Chlorinated Wide-Bandgap Donor Polymer Enabling Annealing Free Nonfullerene Solar Cells with the Efficiency of 11.5.

Abstract

Substituting the hydrogen atoms on the conjugated side chain of a wide-bandgap polymer J52 with chlorine atoms can simultaneously increase the Jsc, Voc, and FF of nonfullerene OSCs, leading to an efficiency boost from 3.78 to 11.53%, which is among the highest efficiencies for as-cast OSCs reported to date. To illustrate the impressive 3-fold PCE enhancement, the chlorination effect on the optical properties and energy levels of polymers, film morphology, and underlying charge dynamics is systematically investigated. Grazing incidence wide-angle X-ray scattering studies show that chlorinated J52-2Cl exhibits strong molecule aggregation, the preferred face-on orientation, and enhanced intermolecular π-π interactions, hence increasing the charge carrier mobility by 1 order of magnitude. Moreover, chlorination modifies the miscibility between the donor and acceptor and consequently optimizes the phase separation morphology of J52-2Cl:ITIC blend films. These results highlight chlorination as a promising approach to achieve highly efficient as-cast OSCs without any extra treatment.