A robust inter‐connecting layer for achiev­­ing high‐performance tandem polymer solar cells is fabricated and demonstrated in polymer tandem solar cells with a PCE of 7.0%. This layer is optically transparent, electrically conductive, and physically strong. It is revealed that, under light illumination, charges are collected and recombined in the interlayer; under dark conditions, charges are generated and extracted from it.

A kink is sometimes seen in the I-V curves for organic solar cells. In literature charge blocking has been speculated to be responsible for such kind of anomalous features. In this manuscript, we use poly(3-hexylthiophene):[6, 6]-phenyl-C61-butyric acid methyl ester as our model polymer system and investigate different device structures using ultraviolet photoelectron spectroscopy as our primary tool to investigate the reason for this S-shaped kink. We attribute this anomalous feature to the presence of strong interface dipoles. We further propose a model based on the standard set of Poisson equation, continuity equation, and current density equations including both drift and diffusion components.

Synthesizing metal oxides through the sol–gel process provides a convenient way for forming a nanostructured layer in wide band gap semiconductors. In this paper, a unique method of introducing dopants into the metal oxide semiconductor is presented. The doped TiO2 is prepared by adding a Cs2CO3 solution to a nanocrystalline TiO2 solution that is synthesized via a non‐hydrolytic sol–gel process. The properties of the TiO2:Cs layer are investigated and the results show stable nanostructure morphology. In addition to providing morphological stability, Cs in TiO2 also gives rise to a more desirable work function for charge transport in organic electronics. Polymer solar cells based on the poly(3‐hexylthiophene) (P3HT): methanofullerene (PC70BM) system with the addition of a TiO2:Cs interfacial layer exhibit excellent characteristics with a power conversion efficiency of up to 4.2%. The improved device performance is attributed to an improved polymer/metal contact, more efficient electron extraction, and better hole blocking properties. The effectiveness of this unique functionality also extends to polymer light emitting devices, where a lower driving voltage, improved efficiency, and extended lifetime are demonstrated.

Nanoscale morphology has been shown to be a critical parameter governing charge transport properties of polymer bulk heterojunction (BHJ) solar cells. Recent results on vertical phase separation have intensified the research on 3D morphology control. In this paper, we intend to modify the distribution of donors and acceptors in a classical BHJ polymer solar cell by making the active layer richer in donors and acceptors near the anode and cathode respectively. Here, we chose [6,6]-phenyl- C(61)-butyric acid methyl ester (PCBM) to be the acceptor material to be thermally deposited on top of [poly(3-hexylthiophene)] P3HT: the PCBM active layer to achieve a vertical composition gradient in the BHJ structure. Here we report on a solar cell with enhanced power conversion efficiency of 4.5% which can be directly correlated with the decrease in series resistance of the device.

Polarizing organic photovoltaic (ZOPV) technology is demonstrated as a novel concept for energy harvesting and recycling technology. Novel, inverted quasi‐bilayer device architecture is utilized to realize the ZOPV device. An anisotropic photovoltaic effect is obtained.