研究了不同化学计量比(x=0.25,0.5,0.75,1.0,1.25)和放氢背压(1×10-4和0.4 MPa)对LiBH4+xMg2NiH4复合体系吸放氢性能的影响.结果表明,随着化学计量比(x)的增加,复合体系的放氢温度逐渐降低,放氢动力学性能得到提高,但放氢容量逐渐降低;其中,在1×10-4和0.4 MPa初始放氢背压下,LiBH4+0.75Mg2NiH4体系具有最佳放氢动力学性能和较高的储氢容量.结果表明,放氢背压和化学计量比均会对高温下液相LiBH4与固态Mg2NiH4的润湿性产生影响,进而影响复合体系的放氢路径和放氢动力学性能.
The effects of stoichiometry(x =0. 25,0. 5,0. 75, 1.0, 1.25) and hydrogen back pressure on the dehydrogenation behavior of LiBH4 +xMg2 NiH4 composites were investigated systematically by methods of X-ray diffraction(XRD) and temperature programmed desorption(TPD) analysis. The results show that the stoichiometry x has a great effect on the dehydriding kinetics of LiBH4+xMg2NiH4 composites. With the increase of x value for the LiBH4 +xMgzNiH4 composites, the decrease of the dehydrogenation temperature and the improvement of the dehydriding kinetics are observed but with a loss of dehydrogenation capacity. Thereinto, LiBH4 + 0. 75Mg2NiH4 composite has the best dehydriding kinetics and a relatively high hydrogen storage capacity under initial hydrogen back pressure of 1 xl0-4 or 0. 4 MPa. The analysis shows that both the stoichiometry x of the LiBH4+xMg2NiH4 mixtures and hydrogen back pressure can influence the wetting between liquid LiBH4 and solid MgzNiH4 , and have a great effect on the dehydrogenation path and kinetics furthermore.