Welcome to the new version of CaltechAUTHORS. Login is currently restricted to library staff. If you notice any issues, please email coda@library.caltech.edu
Published May 5, 2014 | Supplemental Material
Journal Article Open

Dealloyed Pt_(2)Os nanoparticles for enhanced oxygen reduction reaction in acidic electrolytes

Abstract

Carbon-supported Pt2Os (Pt_(2)Os/C) nanoparticles in 3.55 nm sizes are synthesized from a wet chemical reflux process. Subsequently, the Pt_(2)Os/C undergoes a dealloying treatment in which multiple cyclic voltammetric scans are imposed to dissolve the Os atoms selectively from the surface of the Pt_(2)Os nanoparticles. X-ray diffraction signals from the dealloyed sample (DA–Pt_(2)Os/C) indicate a fcc phase and composition analysis suggests Pt4Os. Line scans from the scanning transmission electron microscope confirm that the surface of Pt_(4)Os is depleted with the Os atoms. This agrees with our quantum mechanics (Density Funtional theory) calculations, which predict for the Pt_(3)Os composition that the surface skin layer is pure Pt. The DA–Pt_(2)Os/C shows impressive electrocatalytic behaviors (0.29 mA μgPt^(−1) in mass activity and 1.03 mA cmPt^(−2) in specific activity) for the oxygen reduction reaction (ORR) in oxygen-saturated 0.1 M aqueous HClO_4 solution, as compared to those of commercially available Pt/C and as-synthesized Pt_(2)Os/C. In stability test, the DA–Pt_(2)Os/C demonstrates a better retention of ORR activities and a smaller loss of electrochemical active surface area. We verify experimentally that a four-electron step is responsible for the ORR process occurring on the DA–Pt_(2)Os/C.

Additional Information

© 2014 Elsevier B.V. Received 6 August 2013; Received in revised form 20 November 2013; Accepted 3 January 2014; Available online 10 January 2014. The financial supports from the National Science Council of Taiwan (NSC-100-2221-E009-075-MY3, NSC 101-3113-P-008- 001) and National Science Foundation (CBET-1067848, Caltech) are gratefully acknowledged.

Attached Files

Supplemental Material - Lee_2014p636_SI.pdf

Files

Lee_2014p636_SI.pdf
Files (290.9 kB)
Name Size Download all
md5:36629eca5e9e7401cdbf6967a345eb0d
290.9 kB Preview Download

Additional details

Created:
August 22, 2023
Modified:
October 26, 2023