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结构有序化和掺杂显著提高 PtFe 纳米颗粒的催化性能。

Remarkable Improvement of the Catalytic Performance of PtFe Nanoparticles by Structural Ordering and Doping.

机构信息

Nanocarbon and Manufacturing Innovation Center, School of Mechanical and Power Engineering , East China University of Science and Technology , 130 Meilong Road , Shanghai 200237 , P. R. China.

出版信息

ACS Appl Mater Interfaces. 2019 Mar 27;11(12):11527-11536. doi: 10.1021/acsami.9b01810. Epub 2019 Mar 12.

Abstract

To achieve fuel cell commercialization, the performance improvement and cost reduction of catalysts are still the main challenges. To enhance the catalytic activity and durability for oxygen reduction reaction (ORR), we prepare Au-PtFe particles entrapped in a porous carbon and then convert them to have a fine-grained and highly ordered intermetallic structure. The optimal Au-PtFe particles in catalyzing ORR exhibit initial specific and mass activities 9 times higher than the commercial catalyst of Pt/C. Such a large enhancement is much higher than most of the Pt-based ordered intermetallic catalysts reported in the literature. Accelerated durability testing induces little degradation of the catalytic activity to the ordered structure, particularly the Au-doped one, after potential cycling for many thousands of cycles under harsh electrochemical conditions involving an acidic medium and a high potential range of 0.66-1.3 V. This is in big contrast with the large degradation shown by most previous catalysts. The excellent activity and durability are attributed to synergistic effects of the fine-grained and ordered structure of the particles, the confining support of the porous carbon, and the homogeneous incorporation of a trace amount of Au. The new intermetallic catalyst of Au-PtFe/C represents a new strategy for performance enhancement and cost reduction and thus promotes practical applications of proton-exchange membrane fuel cells.

摘要

为实现燃料电池商业化,提高催化剂的性能和降低成本仍然是主要挑战。为了提高氧还原反应(ORR)的催化活性和耐久性,我们制备了负载在多孔碳中的 Au-PtFe 颗粒,并将其转化为具有精细和高度有序的金属间化合物结构。在催化 ORR 方面,最佳的 Au-PtFe 颗粒的初始比活性和质量活性比商业 Pt/C 催化剂高 9 倍。这种大幅度的增强远远高于文献中报道的大多数基于 Pt 的有序金属间化合物催化剂。经过数千次循环的加速耐久性测试,在涉及酸性介质和 0.66-1.3 V 高电位范围的苛刻电化学条件下,对有序结构的催化活性几乎没有降解,特别是对掺杂 Au 的有序结构。这与大多数先前催化剂显示的大降解形成鲜明对比。优异的活性和耐久性归因于颗粒的精细和有序结构、多孔碳的限制支撑以及痕量 Au 的均匀掺入的协同效应。新型 Au-PtFe/C 金属间化合物催化剂代表了一种提高性能和降低成本的新策略,从而促进质子交换膜燃料电池的实际应用。

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