Tuning Organic Electrochemical Transistor Threshold Voltage using Chemically Doped Polymer Gates.

Organic electrochemical transistors (OECTs) have shown promise as transducers and amplifiers of minute electronic potentials due to their large transconductances. Tuning the OECT threshold voltage is important to achieve low-powered devices with amplification properties within the desired operational voltage range. However, traditional design approaches have struggled to decouple channel and materials properties from threshold voltage, thereby compromising on several other OECT performance metrics, such as electrochemical stability, transconductance, and dynamic range. In this work, simple solution-processing methods are utilized to chemically dope polymer gate electrodes, thereby controlling their work function, which in turn tunes the operation voltage range of the OECTs without perturbing their channel properties. Chemical doping of initially air-sensitive polymer electrodes further improves their electrochemical stability in ambient conditions. Thus, OECTs that are simultaneously low-powered and electrochemically resistant to oxidative side reactions under ambient conditions are demonstrated. This approach shows that threshold voltage, which is once interwoven with other OECT properties, can in fact be an independent design parameter, expanding the design space of OECTs.

Mixed Ionic-Electronic Conduction, a Multifunctional Property in Organic Conductors.

Organic mixed ionic-electronic conductors (OMIECs) have gained recent interest and rapid development due to their versatility in diverse applications ranging from sensing, actuation and computation to energy harvesting/storage, and information transfer. Their multifunctional properties arise from their ability to simultaneously participate in redox reactions as well as modulation of ionic and electronic charge density throughout the bulk of the material. Most importantly, the ability to access charge states with deep modulation through a large extent of its density of states and physical volume of the material enables OMIEC-based devices to display exciting new characteristics and opens up new degrees of freedom in device design. Leveraging the infinite possibilities of the organic synthetic toolbox, this perspective highlights several chemical and structural design approaches to modify OMIECs' properties important in device applications such as electronic and ionic conductivity, color, modulus, etc. Additionally, the ability for OMIECs to respond to external stimuli and transduce signals to myriad types of outputs has accelerated their development in smart systems. This perspective further illustrates how various stimuli such as electrical, chemical, and optical inputs fundamentally change OMIECs' properties dynamically and how these changes can be utilized in device applications.

Electrochemical scanning probe analysis used as a benchmark for carbon forms quality test.

Carbon forms (graphite, pyrolytic graphite, highly oriented pyrolytic graphite (HOPG), glassy carbon, carbon foam, graphene, buckypaper, etc) are a wide class of materials largely used in technology and energy storage. The huge request of carbon compounds with reliable and tunable physical and chemical properties is tackled by contriving new production protocols and/or compound functionalizations. To achieve these goals, new samples must be tested in a trial-and-error strategy with techniques that provide information in terms of both specimen quality and properties. In this work, we prove that electrochemical scanning probe techniques allow testing the performances of carbon compounds when are used as an electrode inside an electrochemical cell. Comparing the results with a reference sample (namely, HOPG) gives an insight on defects in the specimen structure, performances, and possible applications of the new samples. In this study, we concentrate on traditional carbon forms already employed in many fields versus new recently-developed specimens, in view of possible applications to the field of energy storage.

Hyperspectral imaging with deformable gratings fabricated with metal-elastomer nanocomposites.

We report the fabrication and characterization of a simple and compact hyperspectral imaging setup based on a stretchable diffraction grating made with a metal-polymer nanocomposite. The nanocomposite is produced by implanting Ag clusters in a poly(dimethylsiloxane) film by supersonic cluster beam implantation. The deformable grating has curved grooves and is imposed on a concave cylindrical surface, thus obtaining optical power in two orthogonal directions. Both diffractive and optical powers are obtained by reflection, thus realizing a diffractive-catoptric optical device. This makes it easier to minimize aberrations. We prove that, despite the extended spectral range and the simplified optical scheme, it is actually possible to work with a traditional CCD sensor and achieve a good spectral and spatial resolution.

Electroactive Ionic Soft Actuators with Monolithically Integrated Gold Nanocomposite Electrodes.

Electroactive ionic gel/metal nanocomposites are produced by implanting supersonically accelerated neutral gold nanoparticles into a novel chemically crosslinked ion conductive soft polymer. The ionic gel consists of chemically crosslinked poly(acrylic acid) and polyacrylonitrile networks, blended with halloysite nanoclays and imidazolium-based ionic liquid. The material exhibits mechanical properties similar to that of elastomers (Young's modulus ≈ 0.35 MPa) together with high ionic conductivity. The fabrication of thin (≈100 nm thick) nanostructured compliant electrodes by means of supersonic cluster beam implantation (SCBI) does not significantly alter the mechanical properties of the soft polymer and provides controlled electrical properties and large surface area for ions storage. SCBI is cost effective and suitable for the scaleup manufacturing of electroactive soft actuators. This study reports the high-strain electromechanical actuation performance of the novel ionic gel/metal nanocomposites in a low-voltage regime (from 0.1 to 5 V), with long-term stability up to 76 000 cycles with no electrode delamination or deterioration. The observed behavior is due to both the intrinsic features of the ionic gel (elasticity and ionic transport capability) and the electrical and morphological features of the electrodes, providing low specific resistance (<100 Ω cm-2 ), high electrochemical capacitance (≈mF g-1 ), and minimal mechanical stress at the polymer/metal composite interface upon deformation.