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Chemical bonding and electronic structures at magnesium/copper phthalocyanine interfaces

机译:镁/铜酞菁界面的化学键合和电子结构

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Chemistry, electronic structure and electrical behavior at the interfaces between copper phthalocyanine (CuPc) and Mg with a reverse formation sequence were investigated using X-ray photoemission spectroscopy (XPS), ultraviolet photoemission spectroscopy (UPS), and current-voltage (I-V) measurements. A chemical reaction occurs between CuPc and Mg irrespective of the deposition sequence. Despite having different reaction zone thicknesses, both the CuPc-on-Mgo and the Mg-on-CuPc interfaces exhibit chemistry-induced gap states and identical carrier injection barriers, which are confirmed by the symmetric electrical behavior obtained from I-V-characteristics of devices with a structure of Mg/CuPc/Mg. These findings contrast with those expected from physisorptive noble metal-CuPc interfaces and suggest that strong local chemical bonding is a primary factor determining molecular level alignment at reactive metal-CuPc interfaces. (c) 2005 Elsevier B.V. All rights reserved.
机译:使用X射线光电子能谱(XPS),紫外光电子能谱(UPS)和电流-电压(IV)测量研究了铜酞菁(CuPc)和Mg之间具有相反形成顺序的化学,电子结构和电行为。不管沉积顺序如何,CuPc和Mg之间都会发生化学反应。尽管具有不同的反应区厚度,但MPG上的CuPc界面和Mg上的CuPc界面均表现出化学诱导的间隙态和相同的载流子注入势垒,这可以通过以下方法得到证实:从具有Mg / CuPc / Mg的结构。这些发现与从物理上贵金属-CuPc界面预期的结果相反,并表明强烈的局部化学键合是决定反应性金属-CuPc界面分子水平排列的主要因素。 (c)2005 Elsevier B.V.保留所有权利。

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