Title: | Abnormal Metal Bond Distances in PtAu Alloy Nanoparticles : In Situ Back-Illumination XAFS Investigations of the Structure of PtAu Nanoparticles on a Flat HOPG Substrate Prepared by Arc Plasma Deposition |
Authors: | Hu, Bing Browse this author |
Bharate, Bapurao Browse this author |
Jimenez, Juan D. Browse this author |
Lauterbach, Jochen Browse this author |
Todoroki, Naoto Browse this author →KAKEN DB |
Wadayama, Toshimasa Browse this author →KAKEN DB |
Higashi, Kotaro Browse this author →KAKEN DB |
Uruga, Tomoya Browse this author →KAKEN DB |
Iwasawa, Yasuhiro Browse this author →KAKEN DB |
Ariga-Miwa, Hiroko Browse this author →KAKEN DB |
Takakusagi, Satoru Browse this author →KAKEN DB |
Asakura, Kiyotaka Browse this author →KAKEN DB |
Issue Date: | 20-Jan-2022 |
Publisher: | American Chemical Society |
Journal Title: | Journal of physical chemistry c |
Volume: | 126 |
Issue: | 2 |
Start Page: | 1006 |
End Page: | 1016 |
Publisher DOI: | 10.1021/acs.jpcc.1c08393 |
Abstract: | To reveal the origin of the difference between the Pt-Pt bond distance in Au(core)-Pt(shell)-type (PtAu) nanoparticles and that in a Pt overlayer on Au(111), alloy-type PtAu nanoparticles were prepared on a highly oriented pyrolytic graphite (HOPG) surface by arc plasma deposition and their structure was investigated under various electrochemical conditions by bentcrystal Laue analyzer (BCLA)-empowered back-illuminated X-ray absorption fine structure (BCLA + BI-XAFS) and high-energyilluminated X-ray absorption near-edge structure (HERFD + BIXANES) methods. On the basis of the XAFS analysis at both edges, we proposed the formation of a PtAu alloy core covered with a Pt-rich shell at 0.4 VRHE, where the Pt-Pt, Pt-Au, and Au- Au bond lengths were all found to be similar to 2.76 A. The Au-Au bond length was abnormally shorter than that for bulk Au. The Pt shell was dissolved under applied potentials greater than 0.8 VRHE with the aid of the high-intensity X-rays, and the Au-Au distance increased. We concluded that the abnormal bond lengths were due to the strong surface tension from the Pt-rich shell and the relaxation of the lattice distortion. The Pt-Pt bond length in the PtAu nanoparticles decreases as a result of the surface tension of the nanoparticles; this surface tension does not exist on flat Au surfaces, where the lattice distortion between the Pt overlayer and the substrate is the main driving force for the expansion of the Pt-Pt bond length. |
Rights: | This document is the Accepted Manuscript version of a Published Work that appeared in final form in The Journal of Physical Chemistry C, copyright c American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://pubs.acs.org/articlesonrequest/AOR-NGNDHYXZEXYQKJEQXWZF. |
Type: | article (author version) |
URI: | http://hdl.handle.net/2115/87843 |
Appears in Collections: | 触媒科学研究所 (Institute for Catalysis) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)
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