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Printed electronic paper identifies its interest in flexible organic electronics and sustainable and clean energy applications because of its straightforward production method, cost‐effectiveness, and positive environmental impact. However, current limitations include restricted material thickness and the use of supporting substrate for printing. Here, 2D and 3D electronic patterned paper are fabricated from direct ink writing (DIW) nanocellulose and PEDOT:PSS‐based materials using syringe deposition and 3D printing. The conductor patterns are integrated in the bulk of the paper, while non‐conductive sections are used as support to form free‐standing paper. The strong interface between the patterns of electronic patterned paper gives mechanical stability for practical handling. The conductive paper‐based electrode has 202 S cm−1 and is capable of handling electric current up to 0.7 A, which can be used for high‐power devices. Printed supercapacitor papers show high specific energy of 4.05 Wh kg−1, specific power of 4615 W kg−1 at 0.06 A g−1, and capacitance retention above 95% after 2000 cycles. The new design structure of electronic patterned papers presents a solution for additive manufacturing of paper‐based composites for supercapacitors, wearable electronics, or sensors for smart packaging. [ABSTRACT FROM AUTHOR]

The interphase properties in nanocomposites indicate the interaction between filler and matrix, which is dependent on the preparation method, shape, and size of filler and the chemical interaction between two phases. Local chemical environment in polymer matrix give rise to the different dielectric properties compared to that of bulk material. These properties allow the understanding of their effects on the dielectric properties and glass transition (Tg) of the nanocomposites. In this study, interphase power law model was used to predict the interphase properties based on the experimental dielectric constant of polyimide (PI) with BaTiO3, TiO2, and ZrO2 nanocomposites. They were prepared via in situ polymerization of PI whose dielectric constant were increased at interphase filler volume fraction of BaTiO3, TiO2, and ZrO2 at 3.8, 2.05, and 1.7, respectively. These results indicate that PI/ceramics nanocomposites had poor dispersion and weak interphase interaction between the filler and the matrix, as an evidence of scanning electron microscopy and Fourier transform infrared spectroscopy results. However, PI incorporated with high aspect ratio of BaTiO3 nanofiber shows better dispersion than nanocomposites of TiO2 and ZrO2 filled PI; therefore provide higher dielectric constant and Tg. [ABSTRACT FROM AUTHOR]

The rise of internet of things (IoTs) applications has led to the development of a new generation of light‐weight, flexible, and cost‐effective electronics. These devices and sensors have to be simultaneously easily replaceable and disposable while being environmentally sustainable. Thus, the introduction of new functionalized materials with mechanical flexibility that can be processed using large‐area and facile fabrication methods (as, for example, printing technologies) has become a matter of great interest in the scientific community. In this context, cellulose nanofibers (CNFs) are renewable, affordable, robust, and nontoxic materials that are rapidly emerging as components for eco‐friendly electronics. Their combination with conductive polymers (CPs) to obtain conductive nanopapers (CNPs) allows moving their functionality from just substrates to active components of the device. In this work, a route for the inkjet‐printing of organic diodes is outlined. The proposed strategy is based on the use of CNPs as both substrates and bottom electrodes onto which insulator and organic semiconducting layers are deposited to fabricate novel diode structures. Remarkable rectification ratios of up to 1.2 × 103 at |3 V| and a current density up to 5.1 µA cm−2 are achieved. As a proof‐of‐concept of the potentiality of the approach for versatile, low‐temperature, and disposable sensing applications, an NO2 gas sensor is presented. [ABSTRACT FROM AUTHOR]

This work aims to synthesize new series of polysiloxane copolymer through hydrosilylation reaction based on different level of crosslink densities and phenyl content. The results revealed that polysiloxanes resins with phenyl rings increased viscosity up to 3800 cps while displaying a relatively high refractive index of 1.531. The asymmetric phenyl substitution onto chain backbone led to formation of densely packed structure resulting in reduced water absorption and gas permeability of PDMS resins. High level of crosslinking contributed to a high shore A hardness and adhesion strength. It displayed transparency of 97% whose percentage reduction was 1.6% under thermal and 0.6% UV aging. No obvious discoloration was observed during accelerated thermal aging up to 210 min at 80 °C. These results are key attributes that make the synthesized polysiloxane series as ideal candidate for high brightness LED encapsulant. © 2019 Wiley Periodicals, Inc. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019, 136, 47895. [ABSTRACT FROM AUTHOR]