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<p>Owing to their exceptional chemical and electronic tunability, metal–organic frameworks can be designed to develop magnetic ground states — however, the typically weak exchange interactions mediated by the diamagnetic organic ligands result in ordering temperatures confined to the cryogenic limit. The itinerant magnetic ground state realized in the chromium-based framework Cr(tri)<sub>2</sub>(CF<sub>3</sub>SO<sub>3</sub>)<sub>0.33</sub> (Htri, 1<i>H</i>-1,2,3-triazole) is a remarkable exception to this trend, showing a robust ferromagnetic behavior almost at ambient conditions. Here, we use dc SQUID magnetometry, nuclear magnetic resonance, and ferromagnetic resonance to study the magnetic state realized in this material and highlight several thermally-activated relaxation mechanisms for the nuclear magnetization. Most interestingly, we report the development within the paramagnetic regime of mesoscopic magnetic correlated clusters whose slow dynamics in the MHz range are tracked by the nuclear moments, in agreement with the highly unconventional nature of the magnetic transition detected by dc SQUID magnetometry. We discuss the similarity between the clustered phase in the paramagnetic phase and the magnetoelectronic phase segregation leading to colossal magnetoresistance in manganites and cobaltites. These results demonstrate that high-temperature magnetic metal–organic frameworks can serve as a versatile platform for exploring correlated electron phenomena in low-density, chemically tunable materials.</p>

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Magnetic clusters in the paramagnetic phase of a high-temperature ferromagnetic metal–organic framework

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年3月27日

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  • Giacomo Prando,
  • Benjamin Costarella,
  • Matthew S. Dickson,
  • Ryan A. Murphy,
  • Jesse G. Park,
  • Gianrico Lamura,
  • Giuseppe Allodi,
  • Cristian Aloisi,
  • Aëto Apaix,
  • Maria Cristina Mozzati,
  • T. David Harris,
  • Jeffrey R. Long,
  • Pietro Carretta

摘要

Owing to their exceptional chemical and electronic tunability, metal–organic frameworks can be designed to develop magnetic ground states — however, the typically weak exchange interactions mediated by the diamagnetic organic ligands result in ordering temperatures confined to the cryogenic limit. The itinerant magnetic ground state realized in the chromium-based framework Cr(tri)2(CF3SO3)0.33 (Htri, 1H-1,2,3-triazole) is a remarkable exception to this trend, showing a robust ferromagnetic behavior almost at ambient conditions. Here, we use dc SQUID magnetometry, nuclear magnetic resonance, and ferromagnetic resonance to study the magnetic state realized in this material and highlight several thermally-activated relaxation mechanisms for the nuclear magnetization. Most interestingly, we report the development within the paramagnetic regime of mesoscopic magnetic correlated clusters whose slow dynamics in the MHz range are tracked by the nuclear moments, in agreement with the highly unconventional nature of the magnetic transition detected by dc SQUID magnetometry. We discuss the similarity between the clustered phase in the paramagnetic phase and the magnetoelectronic phase segregation leading to colossal magnetoresistance in manganites and cobaltites. These results demonstrate that high-temperature magnetic metal–organic frameworks can serve as a versatile platform for exploring correlated electron phenomena in low-density, chemically tunable materials.