Decomposition of CrN induced by laser-assisted atom probe tomography

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Decomposition of CrN induced by laser-assisted atom probe tomography. / Waldl, Helene; Hans, Marcus; Schiester, Maximilian et al.
In: Ultramicroscopy, Vol. 246.2023, No. April, 113673, 04.2023.

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Waldl H, Hans M, Schiester M, Primetzhofer D, Burtscher M, Schalk N et al. Decomposition of CrN induced by laser-assisted atom probe tomography. Ultramicroscopy. 2023 Apr;246.2023(April):113673. Epub 2022 Dec 27. doi: 10.1016/j.ultramic.2022.113673

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@article{ef94be9ee111450c9d5823fbba5baf5f,
title = "Decomposition of CrN induced by laser-assisted atom probe tomography",
abstract = "It is known that measurement parameters can significantly influence the elemental composition determined by atom probe tomography (APT). Especially results obtained by laser-assisted APT show a strong effect of the laser pulse energy on the apparent elemental composition. Within this study laser-assisted APT experiments were performed on Cr 0.51N 0.49 and thermally more stable (Cr 0.47Al 0.53) 0.49N 0.51, comparing two different base temperatures (i.e. 15 and 60 K), laser wavelengths (i.e. 532 and 355 nm) and systematically modified laser pulse energies. Absolute chemical compositions from laser-assisted APT were compared to data obtained from ion beam analysis. The deduced elemental composition of CrN exhibited a strong increase of the Cr content when the laser pulse energy was increased for both laser wavelengths. For low laser pulse energies Cr, CrN, N and N 2 ions were identified, while the amount of detected Cr ions increased and the amount of N ions strongly decreased at higher laser pulse energies. Further, increased detection of more complex Cr-containing ions such as Cr 2N at the expense of CrN was observed at higher pulse energies. At the highest pulse energy levels used within this work, the resulting Cr content was > 80 at%, dominated by the amount of detected elemental Cr ions. The change of the mass spectrum of the detected ions with increasing laser pulse energy provides evidence that high laser pulse energies initiate the decomposition of CrN during the APT measurement, consistent with the known thermal decomposition path into Cr 2N and subsequently into Cr and gaseous N. In contrast, variation of the laser pulse energy for the thermally more stable CrAlN resulted only in a slight increase of Cr and a decrease of the resulting concentrations of Al and N with increasing laser pulse energy and no change in the type of detected ions. In conclusion, within the present study, the decomposition of a coating material with low thermal stability induced by laser-assisted APT was reported for the first time, emphasizing the importance of the selection of suitable measurement parameters for metastable materials, which are prone to thermal decomposition.",
author = "Helene Waldl and Marcus Hans and Maximilian Schiester and D. Primetzhofer and Michael Burtscher and Nina Schalk and Michael Tkadletz",
note = "Publisher Copyright: {\textcopyright} 2022",
year = "2023",
month = apr,
doi = "10.1016/j.ultramic.2022.113673",
language = "English",
volume = "246.2023",
journal = "Ultramicroscopy",
issn = "0304-3991",
publisher = "Elsevier",
number = "April",

}

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TY - JOUR

T1 - Decomposition of CrN induced by laser-assisted atom probe tomography

AU - Waldl, Helene

AU - Hans, Marcus

AU - Schiester, Maximilian

AU - Primetzhofer, D.

AU - Burtscher, Michael

AU - Schalk, Nina

AU - Tkadletz, Michael

N1 - Publisher Copyright: © 2022

PY - 2023/4

Y1 - 2023/4

N2 - It is known that measurement parameters can significantly influence the elemental composition determined by atom probe tomography (APT). Especially results obtained by laser-assisted APT show a strong effect of the laser pulse energy on the apparent elemental composition. Within this study laser-assisted APT experiments were performed on Cr 0.51N 0.49 and thermally more stable (Cr 0.47Al 0.53) 0.49N 0.51, comparing two different base temperatures (i.e. 15 and 60 K), laser wavelengths (i.e. 532 and 355 nm) and systematically modified laser pulse energies. Absolute chemical compositions from laser-assisted APT were compared to data obtained from ion beam analysis. The deduced elemental composition of CrN exhibited a strong increase of the Cr content when the laser pulse energy was increased for both laser wavelengths. For low laser pulse energies Cr, CrN, N and N 2 ions were identified, while the amount of detected Cr ions increased and the amount of N ions strongly decreased at higher laser pulse energies. Further, increased detection of more complex Cr-containing ions such as Cr 2N at the expense of CrN was observed at higher pulse energies. At the highest pulse energy levels used within this work, the resulting Cr content was > 80 at%, dominated by the amount of detected elemental Cr ions. The change of the mass spectrum of the detected ions with increasing laser pulse energy provides evidence that high laser pulse energies initiate the decomposition of CrN during the APT measurement, consistent with the known thermal decomposition path into Cr 2N and subsequently into Cr and gaseous N. In contrast, variation of the laser pulse energy for the thermally more stable CrAlN resulted only in a slight increase of Cr and a decrease of the resulting concentrations of Al and N with increasing laser pulse energy and no change in the type of detected ions. In conclusion, within the present study, the decomposition of a coating material with low thermal stability induced by laser-assisted APT was reported for the first time, emphasizing the importance of the selection of suitable measurement parameters for metastable materials, which are prone to thermal decomposition.

AB - It is known that measurement parameters can significantly influence the elemental composition determined by atom probe tomography (APT). Especially results obtained by laser-assisted APT show a strong effect of the laser pulse energy on the apparent elemental composition. Within this study laser-assisted APT experiments were performed on Cr 0.51N 0.49 and thermally more stable (Cr 0.47Al 0.53) 0.49N 0.51, comparing two different base temperatures (i.e. 15 and 60 K), laser wavelengths (i.e. 532 and 355 nm) and systematically modified laser pulse energies. Absolute chemical compositions from laser-assisted APT were compared to data obtained from ion beam analysis. The deduced elemental composition of CrN exhibited a strong increase of the Cr content when the laser pulse energy was increased for both laser wavelengths. For low laser pulse energies Cr, CrN, N and N 2 ions were identified, while the amount of detected Cr ions increased and the amount of N ions strongly decreased at higher laser pulse energies. Further, increased detection of more complex Cr-containing ions such as Cr 2N at the expense of CrN was observed at higher pulse energies. At the highest pulse energy levels used within this work, the resulting Cr content was > 80 at%, dominated by the amount of detected elemental Cr ions. The change of the mass spectrum of the detected ions with increasing laser pulse energy provides evidence that high laser pulse energies initiate the decomposition of CrN during the APT measurement, consistent with the known thermal decomposition path into Cr 2N and subsequently into Cr and gaseous N. In contrast, variation of the laser pulse energy for the thermally more stable CrAlN resulted only in a slight increase of Cr and a decrease of the resulting concentrations of Al and N with increasing laser pulse energy and no change in the type of detected ions. In conclusion, within the present study, the decomposition of a coating material with low thermal stability induced by laser-assisted APT was reported for the first time, emphasizing the importance of the selection of suitable measurement parameters for metastable materials, which are prone to thermal decomposition.

UR - http://www.scopus.com/inward/record.url?scp=85145967297&partnerID=8YFLogxK

U2 - 10.1016/j.ultramic.2022.113673

DO - 10.1016/j.ultramic.2022.113673

M3 - Article

VL - 246.2023

JO - Ultramicroscopy

JF - Ultramicroscopy

SN - 0304-3991

IS - April

M1 - 113673

ER -