Abstract

Spintronics are attractive to the utilization in next-generation quantum-computing and memory. Compared with inorganic spintronics, organic spintronics not only controls the spin degree-of-freedom but also possesses advantages such as chemical tailorability, flexibility, and low-cost fabrication process. Besides, the organic spin valve with a sandwich configuration that is composed of two ferromagnetic electrodes and an organic space layer is one of the classical devices in organic spintronics. Greatly enhanced or inversed magnetoresistance (MR) sign appearing in organic spin valve is induced by the unique interfacial effect an organic semiconductor/ferromagnetic interface. The significant enhancement or inversion of MR is later proved to be caused by the spin-dependent hybridization between molecular and ferromagnetic interface, <i>i.e.</i>, the spinterface. The hybridization is ascribed to spin-dependent broadening and shifting of molecular orbitals. The spinterface takes place at one molecular layer when attaching to the surface of ferromagnetic metal. It indicates that the MR response can be modulated artificially in a specific device by converting the nature of spinterface. Despite lots of researches aiming at exploring the mechanism of spinterface, several questions need urgently to be resolved. For instance, the spin polarization, which is difficult to identify and observe with the surface sensitive technique and the inversion or enhancement of MR signal, which is also hard to explain accurately. The solid evidence of spinterface existing in real spintronic device also needs to be further testified. Besides, the precise manipulation of the MR sign by changing the nature of spinterface is quite difficult. According to the above background, this review summarizes the advance in spinterface and prospects future controllable utilization of spinterface. In Section 2, we introduce the basic principle of spintronic device and spinterface. The formation of unique spinterface in organic spin valve is clarified by using the difference in energy level alignment between inorganic and organic materials. Enhancement and inversion of MR sign are related to the broadening and shifting of the molecular level. In Section 3, several examples about identification of spinterface are listed, containing characterization by surface sensitive techniques and identification in real working devices. In Section 4 some methods about the manipulation of spinterface are exhibited, including modulation of ferroelectric organic barrier, interface engineering, regulation of electronic phase separation in ferromagnetic electrodes, etc. Finally, in this review some unresolved questions in spintronics are given, such as multi-functional and room-temperature organic spin valve and improvement of the spin injection efficiency. Spinterface is of great importance for both scientific research and future industrial interest in organic spintronics. The present study paves the way for the further development of novel excellent organic spin valves.

Highlights

  • Schematic diagram of the band structure of inorganic materials and organic materials, and the schematic diagram of the energy difference between inorganic and organic molecule closed to a ferromagnetic electrode[46]

  • 值. 如果用 Jullière 模型进行预测, 以 LSMO 电极 100% 的自旋极化计算, 在 Alq3/Co 界面最大自旋 极化值约为 60%; 由此推断因为 Alq3/Co 电极自 旋界面的存在, 使得磁电阻信号实现了 300% 的增 强 [44]. 文献 [68] 报道了在一端使用非磁电极的 Co (8 nm)/ZMP (40 nm)/Cu(12 nm) 结构中, 自旋依 赖的分子轨道发生移动, 自旋界面起自旋过滤作用

  • SPECIAL TOPIC—Manipulation and applications of solid-state single quantum systems

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Summary

Inorganic At the interface

电极之间相互作用和杂化程度不同, 能级展宽的范 围从毫电子伏特到电子伏特不等 [62]. 此外, 由于与 金属的相互作用, 分子能级的能量会从单个分子起 始位置 e0 偏移到 eeff. 这一偏移取决于金属的态密 度, 也受到界面偶极或镜像力的影响 [63]. 此外, 由于与 金属的相互作用, 分子能级的能量会从单个分子起 始位置 e0 偏移到 eeff. 于铁磁电极来说, 自旋向上和自旋向下的态密度不 同 (D↑FM (E) ̸= DF↓M (E)). 因而自旋向上和自旋向下 的分子能级将会退简并为两种能量 ( ε↑eff= ε↓eff ), 对 应两种不同的展宽宽度 ( Γ ↑ ̸= Γ ↓ ).

At the interface
FM matel
CN NC C
Co Hybrid states LSMO
Positive polarization
LUMO h HOMO
Bulk Co
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