Abstract
The binary molecular system of C60 and copper phthalocyanine(CuPc) molecules has been investigated by scanning tunneling microscopy (STM) at room temperature and at 50 K. As substrate Au(111) was chosen. When C60 and CuPc molecules are sequentially deposited, it is found that well-ordered domains of both molecules may coexist simultaneously. Hence hexagonal ordering of C60 and quadratic ordering of CuPc is observed side by side but no ordered mixed layer of both molecules or heteroepitaxy from one molecule on the other is found. Instead the boundaries of the CuPc domains are often decorated by C60 molecules and for a particular choice of parameters, with regard to the film preparation, individual CuPc molecules may adsorb on top of a C60 layer. The interaction with the underlying C60 layer permits the molecules to perform a localized, hindered rotation. At room temperature the hopping frequency is so high that only the time average of the rotation is seen by STM while at 50 K the rotation is frozen and the CuPc molecule is trapped in one definite position.
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