4.8 Article

Structural and Architectural Evaluation of Bimetallic Nanoparticles: A Case Study of Pt-Ru Core-Shell and Alloy Nanoparticles

Journal

ACS NANO
Volume 3, Issue 10, Pages 3127-3137

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/nn900242v

Keywords

core-shell; nanoparticles; EXAFS; catalysts; structure-property relationships

Funding

  1. National Science Foundation [CHE0401850]
  2. DOE HFI program [DE-FG02-05ER15731]
  3. U.S. Department of Energy [DE-FG02-03ER15476, DE-AC02-98CH10886, DE-FG02-05ER15688, DE-AC02-06CH11357]
  4. NSF MRI [0619191]
  5. Synchrotron Catalysis Consortium
  6. Direct For Mathematical & Physical Scien
  7. Division Of Materials Research [0619191] Funding Source: National Science Foundation

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A comprehensive structural/architectural evaluation of the PtRu (1:1) alloy and Ru@Pt core-shell nanoparticles (NPs) provides spatially resolved structural information on sub-5 nm NPs. A combination of extended X-ray absorption fine structure (EXAFS), X-ray absorption near edge structure (XANES), pair distribution function (PDF) analyses, Debye function simulations of X-ray diffraction (XRD), and field emission transmission electron microscopy/energy dispersive spectroscopy (FE-TEM/EDS) analyses provides complementary information used to construct a detailed picture of the core/shell and alloy nanostructures. The 4.4 nm PtRu (1:1) alloys are crystalline homogeneous random alloys with little twinning in a typical face-centered cubic (fcc) cell. The Pt atoms are predominantly metallic, whereas the Ru atoms are partially oxidized and are presumably located on the NP surface. The 4.0 nm Ru@Pt NPs have highly distorted hcp Ru cores that are primarily in the metallic state but show little order beyond 8 A. In contrast, the 1-2 monolayer thick Pt shells are relatively crystalline but are slightly distorted (compressed) relative to bulk fcc Pt. The homo- and heterometallic coordination numbers and bond lengths are equal to those predicted by the model cluster structure, showing that the Ru and Pt metals remain phase-separated in the core and shell components and that the interface between the core and shell is quite normal.

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