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Colloidal Quantum Dot (CQD) thin films are ad- vantageous for solar energy generation because of their low- cost and size-tunable, solution-processable nature. However, their efficiency in solar cells is limited in part by the performance of the hole transport layer (HTL). Through Solar Cell Capacitance Simulations and Transfer Matrix Method calculations, we show that significant photogeneration occurs in the standard HTL of ethanedithiol-passivated lead sulfide CQDs which is a problem due to the sub-optimal carrier mobility in this material. We report new HTLs composed of chalcogenide-based materials to address these issues, and demonstrate an absolute power conversion efficiency improvement of 1.35% in the best device.
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