Room temperature multiferroics has been a frontier research field by manipulating spin-driven ferroelectricity or charge-order-driven magnetism. Charge-transfer crystals based on electron donor and acceptor assembly, exhibiting simultaneous spin ordering, are drawing significant interests for the development of all-organic magnetoelectric multiferroics. Here, we report that a remarkable anisotropic magnetization and room temperature multiferroicity can be achieved through assembly of thiophene donor and fullerene acceptor. The crystal motif directs the dimensional and compositional control of charge-transfer networks that could switch magnetization under external stimuli, thereby opening up an attractive class of all-organic nanoferronics.
机构:
Hubei Univ, Hubei Collaborat Innovat Ctr Adv Organ Chem Mat, Wuhan 430062, Peoples R China
Hubei Univ, Fac Phys & Elect Technol, Wuhan 430062, Peoples R ChinaHubei Univ, Hubei Collaborat Innovat Ctr Adv Organ Chem Mat, Wuhan 430062, Peoples R China
Yang, Hui
Huang, Zhongbing
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Hubei Univ, Hubei Collaborat Innovat Ctr Adv Organ Chem Mat, Wuhan 430062, Peoples R China
Hubei Univ, Fac Phys & Elect Technol, Wuhan 430062, Peoples R China
Beijing Computat Sci Res Ctr, Beijing 100193, Peoples R ChinaHubei Univ, Hubei Collaborat Innovat Ctr Adv Organ Chem Mat, Wuhan 430062, Peoples R China
Huang, Zhongbing
Gao, Yun
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Hubei Univ, Fac Mat Sci & Engn, Wuhan 430062, Peoples R ChinaHubei Univ, Hubei Collaborat Innovat Ctr Adv Organ Chem Mat, Wuhan 430062, Peoples R China
Gao, Yun
Lin, Haiqing
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Beijing Computat Sci Res Ctr, Beijing 100193, Peoples R ChinaHubei Univ, Hubei Collaborat Innovat Ctr Adv Organ Chem Mat, Wuhan 430062, Peoples R China