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Peer-reviewedCC BY 4.0Dalton Transactions

Phase stability and magnetocaloric properties of Gd 2 OS 2 and γ-Gd 2 S 3 : a combined experimental and theoretical study

Abstract

Modifying the crystal structure of materials through thermal treatment and sulphurisation enables the formation of materials that are chemically challenging to stabilize using classical syntheses. This research investigates the effect of synthesis conditions during thermal treatment starting from the sulphide α-Gd2S3 and examines the structural, magnetic, and magnetocaloric properties of γ-Gd2S3 phase and Gd2OS2-rich sample, obtained in a partially sulphurised atmosphere. Both compounds are known to be chemically unstable, prompting us to calculate their phase diagrams using density functional theory (DFT) to better understand their chemical stability. For the first time, the Néel temperature (TN) of antiferromagnetic (AFM) ordering, the effective magnetic moment (μeff), the magnetocaloric effect (MCE), and the magnetic transition temperature (Tr) corresponding to the maximum MCE are reported for the Gd2OS2 oxysulphide and compared with those of α-Gd2S3 and its sub-phases. DFT investigation of the magnetic exchange interactions Jij was conducted to better understand the antiferromagnetic ordering in these systems. The magnetic phase transition was analyzed using the phenomenological universal curve of magnetic entropy change, revealing a first-order magnetic transition for all samples. The structural change from α-Gd2S3 (Pnma space group) to Gd2OS2 (P21/c space group) lowered TN from 10.0 K to 6.9 K and enhanced the MCE by ∼40%, reaching 79 mJ cm−3 K−1 at 6 K for µ0ΔH = 5 T.

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BibTeX
@article{bouhbou2026phase,
  title = {{Phase stability and magnetocaloric properties of Gd 2 OS 2 and γ-Gd 2 S 3 : a combined experimental and theoretical study}},
  author = {Meriem Bouhbou and Guillaume Durand and Thierry Guizouarn and Thomas Stephant and Odile Merdrignac-Conanec and Xavier Rocquefelte and Pierric Lemoine},
  journal = {Dalton Transactions},
  year = {2026},
  month = oct,
  doi = {10.1039/d6dt01408a},
  url = {https://hal.science/hal-05780203v1},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Phase stability and magnetocaloric properties of Gd 2 OS 2 and γ-Gd 2 S 3 : a combined experimental and theoretical study
AU  - Meriem Bouhbou
AU  - Guillaume Durand
AU  - Thierry Guizouarn
AU  - Thomas Stephant
AU  - Odile Merdrignac-Conanec
AU  - Xavier Rocquefelte
AU  - Pierric Lemoine
PY  - 2026
DA  - 2026/10/09
JO  - Dalton Transactions
DO  - 10.1039/d6dt01408a
UR  - https://hal.science/hal-05780203v1
AB  - Modifying the crystal structure of materials through thermal treatment and sulphurisation enables the formation of materials that are chemically challenging to stabilize using classical syntheses. This research investigates the effect of synthesis conditions during thermal treatment starting from the sulphide α-Gd2S3 and examines the structural, magnetic, and magnetocaloric properties of γ-Gd2S3 phase and Gd2OS2-rich sample, obtained in a partially sulphurised atmosphere. Both compounds are known to be chemically unstable, prompting us to calculate their phase diagrams using density functional theory (DFT) to better understand their chemical stability. For the first time, the Néel temperature (TN) of antiferromagnetic (AFM) ordering, the effective magnetic moment (μeff), the magnetocaloric effect (MCE), and the magnetic transition temperature (Tr) corresponding to the maximum MCE are reported for the Gd2OS2 oxysulphide and compared with those of α-Gd2S3 and its sub-phases. DFT investigation of the magnetic exchange interactions Jij was conducted to better understand the antiferromagnetic ordering in these systems. The magnetic phase transition was analyzed using the phenomenological universal curve of magnetic entropy change, revealing a first-order magnetic transition for all samples. The structural change from α-Gd2S3 (Pnma space group) to Gd2OS2 (P21/c space group) lowered TN from 10.0 K to 6.9 K and enhanced the MCE by ∼40%, reaching 79 mJ cm−3 K−1 at 6 K for µ0ΔH = 5 T.
SN  - 1477-9226
SN  - 1477-9234
ER  -