Gamler Jocelyn T L, Leonardi Alberto, Ashberry Hannah M, Daanen Nicholas N, Losovyj Yaroslav, Unocic Raymond R, Engel Michael, Skrabalak Sara E
Department of Chemistry , Indiana University , 800 East Kirkwood Avenue , Bloomington , Indiana 47405 , United States.
Institute for Multiscale Simulation , Friedrich-Alexander Universität Erlangen-Nürnberg , Cauerstraße 3 , 91058 Erlangen , Germany.
ACS Nano. 2019 Apr 23;13(4):4008-4017. doi: 10.1021/acsnano.8b08007. Epub 2019 Apr 8.
Pt catalysts are widely studied for the oxygen reduction reaction, but their cost and susceptibility to poisoning limit their use. A strategy to address both problems is to incorporate a second transition metal to form a bimetallic alloy; however, the durability of such catalysts can be hampered by leaching of non-noble metal components. Here, we show that random alloyed surfaces can be stabilized to achieve high durability by depositing the alloyed phase on top of intermetallic seeds using a model system with PdCu cores and PtCu shells. Specifically, random alloyed PtCu shells were deposited on PdCu seeds that were either the atomically random face-centered cubic phase (FCC A1, Fm3m) or the atomically ordered CsCl-like phase (B2, Pm3m). Precise control over crystallite size, particle shape, and composition allowed for comparison of these two core@shell PdCu@PtCu catalysts and the effects of the core phase on electrocatalytic durability. Indeed, the nanocatalyst with the intermetallic core saw only an 18% decrease in activity after stability testing (and minimal Cu leaching), whereas the nanocatalyst with the random alloy core saw a 58% decrease (and greater Cu leaching). The origin of this enhanced durability was probed by classical molecular dynamics simulations of model catalysts, with good agreement between model and experiment. Although many random alloy and intermetallic nanocatalysts have been evaluated, this study directly compares random alloy and intermetallic cores for electrocatalysis with the enhanced durability achieved with the intermetallic cores likely general to other core@shell nanocatalysts.
铂催化剂被广泛研究用于氧还原反应,但其成本和易中毒性限制了它们的应用。解决这两个问题的一种策略是引入第二种过渡金属以形成双金属合金;然而,这类催化剂的耐久性可能会因非贵金属组分的浸出而受到阻碍。在此,我们表明,通过使用具有钯铜核和铂铜壳的模型系统,将合金相沉积在金属间化合物籽晶之上,可以使随机合金化表面稳定下来,从而实现高耐久性。具体而言,将随机合金化的铂铜壳沉积在原子无序的面心立方相(FCC A1,Fm3m)或原子有序的类氯化铯相(B2,Pm3m)的钯铜籽晶上。对微晶尺寸、颗粒形状和组成的精确控制使得能够比较这两种核壳结构的钯铜@铂铜催化剂以及核相对电催化耐久性的影响。实际上,具有金属间化合物核的纳米催化剂在稳定性测试后活性仅下降了18%(且铜浸出极少),而具有随机合金核的纳米催化剂活性下降了58%(且铜浸出更多)。通过对模型催化剂进行经典分子动力学模拟探究了这种增强耐久性的起源,模型与实验结果吻合良好。尽管已经评估了许多随机合金和金属间化合物纳米催化剂,但本研究直接比较了用于电催化的随机合金核和金属间化合物核,金属间化合物核实现的增强耐久性可能适用于其他核壳纳米催化剂。