Synthesis and Characterization of Rhieno[3,2-b]pyrrole Based Organic Semiconductors for Organic Field Rffect Transistors


Book Description

Organic semiconductors (OSCs) are used as electro-active materials across numerous different applications, such as organic photovoltaics (OPVs), organic light emitting diodes (OLEDs), and organic field effect transistors (OFETs). This versatility owes to their low cost, light weight, flexibility, solution processability, and ease of large area fabrication. Tremendous efforts have been devoted to designing OSCs with various building blocks in order to obtain more desirable optoelectronic properties. However, there is still a high demand for further improvements in OSC properties. The development of pyrrole-based OSCs for organic electronic applications, fused ring systems containing S,N-heteroacenes, and the working principles of OFETs are discussed in Chapter 1, along with a summary of performance of S,N-heteroacene materials in organic electronic applications. Chapter 2 discusses the tunable optoelectronic properties of thieno[3,2-b]pyrrolebased organic semiconductors synthesized by varying the p-linker. Chapter 3 discusses the effects of using selenophene as a p-spacer in thieno[3,2-b]pyrrole and benzo[c][1,2,5]thiadiazole based donor-acceptor molecule on OFETs parameters. The change of the p-spacer to selenophene in the molecule affects its bond curvature and, consequently the molecule adopted less bond curvature compared to its furan and thiophene analogs. The molecule showed p-type charge carrier mobility characteristics in devices with bottom-gate/bottom-contact configuration. Chapter 4 describes how the change of p-spacer to acquire different backbone curvatures in small molecules synthesized with thieno[3,2-b]pyrrole and benzo[c][1,2,5]thiadiazole impacted p-type OFETs characteristics. Two spacers, bithiophene and thieno[3,2-b]thiophene, produced two different backbone curvature and resulted in a drastic difference in their OFET performance.




Organic Field Effect Transistors


Book Description

Organic Field Effect Transistors presents the state of the art in organic field effect transistors (OFETs), with a particular focus on the materials and techniques useful for making integrated circuits. The monograph begins with some general background on organic semiconductors, discusses the types of organic semiconductor materials suitable for making field effect transistors, the fabrication processes used to make integrated Circuits, and appropriate methods for measurement and modeling. Organic Field Effect Transistors is written as a basic introduction to the subject for practitioners. It will also be of interest to researchers looking for references and techniques that are not part of their subject area or routine. A synthetic organic chemist, for example, who is interested in making OFETs may use the book more as a device design and characterization reference. A thin film processing electrical engineer, on the other hand, may be interested in the book to learn about what types of electron carrying organic semiconductors may be worth trying and learning more about organic semiconductor physics.







Pyrrole Based Donor-acceptor Building Blocks for Organic Field-effect Transistors


Book Description

The class of organic semiconductors is a definite contender for replacing high-cost silicon semiconductors owing to unique advantages such as solution processability, flexibility, lightweight, low cost, and the ability to do multiple structural modifications. Hence, a remarkable amount of scientific research has been carried out to improve the electronic properties of these materials. Throughout the past two decades, many improvements in the field have achieved by designing novel building blocks. There remains the possibility, however, for performance improvement through areas that has paid less attention in both conventional and non-conventional building blocks. Because of the appealing performance of organic semiconductors, it is highly desirable to seek and develop new building blocks for the next generation of organic electronics. In this dissertation, the fundamentals, history, and recent developments of conventional and nonconventional materials are covered briefly in the first chapter. Operation principles, charge transport of organic field effect transistors is introduced. Compared to conventional thiophenebased p-electron donor materials, promising non-conventional pyrrole-based donor materials employed in organic field effect transistors are discussed and summarized. Chapter 2 describes the effect on organic field effect transistor (OFET) properties of a donor-acceptor polymer consist of a branched ester functionalized bithiophene copolymerized with thiophene vinyl thiophene donor. The influence on frontier molecular orbital energy levels, UV-vis absorption, electrochemical properties, OFET parameters and morphological effects were investigated. In chapter 3, the effect of furan spacer group on a thieno[3,2-b]pyrrole and diketopyrrolopyrrole based copolymer is discussed. Upon changing similar flanking groups, the polymer showed a high hole mobility of 0.42 cm2 /V s while the on-to-off ratio exhibited a drastic improvement ~105 . Chapter 4 describes the incorporation of selenium hetero atom in the pyrrole fused rings to yield seleno[3,2-b]pyrrole based small molecules replacing thieno[3,2-b]pyrrole to extend the knowledge of OFETs activity of seleno[3,2-b]pyrrole in banana shaped small molecules. They exhibited moderate charge carrier properties ~10-2 cm2 /V s hole mobility. In the Chapter 5 (attached as an appendix), a study on oxidative degradation of polypropylene mesh in Escherichia coli (E. coli.) environment is disscussed. Medical implants of polypropylene (PP) mesh have demonstrated biodegradation inside the body. Among the many possible factors, bacterial colonization is believed to be one of the causes for biodegradation. To gain insights on this hypothesis PP mesh samples were tested in Luria-Bertani broth containing E. coli and the experimental results demonstrated qualitative and quantitative bioerosion, confirming the oxidative degradation in vitro.