Abstract
Two linear organic A-D-A molecules (DTPT and DTPTT) comprised of electron-donating (D) coplanar heteroacenes as core end-capping with electron-accepting (A) dicyanovinylene were investigated as electron donor materials in organic photovoltaic (OPV) applications. The photophysical and electrochemical properties of these two dyes were examined. The A-D-A configuration renders these two molecules to have intense and red-shifted absorption characteristics for better light-harvesting (higher photocurrent density), while retaining relatively low HOMO energy levels for keeping sufficiently high open circuit voltage (V oc ) in OPV. The optical constants and molecular orientation of thin films were acquired with variable-angle spectroscopic ellipsometry (VASE). Due to the anisotropic behavior observed in thin film, these two organic donors were firstly adopted to combine with electron acceptor C 60 in a vacuum-processed planar heterojunction (PHJ) solar cells. The optimized DTPT-based PHJ device yielded a PCE of 3.01%, whereas the PHJ device based on DTPTT, delivered an inferior PCE of 1.70%. The exciton diffusion length extracted from spectrum-response modeling of PHJ devices is ∼5 nm and ∼4 nm for DTPT and DTPTT, respectively. Replacement of C 60 with C 70 for a better spectral response in 400-500 nm, planar-mixed heterojunction (PMHJ) SMOSCs without a thin donor layer in between the active layer and MoO 3 was found to produce optimum device results. The optimized DTPTT-based device showed a PCE of 3.02%, while the shorter counterpart DTPT delivered a PCE up to 5.64%.