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Organic phototransistors (OPTs) are playing an indispensable role in organic optoelectronics, which greatly show their promising application in optical communication, video imaging, missile guidance, and night vision. However, because the thermally activated mode dominated for thin‐film devices leads to a sharp drop in mobility at low temperatures, until now, most of the studies about OPTs are performed at room temperature, severely hindering their further potential optoelectronic application over a broad range of temperatures, especially at low temperature environment. In this work, the optoelectronic properties of a small molecule (2,6‐diphenylanthracene, DPA) based OPTs with band‐like transport are studied at low temperatures. The devices exhibit outstanding optoelectronic properties in terms of mobility (2.6 cm2 V−1 s−1), on/off ratio (≈104), detectivity (1013 Jones), and external quantum efficiency (2500%) even at 150 K, which is superior to the performance of devices with thermally activated mode. In addition, the organic photodetector at low temperatures is also fabricated. Our results demonstrate that organic π‐conjugated DPA small‐molecule has great potential in low‐temperature application. [ABSTRACT FROM AUTHOR]

Phototransistors combine light detection and signal amplification functions into a single device and are regarded as one of the most important components for optoelectronic integration. In recent years, organic phototransistors (OPTs) have attracted worldwide interest because of their potential advantages of low cost, light weight, excellent flexibility and broadband detection. In this review, a brief description of the working mechanisms and performance metrics of OPTs is presented. Afterwards, the recent progress of OPTs based on the conventional planar field‐effect transistor structure is presented. Furthermore, from the perspective of novel device architectures and interface engineering, strategies for improving the performance of OPTs are discussed. Flexible optoelectronic devices based on OPTs for potential application in next‐generation wearable and human‐friendly electronics are also highlighted. Finally, an outlook for future research directions and challenges for OPTs is provided. [ABSTRACT FROM AUTHOR]

Abstract: The +6 oxidation state of iron generally exists in the form of ferrate(VI) with high redox potential and environmentally friendly nature. Although ferrate(VI) has been known for over a century, its chemistry is still limited to the solvent‐based reactions that suffers from the insolubility/instability of this oxidant and the environmental issues caused by hazardous solvents. Herein, we explore the solvent‐free reactivity of ferrate(VI) under mechanical milling, revealing that its strong oxidizing power is accessible in the “dry” solid state towards a broad variety of substrates, for example, aromatic alcohols/aldehydes and carbon nanotubes. More significantly, solvent‐free mechanochemistry also reshapes the oxidizing ability of ferrate(VI) due to the underlying solvent‐free effect and the promotive mechanical actions. This study opens up a new chemistry of ferrate(VI) with promising application in green oxidative transformation of both organic and inorganic substrates. [ABSTRACT FROM AUTHOR]

Nanosphere lithography is used to process nanopore-structured electrodes, which are applied into the fabrication of bottom-gate, bottom-contact configuration organic field effect transistors (OFETs) to serve as source/drain elecrodes. The introduction of this nanopore-structure electrode facilitates the forming of nanopore-structure pentacene layers with small grain boundaries at the electrode interface, and then reduces the contact resistance, contactinduces the growth of pentacene and accordingly improves the mobility of charge carriers in the OFETs about 20 times as compared with results in literature through enhancing the charge carrier injection. It is believed that this structure of electrode is a valuable approach for improving organic filed effect transistors. [ABSTRACT FROM AUTHOR]

'Regioselectivity deposition' method is developed to pattern silver electrodes facilely and efficiently by solution-process with high resolution (down to 2 μm) on different substrates in A4 paper size. With the help of this method, large-area, flexible, high-performance polymer field-effect transistors based on the silver electrodes and polyimide insulator are fabricated with bottom-contact configuration by all-solution processes. The polymer devices exhibit high performance with average field-effect mobility over 1.0 cm2 V−1 s−1 (the highest mobility up to 1.5 cm2 V−1 s−1) and excellent environmental stability and flexibility, indicating the cost effectiveness of this method for practical applications in organic electronics. [ABSTRACT FROM AUTHOR]

Highlights: [•] Polyimide is used as insulator layers in the process of photolithography for the first time. [•] Large scale, flexible and high-performance transistor arrays and circuits are fabricated. [•] The modified photolithography technique is employed to protect the polyimide in the process of photolithography. [ABSTRACT FROM AUTHOR]

Considering environmental changes and the demand for more sustainable energy sources, stricter requirements have been placed on electrode materials for sodium and potassium‐ion batteries, which are expected to provide higher energy and power density while being affordable and sustainable. Vanadium sulfide‐based materials have emerged as intriguing contenders for the next generation of anode materials due to their high theoretical capacity, abundant reserves, and cost‐effectiveness. Despite these advantages, challenges such as limited cycle life and restricted ion diffusion coefficients continue to impede their effective application in sodium and potassium‐ion batteries. To overcome the limitations associated with electrochemical performance and circumvent bottlenecks imposed by the inherent properties of materials at the bulk scale, this review comprehensively summarizes and analyzes the crystal structures, modification strategies, and energy storage processes of vanadium sulfide‐based electrode materials for sodium and potassium‐ion batteries. The objective is to guide the development of high‐performance vanadium‐based sulfide electrode materials with refined morphologies and/or structures, employing environmentally friendly and cost‐efficient methods. Finally, future perspectives and research suggestions for vanadium sulfide‐based materials are presented to propel practical applications forward. [ABSTRACT FROM AUTHOR]

The study of monolayer organic field‐effect transistors (MOFETs) provides an effective way to investigate the intrinsic charge transport of semiconductors. To date, the research based on organic monolayers on polymeric dielectrics lays far behind that on inorganic dielectrics and the realization of a bulk‐like carrier mobility on pure polymer dielectrics is still a formidable challenge for MOFETs. Herein, a quasi‐monolayer coverage of pentacene film with orthorhombic phase is grown on the poly (amic acid) (PAA) dielectric layer. More significantly, charge density redistribution occurs at the interface between the pentacene and PAA caused by electron transfer from pentacene to the PAA dielectric layer, which is verified by theoretical simulations and experiments. As a consequence, an enhanced hole accumulation layer is formed and pentacene‐based MOFETs on pure polymer dielectrics exhibit bulk‐like carrier mobilities of up to 13.7 cm2 V−1 s−1 from the saturation region at low VGS, 9.1 cm2 V−1 s−1 at high VGS and 7.6 cm2 V−1 s−1 from the linear region, which presents one of the best results of previously reported MOFETs so far and indicates that the monolayer semiconductor growing on pure polymer dielectric could produce highly efficient charge transport. [ABSTRACT FROM AUTHOR]

The front cover artwork is provided by the group of Prof. Tao Li at the School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University (China). The image shows recent advances of organic phototransistors with a planet‐satellite system. Read the full text of the Review at10.1002/cptc.201900198. [ABSTRACT FROM AUTHOR]

The increasing amount of electronic exerts a profound impact on both the environment and human health. Looking forward, it is imperative to develop electronic products that can degrade under mind condition, which largely relies on the development of degradable organic semiconductors (OSCs). Yet, designing degradable OSCs with decent electrical properties is challenging. In this study, two degradable n‐type OSCs based on a dynamic covalent C═C bond formed via the Knoevenagel condensation reaction are reported. The cleavage of Knoevenagel formed C═C bond through a retro‐Knoevenagel process imparts the degradability of these two OSCs in the weak base, particularly in the human‐friendly α‐amino acid of lysine. Meanwhile, the C═C bond formed by Knoevenagel reaction preserves optimal backbone planarity and good electron delocalization of the molecules. This, in turn, endows the OSCs with commendable electron transport performance, achieving an electron mobility of up to 0.57 cm2 V⁻¹ s⁻¹ in organic thin‐film transistors. This work provides a new insight into the molecular design strategy for the development of OSCs with degradability and good electrical properties. [ABSTRACT FROM AUTHOR]

In this paper, we developed a new method to produce large-area single crystal arrays by using the organic semiconductor 9, 10-bis (phenylethynyl) anthracene (BPEA). This method involves an easy operation, is efficient, meets the demands of being low-cost and is independent of the substrate for large-area arrays fabrication. Based on these single crystal arrays, the organic field effect transistors exhibit the superior performance with the average mobility extracting from the saturation region of 0.2 cm2 V−1s−1 (the highest 0.47 cm2 V−1s−1) and on/off ratio exceeding 105. In addition, our single crystal arrays also show a very high photoswitch performance with an on/off current ratio up to 4.1 × 105, which is one of the highest values reported for organic materials. It is believed that this method provides a new way to fabricate single crystal arrays and has the potential for application to large area organic electronics. [ABSTRACT FROM AUTHOR]

[Display omitted] Tissue-equivalent pure organic semiconducting crystals (OSCs) have unique advantages in direct X-ray detectors (DXDs), especially for biological tissue fluoroscopy, but their low carrier mobility and inherent weak absorption restrict the limit-of-detection (LoD) and sensitivity of DXDs. High-mobility OSCs theoretically facilitate charge collection and performance leaps, however, they are rare and suffer from poor solubility due to high conjugation, leading to nearly impossible crystal growth from solution and subsequent device applications. Here we report an ingenious solution-processed crystal-growth and high-performance DXD using 2,6-diphenylanthracene (2,6-DPA), a high-mobility OSC we developed recently. In contrast to previous OSCs, high-mobility 2,6-DPA exhibits low dark current density and large photoconductive gain, resulting in record-breaking LoD of <85 nGy air s−1 and sensitivity of >103 μC Gy air −1 cm−2. Compared with semiconductors containing high- Z atoms (Z is atomic number), the accuracy of 2,6-DPA based DXDs is not affected by near-edge absorption effects. Moreover, the non-linear relationship between irradiation current and dose rate is confirmed as a high injection effect. High mobility and ingenious crystal growth strategy make 2,6-DPA an ideal active material for DXDs and also provide the possibility for more optoelectronic applications. [ABSTRACT FROM AUTHOR]

Small reaction, big application! The silver mirror reaction is a straightforward way to produce silver films, and can be performed using cheap reactants in aqueous solutions. Here, it is successfully introduced into organic electronics by L. Jiang, H. Dong, G. Yu, W. Hu, and co‐workers, and applied to the process of fabricating flexible, high‐performance, large‐area, all‐solution‐processable organic fieldeffect transistors at room temperature with high resolution. [ABSTRACT FROM AUTHOR]

The disordered chain arrangement of polymer dielectrics has complex both internal and external effects on system performance, which generally stimulates the weak acquisition and grain boundaries of vapor‐deposited organic small molecule films (VDOSMFs) with thermally activated charge transport. As a result, achieving "band‐like" transmission of VDOSMs on polymer dielectrics is attempting to prove to be a major challenge. Three types of bi‐polymer dielectrics are developed to modulate charge transport from thermally activated mode to "band‐like" transport at the interfacial level. The bottom consisting of a polyimide layer is critical to interfacial modulation, which shows the selectively binding capability with up‐dielectric layers to realize the modulation of charge transport, as corroborated by interface characterization and density functional‐based tight‐binding calculation. The findings provide an effective strategy for modulating the charge transport through polymer dielectric engineering and also recommend a podium to further comprehend the electrical characteristics of small molecules in organic thin‐film transistors. [ABSTRACT FROM AUTHOR]

Phase‐change semiconductor is one of the best candidates for designing nonvolatile memory, but it has never been realized in organic semiconductors until now. Here, a phase‐changeable and high‐mobility organic semiconductor (3,6‐DATT) is first synthesized. Benefiting from the introduction of electrostatic hydrogen bond (S···H), the molecular conformation of 3,6‐DATT crystals can be reversibly modulated by the electric field and ultraviolet irradiation. Through experimental and theoretical verification, the tiny difference in molecular conformation leads to crystalline polymorphisms and dramatically distinct charge transport properties, based on which a high‐performance organic phase‐change memory transistor (OPCMT) is constructed. The OPCMT exhibits a quick programming/erasing rate (about 3 s), long retention time (more than 2 h), and large memory window (i.e., large threshold voltage shift over 30 V). This work presents a new molecule design concept for organic semiconductors with reversible molecular conformation transition and opens a novel avenue for memory devices and other functional applications. [ABSTRACT FROM AUTHOR]

Organic semiconductors with combinative high carrier mobility and efficient solid‐state emission are full of challenges but urgently pursued for developing new emerging optoelectronics. Herein, by delicately regulating the crystal packing of an anthracene‐based molecular crystal via terminal tert‐butylation, we developed a superior high mobility emissive molecule, 2,6‐di(6‐tert‐butylnaphthyl)anthracene (TBU‐DNA). The unique "slipped herringbone" packing motif of TBU‐DNA enables its appropriate exciton‐exciton coupling and electron‐phonon coupling, thus resulting in remarkably high solid‐state emission (photoluminescence quantum yield, ΦF≈74.9 %) and efficacious charge transport (carrier mobility, μ=5.0 cm2 V−1 s−1). Furthermore, OLETs based on TBU‐DNA show an external quantum efficiency (EQE) of 1.8 %, which is among the highest EQE values for single component OLETs reported till now. This work presents a crystal engineering strategy via exquisite molecular design to realize high mobility emissive organic semiconductors. [ABSTRACT FROM AUTHOR]

Organic semiconductors with combinative high carrier mobility and efficient solid‐state emission are full of challenges but urgently pursued for developing new emerging optoelectronics. Herein, by delicately regulating the crystal packing of an anthracene‐based molecular crystal via terminal tert‐butylation, we developed a superior high mobility emissive molecule, 2,6‐di(6‐tert‐butylnaphthyl)anthracene (TBU‐DNA). The unique "slipped herringbone" packing motif of TBU‐DNA enables its appropriate exciton‐exciton coupling and electron‐phonon coupling, thus resulting in remarkably high solid‐state emission (photoluminescence quantum yield, ΦF≈74.9 %) and efficacious charge transport (carrier mobility, μ=5.0 cm2 V−1 s−1). Furthermore, OLETs based on TBU‐DNA show an external quantum efficiency (EQE) of 1.8 %, which is among the highest EQE values for single component OLETs reported till now. This work presents a crystal engineering strategy via exquisite molecular design to realize high mobility emissive organic semiconductors. [ABSTRACT FROM AUTHOR]

It is generally believed that the incorporation of fluorine functional groups into dielectrics can effectively impede the charge‐trapping process and improve carrier mobility. However, the relationship between the device performance and fluorinated groups is still not clear and also the modulation effect of fluorine functional groups on photogenerated charge carrier in phototransistors has not yet been investigated. Herein, phototransistors are constructed by using three kinds of gate dielectric layers with different fluorinated groups to exploit the effect of fluorine functional groups. It is concluded that the presence of fluorinated groups indeed increases the transistor mobility and optical figures of merit in phototransistors compared to the device with a fluorine‐free dielectric layer. Concurrently, the exciton binding energy is increased with the addition of fluorinated groups, resulting in the decrease of phototransistor performance compared with less content of fluorinated groups due to the synergistic balance effect of fluorine functional groups. The results further clarify how the fluorine functional groups optimize the interface of organic phototransistors and modulate the photoelectric performance. [ABSTRACT FROM AUTHOR]

Integrating high charge‐carrier mobility and low‐threshold lasing action in an organic semiconductor is crucial for the realization of an electrically pumped laser, but remains a great challenge. Herein, we present an organic semiconductor, named as 2,7‐di(2‐naphthyl)‐9H‐fluorene (LD‐2), which shows an unexpected high charge‐carrier mobility of 2.7 cm2 V−1 s−1 and low‐threshold lasing characteristic of 9.43 μJ cm−2 and 9.93 μJ cm−2 and high‐quality factor (Q) of 2131 and 1684 at emission peaks of 420 and 443 nm, respectively. Detailed theoretical calculations and photophysical data analysis demonstrate that a large intermolecular transfer integral of 10.36–45.16 meV together with a fast radiative transition rate of 8.0×108 s−1 are responsible for the achievement of the superior integrated optoelectronic properties in the LD‐2 crystal. These optoelectronic performances of LD‐2 are among the highest reported low‐threshold lasing organic semiconductors with efficient charge transport, suggesting its promise for research of electrically pumped organic lasers (EPOLs). [ABSTRACT FROM AUTHOR]

Integrating high charge‐carrier mobility and low‐threshold lasing action in an organic semiconductor is crucial for the realization of an electrically pumped laser, but remains a great challenge. Herein, we present an organic semiconductor, named as 2,7‐di(2‐naphthyl)‐9H‐fluorene (LD‐2), which shows an unexpected high charge‐carrier mobility of 2.7 cm2 V−1 s−1 and low‐threshold lasing characteristic of 9.43 μJ cm−2 and 9.93 μJ cm−2 and high‐quality factor (Q) of 2131 and 1684 at emission peaks of 420 and 443 nm, respectively. Detailed theoretical calculations and photophysical data analysis demonstrate that a large intermolecular transfer integral of 10.36–45.16 meV together with a fast radiative transition rate of 8.0×108 s−1 are responsible for the achievement of the superior integrated optoelectronic properties in the LD‐2 crystal. These optoelectronic performances of LD‐2 are among the highest reported low‐threshold lasing organic semiconductors with efficient charge transport, suggesting its promise for research of electrically pumped organic lasers (EPOLs). [ABSTRACT FROM AUTHOR]

Molecule design of organic semiconductors (OSCs) for eliminating photoresponse and maintaining high charge mobility concurrently is beneficial to realize intrinsically photostable and high‐performance organic field‐effect transistors (OFETs), which has never been reported. Here, a novel organic semiconductor TFP‐TT‐TPA with a centrosymmetric structure is synthesized. Remarkably, OFETs with TFP‐TT‐TPA show negligible photoresponse under light intensity up to 170.4 mW cm−2 (higher than sunlight intensity, about 138 mW cm−2), which ensures that the devices can work stably under sunlight. Through the single‐crystal structure and exciton dynamics analysis, it is found that the specific structure design can make strong intermolecular D–A interaction that occurs in the aggregate state, which facilitates the process of exciton quenching and thus enables the photostable OFETs. This study provides a new strategy for the design of organic semiconductors with intrinsic photostability and the construction of photostable organic optoelectronic devices for applications in light environment. [ABSTRACT FROM AUTHOR]

Stretchable organic field‐effect transistors (OFETs) are one of the essential building blocks for next‐generation wearable electronics due to the high stretchability of OFET well matching with the large deformation of human skin. In recent years, some significant progress of stretchable OFETs have already been made via the strategies of stretchable molecular design and geometry engineering. However, the main opportunity and challenge of stretchable OFETs is still to simultaneously improve their stretchability and mobility. This review covers the recent advances in the research of stretchable OFETs with high mobility. First, the core stretchable materials are summarized, including organic semiconductors, electrodes, dielectrics, and substrates. Second, the materials and healing mechanism of self‐healing OFET are summarized in detail. Subsequently, their different configurations and the potential applications are summarized. Finally, an outlook of future research directions and challenges in this area is presented. [ABSTRACT FROM AUTHOR]

Polyimide memory materials with a donor–acceptor structure based on a charge‐transfer mechanism exhibit great potential for next‐generation information storage technology due to their outstanding high‐temperature resistance and good dimensional and chemical stability. Precisely controlling memory performance by limited chemical decoration is one of core challenges in this field. Most reported work mainly focuses on designing novel and elaborate electron donors or acceptors for the expected memory behavior of polyimides; this takes a lot of time and is not always efficacious. Herein, we report a series of porphyrinated copolyimides coPI−Znx (x=5, 10, 20, 50, 80), where x represents the mole percentage of Zn ion in the central core of the porphyrin. Experimental and theoretical analysis indicate that the Zn ion could play a vital bridge role in promoting the formation and stabilization of a charge‐transfer complex by enhancing the hybridization of local and charge transfer (HLCT) excitations of porphyrinated polyimides, endowing coPI−Znx with volatile random access memory performance and continuously tunable retention time. This work could provide one simple strategy to precisely regulate memory performance merely by altering the metal content in porphyrinated polyimides. [ABSTRACT FROM AUTHOR]

• By measuring the dielectric properties of 2D confined water and analyzing the relaxation process, the permeation rate of water and the performance of alcohol-water separation can be predicted. • Cationic intercalation can modulate the viscosity of 2D confined water, further impacting water permeation. • Compared with other characterization, dielectric spectroscopy shows the potential for accurate prediction on water permeation without the need of subtracting the adsorbed water. • The prediction on separation performance by dielectric analysis shows universality for other 2D membranes. Attributed to the growing demands for biomass fuels, the alcohol-water separation membranes, particularly the two-dimensional (2D) lamellar structures with high permeability and selectivity have attracted increasing attention. However, owing to the limited tools available for investigating the mass transport in the 2D nanocapillaries, the development of separation membranes mainly relied on theoretical prediction and a summary of experimental performance. In this work, we present an in-operando dielectric study on the pristine and varied ion-crosslinked 2D membranes for alcohol-water separation to establish the relationship between the relaxation process and the separation performance of the membranes. We found that the dielectric relaxation process in the range of 10−2 to 102 Hz, which is related to the viscosity of water in 2D nanocapillaries, can act as an indicator of the separation performance of the membranes. Furthermore, the slowing down of the relaxation process due to the electric field around the cations indicates lower water permeance and separation factor. Compared to the previous characterizations on the surface hydrophilicity or the water absorption, monitoring the dielectric process directly offers insights into the interlayered molecular states and transport, and therefore opens a new avenue towards rational design of 2D selective membranes for alcohol-water separation. [ABSTRACT FROM AUTHOR]

The limited stability, compatibility, and ion transport capacity of SEI remain key challenges in the development of high-energy–density sodium metal batteries. In order to realize the rational design and facile synthesis of SEI, the influencing factors of different challenges were systematically sorted out. By improving SEI chemical/electrochemical stability, mechanical stability, and thermal stability, the voltage window and temperature range of the battery operation can be effectively broadened. Suppressing the volume effect, phase exfoliation, and phase dissolution to enhance SEI compatibility is crucial for extending battery cycle life. The stability of ion transport at the electrode–electrolyte interface is affected by the composition, structure, and homogeneity of the interfacial phase, and fast and uniform interfacial Na+ transport can enable high-rate, high-safety sodium ion battery designs. [Display omitted] • The challenges and design elements of SEI are summarized comprehensively. • The formation mechanism, characteristics, and failure mechanism of SEI are systematically reviewed. • The latest development of SEI regulation strategy is discussed. • The opportunity and research direction of interface design for long lasting sodium metal batteries are prospected. Inhomogeneous and fragile solid electrolyte interphase (SEI) leads to poor battery cycle life and safety hazards, which is a key challenge that limits the practical application of low-cost sodium metal anodes. Although sodium metal batteries based on non-aqueous liquid and solid electrolytes have made great progress in terms of interfacial chemistry and SEI regulation strategies, the relevant evaluation of SEI from the perspective of the electrolyte is not well understood. This paper reviews the formation mechanism, physicochemical properties, and failure mechanism of SEI at the interface between the sodium metal and the liquid/solid electrolyte, focusing on poor stability, compatibility, interfacial ion transport problems, and influencing factors. Recent advances in SEI regulation are summarized in terms of electrolytes, artificial interphases, and electrode engineering to achieve ideal electrochemical reversibility. The effectiveness of the SEI engineering strategies was evaluated based on a comprehensive review of the interfacial stability in different electrolyte systems. Finally, the challenges associated with rational interface design for long-lasting sodium metal batteries are discussed, along with promising avenues for the same. [ABSTRACT FROM AUTHOR]

Abstract: The +6 oxidation state of iron generally exists in the form of ferrate(VI) with high redox potential and environmentally friendly nature. Although ferrate(VI) has been known for over a century, its chemistry is still limited to the solvent‐based reactions that suffers from the insolubility/instability of this oxidant and the environmental issues caused by hazardous solvents. Herein, we explore the solvent‐free reactivity of ferrate(VI) under mechanical milling, revealing that its strong oxidizing power is accessible in the “dry” solid state towards a broad variety of substrates, for example, aromatic alcohols/aldehydes and carbon nanotubes. More significantly, solvent‐free mechanochemistry also reshapes the oxidizing ability of ferrate(VI) due to the underlying solvent‐free effect and the promotive mechanical actions. This study opens up a new chemistry of ferrate(VI) with promising application in green oxidative transformation of both organic and inorganic substrates. [ABSTRACT FROM AUTHOR]

Keywords: Charge Transport; Crystal Engineering; Light Emission; Molecular Crystals; Organic Semiconductor EN Charge Transport Crystal Engineering Light Emission Molecular Crystals Organic Semiconductor 1 1 1 11/03/22 20221107 NES 221107 B An anthracene-based molecular crystal b with a unique "slipped herringbone" packing motif was developed by crystal engineering through terminal I tert i -butylation. Appropriate exciton-exciton coupling/electron-phonon coupling originating from the unique crystal packing induces a remarkably strong solid-state emission and efficient charge transport, as reported by Wenping Hu et al. in their Research Article (e202206825). Appropriate exciton-exciton coupling/electron-phonon coupling originating from the unique crystal packing induces a remarkably strong solid-state emission and efficient charge transport, as reported by Wenping Hu et al. in their Research Article (e202206825). [Extracted from the article]

Organic semiconductors with combinative high carrier mobility and efficient solid‐state emission are full of challenges but urgently pursued for developing new emerging optoelectronics. Herein, by delicately regulating the crystal packing of an anthracene‐based molecular crystal via terminal tert‐butylation, we developed a superior high mobility emissive molecule, 2,6‐di(6‐tert‐butylnaphthyl)anthracene (TBU‐DNA). The unique “slipped herringbone” packing motif of TBU‐DNA enables its appropriate exciton‐exciton coupling and electron‐phonon coupling, thus resulting in remarkably high solid‐state emission (photoluminescence quantum yield, ΦF≈74.9 %) and efficacious charge transport (carrier mobility, μ=5.0 cm2 V−1 s−1). Furthermore, OLETs based on TBU‐DNA show an external quantum efficiency (EQE) of 1.8 %, which is among the highest EQE values for single component OLETs reported till now. This work presents a crystal engineering strategy via exquisite molecular design to realize high mobility emissive organic semiconductors. [ABSTRACT FROM AUTHOR]

An anthracene derivative, 2,6-diphenyl anthracene (DPA), was successfully synthesized with three simple steps and a high yield. The compound was determined to be a durable high performing semiconductor with thin film device mobility over 10 cm2 V−1 s−1. The efficient synthesis and high performance indicates its great potential in organic electronics. [ABSTRACT FROM AUTHOR]