LiAIH4 doped with Ni and Ce（SO4）2 additives and the effect of doping on temperature and hydrogen release were studied by pressure-content-temperature （PCT） experiment and X-ray diffraction （XRD） analysis. It is ...LiAIH4 doped with Ni and Ce（SO4）2 additives and the effect of doping on temperature and hydrogen release were studied by pressure-content-temperature （PCT） experiment and X-ray diffraction （XRD） analysis. It is indicated that doping with Ni induces a significant decrease in temperature in the first step and LiA1H4 doped with 1mol% Ni presents the most absorption of hydrogen. Doping with Ce（S04）2 also causes a marked decrease, while the amount of hydrogen release changes only slightly. The results from X-ray diffraction analysis show that doping does not cause any structural change; Ni and Ce-containing phases are not observed at room temoerature or even at 250℃.展开更多
The catalytic effects of ZrC powder on the dehydrogenation properties of LiAlH4 prepared by designed mixing processes were systematically investigated.The onset dehydrogenation temperatures for the 10 mol% ZrC-doped s...The catalytic effects of ZrC powder on the dehydrogenation properties of LiAlH4 prepared by designed mixing processes were systematically investigated.The onset dehydrogenation temperatures for the 10 mol% ZrC-doped sample are 85.3 and 148.4℃for the first two dehydrogenation stages,decreasing by 90.7 and 57.8℃,respectively,compared with those of the as-received LiAIH4.The isothermal volumetric measurement indicates that adding ZrC powder could significantly enhance the desorption kinetics of LiAlH4.The reaction constant and Avrami index show that the first dehydrogenation stage is controlled by diffusion mechanism with nucleation rate gradually decreasing and the second stage is a freedom nucleation and subsequent growth process.The microstructures and phase transformation characterized by scanning electron microscopy(SEM),X-ray diffraction(XRD),X-ray photoelectron spectroscopy(XPS) and Fourier transform infrared spectroscopy(FTIR) reveal that the improved desorption behavior of LiAlH4 is primarily due to the high density of surface defects and embedded catalyst particles on the surface of LiAlH4 particles during the high-energy mixing process.展开更多
基金supported by the National High-Tech Research and Development Program (No.2006AA05Z132)the Program of the Ministry of Education of China for Changjiang Scholars and Innovative Research Teams in Universities (No.I2P407)
文摘LiAIH4 doped with Ni and Ce（SO4）2 additives and the effect of doping on temperature and hydrogen release were studied by pressure-content-temperature （PCT） experiment and X-ray diffraction （XRD） analysis. It is indicated that doping with Ni induces a significant decrease in temperature in the first step and LiA1H4 doped with 1mol% Ni presents the most absorption of hydrogen. Doping with Ce（S04）2 also causes a marked decrease, while the amount of hydrogen release changes only slightly. The results from X-ray diffraction analysis show that doping does not cause any structural change; Ni and Ce-containing phases are not observed at room temoerature or even at 250℃.
基金financially supported by the National High Technology Research and Development Program of China (No.2006AA05Z132)the National Natural Science Foundation of China (No.51471054)
文摘The catalytic effects of ZrC powder on the dehydrogenation properties of LiAlH4 prepared by designed mixing processes were systematically investigated.The onset dehydrogenation temperatures for the 10 mol% ZrC-doped sample are 85.3 and 148.4℃for the first two dehydrogenation stages,decreasing by 90.7 and 57.8℃,respectively,compared with those of the as-received LiAIH4.The isothermal volumetric measurement indicates that adding ZrC powder could significantly enhance the desorption kinetics of LiAlH4.The reaction constant and Avrami index show that the first dehydrogenation stage is controlled by diffusion mechanism with nucleation rate gradually decreasing and the second stage is a freedom nucleation and subsequent growth process.The microstructures and phase transformation characterized by scanning electron microscopy(SEM),X-ray diffraction(XRD),X-ray photoelectron spectroscopy(XPS) and Fourier transform infrared spectroscopy(FTIR) reveal that the improved desorption behavior of LiAlH4 is primarily due to the high density of surface defects and embedded catalyst particles on the surface of LiAlH4 particles during the high-energy mixing process.
