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Synthesis of hollow Pt–Ag nanoparticles by oxygen-assisted acid etching as electrocatalysts for the oxygen reduction reaction

机译:氧辅助酸刻蚀作为氧还原反应的电催化剂合成空心Pt-Ag纳米粒子

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Hollow bimetallic nanostructures have recently shown promising performance for the oxygen reduction reaction (ORR) in fuel cells. In this work, we report the synthesis of hollow Pt–Ag nanoparticles of varying sizes by O2-assisted acid etching of Ag@Pt core@shell nanostructures at room temperature. With a Pt shell less than 6 nm thick, the O2 dissolved in acetic acid could oxidize the Ag core. Subsequently, silver oxide was dissolved in acetic acid and turned into Ag+ ions. During this process, the Ag atoms diffused into the lattice of the Pt shell, and Ag@Pt core@shell nanostructures evolved into hollow Pt–Ag alloy nanoparticles. The as-synthesized hollow Pt–Ag nanocatalysts maintained specific ORR activities that were enhanced beyond the specific activity for commercial carbon supported Pt nanoparticles. The 5.8 nm hollow Pt–Ag nanoparticles displayed the highest activity of 1.12 mA cm?2. Over the course of an accelerated durability test, the 5.8 nm nanoparticles retained 95% and 87% of their initial electrochemical surface area and specific ORR activity. The enhanced activity and durability can be ascribed to the high surface area of the porous structure and the new d-band center due to the hollow morphology and Pt–Ag alloy formation. This work demonstrates a simple strategy for fabricating small porous nanoparticles, which can be potentially used as electrocatalysts in PEM fuel cells.
机译:中空双金属纳米结构近来已显示出用于燃料电池中的氧还原反应(ORR)的有希望的性能。在这项工作中,我们报道了在室温下通过O 2 辅助酸蚀刻Ag @ Pt核@壳纳米结构,合成了各种尺寸的中空Pt-Ag纳米颗粒。 Pt壳厚度小于6 nm时,溶解在乙酸中的O 2 可以氧化Ag核。随后,将氧化银溶解在乙酸中并变成Ag + 离子。在此过程中,Ag原子扩散到Pt壳的晶格中,而Ag @ Pt核@壳的纳米结构演化为中空的Pt-Ag合金纳米颗粒。合成后的中空Pt-Ag纳米催化剂保持了特定的ORR活性,该活性已增强,超过了商业碳载Pt纳米颗粒的比活性。 5.8 nm的中空Pt-Ag纳米颗粒表现出最高的活性,为1.12 mA cm ?2 。在加速耐久性测试过程中,5.8 nm纳米颗粒保留了其初始电化学表面积和比ORR活性的95%和87%。由于中空形态和Pt-Ag合金的形成,多孔表面的高表面积和新的d带中心可以归因于增强的活性和耐久性。这项工作证明了一种制备小的多孔纳米颗粒的简单策略,该纳米颗粒可以潜在地用作PEM燃料电池中的电催化剂。

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