摘要
首先以葡萄糖为C源,水热法制备了均匀C球,再以乙二醇为溶剂,先后加入醋酸镍、醋酸镁和氯化铈,最终制得Ce-Mg-Ni/C纳米复合储氢材料。采用X射线衍射仪(XRD)分析了溶剂热后复合材料的微观结构,用扫描电镜(SEM)观察了其形貌。通过自动控制的Sieverts设备测试了材料的吸放氢动力学性能。研究表明以均匀C球为载体,预制的Ce、Mg、Ni原子比为2∶1∶2及23∶4∶7的复合材料呈现纳米结构。XRD结果表明,复合材料中出现明显的Ce2MgNi2和Ce23Mg4Ni7的峰值,并伴随有第二相CeMg3和CeNi3出现。通过P-C-T(pressure-composition-temperature)测试实验结果显示,Ce2MgNi2/C和Ce23Mg4Ni7/C复合材料在50℃下的吸附氢量分别可达到1.54%和1.05%(w/w)。
The hydrothermal method was taken to preparing uniform C-sphere from glucose as the C source,then using ethylene glycol as the solvent,and nickel acetate,magnesium acetate and cerium chloride were added successively.Finally,the Ce-Mg-Ni/C nano-composite for hydrogen storage was producing.X-ray diffraction(XRD)and scanning electron microscopy(SEM)were employed to analyze the phase composition and morphology of the solvent-thermal synthesis the nano-composites.Hydrogen adsorption-desorption measurements were performed by an automatic controlled Sieverts.SEM analysis indicated that the pre-fabricated composites with atom radios of 2∶1∶2 and 23∶4∶7 presented a nano-scale structure in uniform C-sphere templates.The XRD analysis showed that Ce2MgNi2 and Ce23Mg4Ni7 have been formed as nano-composite with carbon,and the peaks of the second phase CeMg3 and CeNi3 were presented in XRD patterns.P-C-T(pressure-composition-temperature)test date revealed that the hydrogen adsorption capacity of Ce2MgNi2/C and Ce23Mg4Ni7/C composites reached 1.54%and 1.05%(w/w)at 50℃,respectively.
作者
刘卓承
郭瑞华
阮飞
胡锋
张捷宇
安胜利
LIU Zhuo-Cheng;GUO Rui-Hua;RUAN Fei;HU Feng;ZHANG Jie-Yu;AN Sheng-Li(College of Materials Science and Engineering,Shanghai University,Shanghai 200072,China;Institute of materials and metallurgy,Inner Mongolia University of Science and Technology,Baotou,Inner Mongolia 014010,China)
出处
《无机化学学报》
SCIE
CAS
CSCD
北大核心
2019年第12期2284-2290,共7页
Chinese Journal of Inorganic Chemistry
基金
国家自然科学基金(No.51864040)
内蒙古科技大学创新基金(No.2017QDL-S02)资助项目