An organic flexible temperature-sensor array exhibits great potential in health monitoring and other biomedical applications. The actively addressed 16 × 16 temperature sensor array reaches 100% yield rate and provides 2D temperature information of the objects placed in contact, even if the object has an irregular shape. The current device allows defect predictions of electronic devices, remote sensing of harsh environments, and e-skin applications.

The contact resistance in organic thin-film transistors (TFTs) is the limiting factor in the development of high-frequency organic TFTs. In devices fabricated in the inverted (bottom-gate) device architecture, staggered (top-contact) organic TFTs have usually shown or are predicted to show lower contact resistance than coplanar (bottom-contact) organic TFTs. However, through comparison of organic TFTs with different gate-dielectric thicknesses based on the small-molecule organic semiconductor 2,9-diphenyl-dinaphtho[2,3- b :2’,3’- f ]thieno[3,2- b ]thiophene, we show the potential for bottom-contact TFTs to have lower contact resistance than top-contact TFTs, provided the gate dielectric is sufficiently thin and an interface layer such as pentafluorobenzenethiol is used to treat the surface of the source and drain contacts. We demonstrate bottom-contact TFTs fabricated on flexible plastic substrates with record-low contact resistance (29 Ωcm), record subthreshold swing (62 mV/decade), and signal-propagation delays in 11-stage unipolar ring oscillators as short as 138 ns per stage, all at operating voltages of about 3 V.

This work innovatively develops a dual solution-shearing method utilizing the semiconductor concentration region close to the solubility limit, which successfully generates large-area and high-performance semiconductor monolayer crystals on the millimeter scale. The monolayer crystals with poly(methyl methacrylate) encapsulation show the highest mobility of 10.4 cm 2 V −1 s −1 among the mobility values in the reported solutionprocessed semiconductor monolayers. With similar mobility to multilayer crystals, light is shed on the charge accumulation mechanism in organic field-effect transistors (OFETs), where the first layer on interface bears the most carrier transport task, and the other above layers work as carrier suppliers and encapsulations to the first layer. The monolayer crystals show a very low dependency on channel directions with a small anisotropic ratio of 1.3. The positive mobility-temperature correlation reveals a thermally activated carrier transport mode in the monolayer crystals, which is different from the band-like transport mode in multilayer crystals. Furthermore, because of the direct exposure of highly conductive channels, the monolayer crystal based OFETs can sense ammonia concentrations as low as 10 ppb. The decent sensitivity indicates the monolayer crystals are potential candidates for sensor applications.

Low-cost solution-shearing methods are highly desirable for deposition of organic semiconductor crystals over a large area. To enhance the rate of evaporation and deposition, elevated substrate temperature is commonly employed during shearing processes. However, the Marangoni flow induced by a temperature-dependent surface-tension gradient near the meniscus line shows negative effects on the deposited crystals and its electrical properties. In the current study, the Marangoni effect to improve the shearing process of 2,7-dioctyl[1]benzothieno[3,2-b][1]benzothiophene for organic field-effect transistor (OFET) applications is utilized and regulated. By modifying the gradient of surface tension with different combinations of solvents, the mass transport of molecules is much more favorable, which largely enhances the deposition rate, reduces organic crystal thickness, enlarges grain sizes, and improves coverage. The average and highest mobility of OFETs can be increased up to 13.7 and 16 cm 2 V −1 s −1 . This method provides a simple deposition approach on a large scale, which allows to further fabricate large-area circuits, flexible displays, or bioimplantable sensors.

The contact resistance limits the downscaling and operating range of organic field‐effect transistors (OFETs). Access resistance through multilayers of molecules and the nonideal metal/semiconductor interface are two major bottlenecks preventing the lowering of the contact resistance. In this work, monolayer (1L) organic crystals and nondestructive electrodes are utilized to overcome the abovementioned challenges. High intrinsic mobility of 12.5 cm2 V−1 s−1 and Ohmic contact resistance of 40 Ω cm are achieved. Unlike the thermionic emission in common Schottky contacts, the carriers are predominantly injected by field emission. The 1L‐OFETs can operate linearly from VDS = −1 V to VDS as small as −0.1 mV. Thanks to the good pinch‐off behavior brought by the monolayer semiconductor, the 1L‐OFETs show high intrinsic gain at the saturation regime. At a high bias load, a maximum current density of 4.2 µA µm−1 is achieved by the only molecular layer as the active channel, with a current saturation effect being observed. In addition to the low contact resistance and high‐resolution lithography, it is suggested that the thermal management of high‐mobility OFETs will be the next major challenge in achieving high‐speed densely integrated flexible electronics.

The development of organic thin-film transistors (OTFTs) with low power consumption and high gain will advance many flexible electronics. Here, by combining solution-processed monolayer organic crystal, ferroelectric HfZrOx gating and van der Waals fabrication, we realize flexible OTFTs that simultaneously deliver high transconductance and sub-60 mV/dec switching, under one-volt operating voltage. The overall optimization of transconductance, subthreshold swing and output resistance leads to transistor intrinsic gain and amplifier voltage gain over 5.3 × 104 and 1.1 × 104, respectively, which outperform existing technologies using organics, oxides and low-dimensional nanomaterials. We further demonstrate battery-powered, integrated wearable electrocardiogram (ECG) and pulse sensors that can amplify human physiological signal by 900 times with high fidelity. The sensors are capable of detecting weak ECG waves (undetectable even by clinical equipment) and diagnosing arrhythmia and atrial fibrillation. Our sub-thermionic OTFT is promising for battery/wireless powered yet performance demanding applications such as electronic skins and radio-frequency identification tags, among many others.

The fabrication of electronic circuits on unconventional substrates largely broadens their application areas. For example, green electronics achieved through utilization of biodegradable or recyclable substrates, can mitigate the solid waste problems that arise at the end of their lifespan. Here, we combine screen-printing, high precision laser drilling and thermal evaporation, to fabricate organic field effect transistor (OFET) active-matrix (AM) arrays onto standard printer paper. The devices show a mobility and on/off ratio as high as 0.56 cm2V−1s−1 and 109 respectively. Small electrode overlap gives rise to a cut-off frequency of 39 kHz, which supports that our AM array is suitable for novel practical applications. We demonstrate an 8 × 8 AM light emitting diode (LED) driver with programmable scanning and information display functions. The AM array structure has excellent potential for scaling up.

Organic electrochemical transistors (OECTs) are used as highly sensitive glucose and lactate sensors by modifying the gate electrode with glucose oxidase/lactate oxidase and poly(n-vinyl-2-pyrrolidone)-capped platinum nanoparticles (Pt NPs). The Pt NPs are deposited by using a two-step dip coating method without bias instead of the conventional electrodeposition method and followed by an UV-Ozone post treatment to enhance the catalytic ability of the Pt NPs. The modified OECT sensors have extremely high sensitivity, and can achieve a detection limit of glucose and lactate down to 10 −7 and 10 −6 m, respectively. A polydimethylsiloxane microfluidic channel is successfully integrated with the OECT sensors, which provides a compact chip size of the sensors, a short detection time of around 1 min and extremely low consumption of analyte (30 µ µL). The cross talk between individual sensors in multianalyte sensing devices is also reduced by the dual microfluidic channel structure. Practical applications, such as for detecting glucose in saliva, can therefore be realized, and a prototype of a portable glucose sensor has been successfully created in this study. This portable glucose sensor has excellent potential for real-time and noninvasive glucose sensing applications.