Journal
JOURNAL OF PHYSICAL CHEMISTRY C
Volume 124, Issue 12, Pages 6907-6912Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.9b11412
Keywords
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Funding
- Elements Strategy Initiative for Catalysts and Batteries (ESICB)
- Ministry of Education, Culture, Sports, Science, and Technology (MEXT) of Japan [26248003, 15H01042, 17H05213]
- Japan Society for the Promotion of Science
- CREST, Japan Science and Technology Agency
- [15J09168]
- Grants-in-Aid for Scientific Research [15H01042, 17H05213] Funding Source: KAKEN
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The atomic structures of Au-25( SC2H4Ph)(18), Au-25( SePh)(18), and Au-144(SC2H4Ph)(60), for which the crystal structures have been solved, were examined by aberration-corrected transmission electron microscopy (ACTEM). Time-lapse ACTEM images of Au-25(SePh)(18) exhibited characteristic patterns for the IhAu13 core more frequently compared to Au-25(SC2H4Ph)(18) at a dose rate (DR) = 4 pA/cm(2). In contrast, time-lapse images of Au-144(SC2H4Ph)(60) randomly showed two types of patterns for the Ih and fcc cores at DR = 4 pA/cm(2), indicating that Au-144(SC2H4Ph)(60) can be interconverted between the two isomeric forms without fragmentation. We proposed that the Ih isomer is more stable than the fcc isomer in Au-144(SC2H4Ph)(60) based on population analysis of the images of individual isomers.
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