Automated Author ProfileDr Hiroki Yamamoto
Dr Hiroki Yamamoto
Current S-Index
Sum of Dataset Indices for all datasets
Average Dataset Index per Dataset
Average Dataset Index per dataset
Total Datasets
Total datasets for this author
Average FAIR Score
Average FAIR Score per dataset
Total Citations
Total citations to the author's datasets
Total Mentions
Total mentions of the author's datasets
S-Index Interpretation
The S-Index (Sharing Index) is a comprehensive metric that represents the cumulative impact of all your datasets. It is calculated as the sum of Dataset Index scores across all your claimed datasets.
What it means:
- A higher S-index indicates greater overall impact of your datasets relative to typical datasets in their fields of research
- The S-Index grows as you add more datasets or as existing datasets gain more citations and mentions
- It provides a single number to track your research data impact over time
Current S-Index: 1.9 (sum of 2 datasets Dataset Index scores)
More information here.
S-Index Over Time
Cumulative Citations Over Time
Cumulative Mentions Over Time
Datasets
Topochemical fluorination of A3B2O7, n = 2 Ruddlesden-Popper oxides yields phases of composition A3B2OxFy (5≤x≤7, 2≤y≤4, x+y = 9). The synthesis of these phases has been shown to occur via both the intercalation of F- in the rocksalt layers of the host phases and partial substitution of ‘framework’ oxide ions. Subsequent reduction of these oxyfluorides using LiH yields phases with anionic contents varying from O5F4 to O4F2, none of which can be prepared directly via conventional ceramic synthesis. We propose to collect neutron powder diffraction data from a series of LaSr3CoRuOxFy and La3Ni2OxFy phases to determine the crystal and magnetic structures.
Authors
- Professor Michael Hayward ;
- Dr Ronald Smith ;
- Dr Hiroki Yamamoto ;
- Dr Romain Wernert
Topochemical fluorination of A3B2O7, n = 2 Ruddlesden-Popper oxides yields phases of composition A3B2OxFy (5≤x≤7, 2≤y≤4, x+y = 9). The synthesis of these phases has been shown to occur via both the intercalation of F- in the rocksalt layers of the host phases and partial substitution of ‘framework’ oxide ions. Subsequent reduction of these oxyfluorides using LiH yields phases with anionic contents varying from O5F4 to O4F2, none of which can be prepared directly via conventional ceramic synthesis. We propose to collect neutron powder diffraction data from a series of LaSr3CoRuOxFy and La3Ni2OxFy phases to determine the crystal and magnetic structures.
Authors
- Professor Michael Hayward ;
- Dr Ronald Smith ;
- Dr Hiroki Yamamoto ;
- Dr Romain Wernert