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Human sensory receptors enable the real world to be perceived effortlessly. Hence, massive efforts have been devoted to the development of bionic receptors capable of identifying objects. Unfortunately, most of the existing devices are limited to single sensory emulation and are established on solid-state electronic technologies, which are incompatible with the biological reactions occurring in electrolyte media. Here, an iontronic tactile-gustatory receptor using an all-polymer electrochemical transistor (AECT) is presented. The sensor is biocompatible with the operation voltage of 0.1 V, which is 1 to 2 orders lower than those of reported values. By this study, one receptor is able to accurately recognize various objects perceived by the human tactile and gustatory system without complex circuitry. Additionally, to promote its further application, flexible AECT arrays with channel length of 2 µm and density of 104 167 transistors cm -2 (yield of 97%) are fabricated, 1 to 5 orders higher than those of related works. Finally, a flexible integrated network for electrocardiogram recording is successfully constructed. This study moves a step forward toward state-of-the-art bionic sensors., (© 2023 Wiley-VCH GmbH.)

Polymer semiconductors are promising candidates for wearable and skin-like X-ray detectors due to their scalable manufacturing, adjustable molecular structures and intrinsic flexibility. Herein, we fabricated an intrinsically stretchable n-type polymer semiconductor through spatial nanoconfinement effect for ultrasensitive X-ray detectors. The design of high-orientation nanofiber structures and dense interpenetrating polymer networks enhanced the electron-transporting efficiency and stability of the polymer semiconductors. The resultant polymer semiconductors exhibited an ultrahigh sensitivity of 1.52 × 10 4 μC Gy air -1 cm -2 , an ultralow detection limit of 37.7 nGy air s -1 (comparable to the record-low value of perovskite single crystals), and polymer film X-ray imaging was achieved at a low dose rate of 3.65 μGy air s -1 (about 1/12 dose rate of the commercial medical chest X-ray diagnosis). Meanwhile, the hybrid semiconductor films could sustain 100% biaxial stretching strain with minimal degeneracy in photoelectrical performances. These results provide insights into future high-performance, low-cost e-skin photoelectronic detectors and imaging., (© 2022. The Author(s).)

Competing Interests: Conflict of interest The authors declare that they have no conflict of interest.

Syntheses using classic coupling reactions can be tedious, leading to a dearth of ambipolar semiconducting polymers. Here, we detail the rapid synthesis of balanced ambipolar polymers by using a carbon-hydrogen (C-H) activation strategy. Using this protocol, two C-H reactive hydrogenated monomers and six ambipolar polymers can be rapidly synthesized within 2 h via C-H activation and the optoelectronic properties of the resultant polymers can be characterized. We also describe the fabrication process and performance evaluation of the ambipolar polymers-based organic transistors. For complete details on the use and execution of this protocol, please refer to Shen et al. (2022)., Competing Interests: The authors declare no competing interests., (© 2022 The Author(s).)

The optoelectronic skin is acknowledged as the world's current cutting-edge technology in the fields of wearable healthcare monitoring, soft robotics, artificial retinas, and so on. However, the difficulty in preparing stretchable photosensitive polymers and the high-crystallization nature of most reported photosensitive materials (such as perovskites) severely restrict the development of skin-like optoelectronic devices. Herein, a surface energy-induced self-assembly methodology is proposed to form easily transferrable and flexible perovskite quantum dot (PQD) films with a worm-like morphology. Furthermore, intrinsically stretchable phototransistors (ISTPTs) are fabricated based on a stretchable photosensitive layer heterojunction consisting of worm-like PQD films and hybrid polymer semiconductors. The obtained ISTPTs display highly sensitive response to high-energy photons of X-ray (with a detection limit of 79 nGy s -1 , that is 560 times lower than commercial medical chest X-ray diagnosis) and ultraviolet (with photosensitivity of 5 × 10 6 and detectable light intensity of 50 nW cm -2 among the highest performance of reported photodetectors). In addition, these ISTPTs demonstrate desirable e-skin characteristics with high strain tolerance, high sensing specificity, high optical transparency, and good skin conformability. The surface energy-induced self-assembly methodology for the preparation of ISTPTs is a critical demonstration to enable low-cost and high-performance optoelectronic skins., (© 2021 Wiley-VCH GmbH.)

The lack of ambipolar polymers with balanced hole (μh) and electron mobilities (μe) >10 cm2 V−1 s−1 is the main bottleneck for developing organic integrated circuits. Herein, we show the design and synthesis of a π‐extended selenium‐containing acceptor‐dimeric unit, namely benzo[c][1,2,5]selenadiazol‐4‐yl)ethane (BBSeE), to address this dilemma. In comparison to its sulfur‐counterpart, BBSeE demonstrates enlarged co‐planarity, selective noncovalent interactions, polarized Se−N bond, and higher electron affinity. The successful stannylation of BBSeE offers a great opportunity to access acceptor‐acceptor copolymer pN‐BBSeE, which shows a narrower band gap, lower‐lying lowest unoccupied molecular orbital level (−4.05 eV), and a higher degree of backbone planarity. Consequently, the pN‐BBSeE‐based organic transistors display an ideally balanced ambipolar transporting property with μh and μe of 10.65 and 10.72 cm2 V−1 s−1, respectively. To the best of our knowledge, the simultaneous μh/μe values >10.0 cm2 V−1 s−1 are the best performances ever reported for ambipolar polymers. In addition, pN‐BBSeE shows an excellent shelf‐storage stability, retaining over 85 % of the initial mobility values after two months storage. Our study demonstrates the π‐extended acceptor‐dimeric BBSeE is a promising acceptor building block for constructing high‐performance ambipolar polymers applied in next‐generation organic integrated circuit. [ABSTRACT FROM AUTHOR]

The lack of ambipolar polymers with balanced hole (μh) and electron mobilities (μe) >10 cm2 V−1 s−1 is the main bottleneck for developing organic integrated circuits. Herein, we show the design and synthesis of a π‐extended selenium‐containing acceptor‐dimeric unit, namely benzo[c][1,2,5]selenadiazol‐4‐yl)ethane (BBSeE), to address this dilemma. In comparison to its sulfur‐counterpart, BBSeE demonstrates enlarged co‐planarity, selective noncovalent interactions, polarized Se−N bond, and higher electron affinity. The successful stannylation of BBSeE offers a great opportunity to access acceptor‐acceptor copolymer pN‐BBSeE, which shows a narrower band gap, lower‐lying lowest unoccupied molecular orbital level (−4.05 eV), and a higher degree of backbone planarity. Consequently, the pN‐BBSeE‐based organic transistors display an ideally balanced ambipolar transporting property with μh and μe of 10.65 and 10.72 cm2 V−1 s−1, respectively. To the best of our knowledge, the simultaneous μh/μe values >10.0 cm2 V−1 s−1 are the best performances ever reported for ambipolar polymers. In addition, pN‐BBSeE shows an excellent shelf‐storage stability, retaining over 85 % of the initial mobility values after two months storage. Our study demonstrates the π‐extended acceptor‐dimeric BBSeE is a promising acceptor building block for constructing high‐performance ambipolar polymers applied in next‐generation organic integrated circuit. [ABSTRACT FROM AUTHOR]

Intrinsically stretchable light‐emitting polymer semiconductors are essential building blocks for bioelectronics and display textiles. Stretchability is challenging for rigid conjugated polymers unless sacrificing charge mobility by introducing amorphous domains. High‐performance light‐emitting properties designed with twisted angle are undesirable for conductive materials. Hence, the concurrent strategies hardly satisfy the balance of stretchability, light‐emitting and mobility. Herein, a morphology engineering is proposed by controlling micro‐crystalline and limiting aggregation, that four intrinsically stretchable emissive polymers with good charge mobility based on indacenodithiophene (IDT) are obtained. Polymers reveal good emission properties with high photoluminescence quantum yields (PLQY) of about 20%, while stretchable modulus and charge mobility are tunable by backbone and weight. Specifically emphasizing, IDT‐2T‐H retains high performance of charge mobility and PLQY even at 100% strain. Therefore, organic light emitting diodes are fabricated based on it and showing the luminance of 176.2 cd cm−2, which verifies the potential of technique to reconcile integration of stretchability, light‐emitting, and mobility. This is the first attempt to integrate balanced mechanical, optical, and electrical properties through micro‐crystalline aggregation‐limited morphology in one polymer, offering a feasible approach to advanced integrated circuit and multi‐functional electronics in the future. [ABSTRACT FROM AUTHOR]

This article discusses the recent progress in the development of high-mobility polymer semiconductors with various functionalities. These semiconductors have advantages such as easy solution processing, large-area manufacturing, mechanical strength, and flexibility. The article focuses on the integration of high mobility with stretchability, strong luminescence, photolithography patterning, and efficient thermoelectric conversion. The challenges and future directions in this field are also discussed. The research is supported by various funding sources. [Extracted from the article]

Although the effects of electron‐deficient group substitution on isoindigo on the corresponding conjugated polymers are extensively studied, the modification of isoindigo core with electron‐rich groups has not been investigated. It is envisioned that the introduction of the methoxy group on isoindigo will not only tune the highest occupied molecular orbital (HOMO) energy level of the corresponding polymers but also introduce O···S "conformation lock" to increase the coplanarity of the polymers, which should facilitate hole transport. Herein, the syntheses of two methoxylated isoindigos and the investigations on the charge transport behaviors of their copolymers with bisthiophene (2T) and bisthiazole (2Tz) are reported. It is found that the substitution positions have a drastic influence on the UV–vis absorption and electrochemical properties for both monomers and polymers. Theoretical calculations and single crystal structure analysis confirm the existence of O···S "conformation lock", however, both methoxy substitutions also change the aggregation behaviors of the corresponding polymers to a mixed face‐on/edge‐on orientation which has an adverse effect for charge transport. Among the four polymers, the polymer of 5,5'‐methoxylated isoindigo and 2T exhibit the best hole mobility of 1.9 × 10−1 cm2 V−1 s−1. [ABSTRACT FROM AUTHOR]

The development of polymer semiconductors with strong luminescence and high mobility has always been challenging, and achieving both properties together is considered paradoxical according to molecular design principles. Studies on novel molecular species with unique optoelectrical characteristics are limited. Herein, a novel fully rigid coplanar thiophene‐pyridal[1,2,3]triazole‐thiophene (T‐PT‐T) class structure with considerable intramolecular noncovalent interactions is proposed. To balance luminescence and carrier transport properties, a series of non‐conventional regioregular conjugated polymers (PPTs) with suitable energy gaps (Egs ≈ 1.8 eV) are developed, which exhibit near‐infrared (NIR, 700–1000 nm) light emission and high mobility. One of the synthesized polymers, PPT‐2, exhibits an excellent photoluminescence quantum yield (PLQY) of 9% in the solid‐state and a high mobility reaching 0.35 cm2 V−1 s−1, indicating superior performance compared to other NIR light‐emitting polymer semiconductors. The authors believe that the class structure of fully rigid coplanar "T‐PT‐T" could be harnessed to develop high‐mobility NIR light‐emitting polymer semiconductors. [ABSTRACT FROM AUTHOR]

Large area and highly aligned polymer semiconductor sub-microwires were fabricated using the coaxial focused electrohydrodynamic jet printing technology. As indicated by the results, the sub-microwire arrays have smooth morphology, well reproducibility and controllable with a width of ~110 nm. Analysis shows that the molecular chains inside the sub-microwires mainly exhibited edge-on arrangement and the π-stacking direction (010) of the majority of crystals is parallel to the long axis of the sub-microwires. Sub-microwires based organic field effect transistors showed high mobility with an average of 1.9 cm2 V−1 s−1, approximately 5 times higher than that of thin film based organic field effect transistors. In addition, the number of sub-microwires can be conveniently controlled by the printing technique, which can subsequently concisely control the performance of organic field effect transistors. This work demonstrates that sub-microwires fabricated by the coaxial focused electrohydrodynamic jet printing technology create an alternative path for the applications of high-performance organic flexible device. Here, the authors fabricate large area and highly aligned polymer semiconductor sub-microwires arrays via coaxial focused electrohydrodynamic jet printing technology, achieving high on/off ratio and average mobility that is 5x higher than that of thin film based organic field effect transistors. [ABSTRACT FROM AUTHOR]

The molecular packing and resultant charge transport behaviors of semiconducting polymers are widely known to be temperature‐dependent. Due to the limitation of measurement methods, previous studies on molecular packing behavior have been mainly focused on a very limited temperature range, and therefore cannot support the understanding of charge transport behaviors. In this study, with a homemade temperature‐dependent grazing incidence XRD measurement chamber, the relationship between molecular packing structure and charge transport properties of diketopyrrolopyrrole‐based polymers is investigated across a wide temperature range of 98–623 K. Glass transition temperatures of the alkyl side‐chain and aromatic backbone are identified through the observation of clear transitions in the thermal expansion coefficients of d−d packing and π−π stacking, respectively. A correlation between the π−π stacking distance and charge transport properties is then established using an extended Miller−Abrahams model. The turning point of the charge transport and the failure of the polymer‐based devices are proved to be caused by packing structure changes due to increased temperatures. Such an examination over a wide range of temperatures improves the understanding of the charge transport properties of semiconducting polymers and helps construct thermally stable devices to be used in extreme conditions. [ABSTRACT FROM AUTHOR]

Ambipolar polymer semiconductors are potentially serviceable for logic circuits, light-emitting field-effect transistors (LFETs) and polymer solar cells (PSCs). Although several high-performance ambipolar polymers have been developed, their optoelectronic devices are generally processed from toxic chlorinated solvents. To achieve the commercial applications of organic FETs (OFETs), the polymers should be processed from nonchlorinated solvents, instead of chlorinated solvents. However, most conjugated polymers show poor solubility in nonchlorinated solvents. It is of great importance to develop ambipolar polymers that can be processed from nonchlorinated solvents. Here, we develop a nonchlorinated solvent processed polymer named poly[7-fluoro-N, N′-di(4-decyltetradecyl)-7′-azaisoindigo-6′,6″-(thieno[3,2-b]thiophene-2,5-diyl)-7‴-fluoro-N″, N‴-di(4-decyltetradecyl)-7″-azaisoindigo-6,6‴-([2,2″-bithiophene]-5,5″-diyl)] (PITTI-BT) by designing a monomer with a large molar mass. The polymer displays good solubility in p-xylene (PX). Well-aligned films of PITTI-BT are achieved by an off-center spin-coating (SC) method. Based on the high-quality films, the OFETs fabricated from PX solution achieve record ambipolar performance with hole and electron mobilities of 3.06 and 2.81 cm2 V−1 s−1, respectively. The combination of nonchlorinated solvents and good alignment process offers an effective and eco-friendly approach to obtain high-performance ambipolar transistors. [ABSTRACT FROM AUTHOR]

Application of high‐performance unipolar n‐type polymeric semiconductors lagged behind due to those polymers' poor solubility in green solvents. Traditional methods, such as random copolymerization and asymmetric structuring, enhance solubility but reduce mobility. Here, a universal "lipophilicity strategy" for eco‐friendly processing is reported. This strategy could effectively improve the solubility of polymers without sacrificing crystallinity thus maintaining good mobility of the devices. CF3 group and SCF3 group, which are famous for their high lipophilicity, are introduced to (E)‐1,2‐di(thiophen‐2‐yl)ethane (TVT). The solubility of two monomers is confirmed to be 5 and 16 times higher than the brominated counterpart, respectively. Moreover, CF3TVT and SCF3TVT not only improve solubility of the polymers but also reduce energy levels of donor unit due to their strong electron withdrawing property. By using Ozawa's condition, three unipolar n‐type semiconducting polymers are obtained through direct (hetero)arylation polycondensation (DHAP). Among them, CF3TVT based P2 processed by xylene solutions exhibited the best unipolar n‐type mobility up to 1.37 cm2 V−1 s−1 and reached current on/off ratio of 108, for the first time realizing both green synthesis and nonchlorinated processing. In general, this lipophilicity strategy provides an effective guideline to design high‐performance n‐type polymer with good solubility in nonchlorinated solvents. [ABSTRACT FROM AUTHOR]

The lack of ambipolar polymers with balanced hole (μh) and electron mobilities (μe) >10 cm2 V−1 s−1 is the main bottleneck for developing organic integrated circuits. Herein, we show the design and synthesis of a π‐extended selenium‐containing acceptor‐dimeric unit, namely benzo[c][1,2,5]selenadiazol‐4‐yl)ethane (BBSeE), to address this dilemma. In comparison to its sulfur‐counterpart, BBSeE demonstrates enlarged co‐planarity, selective noncovalent interactions, polarized Se−N bond, and higher electron affinity. The successful stannylation of BBSeE offers a great opportunity to access acceptor‐acceptor copolymer pN‐BBSeE, which shows a narrower band gap, lower‐lying lowest unoccupied molecular orbital level (−4.05 eV), and a higher degree of backbone planarity. Consequently, the pN‐BBSeE‐based organic transistors display an ideally balanced ambipolar transporting property with μh and μe of 10.65 and 10.72 cm2 V−1 s−1, respectively. To the best of our knowledge, the simultaneous μh/μe values >10.0 cm2 V−1 s−1 are the best performances ever reported for ambipolar polymers. In addition, pN‐BBSeE shows an excellent shelf‐storage stability, retaining over 85 % of the initial mobility values after two months storage. Our study demonstrates the π‐extended acceptor‐dimeric BBSeE is a promising acceptor building block for constructing high‐performance ambipolar polymers applied in next‐generation organic integrated circuit. [ABSTRACT FROM AUTHOR]

The lack of ambipolar polymers with balanced hole (μh) and electron mobilities (μe) >10 cm2 V−1 s−1 is the main bottleneck for developing organic integrated circuits. Herein, we show the design and synthesis of a π‐extended selenium‐containing acceptor‐dimeric unit, namely benzo[c][1,2,5]selenadiazol‐4‐yl)ethane (BBSeE), to address this dilemma. In comparison to its sulfur‐counterpart, BBSeE demonstrates enlarged co‐planarity, selective noncovalent interactions, polarized Se−N bond, and higher electron affinity. The successful stannylation of BBSeE offers a great opportunity to access acceptor‐acceptor copolymer pN‐BBSeE, which shows a narrower band gap, lower‐lying lowest unoccupied molecular orbital level (−4.05 eV), and a higher degree of backbone planarity. Consequently, the pN‐BBSeE‐based organic transistors display an ideally balanced ambipolar transporting property with μh and μe of 10.65 and 10.72 cm2 V−1 s−1, respectively. To the best of our knowledge, the simultaneous μh/μe values >10.0 cm2 V−1 s−1 are the best performances ever reported for ambipolar polymers. In addition, pN‐BBSeE shows an excellent shelf‐storage stability, retaining over 85 % of the initial mobility values after two months storage. Our study demonstrates the π‐extended acceptor‐dimeric BBSeE is a promising acceptor building block for constructing high‐performance ambipolar polymers applied in next‐generation organic integrated circuit. [ABSTRACT FROM AUTHOR]