1991
DOI: 10.1016/0168-583x(91)95655-w
|View full text |Cite
|
Sign up to set email alerts
|

Simultaneous conversion electron, conversion X-ray and transmission Mössbauer spectroscopy

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
9
0

Year Published

1998
1998
2010
2010

Publication Types

Select...
5
3

Relationship

1
7

Authors

Journals

citations
Cited by 56 publications
(9 citation statements)
references
References 4 publications
0
9
0
Order By: Relevance
“…The information about the hyperfine interactions of the Mössbauer probe in the investigated material can be extracted from spectra measured in various geometrical arrangements. The Mössbauer spectroscopy in transmission geometry yields information concerning the bulk of a sample; in scattering geometry it allows studying the surface structure up to 30 mm in depth using backscattered g-rays or close surface properties up to approximately 200 nm thick surface layers using backscattered conversion electrons [16]. The use of Mössbauer spectroscopy for observation of the volume changes in solids is known, e.g., from high pressure experiments of crystalline and amorphous solids [17][18][19][20].…”
Section: Introductionmentioning
confidence: 99%
“…The information about the hyperfine interactions of the Mössbauer probe in the investigated material can be extracted from spectra measured in various geometrical arrangements. The Mössbauer spectroscopy in transmission geometry yields information concerning the bulk of a sample; in scattering geometry it allows studying the surface structure up to 30 mm in depth using backscattered g-rays or close surface properties up to approximately 200 nm thick surface layers using backscattered conversion electrons [16]. The use of Mössbauer spectroscopy for observation of the volume changes in solids is known, e.g., from high pressure experiments of crystalline and amorphous solids [17][18][19][20].…”
Section: Introductionmentioning
confidence: 99%
“…Velocity calibration was performed at room temperature with a 25 m ␣-Fe foil, and all isomer shifts are related to the latter. The information depth of CEMS is about 150 nm [12]. The amount of Fe 2+ in the electrolyte has been determined by spectrophotometry using o-phenanthrolin that forms an orangered complex with Fe 2+ (E max at λ = 510 nm).…”
Section: Methodsmentioning
confidence: 99%
“…The conversion and Auger electrons were detected in a He/CH 4 gas-flow proportional counter. The spectra were stored in a multichannel scaler with 1024 channels and fitted according to a least squares fit routine by superimposing Lorentzian lines [12]. Velocity calibration was performed at room temperature with a 25 m ␣-Fe foil, and all isomer shifts are related to the latter.…”
Section: Methodsmentioning
confidence: 99%
“…[14][15][16] The electrons were detected in a He/ CH 4 flow proportional counter. [17][18][19] The spectra were fitted by a hyperfine field distribution calculated with the Normos code [20] or by superimposing Lorentzian lines with the WinISO fitting tool.…”
Section: Analysis Methodsmentioning
confidence: 99%