Photovoltaic technology requires light-absorbing materials that are highly efficient, lightweight, low cost and stable during operation. Organolead halide perovskites constitute a highly promising class of materials, but suffer limited stability under ambient conditions without heavy and costly encapsulation. Here, we report ultrathin (3 μm), highly flexible perovskite solar cells with stabilized 12% efficiency and a power-per-weight as high as 23 W g(-1). To facilitate air-stable operation, we introduce a chromium oxide-chromium interlayer that effectively protects the metal top contacts from reactions with the perovskite. The use of a transparent polymer electrode treated with dimethylsulphoxide as the bottom layer allows the deposition-from solution at low temperature-of pinhole-free perovskite films at high yield on arbitrary substrates, including thin plastic foils. These ultra-lightweight solar cells are successfully used to power aviation models. Potential future applications include unmanned aerial vehicles-from airplanes to quadcopters and weather balloons-for environmental and industrial monitoring, rescue and emergency response, and tactical security applications.

Millenniums-old natural dye indigo--a "new" ambipolar organic semiconductor. Indigo shows balanced electron and hole mobilities of 1 × 10(-2) cm(2) V(-1) s(-1) and good stability against degradation in air. Inverters with gains of 105 in the first and 110 in the third quadrant are demonstrated. Fabricated entirely from natural and biodegradable compounds, these devices show the large potential of such materials for green organic electronics.

Hysteretic effects are investigated in perovskite solar cells in the standard FTO/TiO2/CH3NH3PbI3−xClx/spiro-OMeTAD/Au configuration.We report normal (NH) and inverted hysteresis (IH) in the J-V characteristics occurring for the same device structure, the behavior strictly depending on the pre-poling bias. NH typically appears at pre-poling biases larger than the open circuit bias, while pronounced IH occurs for negative bias pre-poling. The transition from NH to IH is marked by a intermediate mixed hysteresis behavior characterized by a crossing point in the J-V characteristics. The measured J-V characteristics are explained quantitatively by the dynamic electrical model (DEM). Furthermore, the influence of the bias scan rate on the NH/IH hysteresis is discussed based on the time evolution of the non-linear polarization. Introducing a three step measurement protocol, which includes stabilization, pre-poling and measurement, we put forward the difficulties and possible solutions for a correct PCE evaluation.

We describe the history of indigo dye and its derivative Tyrian purple, from their roles in the ancient world to recent research showing the semiconducting properties of indigoids. Indigoids are natural dyes that have been produced for centuries, and indigo is currently the most produced dye worldwide. Herein we review the history of these materials, their chemistry and physical properties, and their semiconducting characteristics in the solid state. Due to hydrogen bonding and π‐stacking, indigo and Tyrian purple form highly‐ordered crystalline thin films. Such films have been used to fabricate high‐performance organic field‐effect transistors with ambipolar charge transport, as well as complementary‐like circuits. Mobility values were found to be in the range of 10−2–0.4 cm2/Vs. With performance on par with the best available organic semiconductors, indigoids demonstrate the potential of sustainable electronics based on biodegradable and biocompatible materials.

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Indigo and its derivatives are industrially-important dyes known for centuries. The low solubility of these compounds limits their applications and hinders potential synthetic chemistry using indigo as a building-block. Herein we report attachment of the tert-butoxy carbonyl (tBOC) thermolabile protecting group to indigos, allowing their processing into neat thin films as well as mixed films with a semiconducting polymer. Photoinduced charge transfer is observed to and from these pigments and the polymer.

Ambipolar organic semiconductors enable complementary-like circuits in organic electronics. Here we show promising electron and hole transport properties in the natural pigment Tyrian Purple (6,6’-dibromoindigo). X-ray diffraction of Tyrian Purple films reveals a highly-ordered structure with a single preferential orientation, attributed to intermolecular hydrogen bonding. This material, with a band gap of ∼1.8 eV, demonstrates high hole and electron mobilities of 0.22 cm2/V·s and 0.03 cm2/V·s in transistors, respectively; and air-stable operation. Inverters with gains of 250 in the first and third quadrant show the large potential of Tyrian Purple for the development of integrated organic electronic circuits

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