Enhanced Cryogenic Magnetocaloric Effect from 4f‐3d Exchange Interaction in B‐Site Ordered Gd2CuTiO6 Double Perovskite Oxide
Magnetic refrigeration based on the principle of the magnetocaloric effect (MCE) in magnetic solids has been considered as a prospective cooling technology. Exploring suitable magnetocaloric materials (MCMs) is a vital prerequisite for practical applications. Herein, an excellent cryogenic MCM—the B...
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Veröffentlicht in: | Advanced functional materials 2024-12, Vol.34 (49), p.n/a |
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Zusammenfassung: | Magnetic refrigeration based on the principle of the magnetocaloric effect (MCE) in magnetic solids has been considered as a prospective cooling technology. Exploring suitable magnetocaloric materials (MCMs) is a vital prerequisite for practical applications. Herein, an excellent cryogenic MCM—the B‐site‐ordered Gd2CuTiO6 double perovskite (DP) oxide—which exhibits the largest MCE among known Gd‐based DP oxides, is identified. Such enhanced cryogenic MCE in the Gd2CuTiO6 DP oxide likely stems from the exchange interaction effect between Gd‐4f and Cu‐3d magnetic sublattices. Under a magnetic field change of 0–7 T, the maximum magnetic entropy change (−ΔSTmax) of the Gd2CuTiO6 DP oxide reaches 51.4 J kg−1 K−1 (378.2 mJ cm−3 K−1), which is much larger than that of the commercialized magnetic refrigerant Gd3Ga5O12, which is 38.3 J kg−1 K−1 (271.2 mJ cm−3 K−1), and it is also superior to most of the recently reported benchmarked cryogenic MCMs, indicating the possibility for practical applications. This work also provides a productive route for future cryogenic MCM design by harnessing 4f–3d exchange interactions.
Herein, an excellent cryogenic magnetocaloric material (MCM) is provided, the B‐site‐ordered Gd2CuTiO6 double perovskite (DP) oxide, which exhibits the largest magnetocaloric effect among the known RE‐based DP oxides and also superior to most of the reported cryogenic MCMs. This research provides a productive route for future MCMs design by harnessing the 4f–3d exchange interactions. |
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ISSN: | 1616-301X 1616-3028 |
DOI: | 10.1002/adfm.202409061 |