Department of Chemistry, Tsinghua University , Beijing 100084, China.
Institut für Physik and IRIS Adlershof, Humboldt-Universität zu Berlin , Berlin 12489, Germany.
J Am Chem Soc. 2017 Jul 26;139(29):9795-9798. doi: 10.1021/jacs.7b05018. Epub 2017 Jul 13.
Here we report a novel approach to synthesize atomically dispersed uniform clusters via a cage-separated precursor preselection and pyrolysis strategy. To illustrate this strategy, well-defined Ru(CO) was separated as a precursor by suitable molecular-scale cages of zeolitic imidazolate frameworks (ZIFs). After thermal treatment under confinement in the cages, uniform Ru clusters stabilized by nitrogen species (Ru/CN) were obtained. Importantly, we found that Ru/CN exhibits excellent catalytic activity (100% conversion), high chemoselectivity (100% for 2-aminobenzaldehyde), and significantly high turnover frequency (TOF) for oxidation of 2-aminobenzyl alcohol. The TOF of Ru/CN (4320 h) is about 23 times higher than that of small-sized (ca. 2.5 nm) Ru particles (TOF = 184 h). This striking difference is attributed to a disparity in the interaction between Ru species and adsorbed reactants.
在这里,我们报告了一种通过笼分离前体预选择和热解策略合成原子分散均匀团簇的新方法。为了说明这一策略,我们通过沸石咪唑酯框架(ZIFs)的适当分子尺度笼将明确的 Ru(CO) 分离为前体。在笼内限制条件下进行热处理后,得到由氮物种稳定的均匀 Ru 团簇(Ru/CN)。重要的是,我们发现 Ru/CN 表现出优异的催化活性(转化率为 100%)、高化学选择性(2-氨基苯甲醛为 100%)和 2-氨基苯甲醇氧化的显著高周转频率(TOF)。Ru/CN 的 TOF(4320 h)大约是小尺寸(约 2.5nm)Ru 颗粒(TOF=184 h)的 23 倍。这种显著的差异归因于 Ru 物种和吸附反应物之间相互作用的差异。