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A flexible, electrochromic, active matrix addressed display (AMAD) is demonstrated. The monolithically integrated AMAD, which contains a 3 × 3 array of organic electrochromic smart pixels (OESPs), is manufactured on a plastic substrate solely using screen printing. Each OESP is based on the combination of one organic electrochromic display (OECD) and one organic electrochemical transistor (OECT), where both devices are screen printed into multilayered vertical architectures. The conduction state of the OECT enables control of the color state of its corresponding OECD, thereby circumventing cross-talk effects in the resulting AMAD device. The manufacturing approach also involves electrical wires, which connect each OECD with its corresponding OECT and also serve as the addressing lines of the resulting AMAD device, that are formed by screen printing of an ink based on either silver or nanocopper., Funding details: European Commission, EC, FP7‐NMP‐2013‐SME‐7, 604568; Funding details: Stiftelsen för Strategisk Forskning, SSF, SE13‐0045; Funding text 1: This project was financially supported by the European Commission (FP7‐NMP‐2013‐SME‐7, project 604568 Printed Logic for Applications of Screen Matrix Activation Systems [PLASMAS]) and the Swedish Foundation for Strategic Research (Silicon‐Organic Hybrid Autarkic Systems, Reference number: SE13‐0045). The authors acknowledge Intrinsiq Materials for providing and sintering the nanocopper‐based screen printing ink.

Two different e-labels were developed to explore the feasibility and to identify scientifi c and engineering challenges of the Real-World-Web platform. First was a printed biosensor e-label, comprising Si-chips with an array of different printegrated devices, and second, an e-label to explore the feasibility of transferring data, through the human body, between a mobile device and different distributed e-labels, adhered onto the body or onto dedicated devices and surfaces of one's ambience. The silicon chips utilized in e-labels, include analogue and digital circuitry to receive and handle sensory input, to perform signal processing, and to transmit information to antennas and displays. When used, the e-label is turned on, and a sample is then added onto the sensor area. The display provides simple instructions and updated information to the user. All data handling, electrical probing, and analysis of the sensor is performed by the Si-chips, and the sensing data is finally shown in the printed display. The second e-label exemplifies an ID-tag for body area networks (BAN) communication applications, which, in part, is manufactured and integrated in the same way as the first e-label, but with another choice of Si-chips and capacitive antennas., Funding details: Knut och Alice Wallenbergs Stiftelse; Funding details: VINNOVA

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-mu Ps) and glycerol dispersed in nanofibrillated cellulose (NFC). NFC, Si-mu Ps 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-mu Ps. 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 x 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., Funding Agencies|Knut and Alice Wallenberg Foundation; Swedish Foundation for Strategic Research; Swedish Government Strategic Research Area in Materials Science on Functional Materials at Linkoping University [2009-00971]

We can control the bandgap of thiophene polymers over 2 eV by choosing the nature, position and regularity of side chain substitutions. Electroluminescence from these polymers cover the full visible spectrum, from the blue into the near infra-red. Blends of these polymer materials allow us to construct voltage controlled variable colour light sources. A newly developed transfer technique allow us to mount thin oriented films of the polymers in polymer LEDs to obtain polarised light sources giving polarisation anisotropys of up to 3. Sub-lambda light sources have been constructed from these polymer materials using nanometer polymer electrodes.

Polarized light sources based on stretch-oriented conjugated polymers are reported. The devices, based on poly 3(4-octylphenyl)-2,2′-bithiophene, show an external quantum efficiency of 0.1% and are produced using a very simple method which may be easily extended to other polymers. The fabrication of the devices is described and factors such as the emission and spectral differences parallel and prependicular to the stretching direction discussed.