State Key Laboratory of Chemical Resource Engineering, Institute of Modern Catalysis, Department of Organic Chemistry, Beijing Engineering Center for Hierarchical Catalysts, School of Science , Beijing University of Chemical Technology , Beijing 100029 , China.
ACS Appl Mater Interfaces. 2018 Jul 5;10(26):22156-22166. doi: 10.1021/acsami.8b05114. Epub 2018 Jun 21.
Carbon-supported Au-Pt Fe nanoparticles were synthesized via microwave heating polyol process, followed by annealing for the formation of the ordered structure. The structure characterizations indicate that Au is alloyed with intermetallic Pt-Fe nanoparticles and therefore the surface electronic properties are tuned. The electrochemical tests show that the microwave heating polyol process is more effective than oil bath heating polyol process for synthesizing the highly active catalysts. The introduction of trace Au (0.2 wt % Au) significantly improves the oxygen reduction reaction (ORR) catalytic activity of Pt Fe catalysts. Au-PtFe/C-H (0.66 A/mg) and Au-PtFe/C-H (0.63 A/mg) prepared in a batch of 10.0 g show significantly improved catalytic activities than their counterparts (PtFe/C-H and PtFe/C-H) as well as commercial Johnson Matthey Pt/C (0.17 A/mg). In addition, the as-prepared Au-PtFe/C-H and Au-PtFe/C-H display highly enhanced stability toward the ORR compared to the commercial Pt/C. The superior catalytic performance is attributed to the synergistic effect of chemically ordered intermetallic structure and Au. This work provides a scalable synthesis of the multimetallic chemically ordered Au-Pt Fe catalysts with high ORR catalytic performance in acidic condition.
通过微波加热多元醇法合成了负载在碳上的 Au-Pt-Fe 纳米粒子,然后进行退火以形成有序结构。结构表征表明 Au 与金属间 Pt-Fe 纳米粒子形成合金,从而调整了表面电子特性。电化学测试表明,与油浴加热多元醇法相比,微波加热多元醇法更有利于合成高活性催化剂。微量 Au(0.2wt%Au)的引入显著提高了 Pt-Fe 催化剂的氧还原反应(ORR)催化活性。在 10.0g 一批量中制备的 Au-PtFe/C-H(0.66A/mg)和 Au-PtFe/C-H(0.63A/mg)的催化活性明显高于其对应物(PtFe/C-H 和 PtFe/C-H)以及商业 Johnson Matthey Pt/C(0.17A/mg)。此外,与商业 Pt/C 相比,所制备的 Au-PtFe/C-H 和 Au-PtFe/C-H 对 ORR 具有更高的增强稳定性。优异的催化性能归因于化学有序金属间结构和 Au 的协同效应。这项工作提供了一种可扩展的方法来合成多金属化学有序的 Au-Pt-Fe 催化剂,在酸性条件下具有高 ORR 催化性能。