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Coverage-dependent structures of cobalt-phthalocyanine molecules adsorbed on Cu(001) surface
Qinmin Guo1, Zhihui Qin, Kan Zang
1State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute of Physics and Mathematics, Chinese Academy of Sciences, Wuhan 430071, PR China.
Abstract:
The morphologies, self-assembly structures, and stability of cobalt-phthalocyanines (CoPc) molecules adsorbed on Cu(001) with coverage ranging from 0.2 monolayer (ML) to 1.6 ML are investigated by ultrahigh-vacuum low-temperature scanning tunneling microscopy (UHV LT-STM) at liquid nitrogen temperature. Upon increasing the deposition of CoPc molecules various structures, such as isolated adsorption, quasi-hexagonal structure, square root(29) x square root(29) structure, are well characterized by the corresponding high-resolution STM images. The CoPc-CoPc intermolecular interaction and CoPc-substrate interfacial interaction dominate the structural evolutions. For the coverage higher than 1 ML, CoPc molecules preferentially locate on top of the molecules underneath and organize into square root(58) x square root(58) structure. As more and more CoPc molecules adsorb on the first layer, in some square root(58) x square root(58) regions molecular insertion leads to the formation of the square root(29) x square root(29) domain to effectively decrease the energy of the whole system.
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