH2  3''  '''')  MgTiO3" target="_blank">">MgTiO3  催化活性  活化能
收稿时间:2014-07-14
修稿时间:2014-10-09

Hydriding/Dehydriding Properties of an MgH2+20%(w) MgTiO3 Composite
WANG Jia-Sheng,HAN Shu-Min,LI Yuan,SHEN Na,ZHANG Wei.Hydriding/Dehydriding Properties of an MgH2+20%(w) MgTiO3 Composite[J].Acta Physico-Chimica Sinica,2015,30(12):2323-2327.
Authors:WANG Jia-Sheng  HAN Shu-Min  LI Yuan  SHEN Na  ZHANG Wei
Institution:1. Hebei Key Laboratory of Applied Chemistry, College of Environmental and Chemical Engineering, Yanshan University, Qinhuangdao 066004, Hebei Province, P. R. China;
2. State Key Laboratory of Metastable Materials Science and Technology, Yanshan University, Qinhuangdao 066004, Hebei Province, P. R. China
Abstract:With the aim of decreasing the dehydriding temperature and improving the hydriding/dehydriding kinetic properties of MgH2, we prepared MgH2+20%(w) MgTiO3 composite via ball-milling, and investigated the hydrogen storage properties of the composite. X- ray diffraction (XRD) results showed that the MgTiO3 decomposed into Mg2TiO4 and TiO2 during the ball-milling. These two resulting compounds remained stable during the hydriding/dehydriding processes, working as catalysts for the hydriding/dehydriding. Temperatureprogrammed- desorption (TPD) and hydriding/dehydriding kinetics tests showed that doping MgH2 with MgTiO3 lowered the onset dehydrogenation temperature of MgH2 from 389 to 249 ℃, as well as increasing the hydrogen absorption amount from 0.977%(w) to 2.902%(w) at 150 ℃, and increasing the desorption amount from 2.319% (w) to 3.653%(w) at 350 ℃. The MgTiO3 additive decreased the dehydriding activation energy of MgH2 from 116 to 95.7 kJ·mol-1. The thermodynamic and kinetic performance of the MgH2+20%(w) MgTiO3 composite was significantly improved compared with pristine MgH2, which was attributed to the high catalytic activity of the (insitu formed) TiO2 and Mg2TiO4 during the ball-milling and dehydriding processes.
Keywords:Hydrogen storage property  2''  '''')  MgH2" target="_blank">">MgH2  3''  '''')  MgTiO3" target="_blank">">MgTiO3  Catalytic activity  Activation energy
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