以NaH粉和Al粉为合成原料,分别采用2%(摩尔分数,X)CeCl3和2%CeCl3/ykH(y=0.02,0.04)为催化添加剂,在室温和3MPa氢压下,通过反应球磨(NaH/AI+CeCl3)和(NaH/AI+CeCl3/ykH)(y=0.02,0.04)复合物成功制备出Na.AI.H配位氢化物.吸放氢性能测试结果表明,KH的加入能有效改善Na-AI-H体系中第二步脱氢反应放氢动力学性能.(NaH/AI+CeCl3/0.02KH)复合物170。C放氢时可在20min内完成脱氢过程,且在较低温度(100—140℃)下具有良好的可逆吸放氢性能.Kissenger方法计算表明,添加KH可降低Na-Al-H体系第二步脱氢反应的表观活化能,降低其放氢峰值温度.相结构分析表明,KH的添加使Na—Al-H体系中Na3AlH。的晶胞体积发生膨胀,进而提高体系的第二步放氢动力学性能.
The Na-AI-H complex hydride was prepared by reactive ball milling (NaH/AI+CeCI3) and (Nail/ AI+CeCIJyKH) (y=0.02, 0.04) composites under a hydrogen pressure of 3 MPa at room temperature, using Nail and AI powder as raw materials, as well as 2% (molar fraction, x) CeCI3 and 2% CeCIJyKH (y=0.02, 0.04) as dopant, respectively. The de-/hydrogenation properties showed that the addition of KH could effectively improve the dehydrogenation kinetics of the second decomposition step for the Na-AI-H system. The (NaH/AI+CeCIJ0.02KH) composite completed the dehydrogenation process within 20 min at 170 ℃, with good de-/hydrogenation cycling performance at relatively low temperatures (100-140 ℃). Calculation by the Kissenger method showed that the addition of KH decreased the apparent activation energy of the second decomposition step of the Na-AI-H system, resulting in a decrease of desorption peak temperatures. Phase structure analysis showed that the enhanced second step dehydrogenation kinetics of the Na-AI-H composite system was mainly ascribed to the lattice volume expansion of Na3AIH6 that resulted from the addition of KH.