Ye Tian-Nan, Park Sang-Won, Lu Yangfan, Li Jiang, Sasase Masato, Kitano Masaaki, Tada Tomofumi, Hosono Hideo
Materials Research Center for Element Strategy, Tokyo Institute of Technology, Yokohama, Japan.
Precursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency, Saitama, Japan.
Nature. 2020 Jul;583(7816):391-395. doi: 10.1038/s41586-020-2464-9. Epub 2020 Jul 15.
Ammonia (NH) is pivotal to the fertilizer industry and one of the most commonly produced chemicals. The direct use of atmospheric nitrogen (N) had been challenging, owing to its large bond energy (945 kilojoules per mole), until the development of the Haber-Bosch process. Subsequently, many strategies have been explored to reduce the activation barrier of the N≡N bond and make the process more efficient. These include using alkali and alkaline earth metal oxides as promoters to boost the performance of traditional iron- and ruthenium-based catalysts via electron transfer from the promoters to the antibonding bonds of N through transition metals. An electride support further lowers the activation barrier because its low work function and high electron density enhance electron transfer to transition metals. This strategy has facilitated ammonia synthesis from N dissociation and enabled catalytic operation under mild conditions; however, it requires the use of ruthenium, which is expensive. Alternatively, it has been shown that nitrides containing surface nitrogen vacancies can activate N (refs. ). Here we report that nickel-loaded lanthanum nitride (LaN) enables stable and highly efficient ammonia synthesis, owing to a dual-site mechanism that avoids commonly encountered scaling relations. Kinetic and isotope-labelling experiments, as well as density functional theory calculations, confirm that nitrogen vacancies are generated on LaN with low formation energy, and efficiently bind and activate N. In addition, the nickel metal loaded onto the nitride dissociates H. The use of distinct sites for activating the two reactants, and the synergy between them, results in the nickel-loaded LaN catalyst exhibiting an activity that far exceeds that of more conventional cobalt- and nickel-based catalysts, and that is comparable to that of ruthenium-based catalysts. Our results illustrate the potential of using vacancy sites in reaction cycles, and introduce a design concept for catalysts for ammonia synthesis, using naturally abundant elements.
氨(NH₃)对化肥工业至关重要,是最常生产的化学品之一。由于大气氮(N₂)的键能很大(每摩尔945千焦),其直接利用一直具有挑战性,直到哈伯-博施法的出现。随后,人们探索了许多策略来降低N≡N键的活化能垒并提高该过程的效率。这些策略包括使用碱金属和碱土金属氧化物作为促进剂,通过从促进剂到氮的反键通过过渡金属的电子转移来提高传统铁基和钌基催化剂的性能。电子化物载体进一步降低了活化能垒,因为其低功函数和高电子密度增强了向过渡金属的电子转移。这种策略促进了由氮解离合成氨,并能够在温和条件下进行催化操作;然而,它需要使用昂贵的钌。另外,已经表明含有表面氮空位的氮化物可以活化N₂(参考文献)。在这里,我们报告负载镍的氮化镧(LaN)能够实现稳定且高效的氨合成,这归因于一种避免常见比例关系的双位点机制。动力学和同位素标记实验以及密度泛函理论计算证实,在LaN上以低形成能产生氮空位,并有效地结合和活化N₂。此外,负载在氮化物上的镍金属使H₂解离。使用不同的位点来活化两种反应物以及它们之间的协同作用,使得负载镍的LaN催化剂表现出远超更传统的钴基和镍基催化剂的活性,并且与钌基催化剂相当。我们的结果说明了在反应循环中使用空位位点的潜力,并引入了一种使用天然丰富元素的氨合成催化剂的设计概念。