Achieving balanced open circuit voltage and short circuit current by tuning the interfacial energetics in organic bulk heterojunction solar cells: A drift-diffusion simulation

Abstract

In organic bulk heterojunction solar cells, the donor/acceptor interfacial energy offset ($ΔE$) is found to provide the driving force for efficient charge separation which gives rise to high short circuit current density ($J_\mathrm{sc}$), but a high $ΔE$ inevitably undermines the open circuit voltage ($V_\mathrm{oc}$). In this paper, employing the device model method we calculated the steady state current density-voltage ($J-V$) and the $J_\mathrm{sc}-ΔE$ curves under two different charge separation mechanisms to investigate the optimum driving force required for achieving sizable $V_\mathrm{oc}$ and $J_\mathrm{sc}$ simultaneously. Under the Marcus charge transfer mechanism, with the increased $ΔE$ the Jsc increases rapidly for $ΔE\leq 0.2$ eV, and then maintains a nearly constant value before decreasing at the Marcus inverted region, which is due to the accumulation of undissociated excitons within their lifetime and is beneficial for obtaining a sizable $J_\mathrm{sc}$ under a $ΔE$ much smaller than the reorganization energy $λ$. For the coherent charge transfer mechanism in which the driving force act as the energy window of accessible charge separated states, with two typical types of density of states for the charge transfer excitons, it is shown that the highest $J_\mathrm{sc}$ can also be achieved under a small $ΔE$ of 0.2\,eV if the high-lying delocalized states are harvested in high proportion. This work demonstrates the existence of the optimum driving force of 0.2\,eV and provides some guidelines for engineering the interfacial energetics to achieve the high balanced $J_\mathrm{sc}$ and $V_\mathrm{oc}$.