Organic Semiconductor Crystals Research Articles

Orienting and shaping organic semiconductor single crystals through selective nanoconfinement.

For organic semiconductor crystals exhibiting anisotropic charge transport along different crystallographic directions, nanoconfinement is a powerful strategy to control crystal orientation by aligning the fast crystallographic growth direction(s) with the unconfined axis(es) of nanoconfining scaffolds. Here, design rules are presented to relate crystal morphology, scaffold geometry, and orientation control in solution-processed small-molecule crystals. Specifically, organic semiconductor triisopropylsilylethynyl pyranthrene needle-like crystals with a dimensionality of n = 1 and perylene platelike crystals with n = 2 were grown from solution within nanoconfining scaffolds comprising cylindrical nanopores with a dimensionality of m = 1, representing one unconfined dimension along the cylinder axis, and those comprising nanopillar arrays with a dimensionality of m = 2. For m = n systems, native crystal growth habits were preserved while the crystal orientation in n = m direction(s) was dictated by the geometry of the scaffold. For n≠m systems, on the other hand, orientation control was restricted within a single plane, either parallel or perpendicular to the substrate surface. Intriguingly, control over crystal shape was also observed for perylene crystals grown in cylindrical nanopores (n > m). Within the nanopores, crystal growth was restricted along a single direction to form a needle-like morphology. Once growth proceeded above the scaffold surface, the crystals adopted their native growth habit to form asymmetric T-shaped single crystals with concave corners. These findings suggest that nanoporous scaffolds with spatially-varying dimensionalities can be used to grow single crystals of complex shapes.

Atomically Smooth Graphene‐Based Hybrid Template for the Epitaxial Growth of Organic Semiconductor Crystals

AbstractAtomically thin 2D materials are good templates to grow organic semiconductor thin films with desirable features. However, the 2D materials typically exhibit surface roughness and spatial charge inhomogeneity due to nonuniform doping, which can affect the uniform assembly of organic thin films on the 2D materials. A hybrid template is presented for preparation of highly crystalline small‐molecule organic semiconductor thin film that is fabricated by transferring graphene onto a highly ordered self‐assembled monolayer. This hybrid graphene template has low surface roughness and spatially uniform doping, and it yields highly crystalline fullerene thin films with grain sizes >300 nm, which is the largest reported grain size for C60 thin films on 2D materials. A graphene/fullerene/pentacene phototransistor fabricated directly on the hybrid template has five times higher photoresponsivity than a phototransistor fabricated on a conventional graphene template supported by a SiO2 wafer.

Surface Doping of Organic Single-Crystal Semiconductors to Produce Strain-Sensitive Conductive Nanosheets.

A highly periodic electrostatic potential, even though established in van der Waals bonded organic crystals, is essential for the realization of a coherent band electron system. While impurity doping is an effective chemical operation that can precisely tune the energy of an electronic system, it always faces an unavoidable difficulty in molecular crystals because the introduction of a relatively high density of dopants inevitably destroys the highly ordered molecular framework. In striking contrast, a versatile strategy is presented to create coherent 2D electronic carriers at the surface of organic semiconductor crystals with their precise molecular structures preserved perfectly. The formation of an assembly of redox‐active molecular dopants via a simple one‐shot solution process on a molecularly flat crystalline surface allows efficient chemical doping and results in a relatively high carrier density of 1013 cm−2 at room temperature. Structural and magnetotransport analyses comprehensively reveal that excellent carrier transport and piezoresistive effects can be obtained that are similar to those in bulk crystals.

Meniscus-controlled printing of single-crystal interfaces showing extremely sharp switching transistor operation.

Meniscus, a curvature of droplet surface around solids, takes critical roles in solution-based thin-film processing. Extension of meniscus shape, and eventual uniform film growth, is strictly limited on highly lyophobic surfaces, although such surface should considerably improve switching characteristics. Here, we demonstrate a technique to control the solution meniscus, allowing to manufacture single-crystalline organic semiconductor (OSC) films on the highest lyophobic amorphous perfluoropolymer, Cytop. We used U-shaped metal film pattern produced on the Cytop surface, to initiate OSC film growth and to keep the meniscus extended on the Cytop surface. The growing edge of the OSC film helped maintain the meniscus extension, leading to a successive film growth. This technique facilitates extremely sharp switching transistors with a subthreshold swing of 63 mV dec-1 owing to the effective elimination of charge traps at the semiconductor/dielectric interface. The technique should expand the capability of print production of functional films and devices.

Sublimely simple method makes ultrathin organic crystals

Forming extremely thin crystals of organic semiconductors under ambient conditions is now possible. The key is a tiny gap. Material is sprayed on a heated surface where it sublimes and rises just 300 µm before condensing to form very thin crystals on the surface above ( 2020, DOI: ). The method uses a simple heater and common organic semiconductor materials to make ultrathin crystals, which have better performance in devices like light-emitting diodes and field-effect transistors because of the resulting film’s low electrical resistance. The method could make fabrication of these thin electronics easier and cheaper. Yang Liu, Xutang Tao, and their colleagues at Shandong University refined a method that they had developed to form pure organic crystals by simply vaporizing material across a gap of a few hundred micrometers ( 2018, DOI: ). The researchers used solid powders as the reservoir material in their first effort, but in the

Crystallization and Organic Field-Effect Transistor Performance of a Hydrogen-Bonded Quaterthiophene.

Crystalline thin films of π-conjugated molecules are relevant as the active layers in organic electronic devices. Therefore, materials with enhanced control over the supramolecular arrangement, crystallinity, and thin-film morphology are desirable. Herein, it is reported that hydrogen-bonded substituents serve as additional structure-directing elements that positively affect crystallization, thin-film morphology, and device performance of p-type organic semiconductors. It is observed that a quaterthiophene diacetamide exhibits a denser packing than that of other quaterthiophenes in the single-crystal structure and, as a result, displays enhanced intermolecular electronic interactions. This feature was preserved in crystalline thin films that exhibited a layer-by-layer morphology, with large domain sizes and high internal order. As a result, organic field-effect transistors of these polycrystalline thin films showed mobilities in the range of the best mobility values reported for single-crystalline quaterthiophenes. The use of hydrogen-bonded groups may, thus, provide an avenue for organic semiconducting materials with improved morphology and performance.

Controlled 2D growth of organic semiconductor crystals by suppressing “coffee-ring” effect

Owing to enhanced charge transport efficiency arising from the ultrathin nature, two-dimensional (2D) organic semiconductor single crystals (OSSCs) are emerging as a fascinating platform for high-performance organic field-effect transistors (OFETs). However, “coffee-ring” effect induced by an evaporation-induced convective flow near the contact line hinders the large-area growth of 2D OSSCs through a solution process. Here, we develop a new strategy of suppressing the “coffee-ring” effect by using an organic semiconductor: polymer blend solution. With the high-viscosity polymer in the organic solution, the evaporation-induced flow is remarkably weakened, ensuring the uniform molecule spreading for the 2D growth of the OSSCs. As an example, wafer-scale growth of crystalline film consisting of few-layered 2,7-didecylbenzothienobenzothiophene (C10-BTBT) crystals was successfully accomplished via blade coating. OFETs based on the crystalline film exhibited a maximum hole mobility up to 12.6 cm2·V−1·s−1, along with an average hole mobility as high as 8.2 cm2·V−1·s−1. Our work provides a promising strategy for the large-area growth of 2D OSSCs toward high-performance organic electronics.

Trap-state suppression and band-like transport in bilayer-type organic semiconductor ultrathin single crystals

Fundamental study of the carrier transport in both the channel layer and the electrode-channel contact of organic semiconductor crystals is indispensable for achieving high-performance organic field-effect transistors. In this paper, we report the temperature-dependent carrier transport of high-mobility organic semiconductors called $2\text{--}\text{decyl}\text{--}7\text{-phenyl-}[1]\text{benzothieno}[3,2\text{--}b][1]\mathrm{benzothiophene}$ (Ph-BTBT-C10) and $3\text{-decyl-}9\text{-phenyl-}[1]\text{benzothieno}[3,2\text{--}b]\text{naphtho}[2,3\text{--}b]\text{thiophene}$ (Ph-BTNT-C10). The use of single-crystal films with controlled bilayer-number thickness enabled the simultaneous study of intralayer and interlayer transport at cryogenic temperatures. Four-probe measurement of two-bilayer- and three-bilayer-thick films of Ph-BTBT-C10 suggests that the access resistance is dominated by tunneling transport across the insulating alkyl-chain layers. Single-crystal thin-film transistors of these materials showed band-like carrier transport down to 80 K and the carrier mobility of Ph-BTBT-C10 reached $34\phantom{\rule{0.16em}{0ex}}\mathrm{c}{\mathrm{m}}^{2}/\mathrm{V}\phantom{\rule{0.16em}{0ex}}\mathrm{s}$. Detailed analysis of the low-temperature characteristics revealed small activation energy of approximately 5 meV and a sharp distribution of band tail states. These findings suggest that high crystallinity owing to the bilayer-type crystal structure effectively suppresses the localization of gate-induced carriers.

Effect of Polymer Molecular Weight on Morphology and Charge Transport of Small-Molecular Organic Semiconductors

The utilization of polymer additives provides an intriguing pathway to tune the electrical performance of solution-grown, small-molecular organic semiconductors. In this study, we report the effect of different polymer molecular weight on the crystal growth, phase segregation and charge transport of the organic semiconductors. A semicrystalline polymer additive polyethylene oxide (PEO) with 8000 and 100 K molecular weight was blended with a well-known organic semiconductor 6,13-bis(triisopropylsilylethynyl) pentacene (TIPS pentacene). Distinctively different thin film morphology of the resultant TIPS pentacene/PEO blend film was identified and quantitatively characterized. In particular, PEO with a higher molecular weight of 100 K exerted a stronger effect on enhancing film formation, crystal coverage and likely mechanical properties, whereas PEO with an 8000 molecular weight yielded more superior crystal alignment and larger crystal sizes. Bottom-gate, top-contact TIPS pentacene/PEO OTFTs were fabricated to test the charge transport, which indicated loading the PEO polymer with molecular weight of 8000 demonstrated a five-fold enhancement in the extracted hole mobilities as compared to the 100 K counterpart. This work of using polymer additives with different molecular weight can be used to tune the crystallization of other solution-processed high-mobility small-molecular organic semiconductors.

Super‐ and Ferroelastic Organic Semiconductors for Ultraflexible Single‐Crystal Electronics

AbstractLike silicon, single crystals of organic semiconductors are pursued to attain intrinsic charge transport properties. However, they are intolerant to mechanical deformation, impeding their application in flexible electronic devices. Such contradictory properties, namely exceptional molecular ordering and mechanical flexibility, are unified in this work. We found that bis(triisopropylsilylethynyl)pentacene (TIPS‐P) crystals can undergo mechanically induced structural transitions to exhibit superelasticity and ferroelasticity. These properties arise from cooperative and correlated molecular displacements and rotations in response to mechanical stress. By utilizing a bending‐induced ferroelastic transition of TIPS‐P, flexible single‐crystal electronic devices were obtained that can tolerate strains (ϵ) of more than 13 % while maintaining the charge carrier mobility of unstrained crystals (μ>0.7 μ0). Our work will pave the way for high‐performance ultraflexible single‐crystal organic electronics for sensors, memories, and robotic applications.

Super- and Ferroelastic Organic Semiconductors for Ultraflexible Single-Crystal Electronics.

Like silicon, single crystals of organic semiconductors are pursued to attain intrinsic charge transport properties. However, they are intolerant to mechanical deformation, impeding their application in flexible electronic devices. Such contradictory properties, namely exceptional molecular ordering and mechanical flexibility, are unified in this work. We found that bis(triisopropylsilylethynyl)pentacene (TIPS-P) crystals can undergo mechanically induced structural transitions to exhibit superelasticity and ferroelasticity. These properties arise from cooperative and correlated molecular displacements and rotations in response to mechanical stress. By utilizing a bending-induced ferroelastic transition of TIPS-P, flexible single-crystal electronic devices were obtained that can tolerate strains (ϵ) of more than 13 % while maintaining the charge carrier mobility of unstrained crystals (μ>0.7 μ0 ). Our work will pave the way for high-performance ultraflexible single-crystal organic electronics for sensors, memories, and robotic applications.

Solution-Processed, Large-Area, Two-Dimensional Crystals of Organic Semiconductors for Field-Effect Transistors and Phototransistors.

Organic electronics with π-conjugated organic semiconductors are promising candidates for the next electronics revolution. For the conductive channel, the large-area two-dimensional (2D) crystals of organic semiconductors (2DCOS) serve as useful scaffolds for modern organic electronics, benefiting not only from long-range order and low defect density nature but also from unique charge transport characteristic and photoelectrical properties. Meanwhile, the solution process with advantages of cost-effectiveness and room temperature compatibility is the foundation of high-throughput print electrical devices. Herein, we will give an insightful overview to witness the huge advances in 2DCOS over the past decade. First, the typical influencing factors and state-of-the-art assembly strategies of the solution-process for large-area 2DCOS over sub-millimeter even to wafer size are discussed accompanying rational evaluation. Then, the charge transport characteristics and contact resistance of 2DCOS-based transistors are explored. Following this, beyond single transistors, the p–n junction devices and planar integrated circuits based on 2DCOS are also emphasized. Furthermore, the burgeoning phototransistors (OPTs) based on crystals in the 2D limits are elaborated. Next, we emphasized the unique and enhanced photoelectrical properties based on a hybrid system with other 2D van der Waals solids. Finally, frontier insights and opportunities are proposed, promoting further research in this field.

Wettability Control of Interfaces for High-Performance Organic Thin-Film Transistors by Soluble Insulating Polymer Films.

Organic small-molecule semiconductors have higher carrier mobility compared to polymer semiconductors, while the actual performances of these materials are susceptible to morphological defects and misalignment of crystalline grains. Here, a new strategy is explored to control the crystallization and morphologies of a solution-processed organic small-molecule semiconductor 2,7-dioctyl[1]benzothieno[3,2-b][1]benzothiophene (C8-BTBT) using soluble polymer films to control the wettability of substrates. Different from the traditional surface modification method, the polymer layer as a modification layer is soluble in the semiconductor solution during the fabrication of organic thin-film transistors (OTFTs). The dissolved polymer alters the state of the semiconductor solution, which in turn, changes the crystallographic morphologies of the semiconductor films. By controlling the solubility and thickness of the polymer modification layers, it is possible to regulate the grain boundary and domain size of C8-BTBT films, which determine the performances of OTFTs. The bottom-gate transistors modified by a thick PS layer exhibit a mobility of >7 cm2/V·s and an on/off ratio of >107. It is expected that this new modification method will be applicable to high-performance OTFTs based on other small molecular semiconductors and dielectrics.

Simple charge transport model for efficient search of high-mobility organic semiconductor crystals

Search for materials with high charge mobilities among the plethora of synthesizable organic semiconductors is of paramount importance for organic electronics, and virtual screening is expected to guide and streamline this process. However, a model for rapid but reliable prediction of charge mobility in organic semiconductors is still lacking. To address this challenge, a simple “diffusion-of-delocalized-polaron” model is suggested in this study. It considers the most essential factors governing the charge transport: intermolecular electronic coupling, electron-phonon interaction, charge delocalization, static and dynamic disorder. The suggested model reproduces experimental charge mobilities in various organic semiconductors remarkably well, and significantly outperforms another approach previously used for screening of organic semiconductors – the Marcus model. Moreover, charge mobility values predicted by our model are closer to the experiment than those provided by the two state-of-the-art approaches – quantum nuclear tunneling model and second-order cumulant expansion of the density matrix – and are on par with the popular transient localization theory. It is thus anticipated that the suggested model is an efficient tool for the search of high-mobility materials, revealing of structure-mobility relationships and rational design of organic semiconductors. Its possible integration with crystal structure prediction can boost the development of organic electronics.

Conjugated Polymer Controlled Morphology and Charge Transport of Small-Molecule Organic Semiconductors

In this study, we report an effective approach to tune the crystallization, microstructure and charge transport of solution-processed organic semiconductors by blending with a conjugated polymer additive poly(3-hexylthiophene) (P3HT). When 6,13-bis(triisopropylsilylethynyl) pentacene (TIPS pentacene) was used as a model semiconductor material to mix with different amount of P3HT, their intermolecular interactions led to distinctive TIPS pentacene film morphologies, including randomly-oriented crystal ribbons, elongated needles with enhanced long-range order, and grass-like curved microwires with interlinkages. Each type of morphology was found to further correlate to considerably different charge transport and device performance. As compared to pristine TIPS pentacene devices, bottom-gate, top-contact OTFTs with 2% in weight P3HT additive showed a 2-fold and 5-fold improvement of average field-effect mobility and performance consistency (defined as the ratio of average mobility to the standard deviation), respectively. The improvement in transistor electrical performance can be attributed to the combined effect of enhanced crystal orientation and uniformity, as well as increased areal coverage. This work can be applied beyond the particular example demonstrated in this study and to tune the charge transport of other small-molecule organic semiconductors in general.

Organic Semiconductors: Charge‐Transfer‐Controlled Growth of Organic Semiconductor Crystals on Graphene (Adv. Sci. 6/2020)

In article number 1902315, Kilwon Cho and co-workers investigate the growth of C60 thin films on graphene. The crystallinity of C60 thin film is significantly improved when it is grown on p-doped graphene where electron transfer from graphene to C60 is suppressed.

Charge-Transfer-Controlled Growth of Organic Semiconductor Crystals on Graphene.

Controlling the growth behavior of organic semiconductors (OSCs) is essential because it determines their optoelectronic properties. In order to accomplish this, graphene templates with electronic‐state tunability are used to affect the growth of OSCs by controlling the van der Waals interaction between OSC ad‐molecules and graphene. However, in many graphene‐molecule systems, the charge transfer between an ad‐molecule and a graphene template causes another important interaction. This charge‐transfer‐induced interaction is never considered in the growth scheme of OSCs. Here, the effects of charge transfer on the formation of graphene–OSC heterostructures are investigated, using fullerene (C60) as a model compound. By in situ electrical doping of a graphene template to suppress the charge transfer between C60 ad‐molecules and graphene, the layer‐by‐layer growth of a C60 film on graphene can be achieved. Under this condition, the graphene–C60 interface is free of Fermi‐level pinning; thus, barristors fabricated on the graphene–C60 interface show a nearly ideal Schottky–Mott limit with efficient modulation of the charge‐injection barrier. Moreover, the optimized C60 film exhibits a high field‐effect electron mobility of 2.5 cm2 V−1 s−1. These results provide an efficient route to engineering highly efficient optoelectronic graphene–OSC hybrid material applications.

AFM-IR and IR-SNOM for the Characterization of Small Molecule Organic Semiconductors

Vibrational spectroscopies, such as Raman and Fourier-transform infrared spectroscopy (FT-IR), are powerful tools for the characterization of organic semiconductor thin films and crystals in additi...

Laser oscillation at an intended wavelength from a distributed feedback structure on anisotropic organic crystals

An organic laser device is constructed as distributed feedback (DFB) type using an anisotropic single crystal of an organic semiconductor oligomer BP3T. The DFB structure is formed on top of the crystal via an interference exposure technique of a positive type photoresist. In the DFB structure, both the phase matching condition and waveguide condition must be fulfilled. Under these conditions, the effective refractive indices can be precisely predicted for a BP3T crystal, and they vary depending upon the crystal thickness. As a result, the device produces a single-mode laser oscillation at an intended wavelength (typically ∼569 nm). The present study enables us to design a down-to-earth laser device based on an anisotropic organic semiconductor crystal toward practical use.

Crystallization Mechanism of 9,9-Diphenyl-dibenzosilole from Solids.

Organic semiconductor (OSC) crystals have great potential to be applied in many fields, as they can be flexibly designed according to the demands and show an outstanding device performance. However, OSCs with the capacity of solid-state crystallization (SSC) are developing too slowly to meet demands in productions and applications, due to their difficulties in molecular design and synthesis, unclear mechanism and high dependence on experimental conditions. In this work, in order to solve the problems, we synthesized an organic semiconductor capable of SSC at room temperature by adjusting the relationship between conjugated groups and functional groups. The thermodynamic and kinetic properties have been studied to discover the model of film SSC. Moreover, it can be purposefully controlled to prepare the high-quality crystals, and their corresponding organic electronic devices were further fabricated and discussed.