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The potential of the screen printing method for large-scale production of organic electrochemical transistors (OECTs), combining high production yield with low cost, is here demonstrated. Fully screen-printed OECTs of 1 mm 2 area, based on poly(3,4-ethylenedioxythiophene) doped with poly(styrensulfonate) (PEDOT:PSS), have been manufactured on flexible polyethylene terephthalate (PET) substrates. The goal of this project effort has been to explore and develop the printing processing to enable high yield and stable transistor parameters, targeting miniaturized digital OECT circuits for large-scale integration (LSI). Of the 760 OECTs manufactured in one batch on a PET sheet, only two devices were found malfunctioning, thus achieving an overall manufacturing yield of 99.7%. A drain current ON/OFF ratio at least equal to 400 was applied as the strict exclusion principle for the yield, motivated by proper operation in LSI circuits. This consistent performance of low-footprint OECTs allows for the integration of PEDOT:PSS-based OECTs into complex logic circuits operating at high stability and accuracy.

The nature of mass transport in plants has recently inspired the development of low-cost and sustainable wood-based electronics. Herein, we report a wood electrochemical transistor (WECT) where all three electrodes are fully made of conductive wood (CW). The CW is prepared using a two-step strategy of wood delignification followed by wood amalgamation with a mixed electron-ion conducting polymer, poly(3,4-ethylenedioxythiophene)–polystyrene sulfonate (PEDOT:PSS). The modified wood has an electrical conductivity of up to 69 Sm−1 induced by the formation of PEDOT:PSS microstructures inside the wood 3D scaffold. CW is then used to fabricate the WECT, which is capable of modulating an electrical current in a porous and thick transistor channel (1 mm) with an on/off ratio of 50. The device shows a good response to gate voltage modulation and exhibits dynamic switching properties similar to those of an organic electrochemical transistor. This wood-based device and the proposed working principle demonstrate the possibility to incorporate active electronic functionality into the wood, suggesting different types of bio-based electronic devices.

The increasing demands to further electrify and digitalize our society set demands for a green electrical energy storage technology that can be scaled between very small, and heavily distributed electrical energy sources, to very large volumes. Such technology must be compatible with fast-throughput, large-volume and low-cost fabrication processes, such as using printing and coating techniques. Here, we demonstrate a sequential production protocol to fabricate supercapacitors including electrodes based on cellulose nanofibrils (CNF) and the conducting polymer PEDOT:PSS. Thin and lightweight paper electrodes, carbon adhesion layers and the gel electrolyte are fabricated using spray coating, screen printing, and bar coating, respectively. These all solid-state supercapacitors are flexible, mechanically robust and exhibit a low equivalent series resistance (0.22 Ω), thus resulting in a high power density (∼10 4  W/kg) energy technology. The supercapacitors are combined and connected to a power management circuit to demonstrate a smart packaging application. This work shows that operational and embedded supercapacitors can be manufactured in a manner to allow for the integration with, for instance smart packaging solutions, thus enabling powered, active internet-of-things (IoT) devices in a highly distributed application.

A mixed ionic–electronic conductor based on nanofibrillated cellulose composited with poly(3,4‐ethylene‐dioxythio­phene):­poly(styrene‐sulfonate) along with high boiling point solvents is demonstrated in bulky electrochemical devices. The high electronic and ionic conductivities of the resulting nanopaper are exploited in devices which exhibit record values for the charge storage capacitance (1F) in supercapacitors and transconductance (1S) in electrochemical transistors.

Printed electronics are considered for wireless electronic tags and sensors within the future Internet-of-things (IoT) concept. As a consequence of the low charge carrier mobility of present printable organic and inorganic semiconductors, the operational frequency of printed rectifiers is not high enough to enable direct communication and powering between mobile phones and printed e-tags. Here, we report an all-printed diode operating up to 1.6 GHz. The device, based on two stacked layers of Si and NbSi ₂ particles, is manufactured on a flexible substrate at low temperature and in ambient atmosphere. The high charge carrier mobility of the Si microparticles allows device operation to occur in the charge injection-limited regime. The asymmetry of the oxide layers in the resulting device stack leads to rectification of tunneling current. Printed diodes were combined with antennas and electrochromic displays to form an all-printed e-tag. The harvested signal from a Global System for Mobile Communications mobile phone was used to update the display. Our findings demonstrate a new communication pathway for printed electronics within IoT applications.

The quest for eco‐friendly materials with anticipated positive impact for sustainability is crucial to achieve the UN sustainable development goals. Classical strategies of composite materials can be applied on novel nanomaterials and green materials. Besides the actual technology and applications also processing and manufacturing methods should be further advanced to make entire technology concepts sustainable. Here, they show an efficient way to combine two low‐cost materials, cellulose and zinc oxide (ZnO), to achieve novel functional and “green” materials via paper‐making processes. While cellulose is the most abundant and cost‐effective organic material extractable from nature. ZnO is cheap and known of its photocatalytic, antibacterial, and UV absorption properties. ZnO nanowires are grown directly onto cellulose fibers in water solutions and then dewatered in a process mimicking existing steps of large‐scale papermaking technology. The ZnO NW paper exhibits excellent photo‐conducting properties under simulated sunlight with good ON/OFF switching and long‐term stability (90 minutes). It also acts as an efficient photocatalyst for hydrogen peroxide (H 2 O 2 ) generation (5.7 × 10 −9   m s −1 ) with an envision the possibility of using it in buildings to enable large surfaces to spontaneously produce H 2 O 2 at its outer surface. Such technology promise for fast degradation of microorganisms to suppress the spreading of diseases.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

The redox flow battery (RFB) has emerged as one of the promising rechargeable energy storage devices. Ion-selective membranes play a pivotal role in RFB regarding their capacity, cycle performance, and cost of production. However, to achieve large-scale commercialization of RFB, it is imperative but remains challenging to develop the next generation of economically efficient and environmentally friendly membranes with outstanding ion transport performance. Here, we report a renewable ion-selective membrane fabricated from wood-derived nanocellulose. The appropriate nanopore size combined with abundant surface charge realized by a chemical cross-linking approach enables membranes with ultralow permeability of redox molecules. As a result, this nanocellulose membrane demonstrates excellent feasibility in an aqueous organic redox flow battery (AORFB) by using 4,5-dihydroxybenzene-1,3-disulfonate as catholyte and alizarin red S as anolyte. More significantly, the nanocellulose membrane indeed outperforms the commercial Nafion 115 membrane including higher capacity and better cycle stability. In addition to the highlighted electrochemical performance of nanocellulose membranes in RFBs, the renewable nanocellulose materials will facilitate AORFB toward sustainable development.

Electrochromic devices have important implications as smart windows for energy efficient buildings, internet of things devices, and in low-cost advertising applications. While inorganics have so far dominated the market, organic conductive polymers possess certain advantages such as high throughput and low temperature processing, faster switching, and superior optical memory. Here, we present organic electrochromic devices that can switch between two high-resolution images, based on UV-patterning and vapor phase polymerization of poly(3,4-ethylenedioxythiophene) films. We demonstrate that this technique can provide switchable greyscale images through the spatial control of a UV-light dose. The color space was able to be further altered via optimization of the oxidant concentration. Finally, we utilized a UV-patterning technique to produce functional paper with electrochromic patterns deposited on porous paper, allowing for environmentally friendly electrochromic displays.

Low cost and flexible devices such as wearable electronics, e-labels and distributed sensors will make the future “internet of things” viable. To power and communicate with such systems, high frequency rectifiers are crucial components. We present a simple method to manufacture flexible diodes, operating at GHz frequencies, based on self-adhesive composite films of silicon micro-particles (Si-μPs) and glycerol dispersed in nanofibrillated cellulose (NFC). NFC, Si-μPs and glycerol are mixed in a water suspension, forming a self-supporting nanocellulose-silicon composite film after drying. This film is cut and laminated between a flexible pre-patterned Al bottom electrode and a conductive Ni-coated carbon tape top contact. A Schottky junction is established between the Al electrode and the Si-μPs. The resulting flexible diodes show current levels on the order of mA for an area of 2 mm 2 , a current rectification ratio up to 4 × 10 3 between 1 and 2 V bias and a cut-off frequency of 1.8 GHz. Energy harvesting experiments have been demonstrated using resistors as the load at 900 MHz and 1.8 GHz. The diode stack can be delaminated away from the Al electrode and then later on be transferred and reconfigured to another substrate. This provides us with reconfigurable GHz-operating diode circuits.