Fan Hua, Folke Jan Markus, Liu Zigeng, Girgsdies Frank, Imlau Robert, Ruland Holger, Heumann Saskia, Granwehr Josef, Eichel Rüdiger-A, Schlögl Robert, Frei Elias, Huang Xing
Department of Heterogeneous Reactions, Max Planck Institute for Chemical Energy Conversion, 45470 Mülheim an der Ruhr, Germany.
Department of Inorganic Chemistry, Fritz-Haber Institute of Max Planck Society, Faradayweg 4-6, 14195 Berlin, Germany.
ACS Appl Mater Interfaces. 2021 Jun 30;13(25):30187-30197. doi: 10.1021/acsami.1c06771. Epub 2021 Jun 15.
Developing high-performance Fe-based ammonia catalysts through simple and cost-efficient methods has received an increased level of attention. Herein, we report for the first time, the synthesis of two-dimensional (2D) FeOOH nanoflakes encapsulated by mesoporous SiO (mSiO) via a simple solution-based method for ammonia synthesis. Due to the sticking of the mSiO coating layers and the limited spaces in between, the Fe after reduction retains the 2D morphology, showing high resistance against the sintering in the harsh Haber-Bosch process. Compared to supported Fe particles dispersed on mSiO spheres, the coated catalyst shows a significantly improved catalytic activity by 50% at 425 °C. Thermal desorption spectroscopy (TDS) reveals the existence of a higher density of reactive sites for N activation in the 2D Fe catalyst, which is possibly coupled to a larger density of surface defect sites (kinks, steps, point defects) that are generally considered as active centers in ammonia synthesis. Besides the structural impact of the coating on the 2D Fe, the electronic one is elucidated by partially substituting Si with Al in the coating, confirmed by Si and Al magic-angle spinning nuclear magnetic resonance (MAS NMR). An increased apparent activation energy () of the Al-containing catalyst evidences an influence on the nature of the active site. The herein-developed stable 2D Fe nanostructures can serve as an example of a 2D material applied in catalysis, offering the chance of a rational catalyst design based on a stepwise introduction of various promoters, in the coating and on the metal, maintaining the spatial control of the active centers.
通过简单且经济高效的方法开发高性能铁基氨合成催化剂受到了越来越多的关注。在此,我们首次报道了通过一种基于溶液的简单方法合成由介孔SiO(mSiO)包覆的二维(2D)FeOOH纳米片用于氨合成。由于mSiO涂层的粘连以及其间有限的空间,还原后的铁保留了二维形态,在苛刻的哈伯-博施法过程中表现出高抗烧结性。与分散在mSiO球上的负载型铁颗粒相比,包覆催化剂在425℃时的催化活性显著提高了50%。热脱附光谱(TDS)揭示了二维铁催化剂中存在更高密度的用于氮活化的活性位点,这可能与更大密度的表面缺陷位点(扭结、台阶、点缺陷)相关,这些缺陷位点通常被认为是氨合成中的活性中心。除了涂层对二维铁的结构影响外,通过在涂层中用铝部分替代硅来阐明电子影响,这通过硅和铝的魔角旋转核磁共振(MAS NMR)得到证实。含铝催化剂的表观活化能增加证明了对活性位点性质的影响。本文开发的稳定二维铁纳米结构可作为二维材料应用于催化的一个例子,为基于逐步引入各种促进剂进行合理催化剂设计提供了机会,这些促进剂可在涂层中和金属上,同时保持对活性中心的空间控制。