• Energy Research

Organic solar cells utilize an energy-level offset to generate free charge carriers. Although a very small energy-level offset increases the open-circuit voltage, it remains unclear how exactly charge generation is affected. Here we investigate organic solar cell blends with highest occupied molecular orbital energy-level offsets (∆EHOMO) between the donor and acceptor that range from 0 to 300 meV. We demonstrate that exciton quenching at a negligible ∆EHOMO takes place on timescales that approach the exciton lifetime of the pristine materials, which drastically limits the external quantum efficiency. We quantitatively describe this finding via the Boltzmann stationary-state equilibrium between charge-transfer states and excitons and further reveal a long exciton lifetime to be decisive in maintaining an efficient charge generation at a negligible ∆EHOMO. Moreover, the Boltzmann equilibrium quantitatively describes the major reduction in non-radiative voltage losses at a very small ∆EHOMO. Ultimately, highly luminescent near-infrared emitters with very long exciton lifetimes are suggested to enable highly efficient organic solar cells. Donor–acceptor systems with low energy-level offset enable high power efficiency in organic solar cells yet it is unclear what drives charge generation. Classen et al. show that long exciton lifetimes enable efficient exciton splitting and thus generation of free charges while also suppressing voltage losses.

High definition of all-small molecule materials for organic solar cells allows slow separation of localized charges.

Geminate recombination rates are successfully predicted for series of small-molecule bulk heterojunction solar cells applying the Marcus–Levich–Jortner equation.

The power conversion efficiencies of organic solar cells (OSCs) have reached over 19%. However, the combination of high efficiency and long-term stability is still a major conundrum of commercialization. Here a Y6-analogue and a 2,2′-bithiophene unit are utilized to construct a series of oligomer acceptors to investigate the effect of molecular size and packing properties on photovoltaic performance. By altering the molecular chain length, we modify the thermal properties, crystallization behaviours and molecular packing and achieve an optimal microstructure and a more stable morphology in blend films. A combination of efficiencies over 15% and an extrapolated T80 lifetime over 25,000 h, which equates to an average lifetime exceeding 16 years in Guangzhou, is achieved for binary OSCs based on an oligomer acceptor. This work emphasizes the importance of oligomeric strategy in tuning molecular packing behaviours and blend morphology, leading to development of novel non-fullerene acceptors for stable and efficient OSCs.

AbstractMultijunction solar cells offer a path to very high conversion efficiency, exceeding 60% in theory. Under ideal conditions, efficiency increases monotonically with the number of junctions. In this study, we explore technical and economic mechanisms acting on tandem solar cells. We find that these mechanisms produce limitations that are the more pronounced the greater the number of junction is and, hence, limit the ideal number of junctions, as well as the corresponding efficiencies. Spectral variations induce current losses in series‐connected tandem solar cells. For Denver, we find that these losses reduce achievable harvesting efficiencies to 51% for non‐concentrated light and that they restrict the ideal number of junctions to less than nine. Independently operated solar cells suffer from optical losses with similar consequences. Even high optical efficiencies of 99% restrict the ideal number of junctions to below 10 and reduce achievable efficiencies by more than 10%. Only architectures with a sequential cell illumination are more resilient to these losses. Restricting available materials reveals that a sufficiently low band gap for the bottom cell of 0.9 eV or below is expedient to realize high efficiencies. Economic considerations show that five junctions or less are economically ideal for most conceivable applications.

This work introduces nickel(ii) dibutyldithiocarbamate as a broadband and universal antioxidant for conjugated polymer semiconductors.