Energy Systems Division, Argonne National Laboratory, Argonne, IL 60439, USA.
Acc Chem Res. 2013 Aug 20;46(8):1806-15. doi: 10.1021/ar300229c. Epub 2013 Mar 12.
Supported metal nanoparticles are among the most important catalysts for many practical reactions, including petroleum refining, automobile exhaust treatment, and Fischer-Tropsch synthesis. The catalytic performance strongly depends on the size, composition, and structure of the metal nanoparticles, as well as the underlying support. Scientists have used conventional synthesis methods including impregnation, ion exchange, and deposition-precipitation to control and tune these factors, to establish structure-performance relationships, and to develop better catalysts. Meanwhile, chemists have improved the stability of metal nanoparticles against sintering by the application of protective layers, such as polymers and oxides that encapsulate the metal particle. This often leads to decreased catalytic activity due to a lack of precise control over the thickness of the protective layer. A promising method of catalyst synthesis is atomic layer deposition (ALD). ALD is a variation on chemical vapor deposition in which metals, oxides, and other materials are deposited on surfaces by a sequence of self-limiting reactions. The self-limiting character of these reactions makes it possible to achieve uniform deposits on high-surface-area porous solids. Therefore, design and synthesis of advanced catalysts on the nanoscale becomes possible through precise control over the structure and composition of the underlying support, the catalytic active sites, and the protective layer. In this Account, we describe our advances in the synthesis and stabilization of supported metal catalysts by ALD. After a short introduction to the technique of ALD, we show several strategies for metal catalyst synthesis by ALD that take advantage of its self-limiting feature. Monometallic and bimetallic catalysts with precise control over the metal particle size, composition, and structure were achieved by combining ALD sequences, surface treatments, and deposition temperature control. Next, we describe ALD oxide overcoats applied with atomically precise thickness control that stabilize metal catalysts while preserving their catalytic function. We also discuss strategies for generation and control over the porosity of the overcoats that allow the embedded metal particles to remain accessible by reactants, and the details for ALD alumina overcoats on metal catalysts. Moreover, using methanol decomposition and oxidative dehydrogenation of ethane as probe reactions, we demonstrate that selectively blocking low coordination metal sites by oxide overcoats can provide another strategy to enhance both the durability and selectivity of metal catalysts.
负载型金属纳米粒子是许多实际反应(包括石油炼制、汽车尾气处理和费托合成)中最重要的催化剂之一。催化剂的催化性能强烈依赖于金属纳米粒子的尺寸、组成和结构,以及载体的性质。科学家们已经使用传统的合成方法,包括浸渍、离子交换和沉积沉淀,来控制和调节这些因素,建立结构-性能关系,并开发更好的催化剂。同时,化学家们通过应用聚合物和氧化物等保护层来提高金属纳米粒子的抗烧结稳定性,从而包裹金属颗粒。然而,这通常会导致催化活性的降低,因为无法精确控制保护层的厚度。原子层沉积(ALD)是一种很有前途的催化剂合成方法。ALD 是化学气相沉积的一种变体,其中金属、氧化物和其他材料通过一系列自限制反应在表面上沉积。这些反应的自限制性质使得在高表面积多孔固体上实现均匀的沉积物成为可能。因此,通过精确控制载体的结构和组成、催化活性位和保护层,可以实现纳米尺度上先进催化剂的设计和合成。在本综述中,我们描述了通过 ALD 在负载型金属催化剂的合成和稳定化方面的进展。在简要介绍 ALD 技术之后,我们展示了几种利用其自限制特性的金属催化剂合成策略。通过组合 ALD 序列、表面处理和沉积温度控制,实现了对金属颗粒尺寸、组成和结构的精确控制的单金属和双金属催化剂。接下来,我们描述了具有原子级精度厚度控制的 ALD 氧化物覆盖层,该覆盖层稳定金属催化剂的同时保持其催化功能。我们还讨论了生成和控制覆盖层多孔性的策略,这使得嵌入的金属颗粒仍然可以与反应物接触,并详细介绍了金属催化剂上的 ALD 氧化铝覆盖层。此外,我们使用甲醇分解和乙烷氧化脱氢作为探针反应,证明通过氧化物覆盖层选择性地封闭低配位金属位可以提供另一种策略,以提高金属催化剂的耐久性和选择性。