Fossil fuel alternatives, such as solar energy, are moving to the forefront in a variety of research fields. Polymer-based organic photovoltaic systems hold the promise for a cost-effective, lightweight solar energy conversion platform, which could benefit from simple solution processing of the active layer. The function of such excitonic solar cells is based on photoinduced electron transfer from a donor to an acceptor. Fullerenes have become the ubiquitous acceptors because of their high electron affinity and ability to transport charge effectively. The most effective solar cells have been made from bicontinuous polymer–fullerene composites, or so-called bulk heterojunctions. The best solar cells currently achieve an efficiency of about 5 %, thus significant advances in the fundamental understanding of the complex interplay between the active layer morphology and electronic properties are required if this technology is to find viable application.

Polymer–Fullerene Composite Solar Cells

2.2. Materials 929 2.3. Factors Influencing Charge Mobility 931 2.3.1. Molecular Packing 931 2.3.2. Disorder 932 2.3.3. Temperature 933 2.3.4. Electric Field 934 2.3.5. Impurities 934 2.3.6. Pressure 934 2.3.7. Charge-Carrier Density 934 2.3.8. Size/molecular Weight 935 3. The Charge-Transport Parameters 935 3.1. Electronic Coupling 936 3.1.1. The Energy-Splitting-in-Dimer Method 936 3.1.2. The Orthogonality Issue 937 3.1.3. Impact of the Site Energy 937 3.1.4. Electronic Coupling in Oligoacene Derivatives 938

Charge transport in organic semiconductors.

Since the discovery of highly conducting polyacetylene by Shirakawa, MacDiarmid, and Heeger in 1977, π-conjugated systems have attracted much attention as futuristic materials for the development and production of the next generation of electronics, that is, organic electronics. Conceptually, organic electronics are quite different from conventional inorganic solid state electronics because the structural versatility of organic semiconductors allows for the incorporation of functionality by molecular design. This versatility leads to a new era in the design of electronic devices. To date, the great number of π-conjugated semiconducting materials that have either been discovered or synthesized generate an exciting library of π-conjugated systems for use in organic electronics. 11 However, some key challenges for further advancement remain: the low mobility and stability of organic semiconductors, the lack of knowledge regarding structure property relationships for understanding the fundamental chemical aspects behind the structural design, and realization of desired properties. Organic field-effect transistors (OFETs) are a kind of device consisting of an organic semiconducting layer, a gate insulator layer, and three terminals (drain, source, and gate electrodes). OFETs are not only essential building blocks for the next generation of cheap and flexible organic circuits, but they also provide an important insight into the charge transport of πconjugated systems. Therefore, they act as strong tools for the exploration of the structure property relationships of πconjugated systems, such as parameters of field-effect mobility (μ, the drift velocity of carriers under unit electric field), current on/off ratio (the ratio of the maximum on-state current to the minimum off-state current), and threshold voltage (the minimum gate voltage that is required to turn on the transistor). 17 Since the discovery of OFETs in the 1980s, they have attracted much attention. Research onOFETs includes the discovery, design, and synthesis of π-conjugated systems for OFETs, device optimization, development of applications in radio frequency identification (RFID) tags, flexible displays, electronic papers, sensors, and so forth. It is beyond the scope of this review to cover all aspects of π-conjugated systems; hence, our focus will be on the performance analysis of π-conjugated systems in OFETs. This should make it possible to extract information regarding the fundamental merit of semiconducting π-conjugated materials and capture what is needed for newmaterials and what is the synthesis orientation of newπ-conjugated systems. In fact, for a new science with many practical applications, the field of organic electronics is progressing extremely rapidly. For example, using “organic field effect transistor” or “organic field effect transistors” as the query keywords to search the Web of Science citation database, it is possible to show the distribution of papers over recent years as shown in Figure 1A. It is very clear

Semiconducting π-conjugated systems in field-effect transistors: a material odyssey of organic electronics.

Functionalized acenes and heteroacenes for organic electronics.

Organic semiconductors have been the subject of active research for over a decade now, with applications emerging in light-emitting displays and printable electronic circuits. One characteristic feature of these materials is the strong trapping of electrons but not holes1: organic field-effect transistors (FETs) typically show p-type, but not n-type, conduction even with the appropriate low-work-function electrodes, except for a few special high-electron-affinity2,3,4 or low-bandgap5 organic semiconductors. Here we demonstrate that the use of an appropriate hydroxyl-free gate dielectric—such as a divinyltetramethylsiloxane-bis(benzocyclobutene) derivative (BCB; ref. 6)—can yield n-channel FET conduction in most conjugated polymers. The FET electron mobilities thus obtained reveal that electrons are considerably more mobile in these materials than previously thought. Electron mobilities of the order of 10-3 to 10-2 cm2 V-1 s-1 have been measured in a number of polyfluorene copolymers and in a dialkyl-substituted poly(p-phenylenevinylene), all in the unaligned state. We further show that the reason why n-type behaviour has previously been so elusive is the trapping of electrons at the semiconductor–dielectric interface by hydroxyl groups, present in the form of silanols in the case of the commonly used SiO2 dielectric. These findings should therefore open up new opportunities for organic complementary metal-oxide semiconductor (CMOS) circuits, in which both p-type and n-type behaviours are harnessed.

General observation of n-type field-effect behaviour in organic semiconductors

We demonstrate thin-film ferroelectric transistors, made entirely from organic materials that are processed from solution. The devices consist of thin ferroelectric poly(vinylidene fluoride/trifluoroethylene) films sandwiched between electrodes made of conducting poly(3,4-ethylenedioxythiophene) stabilized with polystyrene-4-sulphonic acid. On top of this stack, an organic semiconductor is applied. The ferroelectric transistors, constructed using unipolar p- or n-type semiconductor channels, have remnant current modulations of ∼103 with a retention time of hours. They can be switched in 0.1–1ms at operating voltages less than 10V.

/pdf/all-polymer-ferroelectric-transistors-2ege4ge8i2.pdf

All-polymer ferroelectric transistors

https://pure.rug.nl/ws/files/6745033/2010OrgElectrAndringa.pdf

Gas sensing with self-assembled monolayer field-effect transistors

https://pure.rug.nl/ws/files/14624677/2009BiosensBioelectronStoliar.pdf

DNA adsorption measured with ultra-thin film organic field effect transistors.

Complex digital circuits reliably work when the noise margin of the logic gates is sufficiently high. For p-type only inverters, the noise margin is typically about 1 V. To increase the noise margin, we fabricated inverters with dual gate transistors. The top gate is advantageously used to independently tune the threshold voltage.

/pdf/increasing-the-noise-margin-in-organic-circuits-using-dual-14lmnyxho5.pdf

Increasing the noise margin in organic circuits using dual gate field-effect transistors

Fullerene-containing polyesters have been prepared by polycondensation of bifunctional fullerene adducts with tetraethyleneglycol or polyethyleneglycol. The molecular weights of these polymers have been determined by size exclusion chromatography coupled with light scattering. The polymers have also been characterized by NMR, UV/Vis and FTIR spectroscopies. Thanks to their good solubility in common organic solvents and to their good film-forming properties, these fullerene-containing polyesters are easy to process and could be used to evaluate their potential for the preparation of all-polymer donor/acceptor bulk heterojunction photovoltaic cells.

Sepas Setayesh

Papers

All-polymer ferroelectric transistors

Gas sensing with self-assembled monolayer field-effect transistors

DNA adsorption measured with ultra-thin film organic field effect transistors.

Increasing the noise margin in organic circuits using dual gate field-effect transistors

Fullerene-functionalized polyesters: synthesis, characterization and incorporation in photovoltaic cells