Over the past three decades, significant research efforts have focused on improving the charge carrier mobility of organic thin-film transistors (OTFTs). In recent years, a commonly observed nonlinearity in OTFT current-voltage characteristics, known as the "kink" or "double slope," has led to widespread mobility overestimations, contaminating the relevant literature. Here, published data from the past 30 years is reviewed to uncover the extent of the field-effect mobility hype and identify the progress that has actually been achieved in the field of OTFTs. Present carrier-mobility-related challenges are identified, finding that reliable hole and electron mobility values of 20 and 10 cm V s , respectively, have yet to be achieved. Based on the analysis, the literature is then reviewed to summarize the concepts behind the success of high-performance p-type polymers, along with the latest understanding of the design criteria that will enable further mobility enhancement in n-type polymers and small molecules, and the reasons why high carrier mobility values have been consistently produced from small molecule/polymer blend semiconductors. Overall, this review brings together important information that aids reliable OTFT data analysis, while providing guidelines for the development of next-generation organic semiconductors.

We report the synthesis of two new selenophene-containing ladder-type monomers, cyclopentadiselenophene (CPDS) and indacenodiselenophene (IDSe), via a 2-fold and 4-fold Pd-catalyzed coupling with a 1,1-diborylmethane derivative. Copolymers with benzothiadiazole were prepared in high yield by Suzuki polymerization to afford materials which exhibited excellent solubility in a range of nonchlorinated solvents. The CPDS copolymer exhibited a band gap of just 1.18 eV, which is among the lowest reported for donor-acceptor polymers. Thin-film transistors were fabricated using environmentally benign, nonchlorinated solvents, with the CPDS and IDSe copolymers exhibiting hole mobility up to 0.15 and 6.4 cm V s, respectively. This high performance was achieved without the undesirable peak in mobility often observed at low gate voltages due to parasitic contact resistance.

The synthesis of a novel fluorinated n-type small molecule based on an indacenodithiophene core is reported. Fluorination is found to have a significant impact on the physical properties, including a surprisingly dramatic improvement in solubility, in addition to effectively stabilizing the lowest-unoccupied molecular orbital energy (−4.24 eV). Single-crystal analysis and density functional theory calculations indicate the improved solubility can be attributed to backbone torsion resulting from the positioning of the fluorine group in close proximity to the strongly electron-withdrawing dicyanomethylene group. Organic thin-film transistors made via blade coating display high electron mobility (up to 0.49 cm 2 V −1 s −1 ) along with good retention of performance in ambient conditions.

A new method to synthesize an electron-rich building block cyclopentadithienothiophene (9H-thieno-[3,2-b]thieno[2″,3″:4′,5′]thieno[2′,3′:3,4] cyclopenta[1,2-d]thiophene, CDTT) via a facile aromatic extension strategy is reported. By combining CDTT with 1,1-dicyanomethylene-3-indanone endgroups, a promising nonfullerene small molecule acceptor (CDTTIC)is prepared. As-cast, single-junction nonfullerene organic solar cells based on PFBDB-T: CDTTIC blends exhibit very high short-circuit currents up to 26.2 mA cm −2 in combination with power conversion efficiencies over 11% without any additional processing treatments. The high photocurrent results from the near-infrared absorption of the CDTTIC acceptor and the well-intermixed blend morphology of polymer donor PFBDB-T and CDTTIC. This work demonstrates a useful fused ring extension strategy and promising solar cell results, indicating the great potential of the CDTT derivatives as electron-rich building blocks for constructing high-performance small molecule acceptors in organic solar cells.

Two PDI tetramers with a central tetrathienylethene core were investigated as non-fullerene acceptors in organic photovoltaics and the dramatic differences in their optical absorption spectra were rationalised on the basis of DFT calculations.

A straightforward synthesis is reported for four structurally simple donor–acceptor conjugated polymers based on an alkylated difluorobenzotriazole and either unsubstituted bithiophene (T2) or thienylvinylthiophene (TVT) co‐monomers. Two solubilizing sidechains are investigated in which the position of the branching point is moved away from the conjugated backbone. Optoelectronic measurements and density functional theory calculations show very similar energetic properties between the polymers, with a slightly narrower bandgap for the vinylene incorporating TVT polymers as a result of extended conjugation. Transistor measurements demonstrate that the simplest polymer, containing a readily available 2‐decyltetradecyl sidechain with a T2 co‐monomer, exhibits the best device performance, with an average saturated mobility of 0.2 cm2 V−1 s−1.

The synthesis of two novel n-type molecular organic semiconductors based on a fluorinated indacenodithiophene core in combination with an electron withdrawing N-cyanoimine group is reported, and the influence of the...

Three copolymers based alkylated indacenodithieno[3,2-b]thiophene (IDTT) are reported.