Delayed Triplet-State Formation through Hybrid Charge Transfer Exciton at Copper Phthalocyanine/GaAs Heterojunction

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Light absorption in organic molecules on an inorganic substrate and subsequent electron transfer to the substrate create so-called hybrid charge transfer exciton (HCTE). The relaxation process of the HCTE states largely determines charge separation efficiency or optoelectronic device performance. Here, the study on energy and time-dispersive behavior of photoelectrons at the hybrid interface of copper phthalocyanine (CuPc)/p-GaAs(001) upon light excitation of GaAs reveals a clear pathway for HCTE relaxation and delayed triplet-state formation. According to the ground-state energy level alignment at the interface, CuPc/p-GaAs(001) shows initially fast hole injection from GaAs to CuPc. Thus, the electrons in GaAs and holes in CuPc form an unusual HCTE state manifold. Subsequent electron transfer from GaAs to CuPc generates the formation of the triplet state in CuPc with a few picoseconds delay. Such two-step charge transfer causes delayed triplet-state formation without singlet excitation and subsequent intersystem crossing within the CuPc molecules.
Publisher
AMER CHEMICAL SOC
Issue Date
2017-10
Language
English
Article Type
Article
Keywords

SURFACE PHOTOVOLTAGE; ENERGY-TRANSFER; SOLAR-CELLS; THIN-FILMS; SEMICONDUCTOR; INTERFACES; SEPARATION; TRANSPORT; DYNAMICS; WIRES

Citation

JOURNAL OF PHYSICAL CHEMISTRY LETTERS, v.8, no.19, pp.4763 - 4768

ISSN
1948-7185
DOI
10.1021/acs.jpclett.7b02111
URI
http://hdl.handle.net/10203/226824
Appears in Collection
CH-Journal Papers(저널논문)
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