There is, I think, something ethereal about i —the square root of minus one. I remember first hearing about it at school. It seemed an odd beast at that time—an intruder hovering on the edge of reality.

Usually familiarity dulls this sense of the bizarre, but in the case of i it was the reverse: over the years the sense of its surreal nature intensified. It seemed that it was impossible to write mathematics that described the real world in …

I and i

The need to develop inexpensive renewable energy sources stimulates scientific research for efficient, low-cost photovoltaic devices.1 The organic, polymer-based photovoltaic elements have introduced at least the potential of obtaining cheap and easy methods to produce energy from light.2 The possibility of chemically manipulating the material properties of polymers (plastics) combined with a variety of easy and cheap processing techniques has made polymer-based materials present in almost every aspect of modern society.3 Organic semiconductors have several advantages: (a) lowcost synthesis, and (b) easy manufacture of thin film devices by vacuum evaporation/sublimation or solution cast or printing technologies. Furthermore, organic semiconductor thin films may show high absorption coefficients4 exceeding 105 cm-1, which makes them good chromophores for optoelectronic applications. The electronic band gap of organic semiconductors can be engineered by chemical synthesis for simple color changing of light emitting diodes (LEDs).5 Charge carrier mobilities as high as 10 cm2/V‚s6 made them competitive with amorphous silicon.7 This review is organized as follows. In the first part, we will give a general introduction to the materials, production techniques, working principles, critical parameters, and stability of the organic solar cells. In the second part, we will focus on conjugated polymer/fullerene bulk heterojunction solar cells, mainly on polyphenylenevinylene (PPV) derivatives/(1-(3-methoxycarbonyl) propyl-1-phenyl[6,6]C61) (PCBM) fullerene derivatives and poly(3-hexylthiophene) (P3HT)/PCBM systems. In the third part, we will discuss the alternative approaches such as polymer/polymer solar cells and organic/inorganic hybrid solar cells. In the fourth part, we will suggest possible routes for further improvements and finish with some conclusions. The different papers mentioned in the text have been chosen for didactical purposes and cannot reflect the chronology of the research field nor have a claim of completeness. The further interested reader is referred to the vast amount of quality papers published in this field during the past decade.

Conjugated polymer-based organic solar cells

Research in the use of organic polymers as the active semiconductors in light-emitting diodes has advanced rapidly, and prototype devices now meet realistic specifications for applications. These achievements have provided insight into many aspects of the background science, from design and synthesis of materials, through materials fabrication issues, to the semiconductor physics of these polymers.

Electroluminescence in conjugated polymers

Aggregation-induced emission: phenomenon, mechanism and applications.

Direct printing of functional electronic materials may provide a new route to low-cost fabrication of integrated circuits. However, to be useful it must allow continuous manufacturing of all circuit components by successive solution deposition and printing steps in the same environment. We demonstrate direct inkjet printing of complete transistor circuits, including via-hole interconnections based on solution-processed polymer conductors, insulators, and self-organizing semiconductors. We show that the use of substrate surface energy patterning to direct the flow of water-based conducting polymer inkjet droplets enables high-resolution definition of practical channel lengths of 5 micrometers. High mobilities of 0.02 square centimeters per volt second and on-off current switching ratios of 10 5 were achieved.

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High-Resolution Inkjet Printing of All-Polymer Transistor Circuits

Highly efficient perovskite solar cells for light harvesting under indoor illumination via solution processed SnO2/MgO composite electron transport layers

We present contact-angle hysteresis and surface energy of differently treated indium–tin–oxide (ITO) thin films obtained from contact angles for liquids with different polar character We find that the hysteresis and the polar and dispersion component of the surface energy depend strongly on the surface treatments Oxygen-plasma treatments induce the highest polarity and the highest total surface energy, and we suggest that this improves the interface formation with polymers, and therefore, the performance of light-emitting diodes We discuss the results in relation to the ITO surface roughness and chemical heterogeneity modified by the different treatments

Surface energy and polarity of treated indium–tin–oxide anodes for polymer light-emitting diodes studied by contact-angle measurements

X-ray photoelectron spectroscopy of surface-treated indium-tin oxide thin films

We report electroabsorption and electroluminescence investigations of polymer light-emitting diodes featuring a LiF/Ca/Al cathode, for efficient electron injection into the electroluminescent polymer layer. Our measurement of the built-in potential gives direct evidence of a sizeable reduction of the cathodic barrier height not only with respect to Ca, but also versus LiF/Al or CsF/Al bilayer cathodes, currently amongst the most efficient electron injectors for low electron affinity polymers. In blue-emitting (∼2.7 at peak) polyfluorene-based LEDs, with poly(ethylenedioxythiophene)/poly(styrene sulphonic acid) anodes and LiF/Ca/Al cathodes, we measure a built-in potential of 2.7 V, a luminance of ∼1600 cd/m2 (the highest among the devices studied here) at a driving voltage of 5 V, and efficiencies as high as ∼3 lm/W. We also find that the turn-on voltage essentially coincides with the built-in potential within the experimental error.

Efficient electron injection in blue-emitting polymer light-emitting diodes with LiF/Ca/Al cathodes

We report the characteristics of a series of polymer light-emitting diodes, fabricated with LiF/Al cathodes and differing only by the thickness of the LiF interlayer (0 nm⩽d⩽11 nm). Electroabsorption studies of the internal electrostatic potential give direct evidence of a sizable reduction of the cathodic barrier height brought about by the LiF films. These results also correlate with photoemission experiments [S. E. Shaheen, G. E. Jabbour, M. M. Morrell, Y. Kawabe, B. Kippelen, N. Peyghambarian, M. F. Nabor, R. Schlaf, E. A. Mash, and N. R. Armstrong, J. Appl. Phys. 84, 2324 (1998)] and with the electroluminescence performance of the diodes.

Franco Cacialli

Papers

Highly efficient perovskite solar cells for light harvesting under indoor illumination via solution processed SnO2/MgO composite electron transport layers

Surface energy and polarity of treated indium–tin–oxide anodes for polymer light-emitting diodes studied by contact-angle measurements

X-ray photoelectron spectroscopy of surface-treated indium-tin oxide thin films

Efficient electron injection in blue-emitting polymer light-emitting diodes with LiF/Ca/Al cathodes

LiF/Al cathodes and the effect of LiF thickness on the device characteristics and built-in potential of polymer light-emitting diodes