Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Originally published in Science Express on 14 May 2009
Science 5 June 2009:
Vol. 324. no. 5932, pp. 1302 - 1305
DOI: 10.1126/science.1170377

Reports

Pd-Pt Bimetallic Nanodendrites with High Activity for Oxygen Reduction

Byungkwon Lim,1 Majiong Jiang,2 Pedro H. C. Camargo,1 Eun Chul Cho,1 Jing Tao,3 Xianmao Lu,1 Yimei Zhu,3 Younan Xia1,*

Controlling the morphology of Pt nanostructures can provide a great opportunity to improve their catalytic properties and increase their activity on a mass basis. We synthesized Pd-Pt bimetallic nanodendrites consisting of a dense array of Pt branches on a Pd core by reducing K2PtCl4 with L-ascorbic acid in the presence of uniform Pd nanocrystal seeds in an aqueous solution. The Pt branches supported on faceted Pd nanocrystals exhibited relatively large surface areas and particularly active facets toward the oxygen reduction reaction (ORR), the rate-determining step in a proton-exchange membrane fuel cell. The Pd-Pt nanodendrites were two and a half times more active on the basis of equivalent Pt mass for the ORR than the state-of-the-art Pt/C catalyst and five times more active than the first-generation supportless Pt-black catalyst.

1 Department of Biomedical Engineering, Washington University, St. Louis, MO 63130, USA.
2 Department of Chemistry, Washington University, St. Louis, MO 63130, USA.
3 Condensed Matter Physics and Materials Science Department, Brookhaven National Laboratory, Upton, NY 11973, USA.

* To whom correspondence should be addressed. E-mail: xia{at}biomed.wustl.edu

Read the Full Text





To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)