Control of Covalent Bond Enables Efficient Magnetic Cooling

作者：Xin Tang, Yoshio Miura, Noriki Terada, Enda Xiao, Shintaro Kobayashi, Allan M. Döring, Terumasa Tadano, A. Martín-Cid, Takuo Ohkochi, Shogo Kawaguchi, Yoshitaka Matsushita, Tadakatsu Ohkubo, Tetsuya Nakamura, Konstantin Skokov, Oliver Gutfleisch, K. Hono, H. Sepehri‐Amin · 发表于：Advanced Materials · 年份：2025 · DOI：10.1002/adma.202514295 · 被引用次数：4 · 研究领域：Magnetic and transport properties of perovskites and related materials、Shape Memory Alloy Transformations、Thermal Expansion and Ionic Conductivity

Abstract Magnetic cooling, harnessing the temperature change in matter when exposed to a magnetic field, presents an energy‐efficient and climate‐friendly alternative to traditional vapor‐compression refrigeration systems, with a significantly lower global warming potential. The advancement of this technology would be accelerated if irreversible losses arising from hysteresis in magnetocaloric materials are minimized. Despite extensive efforts to manipulate crystal lattice constants at the unit‐cell level, mitigating hysteresis often compromises cooling performance. Herein, we address this persistent challenge by forming Sn(Ge) 3 −Sn(Ge) 3 bonds within the unit cell of the Gd 5 Ge 4 compound. This approach enables an energetically favorable phase transition, leading to the elimination of thermal hysteresis. Consequently, we achieve a synergistic improvement of two key magnetocaloric figures of merit: a larger magnetic entropy change and a twofold increase in the reversible adiabatic temperature change (from 3.8 to 8 K) in the Gd 5 Sn 2 Ge 2 compound. Such synergies can be extended over a wide temperature range of 40–160 K. This study demonstrates a paradigm shift in mastering hysteresis toward simultaneously achieving exceptional magnetocaloric metrics and opens up promising avenues for gas liquefaction applications in the longstanding pursuit of sustainable energy solutions.