2015
DOI: 10.1063/1.4939078
|View full text |Cite
|
Sign up to set email alerts
|

Electronic ground states of Fe2+ and Co2+ as determined by x-ray absorption and x-ray magnetic circular dichroism spectroscopy

Abstract: The 6 Π electronic ground state of the Co + 2 diatomic molecular cation has been assigned experimentally by x-ray absorption and x-ray magnetic circular dichroism

Help me understand this report
View preprint versions

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

1
36
0

Year Published

2016
2016
2023
2023

Publication Types

Select...
5
2

Relationship

0
7

Authors

Journals

citations
Cited by 17 publications
(37 citation statements)
references
References 70 publications
1
36
0
Order By: Relevance
“…1 Apart from in depth studies of the X-ray absorption process itself, effective and simplified rules have been proposed for the spectral analysis and applied for a wide range of species, like one-center rules, building block and bond length with ruler principles, and, for fixed in space species, orientational probing. [1][2][3][4] Owing to recently improved techniques to trap molecular cations in sufficient amount and time to be measurable by X-ray synchrotron beams, [5][6][7][8][9][10][11] highresolution NEXAFS of such species has now become a realistic proposition.…”
Section: Introductionmentioning
confidence: 99%
“…1 Apart from in depth studies of the X-ray absorption process itself, effective and simplified rules have been proposed for the spectral analysis and applied for a wide range of species, like one-center rules, building block and bond length with ruler principles, and, for fixed in space species, orientational probing. [1][2][3][4] Owing to recently improved techniques to trap molecular cations in sufficient amount and time to be measurable by X-ray synchrotron beams, [5][6][7][8][9][10][11] highresolution NEXAFS of such species has now become a realistic proposition.…”
Section: Introductionmentioning
confidence: 99%
“…[13,15] In t ho e calculation , the orbital magnetic moments per atom, f.LL :::; 0.7 f.LB , determined by XMCD, of small Co;t clusters with n 2: 8 and of the cobalt diatomic molecular cation (f.LL = 1 f.LB) were already used as a benchmark. [18,10,8] While in the meantime f.Ls and f.LL from XMCD measurements have also been reported for the cobalt trimer cation [1 9] with f.LL :::; 0.5 f.LB per atom, accura te experimental values for the cluster size range from n = 4 -9, where 3D cluster sLrucL ures appear, are sL ill missing. In the case of iron, already the smallest clusters have largely quenched orbital magnetic moments.…”
Section: Lntrod Uctionmentioning
confidence: 95%
“…Instead, t he small orbital magnetic moment in Cot is due to its electronic configuration with three electrons in a doubly degenerate orbital of 1r symmetry with ml = ± 1. [18] The considerable difference between the orbital-to-spin magnetic moment ratio of Cot 5 and Cot indicaLes an abrupL change in the symmetry of Lhe 3d derived ' states between n = 5 and n = 6. Overall the ratio in the n = 2 15 cluster size range is considerably higher, by a factor of two to nine, than in bulk cobalt [3] , as indicated in figure 2.…”
Section: X-ray Absorption and Xmcd Spectroscopymentioning
confidence: 99%
See 2 more Smart Citations