Department of Chemistry, State University of New York at Binghamton, Binghamton, NY 13902, USA.
Acc Chem Res. 2013 Aug 20;46(8):1867-77. doi: 10.1021/ar3002238. Epub 2013 Mar 5.
Due to the increasing worldwide energy demand and environ-mental concerns, the need for alternative energy sources is growing stronger, and platinum catalysts in fuel cells may help make the technologies a reality. However, the pursuit of highly active Pt-based electrocatalysts continues to be a challenge. Scientists developing electrocatalysts continue to focus on characterizing and directing the construction of nanocrystals and advancing their electrochemical applications. Although chemists have worked on Pt-based bimetallic (Pt-M) preparations in the past, more recent research shows that both shape-controlled Pt-M nanocrystals and the assembly of these nanocrystals into supercrystals are promising new directions. A solution-based synthesis approach is an effective technique for preparing crystallographic facet-directed nanocatalysts. This is aided by careful selection of the metal precursor, capping ligand, reducing agent, and solvent. Incorporating a secondary metal M into the Pt lattice and manipulating the crystal facets on the surface cooperatively alter the electrocatalytic behavior of these Pt-M bimetallic nanocrystals. Specifically, chemists have extensively studied the {111}- and {100}-terminated crystal facets because they show unique atomic arrangement on surfaces, exhibit different catalytic performance, and possess specific resistance to toxic adsorbed carbon monoxide (COads). For catalysts to have maximum efficiency, they need to have resistance to COads and other poisonous carbon-containing intermediates when the catalysts operate under harsh conditions. A necessary design to any synthesis is to clearly understand and utilize the role of each component in order to successfully induce shape-controlled growth. Since chemists began to understand Pt nanocrystal shape-dependent electrocatalytic activity, the main obstacles blocking proton exchange membrane fuel cells are anode poisoning, sluggish kinetics at the cathode, and low activity. In this Account, we discuss the basic concepts in preparation of Pt-M bimetallic nanocrystals, focusing on several immaculate examples of manipulation at the nanoscale. We briefly introduce the prospects for applying Pt-M nanocrystals as electrocatalysts based on the electronic and geometric standpoints. In addition, we discuss several key parameters in the solution-based synthesis approach commonly used to facilitate Pt-M nanocrystals, such as reaction temperature and time, the combination of organic amines and acids, gaseous adsorbates, anionic species, and solvent. Each example features various nanoscale morphologies, such as spheres, cubes, octahedrons, and tetrahedrons. Additionally, we outline and review the superior electrocatalytic performances of the recently developed high-index Pt-M nanostructures. Next, we give examples of the electrocatalytic capabilities from these shape-defined Pt-M architectures by highlighting significant accomplishments in specific systems. Then, using several typical cases, we summarize electrochemical evaluations on the Pt-based shape-/composition-dependent nanocatalysts toward reactions on both the anode and the cathode. Lastly, we provide an outlook of current challenges and promising directions for shape-controlled Pt-M bimetallic electrocatalysts.
由于全球能源需求不断增长和环境问题日益严重,对替代能源的需求越来越强烈,燃料电池中的铂催化剂可能有助于使这些技术成为现实。然而,寻找高活性的基于铂的电催化剂仍然是一个挑战。科学家们一直在研究电催化剂,继续致力于表征和指导纳米晶体的构建,并推进其电化学应用。尽管化学家过去曾致力于研究基于铂的双金属(Pt-M)制剂,但最近的研究表明,形状控制的 Pt-M 纳米晶体和这些纳米晶体组装成超晶体都是很有前途的新方向。基于溶液的合成方法是制备结晶面导向纳米催化剂的有效技术。这得益于对金属前体、封端配体、还原剂和溶剂的精心选择。将辅助金属 M 掺入 Pt 晶格并协同改变表面的晶面可以改变这些 Pt-M 双金属纳米晶体的电催化行为。具体来说,化学家已经广泛研究了 {111} 和 {100} 终止晶面,因为它们在表面上表现出独特的原子排列,表现出不同的催化性能,并对有毒吸附的一氧化碳(COads)具有特定的抵抗力。为了使催化剂具有最高的效率,当催化剂在苛刻的条件下运行时,它们需要具有对 COads 和其他有毒含碳中间体的抵抗力。任何合成的必要设计都是要清楚地理解和利用每个组件的作用,以便成功地诱导形状控制生长。自从化学家开始了解 Pt 纳米晶体形状依赖性电催化活性以来,阻碍质子交换膜燃料电池的主要障碍是阳极中毒、阴极动力学缓慢和活性低。在本专题介绍中,我们讨论了制备 Pt-M 双金属纳米晶体的基本概念,重点介绍了在纳米尺度上进行的几个完美操作实例。我们简要介绍了基于电子和几何观点的 Pt-M 纳米晶体作为电催化剂的应用前景。此外,我们还讨论了在基于溶液的合成方法中常用的几个关键参数,例如反应温度和时间、有机胺和酸的组合、气态吸附物、阴离子和溶剂。每个实例都具有各种纳米级形态,例如球体、立方体、八面体和四面体。此外,我们还概述和回顾了最近开发的高指数 Pt-M 纳米结构的优越电催化性能。接下来,我们通过突出特定系统中的重要成就,给出了这些形状定义的 Pt-M 结构的电催化能力的例子。然后,使用几个典型案例,我们总结了基于 Pt 的形状/组成依赖性纳米催化剂对阳极和阴极反应的电化学评价。最后,我们提供了对形状控制的 Pt-M 双金属电催化剂当前挑战和有前景的方向的展望。