اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدElectronic properties and morphology of Cu-Phthalocyanine - C$_{60}$ composite mixtures
146
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
Phthalocyanines in combination with C$_{60}$ are benchmark materials for organic solar cells. Here we have studied the morphology and electronic properties of co-deposited mixtures (blends) of these materials forming a bulk heterojunction as a function of the concentration of the two constituents. For a concentration of 1:1 of CuPc:C$_{60}$ a phase separation into about 100 nm size domains is observed, which results in electronic properties similar to layered systems. For low C$_{60}$ concentrations (10:1 CuPc:C$_{60}$) the morphology, as indicated by Low-Energy Electron Microscopy (LEEM) images, suggests a growth mode characterized by (amorphous) domains of CuPC, whereby the domain boundaries are decorated with C$_{60}$. Despite of these markedly different growth modes, the electronic properties of the heterojunction films are essentially unchanged.
قيم البحث
اقرأ أيضاً
The electronic properties of co-evaporated mixtures (blends) of manganese phthalocyanine and the fullerene C$_{60}$ (MnPc:C$_{60}$) have been studied as a function of the concentration of the two constituents using two supplementary electron spectros
copic methods, photoemission spectroscopy (PES) as well as electron energy-loss spectroscopy (EELS) in transmission. Our PES measurements provide a detailed picture of the electronic structure measured with different excitation energies as well as different mixing ratios between MnPc and C$_{60}$. Besides a relative energy shift, the occupied electronic states of the two materials remain essentially unchanged. The observed energy level alignment is different compared to that of the related CuPc:C$_{60}$ bulk heterojunction. Moreover, the results from our EELS investigations show that despite of the rather small interface interaction the MnPc related electronic excitation spectrum changes significantly by admixing C$_{60}$ to MnPc thin films.
The signature of magnetism without a ferromagnet in a non-magnetic heterostructure is novel as well as fascinating from fundamental research point of view. It has been shown by AlMari et al: that magnetism can be induced at the interface of Cu/C60 du
e to change in density of states. However, the quantification of such interfacial magnetic moment has not been performed yet. In order to quantify the induced magnetic moment in Cu, we have performed X-ray magnetic circular dichroism (XMCD) measurements on Cu/C$_{60}$ multilayers. We have observed room temperature ferromagnetism in Cu/C$_{60}$ stack. Further XMCD measurements show that ~0.01 $mu_B$/atom magnetic moment has been induced in Cu at the Cu/C$_{60}$ interface.
The magnetic and transport properties of the metal phthalocyanine (MPc) and F$_{16}$MPc (M = Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn and Ag) families of molecules in contact with S-Au wires are investigated by density functional theory within the local
density approximation, including local electronic correlations on the central metal atom. The magnetic moments are found to be considerably modified under fluorination. In addition, they do not depend exclusively on the configuration of the outer electronic shell of the central metal atom (as in isolated MPc and F$_{16}$MPc) but also on the interaction with the leads. Good agreement between the calculated conductance and experimental results is obtained. For M = Ag, a high spin filter efficiency and conductance is observed, giving rise to a potentially high sensitivity for chemical sensor applications.
The paper has been withdrawn
Ambipolar charge carrier transport in Copper phthalocyanine (CuPc) is studied experimentally in field-effect transistors and metal-insulator-semiconductor diodes at various temperatures. The electronic structure and the transport properties of CuPc a
ttached to leads are calculated using density functional theory and scattering theory at the non-equilibrium Greens function level. We discuss, in particular, the electronic structure of CuPc molecules attached to gold chains in different geometries to mimic the different experimental setups. The combined experimental and theoretical analysis explains the dependence of the mobilityand the transmission coefficient on the charge carrier type (electrons or holes) and on the contact geometry. We demonstrate the correspondence between our experimental results on thick films and our theoretical studies of single molecule contacts. Preliminary results for fluorinated CuPc are discussed.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
