Significant progress in power conversion efficiencies and stabilities of polymer solar cells has been achieved using semiconducting metal oxides as charge extraction interlayers. Both n- and p-type transition metal oxides with good transparency in the visible as well as infrared region make good Ohmic contacts to both donors and acceptors in polymer bulk heterojunction solar cells. Their compatibility with roll-to-roll processing makes them very attractive for low cost manufacturing of polymer solar cells. In this review, we will present the recent results on synthesis and characterization of these metal oxides along with the device performance of the solar cells using these metal oxides as interlayers.

The operating lifetime of blue quantum-dot light-emitting diodes (QLED) is currently a short slab for this emerging display technology. To pinpoint the origin of device degradation, here we apply multiple techniques to monitor the electric-field distribution and space-charge accumulation across the multilayered structure before and after lifetime tests. Evident by charge-modulated electro-absorption and capacitance-voltage characteristics, the excited electrons in blue quantum dots (QD) are prone to cross the type II junction between the QD emission layer and the electron-transporting layer (ETL) due to the offset of conduction band minimum, leading to space-charge accumulation and operating-voltage rise in the ETL. Therefore, unlike those very stable red devices, of which the lifetime is primarily limited by the slow degradation of hole-transporting layer, the poor lifetime of blue QLED originates from the fast degradation at the QD-ETL junction. Materials engineering for efficient electron injection is prerequisite for the boost of operating lifetime.