Pentacene

About: Pentacene is a research topic. Over the lifetime, 5051 publications have been published within this topic receiving 161481 citations. The topic is also known as: 2,3:6,7-dibenzanthracene & benzo[b]naphthacene.

Remarkable Enhancement of the Hole Mobility in Several Organic Small-Molecules, Polymers, and Small-Molecule:Polymer Blend Transistors by Simple Admixing of the Lewis Acid p-Dopant B(C6F5)3.

Abstract: Improving the charge carrier mobility of solution-processable organic semiconductors is critical for the development of advanced organic thin-film transistors and their application in the emerging sector of printed electronics. Here, a simple method is reported for enhancing the hole mobility in a wide range of organic semiconductors, including small-molecules, polymers, and small-molecule:polymer blends, with the latter systems exhibiting the highest mobility. The method is simple and relies on admixing of the molecular Lewis acid B(C6F5)3 in the semiconductor formulation prior to solution deposition. Two prototypical semiconductors where B(C6F5)3 is shown to have a remarkable impact are the blends of 2,8-difluoro-5,11-bis(triethylsilylethynyl)anthradithiophene:poly(triarylamine) (diF-TESADT:PTAA) and 2,7-dioctyl[1]-benzothieno[3,2-b][1]benzothiophene:poly(indacenodithiophene-co-benzothiadiazole) (C8-BTBT:C16-IDTBT), for which hole mobilities of 8 and 11 cm2 V-1 s-1, respectively, are obtained. Doping of the 6,13-bis(triisopropylsilylethynyl)pentacene:PTAA blend with B(C6F5)3 is also shown to increase the maximum hole mobility to 3.7 cm2 V-1 s-1. Analysis of the single and multicomponent materials reveals that B(C6F5)3 plays a dual role, first acting as an efficient p-dopant, and secondly as a microstructure modifier. Semiconductors that undergo simultaneous p-doping and dopant-induced long-range crystallization are found to consistently outperform transistors based on the pristine materials. Our work underscores Lewis acid doping as a generic strategy towards high performance printed organic microelectronics.

Analysis of improved photovoltaic properties of pentacene/C60 organic solar cells: Effects of exciton blocking layer thickness and thermal annealing

Abstract: We report on the photovoltaic properties of organic solar cells based on pentacene and C 60 thin films with a focus on their spectral responses and the effect of thermal annealing. Spectra of external quantum efficiency (EQE) are measured and analyzed with a one-dimensional exciton diffusion model dependent upon the complex optical functions of pentacene films, which are measured by spectroscopic ellipsometry. An improvement in EQE is observed when the thickness of the bathocuproine (BCP) layer is decreased from 12 nm to 6 nm. Detailed analysis of the EQE spectra indicates that large exciton diffusion lengths in the pentacene films are responsible for the overall high EQE values near wavelengths of 668 nm. Analysis also shows that improvement in the EQE of devices with the thinner BCP layer can be attributed to a net gain in optical field distribution and improvement in carrier collection efficiency. An improvement in open-circuit voltage ( V OC ) is also achieved through a thermal annealing process, leading to a net increase in power conversion efficiency. Integration of the EQE spectrum with an AM1.5 G spectrum yields a predicted power conversion efficiency of 1.8 ± 0.2%. The increase in V OC is attributed to a significant reduction in the diode reverse saturation current upon annealing.

On the interface dipole at the pentacene-fullerene heterojunction : A theoretical study

Abstract: The electronic structure at organic/organic interfaces plays a key role, among others, in defining the quantum efficiency of organics-based photovoltaic cells. Here, we perform quantum-chemical and microelectrostatic calculations on molecular aggregates of various sizes and shapes to characterize the interfacial dipole moment at pentacene/C60 heterojunctions. The results show that the interfacial dipole mostly originates in polarization effects due to the asymmetry in the multipolar expansion of the electronic density distribution between the interacting molecules, rather than in a charge transfer from donor to acceptor. The local dipole is found to fluctuate in sign and magnitude over the interface and appears as a sensitive probe of the relative arrangements of the pentacene and C60 molecules (and of the resulting local electrical fields sensed by the molecular units).