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The fabrication of the Screen‐Printed Electrode (SPE) was performed using the graphite ink to print the working (WE) and counter electrodes (CE), and silver/silver chloride path as reference electrode (RE). All the electrodes are printed in a paper substrate using screen‐printing technique. The resulting SPE is characterized using scanning electron microscopy, showing all the ink layer, and subsequently optimized. The paper sample presented the cellulose fibers entanglement, extremely rough, with highly porous network. Then the graphite ink was deposited and the surface became flat, thinner and very smooth. When the silver ink was painted on top of the graphite ink, the spherical silver particles, ranged from 2–3.5 μm in size, were observed. And finally, the silver ink was covered with a AgCl layer and the particle size becomes larger with an irregular sphere‐like phase. The images showed that the layers appear to be homogeneously distributed with good coverage. Then fabrication process was optimized concerning type of paper, the sanding process, the hydrophobic barrier, the electrode design and size. In summary, the optimized values included using the previously sanded matte paper with a mineral spirit layer. The design and size of the electrode were also tested to achieve the best electrochemical performance (design 3 with 3.5 cm). The final SPE was a miniaturized and flexible paper‐based electrochemical electrode. In order to evaluate the electrical properties, the ohmic resistance of each ink was tested using a multimeter and the obtained values were 2.18 kΩ for the graphite ink, 2.27 Ω for the silver ink and 38.33 kΩ for the silver/silver chloride ink. That can indicate the good conductivity of each ink used in the fabrication of the electrode and the correct deposition of Ag/AgCl. Finally, the electrode was used to measure the electrochemical response of K4[Fe(CN)6] in different concentrations. Then a calibration curve was obtained from the voltammograms and a linearity was observed between the current and concentration in the range of 0.50–2.00 mM. That indicates that the SPE has potential to be used as a voltammetric electrode. [ABSTRACT FROM AUTHOR]

Nanocellulose has received enormous scientific interest for its abundance, easy manufacturing, biodegradability, and low cost. Cellulose nanocrystals (CNCs) and cellulose nanofibers (CNFs) are ideal candidates to replace plastic coating in the textile and paper industry. Thanks to their capacity to form an interconnected network kept together by hydrogen bonds, nanocelluloses perform an unprecedented strengthening action towards cellulose‐ and other fiber‐based materials. Furthermore, nanocellulose use implies greener application procedures, such as deposition from water. The surface chemistry of nanocellulose plays a pivotal role in influencing the performance of the coating: tailored surface functionalization can introduce several properties, such as gas or grease barrier, hydrophobicity, antibacterial and anti‐UV behavior. This review summarizes recent achievements in the use of nanocellulose for paper and textile coating, evidencing critical aspects of coating performances related to deposition technique, nanocellulose morphology, and surface functionalization. Furthermore, beyond focusing on the aspects strictly related to large‐scale coating applications for paper and textile industries, this review includes recent achievements in the use of nanocellulose coating for the safeguarding of Cultural Heritage, an extremely noble and interesting emerging application of nanocellulose, focusing on consolidation of historical paper and archaeological textile. Finally, nanocellulose use in electronic devices as an electrode modifier is highlighted. [ABSTRACT FROM AUTHOR]

Laser‐induced graphene (LIG) produced by irradiation of paper (paper‐LIG)holds substantial promise for flexible devices. This article presents paper‐LIG humidity and temperature sensors fabricated by single‐step irradiation of common filter paper with a pulsed UV laser (355 nm). The influence of the process parameters on the conversion of cellulose fibers into LIG is discussed based on the resulting morphology, structure, conductivity, and chemical composition, revealing a distinct barrier to transformation and a propagation behavior not seen under CO2 laser irradiation. The obtained material is constituted by a porous, electrically conductive network of fibers. The paper‐LIG relative humidity (RH) and temperature sensors with sensitivities of up to 1.3 × 10−3%RH−1 and ‐ 2.8 × 10−3 °C−1, respectively, are examined in terms of their linearity, reproducibility, and response time. A detailed discussion on the response mechanism is presented in the context of literature, pointing towards the absorption of water molecules in the interlayer spacing of graphene as the main reason for the increase in resistance with RH. Additionally, a contribution from variable range hopping along the ab plane of graphene at high RH is suggested. These results demonstrate the potential of paper‐LIG for low‐cost, sustainable, and environmentally friendly sensing. [ABSTRACT FROM AUTHOR]

The absolute dating of documents is still one of the most important challenges for forensic document examiners (FDE). The potential difference between the date on a questioned document and the actual year of production of the used paper can be only 1 to 5 years. Until now, there was no analytical method with this accuracy available. This study demonstrates a method for an absolute dating of paper by using the 14C bomb peak and dating the starch in the paper. Accelerator mass spectroscopy (AMS) radiocarbon measurements were performed on starch extracts and cellulose fibers from 50 paper samples with known production year from 1950 to 2018. For most of the paper samples, the measured 14C concentration values in the starch extracts were highly correlated with the data of the 14C bomb peak calibration curve. The differences between the calibrated ages and the actual harvest years of the starch‐containing plants were only up to 3 years. The 14C concentration in the paper fibers showed a lower but significant correlation with the production year of the papers and can be used to support the dating results of the starch extracts. In order to secure the accuracy of the dating, aside from the radiocarbon measurements of the extracted starch other analytical methods or data are used, like a detailed chemical analysis of the paper composition including fiber composition and the spectroscopic analysis of the purity of the starch extracts. In practice, only starch extracts without contaminations are used for the paper dating. [ABSTRACT FROM AUTHOR]

Inkjet printing (IJP) is the most widespread direct‐write technique in paper electronics. However, this technique cannot be used for printing devices on untreated regular paper, since its low‐viscosity nanoinks leak through the cellulose fibers. Thus, a planarization coating is frequently used as a barrier, even though this makes substrates more expensive and less eco‐friendly. Alternatively, high solid content screen printing (SP) inks could allow printing on regular paper due to their high viscosity and large particle size; however, they cannot be printed through IJP. Another digital technique is then required: laser‐induced forward transfer (LIFT). This work aims at proving the feasibility of LIFT for printing devices on regular paper. The main transfer parameters are systematically varied to obtain uniform Ag‐SP interconnects, whose performance is improved by a multiple‐printing approach. It results in low resistances with much better performance than those typical of IJP. After optimizing the functionality of the printed lines, a proof‐of‐concept consisting of a radio‐frequency inductor is provided. The characterization of the device shows a substantially higher performance than that of the same device printed with IJP ink in similar conditions, which proves the potential of LIFT for digitally fabricating devices on regular paper. [ABSTRACT FROM AUTHOR]

Nanostructured composites built with microporous cellulose fibers and carbon nanotubes (CNTs) have potential impacts in the fields of energy storage, sensors, and flexible electronics. Few results have been shown for high mechanoelectrical sensitivity of CNT‐paper composite because of numerous current paths in the network. Here, CNT‐paper‐based nanostructured composite sensors whose sensitivities are generated by controlled tensile fracture of the composite are presented. Under uniaxial load, the cellulose fibers in the paper experience straightening, stiffening, and fracture. The cellulose fibers originally parallel to the tension are fractured while those inclined and perpendicular to the tension are reorganized to form crossbar junctions in the vicinity of a crack. The cross junctions exhibit resistive and capacitive sensitivity to the out‐of‐plane force by the compression of the junctions. Such piezoresistive and piezocapacitive sensitivities are characterized and evaluated for human behavior monitoring. [ABSTRACT FROM AUTHOR]

This paper describes the design and fabrication of electrically controlled paper actuators that operate based on the dimensional changes that occur in paper when the moisture absorbed on the surface of the cellulose fibers changes. These actuators are called 'Hygroexpansive Electrothermal Paper Actuators' (HEPAs). The actuators are made from paper, conducting polymer, and adhesive tape. They are lightweight, inexpensive, and can be fabricated using simple printing techniques. The central element of the HEPAs is a porous conducting path (used to provide electrothermal heating) that changes the moisture content of the paper and causes actuation. This conducting path is made by embedding a conducting polymer (PEDOT:PSS) within the paper, and thus making a paper/polymer composite that retains the porosity and hydrophilicity of paper. Different types of HEPAs (straight, precurved, and creased) achieved different types of motions (e.g., bending motion, accordion type motion). A theoretical model for their behavior is proposed. These actuators have been used for the manipulation of liquids and for the fabrication of an optical shutter. [ABSTRACT FROM AUTHOR]