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通过原位电置换反应制备用于氧电催化的PtNi空心纳米颗粒的形成机制及克级生产

Formation Mechanism and Gram-Scale Production of PtNi Hollow Nanoparticles for Oxygen Electrocatalysis through In Situ Galvanic Displacement Reaction.

作者信息

Kang Yun Sik, Jung Jae Young, Choi Daeil, Sohn Yeonsun, Lee Soo-Hyoung, Lee Kug-Seung, Kim Nam Dong, Kim Pil, Yoo Sung Jong

机构信息

Center for Hydrogen·Fuel Cell Research, Korea Institute of Science and Technology, Seoul 02792, Republic of Korea.

School of Chemical Engineering, School of Semiconductor and Chemical Engineering, Solar Energy Research Center, Chonbuk National University, Jeonju 54896, Republic of Korea.

出版信息

ACS Appl Mater Interfaces. 2020 Apr 8;12(14):16286-16297. doi: 10.1021/acsami.9b22615. Epub 2020 Mar 24.

DOI:10.1021/acsami.9b22615
PMID:32167736
Abstract

Galvanic displacement reaction has been considered a simple method for fabricating hollow nanoparticles. However, the formation of hollow interiors in nanoparticles is not easily achieved owing to the easy oxidization of transition metals, which results in mixed morphologies, and the presence of surfactants on the nanoparticle surface, which severely deteriorates the catalytic activity. In this study, we developed a facile gram-scale methodology for the one-pot preparation of carbon-supported PtNi hollow nanoparticles as an efficient and durable oxygen reduction electrocatalyst without using stabilizing agents or additional processes. The hollow structures were evolved from sacrificial Ni nanoparticles via an in situ galvanic displacement reaction with a Pt precursor, directly following a preannealing process. By sampling the PtNi/C hollow nanoparticles at various reaction times, the structural formation mechanism was investigated using transmission electron microscopy with energy-dispersive X-ray spectroscopy mapping/line-scan profiling. We found out that the structure and morphology of the PtNi hollow nanoparticles were controlled by the acidity of the metal precursor solution and the nanoparticle core size. The synthesized PtNi hollow nanoparticles acted as an oxygen reduction electrocatalyst, with a catalytic activity superior to that of a commercial Pt catalyst. Even after 10 000 cycles of harsh accelerated durability testing, the PtNi/C hollow electrocatalyst showed high performance and durability. We concluded that the Pt-rich layers on the PtNi hollow nanoparticles improved the catalytic activity and durability considerably.

摘要

电置换反应被认为是制备空心纳米颗粒的一种简单方法。然而,由于过渡金属容易氧化导致形态混合,以及纳米颗粒表面存在表面活性剂严重降低催化活性,在纳米颗粒中形成中空内部并不容易实现。在本研究中,我们开发了一种简便的克级方法,用于一锅法制备碳载PtNi空心纳米颗粒,作为一种高效耐用的氧还原电催化剂,无需使用稳定剂或额外的工艺。在预退火过程之后,通过与Pt前驱体的原位电置换反应,牺牲性Ni纳米颗粒演变成中空结构。通过在不同反应时间对PtNi/C空心纳米颗粒进行取样,利用透射电子显微镜结合能量色散X射线光谱映射/线扫描分析研究了结构形成机制。我们发现PtNi空心纳米颗粒的结构和形态受金属前驱体溶液的酸度和纳米颗粒核尺寸的控制。合成的PtNi空心纳米颗粒用作氧还原电催化剂,其催化活性优于商业Pt催化剂。即使经过10000次苛刻的加速耐久性测试循环后,PtNi/C空心电催化剂仍表现出高性能和耐久性。我们得出结论,PtNi空心纳米颗粒上的富Pt层显著提高了催化活性和耐久性。

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