Department of Applied Chemistry, Faculty of Engineering, Oita University, 700 Dannoharu, Oita 870-1154, Japan.
Elements Strategy Initiative for Catalysts and Batteries, Kyoto University, 1-30 Goryo-Ohara, Nishikyo-ku, Kyoto 615-8245, Japan.
Sci Adv. 2017 Apr 28;3(4):e1602747. doi: 10.1126/sciadv.1602747. eCollection 2017 Apr.
Ammonia has been suggested as a carbon-free hydrogen source, but a convenient method for producing hydrogen from ammonia with rapid initiation has not been developed. Ideally, this method would require no external energy input. We demonstrate hydrogen production by exposing ammonia and O at room temperature to an acidic RuO/γ-AlO catalyst. Because adsorption of ammonia onto the catalyst is exothermic, the catalyst bed is rapidly heated to the catalytic ammonia autoignition temperature, and subsequent oxidative decomposition of ammonia produces hydrogen. A differential calorimeter combined with a volumetric gas adsorption analyzer revealed a large quantity of heat evolved both with chemisorption of ammonia onto RuO and acidic sites on the γ-AlO and with physisorption of multiple ammonia molecules.
氨被认为是一种无碳的氢源,但尚未开发出一种方便的方法,可将氨快速转化为氢气,且无需外部能量输入。我们在室温下将氨和氧气暴露于酸性 RuO/γ-AlO 催化剂上,从而实现了氢气的生产。由于氨在催化剂上的吸附是放热的,因此催化剂床迅速被加热到催化氨自燃温度,随后氨的氧化分解产生氢气。差示量热计与体积气体吸附分析仪相结合,揭示了大量的热与氨在 RuO 上的化学吸附以及在 γ-AlO 上的酸性位和多个氨分子的物理吸附有关。