Brumbach, Michael and Placencia, Diogenes and Armstrong, Neal R. (2008) Titanyl phthalocyanine/C-60 heterojunctions: Band-edge offsets and photovoltaic device performance. JOURNAL OF PHYSICAL CHEMISTRY C, 112 (8). pp. 3142-3151.
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Official URL: http://pubs.acs.org/doi/abs/10.1021/jp0772171
Planar heterojunction organic photovoltaic devices have been created using oxo-titanium phthalocyanine (TiOPc) as the donor layer and fullerene (C-60) as the acceptor layer, with comparisons to devices based on copper phthalocyanine (CuPc) as the donor. TiOPC/C-60 and CuPC/C-60 heterojunctions were first characterized by a combination of UV-photoelectron spectroscopy (UPS) and X-ray photoelectron spectroscopy (XPS) to estimate the frontier orbital energy offset (E-HOMO(D) - E-LUMO(A)), which is related to the open-circuit photopotential (V-OC). A small interface dipole effect was seen at the TiOPc/C-60 interface (eD approximate to 0.02 eV), whereas a significant interface dipole was observed for the CuPC/C-60 interface (eD approximate to 0.3 eV). On the basis of the work presented here and previously reported electrochemical and UPS/XPS studies, we estimate an E-HOMO(D) - E-LUMO(A) energy offset of ca. 1.1 eV for the TiOPc/C-60 heterojunction and 0.7 eV for the CuPC/C-60 heterojunction. Maximum V-OC values observed at room temperature for corresponding planar heterojunction photovoltaic devices were 0.3-0.4 V lower than the energy offset potentials, even at high light intensities, where the maximum V-OC, at room temperature, was achieved. TiOPc/C-60 heterojunctions offer higher V-OC values than CuPC/C-60 heterojunctions, but with a lower intrinsic driving force for exciton dissociation (photoinduced charge transfer).
|Subjects:||Analytical Science > Microscopy and probe methods|
Technology > Nanotechnology and energy applications
Physical Science > Photonics
|Deposited By:||Farnush Anwar|
|Deposited On:||13 Jan 2009 16:40|
|Last Modified:||27 Jan 2009 12:11|
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