Entropy and disorder enable charge separation in organic solar cells
arXiv:1603.06304 · doi:10.1021/acs.jpclett.6b02178
Abstract
Although organic heterojunctions can separate charges with near-unity efficiency and on a sub-picosecond timescale, the full details of the charge-separation process remain unclear. In typical models, the Coulomb binding between the electron and the hole can exceed the thermal energy by an order of magnitude, suggesting that it is impossible for the charges to separate before recombining. Here, we consider the entropic contribution to charge separation in the presence of disorder and find that even modest amounts of disorder have a decisive effect, reducing the charge-separation barrier to about or eliminating it altogether. Therefore, the charges are usually not thermodynamically bound at all and could separate spontaneously if the kinetics otherwise allowed it. Our conclusion holds despite the worst-case assumption of localised, thermalised carriers, and is only strengthened if mechanisms like delocalisation or `hot' states are also present.
References in corpus (4)
- The Role of Driving Energy and Delocalised States for Charge Separation in Organic Semiconductors
- Origin of the Efficient Polaron Pair Dissociation in Polymer--Fullerene Blends
- Noise-induced quantum coherence drives photocarrier generation dynamics at polymeric semiconductor heterojunctions
- Kramers rate theory of ionization and dissociation of bound states
Cited by in corpus (14)
- Charge Photogeneration in Non-Fullerene Organic Solar Cells: Influence of Excess Energy and Electrostatic Interactions
- Delocalised kinetic Monte Carlo for simulating delocalisation-enhanced charge and exciton transport in disordered materials
- Even a little delocalization produces large kinetic enhancements of charge-separation efficiency in organic photovoltaics
- Charge separation in donor-C60 complexes with real-time Green's functions: The importance of nonlocal correlations
- Energetics and Kinetics Requirements for Organic Solar Cells to 2 Break the 20% Power Conversion Efficiency Barrier
- Delocalisation enables efficient charge generation in organic photovoltaics, even with little to no energetic offset
- The interplay of interfaces, supramolecular assembly, and electronics in organic semiconductors
- Exciton Dissociation and Charge Separation at Donor-Acceptor Interfaces from Quantum-Classical Dynamics Simulations
- Identification of Ultrafast Photophysical Pathways in Photoexcited Organic Heterojunctions
- Model for the dynamics of carrier injection in a band with polaronic states: Application to exciton dissociation in organic solar cells
- Manipulation of Charge Delocalization in a Bulk Heterojunction Material Using a Mid-Infrared Push Pulse
- General Rules for the Impact of Energetic Disorder and Mobility on Nongeminate Recombination in Phase-Separated Organic Solar Cells
- Exciton transport in amorphous polymers and the role of morphology and thermalisation
- The Enhancement of Interfacial Exciton Dissociation by Energetic Disorder is a Nonequilibrium Effect