Co/Pt multilayers with perpendicular anisotropy were deposited using a dc magnetron sputtering system under high vacuum.Magnetization process was investigated by the measurement of magnetic components parallel and perpendicular to the applied field.A dependence of the coercivity of Co/Pt multilayers on the Co layer thickness was reported,in which the total thickness of Co layers kept constant.It is observed that the coercivity increases with the increment of Co layer thickness.For the samples with the same Co layer thickness while different total Co layer thickness,the coercivity first increases and then decreases with the increase of the total thickness of Co layers.This effect could be attributed to the competition between the reduction of HC related to incoherent reversal and the step-up of HC contributed by the magnetic polarization of Pt atoms at the interface of Co and Pt layers during magnetization reversal.The results show that the change of the coercivity is strongly related to the Co layer thickness,but not the total thickness of Co layers.The dependence of the coercivity on the angle between an applied field and the easy axis shows that the nucleation mode is dominant in magnetization reversal process of the samples.
We herein report the effective performance enhancement of the pentacene-based organic thin film transistors with silicon di- oxide dielectric by inserting a thin metal phthalocyanines interlayer between Au source/drain electrodes and the pentacene active layer. The threshold voltage decreased remarkably from ca. -20 V to a few volts （below -7.6 V） while the mobility in- creased 1.5-3 times after the insertion of the interlayer of only ca. 2 nm, which could be attributed to the reduction of the car- tier injection barrier. The results suggest a simple and effective way to achieve low-threshold-voltage pentacene-based organic thin film transistors with high mobility on silicon dioxide dielectric.
LI YiLIU QiWANG XiZhangSEKITANI TsuyoshiSOMEYA TakaoHU Zheng
Sheet-like carbon-nitrogen (CNx)/graphene composites with a high content of nitrogen (x≤0.15) was prepared by the carbonization of polypyrrole (PPy)/reduced-graphene-oxide (rGO) composite at 600-800°C. We used rGO instead of graphene oxide (GO) sheets as a template and a substrate to immobilize PPy since the PPy/GO composite agglomerates easily because of the dehydration of excess oxygen-containing groups on the GO sheets during the drying process. The dried PPy/rGO intermediate and its derived CNx/graphene products retain their high dispersion and loose-powder features. The as-prepared CNx/graphene composites have a total nitrogen content of about 10 at% and their nitrogen state is mainly of pyridinic and graphitic type. CNx/graphene composites exhibit excellent performance for the oxygen reduction reaction (ORR) in terms of electrocatalytic activity, stability and immunity towards methanol crossover and CO poisoning, suggesting their potential as metal-free electrocatalysts for the ORR.
MA YanWenZHANG LingRongLIJuanJuanNI HaiTaoLI MengZHANG JinLeiFENG XiaoMiaoFAN QuLiHU ZhengHUANG Wei
