Center for Energy Materials, Interdisciplinary Nanoscience Center and Department of Chemistry, Aarhus University, DK-8000 Aarhus, Denmark.
Dalton Trans. 2013 Jan 21;42(3):680-7. doi: 10.1039/c2dt31591b.
Ammonium borohydride, NH(4)BH(4), has a high hydrogen content of ρ(m) = 24.5 wt% H(2) and releases 18 wt% H(2) below T = 160 °C. However, the half-life of bulk NH(4)BH(4) at ambient temperatures and pressures, ~6 h, is insufficient for practical applications. The decomposition of NH(4)BH(4) (ABH(2)) was studied at variable hydrogen and argon back pressures to investigate possible pressure mediated stabilization effects. The hydrogen release rate from solid ABH(2) at ambient temperatures is reduced by ~16% upon increasing the hydrogen back pressure from 5 to 54 bar. Similar results were obtained using argon pressure and the observed stabilization may be explained by a positive volume of activation, ca. 73 ± 17 cc mol(-1), in the transition state leading to hydrogen release. Nanoconfinement in mesoporous silica, MCM-41, was investigated as alternative means to stabilize NH(4)BH(4). However, other factors appear to significantly destabilize NH(4)BH(4) and it rapidly decomposes at ambient temperatures into [(NH(3))(2)BH(2)][BH(4)] (DADB) in accordance with the bulk reaction scheme. The hydrogen desorption kinetics from nanoconfined [(NH(3))(2)BH(2)][BH(4)] is moderately enhanced as evidenced by a reduction in the DSC decomposition peak temperature of ΔT = -13 °C as compared to the bulk material. Finally, we note a surprising result, storage of DADB at temperature <-30 °C transformed, reversibly, the [(NH(3))(2)BH(2)][BH(4)] into a new low temperature polymorph as revealed by both XRD and solid state MAS (11)B MAS NMR.
硼氢化铵,NH(4)BH(4),具有高的氢含量 ρ(m) = 24.5wt% H(2),在 T = 160°C 以下释放 18wt% H(2)。然而,在环境温度和压力下,块状 NH(4)BH(4 的半衰期,~6h,对于实际应用来说是不够的。研究了 NH(4)BH(4 (ABH(2))在可变氢气和氩气背压下的分解,以研究可能的压力介导稳定化效应。在环境温度下,从固态 ABH(2)中释放氢气的速率在氢气背压从 5 增加到 54 巴时降低了约 16%。使用氩气压也得到了类似的结果,观察到的稳定化作用可以通过在导致氢气释放的过渡态中,正的活化体积,约 73 ± 17 cc mol(-1)来解释。介孔二氧化硅 MCM-41 中的纳米约束被研究为稳定 NH(4)BH(4 的替代方法。然而,其他因素似乎显著使 NH(4)BH(4 不稳定,它在环境温度下迅速分解为 [(NH(3))(2)BH(2)][BH(4)] (DADB),与块状反应方案一致。与块状材料相比,从纳米约束的 [(NH(3))(2)BH(2)][BH(4)]中解吸氢气的动力学适度增强,这表现在 DSC 分解峰温度降低了 ΔT = -13°C。最后,我们注意到一个令人惊讶的结果,在温度 <-30°C 下储存 DADB 可使 [(NH(3))(2)BH(2)][BH(4)]可逆地转变为一种新的低温多晶型物,这一点通过 XRD 和固态 MAS(11)B MAS NMR 都得到了证实。