Gao Mingsheng, Lu Xiangqian, Yang Yuying, Qin Wei
School of Physics, State Key Laboratory of Crystal Materials, Shandong University, Jinan, 250100, China.
Adv Mater. 2024 Aug;36(33):e2405024. doi: 10.1002/adma.202405024. Epub 2024 May 17.
Organic multiferroic heterostructure is one of the most promising structures for the future design of high-density flexible energy-efficient data storage. Here, organic ferromagnetic metal(tetracyanoethylene) (M(TCNE))/ferroelectric poly(vinylidene fluoride-co-trifluoroethylene) (P(VDF-TrFE)) multiferroic heterostructures are fabricated, where the excited state in M(TCNE) interacted with localized dipole in P(VDF-TrFE) provides a key link for the interfacial coupling. Thus, aligned dipoles in P(VDF-TrFE) by external electric field can affect the magnetization of Fe(TCNE) effectively to result in a pronounced magnetization-voltage (M-V) hysteresis loop. Moreover, light-induced electron-hole pairs in Fe(TCNE) with long lifetime effectively interact with the dipoles in P(VDF-TrFE) to lead to an effect in external light control of electric polarization of P(VDF-TrFE). Overall, the organic multiferroic heterostructure provides the possibility of realizing two storage modes, light control of dipole as well as electric field control of spin, which can broaden multifunctional applications of organic multiferroic materials in the area of multistate storage.
有机多铁异质结构是未来高密度灵活节能数据存储设计中最具前景的结构之一。在此,制备了有机铁磁金属(四氰基乙烯)(M(TCNE))/铁电聚偏二氟乙烯-三氟乙烯共聚物(P(VDF-TrFE))多铁异质结构,其中M(TCNE)中的激发态与P(VDF-TrFE)中的局域偶极相互作用为界面耦合提供了关键联系。因此,通过外部电场使P(VDF-TrFE)中的偶极排列整齐,能够有效影响Fe(TCNE)的磁化,从而产生明显的磁化-电压(M-V)磁滞回线。此外,Fe(TCNE)中具有长寿命的光致电子-空穴对与P(VDF-TrFE)中的偶极有效相互作用,导致对P(VDF-TrFE)的极化进行外部光控的效应。总体而言,有机多铁异质结构提供了实现两种存储模式的可能性,即偶极的光控以及自旋的电场控制,这可以拓宽有机多铁材料在多态存储领域中的多功能应用。