Charge transport and collection in organic solar cells are heavily influenced by traps which ultimately limit the ability to harvest all photogenerated carriers. We investigate photocurrent responses of organic solar cells subjected to varying degrees of aging from time-and frequency-domain perspectives. Intensitymodulated photocurrent spectroscopy (IMPS) is primarily used here to resolve the effect of trap-assisted nongeminate charge recombination over a broad frequency range (e.g., ∼1 mHz−1 MHz). We use a combination of IMPS and time-dependent photocurrent transients to understand characteristic degradation signatures (i.e., positive, low-frequency imaginary component and "gain peak" where the real photocurrent exhibits a characteristic maximum, I max , at high frequencies) unique to organic solar cells. As trap densities and occupation increase with aging and light intensity, the photocurrent contrast (i.e., maximum/steady-state photocurrent, I max /I DC ) and the size of the low-frequency imaginary contribution increase. Substantial harmonic content underlies this trend which becomes more prominent as modulation frequencies and trap levels increase. We then use drift-diffusion simulations to describe IMPS responses and photocurrent transient signals over the entire frequency sampling window for aged devices that show excellent agreement with experiment. The results provide deeper insights into trap-related phenomena over a larger frequency bandwidth and further demonstrate the effectiveness of IMPS in its ability to identify mechanistic and kinetic details of degradation.

Resolving the population dynamics of multiple triplet excitons on time scales comparable to their lifetimes is a key challenge for multiexciton harvesting strategies, such as singlet fission. We show that this information can be obtained from fluorescence quenching dynamics and stochastic kinetic modeling simulations of single nanoparticles comprising self-assembled aggregated chains of poly(3-hexylthiophene) (P3HT). These multichromophoric structures exhibit the elusive J-aggregate type excitonic coupling leading to delocalized intrachain excitons that undergo facile triplet formation mediated by interchain charge transfer states. We propose that P3HT J-aggregates can serve as a useful testbed for elucidating the presence of multiple triplets and understanding factors governing their interactions over a broad range of time scales. Stochastic kinetic modeling is then used to simulate discrete population dynamics and estimate higher order rate constants associated with triplet-triplet and singlet-triplet annihilation. Together with the quasi-CW nature of the experiment, the model reveals the expected amounts of triplets at equilibrium per molecule. Our approach is also amenable to a variety of other systems, e.g., singlet fission active molecular arrays, and can potentially inform design and optimization strategies to improve triplet harvesting yields.

We investigate the degradation phenomena of organic solar cells based on nonfullerene electron acceptors (NFA) using intensity-modulated photocurrent spectroscopy (IMPS). Devices composed of NIR absorbing blends of a polymer (PTB7) and NFA molecules (COi8DFIC) were operated in air for varying periods of time that display unusual degradation trends. Light aging (e.g., ∼3 days) results in a characteristic first quadrant (positive phase shifts) degradation feature in IMPS Nyquist (Bode) plots that grow in amplitude and frequency with increasing excitation intensity and then subsequently turns over and vanishes. By contrast, devices aged and operated in air for longer times (>5 days) display poor photovoltaic performance and have a dominant first quadrant IMPS component that grows nonlinearly with excitation intensity. We analyze these degradation trends using a simple model with descriptors underlying the first quadrant feature (i.e., trap lifetime and occupancy). The results indicate that the quasi first-order recombination rate constant, k rec, is significantly slower in addition to lower trap densities in devices exhibiting light aging effects that are overcome by increasing carrier densities (viz. excitation intensity). By contrast, larger trap densities and distributions coupled with larger k rec values are found to be responsible for the continuous growth of the first quadrant with light intensity. We believe that defect formation and charge recombination at device contact interfaces is chiefly responsible for performance degradation, which offers several directions for materials and device optimization strategies to minimize long-term detrimental factors.