Bueno Sandra L A, Ashberry Hannah M, Shafei Ibrahim, Skrabalak Sara E
Department of Chemistry, Indiana University-Bloomington, 800 E. Kirkwood Ave., Bloomington, Indiana 47405, United States.
Acc Chem Res. 2021 Apr 6;54(7):1662-1672. doi: 10.1021/acs.accounts.0c00655. Epub 2020 Dec 30.
ConspectusWhen combined with earth-abundant metals, Pt-based alloy nanoparticles (NPs) can be cost-effective electrocatalysts. However, these NPs can experience leaching of non-noble-metal components under harsh electrocatalytic conditions. The Skrabalak group has demonstrated a novel NP construct in which Pt-based random alloy surfaces are stabilized against non-noble-metal leaching by their deposition onto intermetallic seeds. These core@shell NPs are highly durable electrocatalysts, with the ability to tune catalytic performance by the core@shell architecture, surface alloy composition, and NP shape. This versatility was demonstrated in a model system in which random alloy () PtM surfaces were deposited onto ordered intermetallic () PdCu seeds using seed-mediated co-reduction (SMCR). In the initial demonstration, PtCu shells were deposited on PdCu seeds, with these core@shell NPs exhibiting higher specific and mass activities for the oxygen reduction reaction (ORR) when compared to similarly sized PtCu NPs. These NPs also showed outstanding durability, maintaining ∼85% in specific activity after 5000 cycles. Characterization of the NPs after use revealed minimal loss of Cu. The activity enhancement was attributed to the strained surface that arises from the lattice mismatch between the intermetallic core and random alloy surface. The outstanding durability was attributed to the ordered structure of the intermetallic core.The origin of this durability enhancement was investigated by classical molecular dynamics simulations, where Pt atoms were found to have a lower potential energy when deposited on an intermetallic core than when deposited on a random alloy core. Also, ordering of Cu atoms at the core@shell interface appears to enhance the overall binding between the core and the shell materials. Inspired by this initial demonstration, SMCR has been used to achieve shells of different random alloy compositions, PtM (M = Ni, Co, Cu, or Fe). This advance is significant because ligand effects vary as a function of PtM identity and Pt/M ratio. These features also influence the degree of surface strain imparted from the lattice mismatch between the core and shell materials. Like the initial demonstration, standout features of these core@shell NPs were high durability and resistance to non-noble metal leaching.Moving forward, efforts have been directed toward integrating shape-control to this core@shell NP construct. This integration is motivated by the shape-dependent catalytic performance of NPs derived from the selective expression of specific facets. Considering the initial PdCu@PtCu system, NPs with a cubic shape have been achieved by judicious selection of capping ligands during SMCR. Evaluation of these NPs as catalysts for the electrooxidation of formic acid found that the nanocubic shape enhances catalytic performance compared to similar core@shell NPs with a spherical morphology. We envision that SMCR can be applied to other NP systems to achieve highly durable catalysts as the syntheses of monodisperse and shape-controlled intermetallic seeds are advanced. This Account highlights the role of intermetallic cores in providing more durable electrocatalysts. More broadly, the versatility of SMCR is highlighted as a route to integrate architecture, alloy surfaces, and shape within one NP system, and how this achievement is inspiring new high-performance and robust catalysts is discussed.
概述
当与储量丰富的金属结合时,铂基合金纳米颗粒(NPs)可成为具有成本效益的电催化剂。然而,在苛刻的电催化条件下,这些纳米颗粒可能会出现非贵金属成分的浸出。斯克拉巴拉克团队展示了一种新型的纳米颗粒结构,其中铂基随机合金表面通过沉积在金属间化合物晶种上而得以稳定,防止非贵金属浸出。这些核壳纳米颗粒是高度耐用的电催化剂,能够通过核壳结构、表面合金组成和纳米颗粒形状来调节催化性能。这种多功能性在一个模型系统中得到了证明,在该系统中,随机合金()PtM表面通过晶种介导的共还原(SMCR)沉积在有序金属间化合物()PdCu晶种上。在最初的演示中,PtCu壳层沉积在PdCu晶种上,与尺寸相似的PtCu纳米颗粒相比,这些核壳纳米颗粒在氧还原反应(ORR)中表现出更高的比活性和质量活性。这些纳米颗粒还表现出出色的耐久性,在5000次循环后比活性保持在约85%。使用后对纳米颗粒的表征显示铜的损失最小。活性增强归因于金属间化合物核与随机合金表面之间的晶格失配所产生的应变表面。出色的耐久性归因于金属间化合物核的有序结构。
通过经典分子动力学模拟研究了这种耐久性增强的起源,发现铂原子沉积在金属间化合物核上时的势能比沉积在随机合金核上时更低。此外,核壳界面处铜原子的有序排列似乎增强了核与壳材料之间的整体结合。受此初步演示的启发,SMCR已被用于制备不同随机合金组成的壳层,PtM(M = Ni、Co、Cu或Fe)。这一进展意义重大,因为配体效应会随着PtM身份和Pt/M比例的变化而变化。这些特性还会影响核壳材料之间晶格失配所产生的表面应变程度。与最初的演示一样,这些核壳纳米颗粒的突出特点是高耐久性和抗非贵金属浸出。
展望未来,人们致力于将形状控制集成到这种核壳纳米颗粒结构中。这种集成的动机源于纳米颗粒的形状依赖催化性能,这种性能源于特定晶面的选择性表达。考虑到最初的PdCu@PtCu系统,通过在SMCR过程中明智地选择封端配体,已经制备出了立方形状的纳米颗粒。将这些纳米颗粒作为甲酸电氧化催化剂进行评估发现,与具有球形形态的类似核壳纳米颗粒相比,纳米立方形状增强了催化性能。我们设想,随着单分散和形状可控金属间化合物晶种的合成取得进展,SMCR可应用于其他纳米颗粒系统,以制备高度耐用的催化剂。本综述强调了金属间化合物核在提供更耐用电催化剂方面的作用。更广泛地说,突出了SMCR作为一种在一个纳米颗粒系统中整合结构、合金表面和形状的途径的多功能性,并讨论了这一成果如何激发新型高性能和稳健催化剂的产生。