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Interface-Induced Spin and Dipole Ordering of the Copper Spin 1/2 Molecule: Bis(4-cyano-2,2,6,6-tetramethyl-3,5-heptanedionato)copper(II)
Author(s) -
David Wisbey,
Ning Wu,
Danqin Feng,
Anthony N. Caruso,
J.A. Belot,
Yaroslav Losovyj,
E. Vescovo,
P. A. Dowben
Publication year - 2008
Publication title -
the journal of physical chemistry c
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.401
H-Index - 289
eISSN - 1932-7455
pISSN - 1932-7447
DOI - 10.1021/jp804251b
Subject(s) - copper , dipole , molecule , metal , polarization (electrochemistry) , crystallography , spin (aerodynamics) , spin polarization , materials science , chemistry , adsorption , condensed matter physics , electron , physics , organic chemistry , thermodynamics , quantum mechanics
Using light-polarization-dependent angle-resolved photoemission, the metal-organic molecule bis(4-cyano-2,2,6,6-tetramethyl-3,5-heptanedionato)copper(II) (or Cu(CNdpm) 2 , i.e., C 24 H 36 N 2 O 4 Cu, Cu(II)) is observed to adopt a preferential orientation that depends on the film thickness and substrate when adsorbed on Co(111) and Cu(111). In addition, the final-state binding energies change with film thickness, suggesting the substrates affect the screening or charging in the photoemission final state. For Cu(CNdpm) 2 deposited on Co(111), the induced spin polarization was found to depend strongly on the molecular orbital contributions.

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