Boddien Albert, Loges Björn, Junge Henrik, Beller Matthias
Leibniz-Institut für Katalyse e.V. an der Universität Rostock, Albert-Einstein-Strasse 29a, 18059 Rostock, Germany.
ChemSusChem. 2008;1(8-9):751-8. doi: 10.1002/cssc.200800093.
The efficient generation of hydrogen from formic acid/amine adducts at ambient temperature is demonstrated. The highest catalytic activity (TOF up to 3630 h(-1) after 20 min) was observed in the presence of in situ generated ruthenium phosphine catalysts. Compared to the previously known methods to generate hydrogen from liquid feedstocks, the systems presented here can be operated at room temperature without the need for any high-temperature reforming processes, and the hydrogen produced can then be directly used in fuel cells. A variety of Ru precursors and phosphine ligands were investigated for the decomposition of formic acid/amine adducts. These catalytic systems are particularly interesting for the generation of H2 for new applications in portable electric devices.
本文展示了在室温下由甲酸/胺加合物高效制氢的过程。原位生成的钌膦催化剂存在时,观察到最高催化活性(20分钟后TOF高达3630 h⁻¹)。与先前已知的从液体原料制氢的方法相比,本文介绍的体系可在室温下运行,无需任何高温重整过程,所产生的氢气可直接用于燃料电池。研究了多种钌前驱体和膦配体用于甲酸/胺加合物的分解。这些催化体系对于为便携式电子设备的新应用生成氢气尤为有趣。