DOI: https://doi.org/10.29363/nanoge.hopv.2026.117
Publication date: 11th March 2026
All-polymer solar cells offer potential advantages in mechanical robustness and morphological stability, yet they remain less efficient than state-of-the-art small-molecule non-fullerene acceptor–based organic solar cells. In this work, we investigate the efficiency-limiting processes in all-polymer bulk heterojunction devices based on the donor polymers PBDB-T and PBDB-T-2F (PM6) blended with the polymer acceptors PYN-BDT and PYN-BDTF. Owing to π-extended naphthalene units, the acceptor polymers exhibit strong absorption extending to approximately 900 nm. A combination of steady-state spectroscopy and time-resolved techniques—including transient absorption, time-resolved photoluminescence, photoluminescence-detected magnetic resonance, and time-delayed collection field measurements—enables a quantitative analysis of charge-generation and loss processes. Kinetic parameters and process yields derived from pulsed-laser spectroscopy reproduce the measured current–voltage characteristics, confirming the consistency of the approach. The results show that moderate fill factors arise from non-geminate recombination competing with charge extraction and from field-dependent charge generation, with the relative importance of these processes depending on the polymer acceptor. The methodology provides a general framework for quantifying loss mechanisms in bulk heterojunction organic solar cells.
