A number of complementary, synergistic advances are reported herein. First, we describe the ‘first-time’ synthesis of ultrathin Ru 2 Co 1 nanowires (NWs) possessing average diameters of 2.3 ± 0.5 nm using a modified surfactant-mediated protocol. Second, we utilize a combination of quantitative EDS, EDS mapping (along with accompanying line-scan profiles), and EXAFS spectroscopy results to probe the local atomic structure of not only novel Ru 2 Co 1 NWs but also ‘control’ samples of analogous ultrathin Ru 1 Pt 1 , Au 1 Ag 1 , Pd 1 Pt 1 , and Pd 1 Pt 9 NWs. We demonstrate that ultrathin NWs possess an atomic-level geometry that is fundamentally dependent upon their intrinsic chemical composition. In the case of the PdPt NW series, EDS mapping data are consistent with the formation of a homogeneous alloy, a finding further corroborated by EXAFS analysis. By contrast, EXAFS analysis results for both Ru 1 Pt 1 and Ru 2 Co 1 imply the generation of homophilic structures in which there is a strong tendency for the clustering of ‘like’ atoms; associated EDS results for Ru 1 Pt 1 convey the same conclusion, namely the production of a heterogeneous structure. Conversely, EDS mappingmore »
Adaptive kinetic Monte Carlo simulations of surface segregation in PdAu nanoparticles
Surface segregation in bimetallic nanoparticles (NPs) is critically important for their catalytic activity because the activity is largely determined by the surface composition. Little, however, is known about the atomic scale mechanisms and kinetics of surface segregation. One reason is that it is hard to resolve atomic rearrangements experimentally. It is also difficult to model surface segregation at the atomic scale because the atomic rearrangements can take place on time scales of seconds or minutes – much longer than can be modeled with molecular dynamics. Here we use the adaptive kinetic Monte Carlo (AKMC) method to model the segregation dynamics in PdAu NPs over experimentally relevant time scales, and reveal the origin of kinetic stability of the core@shell and random alloy NPs at the atomic level. Our focus on PdAu NPs is motivated by experimental work showing that both core@shell and random alloy PdAu NPs with diameters of less than 2 nm are stable, indicating that one of these structures must be metastable and kinetically trapped. Our simulations show that both the Au@Pd and the PdAu random alloy NPs are metastable and kinetically trapped below 400 K over time scales of hours. These AKMC simulations provide insight into the energy more »
- Award ID(s):
- 1764230
- Publication Date:
- NSF-PAR ID:
- 10108303
- Journal Name:
- Nanoscale
- Volume:
- 11
- Issue:
- 21
- Page Range or eLocation-ID:
- 10524 to 10535
- ISSN:
- 2040-3364
- Sponsoring Org:
- National Science Foundation
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