Qi Haifeng, Yang Ji, Liu Fei, Zhang LeiLei, Yang Jingyi, Liu Xiaoyan, Li Lin, Su Yang, Liu Yuefeng, Hao Rui, Wang Aiqin, Zhang Tao
CAS Key Laboratory of Science and Technology on Applied Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, China.
University of Chinese Academy of Sciences, Beijing, China.
Nat Commun. 2021 Jun 2;12(1):3295. doi: 10.1038/s41467-021-23429-w.
Single-atom catalysts (SACs) have emerged as a frontier in heterogeneous catalysis due to the well-defined active site structure and the maximized metal atom utilization. Nevertheless, the robustness of SACs remains a critical concern for practical applications. Herein, we report a highly active, selective and robust Ru SAC which was synthesized by pyrolysis of ruthenium acetylacetonate and N/C precursors at 900 °C in N followed by treatment at 800 °C in NH. The resultant Ru-N structure exhibits moderate capability for hydrogen activation even in excess NH, which enables the effective modulation between transimination and hydrogenation activity in the reductive amination of aldehydes/ketones towards primary amines. As a consequence, it shows superior amine productivity, unrivalled resistance against CO and sulfur, and unexpectedly high stability under harsh hydrotreating conditions compared to most SACs and nanocatalysts. This SAC strategy will open an avenue towards the rational design of highly selective and robust catalysts for other demanding transformations.
单原子催化剂(SACs)因其明确的活性位点结构和最大化的金属原子利用率,已成为多相催化领域的前沿研究方向。然而,SACs的稳定性仍是实际应用中的关键问题。在此,我们报道了一种高活性、高选择性且稳定的Ru SAC,它是通过乙酰丙酮钌和N/C前驱体在900℃的氮气中热解,随后在800℃的氨气中处理而合成的。所得的Ru-N结构即使在过量氨气存在的情况下也具有适度的氢活化能力,这使得醛/酮向伯胺的还原胺化反应中,转亚胺化和氢化活性之间能够实现有效调控。因此,与大多数SACs和纳米催化剂相比,它表现出卓越的胺生成率、无与伦比的抗CO和抗硫性能,以及在苛刻加氢处理条件下出人意料的高稳定性。这种SAC策略将为合理设计用于其他苛刻转化反应的高选择性和稳定催化剂开辟一条途径。