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作 者:方方[1] 李永涛[1] 宋云[1] 査俊[1] 赵斌[1] 孙大林[1]
出 处:《物理化学学报》2011年第6期1537-1542,共6页Acta Physico-Chimica Sinica
基 金:国家自然科学基金(51001028);上海市自然科学基金(10ZR1404300);中央高校基本科研业务费专项资金资助~~
摘 要:以LiBH4和MnCl2为初始原料,采用反应球磨法制备了LiMn(BH4)3/2LiCl复合物,并系统地研究了该复合物的脱氢性能及含钛催化剂的掺杂对其脱氢性能的影响.结果表明:LiMn(BH4)3/2LiCl复合物是由非晶态的LiMn(BH4)3和晶态的LiCl组成,在135-190°C分解,分解反应的活化能为114.0kJ·mol-1;LiMn(BH4)3/2LiCl复合物分解失重约7.0%(w).组分分析表明除H2外,释放的气体中还含有4.0%(摩尔分数,x)的B2H6.B2H6的生成是该复合物失重超过其理论储氢容量6.3%(w)的原因;进一步研究发现,含钛催化剂(TiF3、TiC、TiN和TiO2)中,仅TiF3能够催化LiMn(BH4)3/2LiCl复合物的分解反应,使其起始分解温度和分解反应活化能分别降低至125°C和104.0kJ·mol-1.这主要归因于TiF3中的Ti原子取代了LiMn(BH4)3中的部分Li原子,并在局域形成了易于分解的Ti(BH4)3.A LiMn(BH4)3/2LiCl composite was prepared by reactive ball-milling a mixture of LiBH4 and MnCl2, and its dehydrogenation properties were investigated. The results indicate that the LiMn(BH4)3/2LiCl composite consists of crystalline LiCl and amorphous LiMn(BH4)3, and decomposes at 135-190 °C with an activation energy of 114.0 kJ·mol-1, resulting in an emission of 7.0% (w) gas. The released gases contain 96.0% H2 and 4.0% B2H6 (mole fraction, x), which is the reason for why the mass loss of the LiMn(BH4)3/2LiCl composite is larger than that of theoretical hydrogen capacity of 6.3% (w). Moreover, the influence of various Ti-containing dopants on the decomposition of the LiMn(BH4)3/2LiCl composite was studied. We found that among TiF3, TiC, TiN, and TiO2, only TiF3 achieved a reduction in decomposition temperature. Compared with the undoped LiMn(BH4)3/2LiCl composite, the onset decomposition temperature and the activation energy of the TiF3-doped composite are reduced to 125 °C and to 104.0 kJ·mol-1, respectively. These are attributed to the formation of Ti(BH4)3 in some local regions of the TiF3-doped composite by the partial substitution of Ti for Li in LiMn(BH4)3.
关 键 词:硼氢化物 反应球磨 LiMn(BH4)3 脱氢性能 催化
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