Tunable Tribotronic Dual‐Gate Logic Devices Based on 2D MoS2 and Black Phosphorus

With the Moore's law hitting the bottleneck of scaling‐down in size (below 10 nm), personalized and multifunctional electronics with an integration of 2D materials and self‐powering technology emerge as a new direction of scientific research. Here, a tunable tribotronic dual‐gate logic device based on a MoS₂ field‐effect transistor (FET), a black phosphorus FET and a sliding mode triboelectric nanogenerator (TENG) is reported. The triboelectric potential produced from the TENG can efficiently drive the transistors and logic devices without applying gate voltages. High performance tribotronic transistors are achieved with on/off ratio exceeding 106 and cutoff current below 1 pA μm^–1. Tunable electrical behaviors of the logic device are also realized, including tunable gains (improved to ≈13.8) and power consumptions (≈1 nW). This work offers an active, low‐power‐consuming, and universal approach to modulate semiconductor devices and logic circuits based on 2D materials with TENG, which can be used in microelectromechanical systems, human–machine interfacing, data processing and transmission.     

Bis‐Diketopyrrolopyrrole Moiety as a Promising Building Block to Enable Balanced Ambipolar Polymers for Flexible Transistors

A bis‐diketopyrrolopyrrole (DPP dimer, 2DPP) core is synthesized with much stronger electron deficiency than DPP by homocoupling of DPP. 2DPP‐based polymers, P2DPP‐BT, P2DPP‐TT, P2DPP‐TVT, and P2DPP‐BDT, are obtained. Top‐gated organic field‐effect transistors on plastic substrate are fabricated. Compared with their mono‐DPP‐based polymers, remarkable improvement of electron mobilities of P2DPPs is achieved. Meanwhile, their p‐channel performance becomes higher.     

Single-Component CMOS-Like Logic using Diketopyrrolopyrrole-Based Ambipolar Organic Electrochemical Transistors

Complementary circuits based on organic electrochemical transistors (OECTs) are attractive for the development of inexpensive and disposable point-of-care bioelectronic devices. Ambipolar OECTs, which employ a single channel material, could decrease the fabrication complexity and manufacturing costs of such circuits. An ideal channel material for ambipolar OECTs should be electrochemically stable in aqueous environments, afford facile ion insertion for both cations and anions, and also facilitate high and balanced electron and hole transport. In this study, triethylene glycol functionalized diketopyrrolopyrrole (DPP)-based polymer is proposed for the development of ambipolar OECTs. It is shown that DPP-based OECTs have a high and comparable figure of merit for both n- and p-type operations. Logic NOT, NAND, and NOR operations with corresponding complementary circuits constructed from identical DPP-based OECT devices are demonstrated. This study is an important step toward the development of sophisticated complementary metal–oxide–semiconductor-like logic circuits using single-component OECTs.     

WSe2场效应晶体管的源漏接触特性研究

二硒化钨(WSe2)具有双极导电特性,可以通过外界掺杂或改变源漏金属来调节载流子传输类型,是一类特殊的二维纳米材料,有望在未来集成电路中成为硅(Si)的替代材料.文章采用理论与实验相结合的方式系统分析了 WSe2场效应晶体管中的源漏接触特性对器件导电类型及载流子传输特性的影响,通过制备不同金属作为源漏接触电极的WSe2场效应晶体管,发现金属/WSe2接触的实际肖特基接触势垒高低极大地影响了晶体管的开态电流.源漏金属/WSe2接触特性不仅取决于接触前理想的费米能级差,还受到界面特性,特别是费米能级钉扎效应的影响.     

Solution‐Processed High‐Performance Tetrathienothiophene‐Based Small Molecular Blends for Ambipolar Charge Transport

Four soluble dialkylated tetrathienoacene ( TTAR) ‐based small molecular semiconductors featuring the combination of a TTAR central core, π‐conjugated spacers comprising bithiophene ( bT ) or thiophene ( T ), and with/without cyanoacrylate ( CA ) end‐capping moieties are synthesized and characterized. The molecule DbT‐TTAR exhibits a promising hole mobility up to 0.36 cm² V^?1 s^?1 due to the enhanced crystallinity of the microribbon‐like films. Binary blends of the p‐type DbT‐TTAR and the n‐type dicyanomethylene substituted dithienothiophene‐quinoid ( DTTQ‐11 ) are investigated in terms of film morphology, microstructure, and organic field‐effect transistor (OFET) performance. The data indicate that as the DbT‐TTAR content in the blend film increases, the charge transport characteristics vary from unipolar (electron‐only) to ambipolar and then back to unipolar (hole‐only). With a 1:1 weight ratio of DbT‐TTAR DTTQ‐11 in the blend, well‐defined pathways for both charge carriers are achieved and resulted in ambipolar transport with high hole and electron mobilities of 0.83 and 0.37 cm² V^?1 s^?1, respectively. This study provides a viable way for tuning microstructure and charge carrier transport in small molecules and their blends to achieve high‐performance solution‐processable OFETs.     

Effect of side‐chain functionality on the organic field‐effect transistor performance of oligo(p‐phenylenevinylene) derivatives

In order to observe the effects of the substitution of electronegative flourine with aromatic groups in oligo(p ‐phenylenevinylene) compounds on their packing, morphology, and charge carrier mobility, we have synthesized napthol‐substituted oligo(p ‐phenylenevinylene) compounds and examined their solubility, redox properties, thin film morphologies, and charge carrier properties. To date, very few examples of conjugated oligomers bearing napthol side groups have been reported in the literature. After annealing at 150 °C, the mobility of S1, S2, and S3 was 4.0 × 10^?2 cm² V^?1 s^?1, 1.2 × 10^?2 cm² V^?1 s^?1, and 2.6 × 10^?3 cm² V^?1 s^?1, respectively. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44825.