Yan Hanxue, Gao Wenbo, Wang Qianru, Guo Jianping, Chen Ping
Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, China.
University of Chinese Academy of Sciences, Beijing, China.
Faraday Discuss. 2023 Jul 19;243(0):55-64. doi: 10.1039/d2fd00142j.
Noble metal elements are focal catalytic candidates for many chemical processes, but have received little attention in the field of nitrogen fixation except ruthenium and osmium. Iridium (Ir), as a representative, has been shown to be catalytically inactive for ammonia synthesis because of its weak nitrogen adsorption and severe competitive adsorption of H over N that strongly inhibits the activation of N molecules. Here we show that, upon compositing with lithium hydride (LiH), iridium can catalyze ammonia formation at much enhanced reaction rates. The catalytic performance of the LiH-Ir composite can be further improved by dispersion on a MgO support with a high specific surface area. At 400 °C and 10 bar, the MgO-supported LiH-Ir (LiH-Ir/MgO) catalyst shows a 100-fold increase in activity compared to the bulk LiH-Ir composite and the MgO-supported Ir metal catalyst (Ir/MgO). The formation of a lithium-iridium complex hydride phase was identified and characterized, and this phase may be responsible for the activation and hydrogenation of N to NH.
贵金属元素是许多化学过程中重要的催化候选物,但除了钌和锇之外,在固氮领域很少受到关注。以铱(Ir)为例,由于其对氮的吸附较弱以及氢对氮的严重竞争性吸附强烈抑制了氮分子的活化,已证明铱对氨合成没有催化活性。在此我们表明,与氢化锂(LiH)复合后,铱能够以大大提高的反应速率催化氨的形成。通过分散在具有高比表面积的氧化镁(MgO)载体上,LiH-Ir复合材料的催化性能可以进一步提高。在400℃和10巴的条件下,MgO负载的LiH-Ir(LiH-Ir/MgO)催化剂的活性比块状LiH-Ir复合材料和MgO负载的铱金属催化剂(Ir/MgO)提高了100倍。已鉴定并表征了锂 - 铱复合氢化物相的形成,并且该相可能是氮活化和氢化生成氨的原因。