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This study develops a simple and low-cost 3D paper-based analytical device (3D PAD) for the detection of available phosphate in soil. Epoxy resin is presented as a new hydrophobic material for low-cost mass production of PADs using the screen-printing method. An optimized concentration of epoxy resin solution is screen printed onto Whatman filter paper no. 1 in an easy one-step process to create hydrophobic patterns on PADs. The epoxy resin is air dried at room temperature, without heating or UV curing. This method delivers high reproducibility, resolution, and stability, and the epoxy resin barrier is compatible with both organic solvents and aqueous solutions. The molybdenum blue method is used in this PAD to measure phosphate in a colorimetric assay. The developed 3D PAD attains a linear range of 0.5-40 mg L

This work reports on the development and performance evaluation of newly developed paper sheets coated, on both sides, with thin films of biodegradable poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) for applications of food packaging. For this, PHBV/paper/PHBV multilayers were first prepared by the thermo-sealing technique, optimizing the process variables of temperature and time. Thereafter, the multilayer sheets were characterized in terms of their morphological, optical, thermal, mechanical, and barrier properties and compared with equivalent paper structures double coated with high-barrier multilayer films of petrochemical polymers. The results indicated that the double coatings of PHBV successfully improved the mechanical resistance and ductility, protected from moisture, and also reduced the aroma and oxygen permeances of paper, having a minimal effect on its optical and thermal properties. Finally, the compostability of the resultant multilayer sheets was analyzed, confirming that the presence of the PHBV coatings slightly delayed the aerobic biodegradation and disintegration of paper.

In this study, the effect of air plasma on the surface properties of printed and coated cardboard was investigated. The material was activated by low-pressure cold plasma for 1, 10, 20, and 30 s. Wettability changes on the surface were examined by contact angle measurements using the sessile droplet technique. The differences in the surface free energy were calculated using the Lifshitz–van derWaals/acid–base and Contact Angle Hysteresis approaches. Optical profilometry was used for the surface roughness evaluation and an X-ray photoelectron spectroscopy analysis was performed to find changes in surface chemistry. Adhesive strength tests were carried out to estimate the adhesion changes after the material’s modification. It was found that the water and formamide contact angles increased after the plasma treatment while the diiodomethane contact angle did not change. As a result of the modification, the surface free energy also increased significantly and the surface roughness increased. The pull-off tests confirmed the improvement in the material’s surface properties. Moreover, it was demonstrated that the optimal effect can be obtained after just 10 s of the plasma process.

In this paper we propose an approach for performing fault detection and identification in clock ensembles based on the generalized likelihood ratio test. We show that by applying a set of purposefully-designed statistical tests, one can successfully detect faults occurring in a clock of the ensemble, and identify which measurement in the ensemble is most likely to have triggered the detection. We first develop the theoretical framework for the characterization of the detectors and their performance, and validate the derivations via Monte Carlo simulations. Then, we apply the statistical tests to an ensemble of cesium clocks, aiming at detecting and identifying three types of non-nominal behaviors. The faulty conditions are obtained by injecting a pattern of phase steps, a phase and frequency drift, and an oscillatory phase component.

We present an x-ray Computed Tomography setup that integrates a seven degrees of freedom robotic arm as a sample holder within an existing laboratory x-ray computed tomography setup. We aim to provide a flexible sample holder that is able to execute non-standard and task-specific trajectories for complex samples. The robotic arm is integrated with a unified software package that allows for path planning, collision detection, geometric calibration and reconstruction of the sample. The calibration is necessary to identify the accurate pose of the sample which deviates from the expected pose due to inaccurate placement of the robotic arm. With our software the user is able to command the robotic arm to execute arbitrary trajectories for a given sample in a safe manner and output its reconstruction to the user. We present experimental results with a circular trajectory where the robotic sample holder achieves identical visual quality compared to a conventional sample holder.

We present a facile paper-based microfluidic device fabrication technique leveraging off-the-shelf carbon paper for the deposition of hydrophobic barriers using a novel "stencil scratching" method. This exceedingly frugal approach (0.05$) requires practically no technical training to employ. Hydrophobic barriers fabricated using this approach offer a width of 3 mm and a hydrophilic channel width of 849 μm, with an ability to confine major aqueous solvents without leakage. The utility of the device is demonstrated by porting a cell viability assay showing a limit-of-detection (LOD) of 0.6 × 108 CFU mL-1 and bilirubin assay with human serum showing a detection range of 1.76-6.9 mg dL-1 and a limit-of-detection (LOD) of 1.76 mg dL-1. The intuitiveness and economic viability of the fabrication method afford it great potential in the field of point-of-care diagnostics geared towards providing testing infrastructure in resource-scarce regions globally.

Membrane emulsification is a promising new technique that can be deployed as a scalable modular conduit for the consistent and continuous production of single and complex emulsions. This work reports on the development of a manufacturing platform based on membrane emulsification for the first time for microcapsule-based self-healing cementitious materials. The feasibility of single and double emulsion production with wall formation as a secondary step through UV radical polymerisation was explored using a discrete membrane emulsification dispersion cell. The operational parameters (pressure, dispersed phase flux, temperature, shear rate) were established for the specific phase characteristics (viscosity, density, interfacial tension) to achieve control of emulsion droplets and maintain a high encapsulation of core content (high payload). Microcapsules with sodium silicate core and an average diameter of ∼130 μm were produced. Microcapsules were shown to achieve high payload (∼89%). Moreover their thermal stability was characterised and their release performance in the cementitious matrix established. The results demonstrated the capability of membrane emulsification to produce microcapsules with an aqueous core for use in self-healing of cementitious materials.

Researchers from academia and the corporate-sector rely on scholarly digital libraries to access articles. Attackers take advantage of innocent users who consider the articles' files safe and thus open PDF-files with little concern. In addition, researchers consider scholarly libraries a reliable, trusted, and untainted corpus of papers. For these reasons, scholarly digital libraries are an attractive-target and inadvertently support the proliferation of cyber-attacks launched via malicious PDF-files. In this study, we present related vulnerabilities and malware distribution approaches that exploit the vulnerabilities of scholarly digital libraries. We evaluated over two-million scholarly papers in the CiteSeerX library and found the library to be contaminated with a surprisingly large number (0.3-2%) of malicious PDF documents (over 55% were crawled from the IPs of US-universities). We developed a two layered detection framework aimed at enhancing the detection of malicious PDF documents, Sec-Lib, which offers a security solution for large digital libraries. Sec-Lib includes a deterministic layer for detecting known malware, and a machine learning based layer for detecting unknown malware. Our evaluation showed that scholarly digital libraries can detect 96.9% of malware with Sec-Lib, while minimizing the number of PDF-files requiring labeling, and thus reducing the manual inspection efforts of security-experts by 98%.

Paper-based strain sensors have attracted attention as a cost-effective and environmentally friendly approach to wearable electronic devices. This paper proposes a paper-based strain sensor created solely using hand-painting, which is a simple, equipment-free process utilized in green electronics. Commercial printing paper is coated with polydimethylsiloxane diluted with heptane, which provides moisture resistance and mechanical robustness while increasing the hydrophobicity of the surface. The electrodes and conduction channels are fabricated using a pencil for graphite deposition and a brush for the deposition of tin-doped indium oxide nanoparticles, respectively. With a gauge factor of 41.98 in tensile strain tests and 21.36 in compressive strain tests, our strain sensor exhibits a good sensitivity that is similar to that of previously reported paper-based sensors. We also demonstrate that our proposed strain sensor can be used as a weak motion detection device for humans and robots.

Molecular simulation technology is a new technology emerging with the rapid development of computer technology. It has the advantages of clear microscopic models, in-depth and precise calculation etc., it has been widely used in the oil–paper insulation system of transformer in recent years. Based on the application of molecular simulation technology in the oil–paper insulation system of transformers in this study, the current research status and progress of molecular simulation in these area are elaborated in detail from the aspects of transformer insulating oil and insulating paper according to the domestic and foreign literature, and the application of molecular simulation technology in plant insulating oil and nano-modified insulating oil is emphatically analysed. The complementing research method of molecular simulation and experiment is pointed out, which provides certain reference for solving many problems existing in the field of oil–paper insulation system of transformers.

Colorimetric tests for at-home health monitoring became popular 50 years ago with the advent of the urinalysis test strips, due to their reduced costs, practicality, and ease of operation. However, developing digital systems that can interface these sensors in an efficient manner remains a challenge. Efforts have been put towards the development of portable optical readout systems, such as smartphones. However, their use in daily settings is still limited by their error-prone nature associated to optical noise from the ambient lighting, and their low sensitivity. Here, a smartphone application (Colourine) to readout colorimetric signals was developed on Android OS and tested on commercial urinalysis test strips for pH, proteins, and glucose detection. The novelty of this approach includes two features: a pre-calibration step where the user is asked to take a photo of the commercial reference chart, and a CIE-RGB-to-HSV color space transformation of the acquired data. These two elements allow the background noise given by environmental lighting to be minimized. The sensors were characterized in the ambient light range 100-400 lx, yielding a reliable output. Readouts were taken from urine strips in buffer solutions of pH (5.0-9.0 units), proteins (0-500 mg dL(-1)) and glucose (0-1000 mg dL(-1)), yielding a limit of detection (LOD) of 0.13 units (pH), 7.5 mg dL(-1) (proteins) and 22 mg dL(-1) (glucose), resulting in an average LOD decrease by about 2.8 fold compared to the visual method., Engineering and Physical Sciences Research Council (EPSRC) New Investigator Award; Central Universities Fundamental Research Funds; KU-KAIST Joint Research Center; Sandooq Al Watan LLC (SWARD)

Plasmonic metafilms have been widely utilized to generate vivid colors, but making them both active and flexible simultaneously remains a great challenge. Here flexible active plasmonic metafilms constructed by printing electrochromic nanoparticles onto ultrathin metal films (, Commercially available printing techniques offer fullyprinted flexible plasmonic metafilms, which show electrically‐tunable omni‐ or bi‐directional color dynamics engineered with structural geometries. Such activelycontrolled directional color dynamics in flexible plasmonics significantly unlocks the full potential of plasmonics for flexible/wearable devices.

Microfluidic magnetophoresis is a powerful technique that is used to separate and/or isolate cells of interest from complex matrices for analysis. However, mechanical pumps are required to drive flow, limiting portability and making translation to point-of-care (POC) settings difficult. Microfluidic paper-based analytical devices (μPADs) offer an alternative to traditional microfluidic devices that do not require external pumps to generate flow. However, μPADs are not typically used for particle analysis because most particles become trapped in the porous fiber network. Here we report the ability of newly developed fast-flow microfluidic paper-based analytical devices (ffPADs) to perform magnetophoresis. ffPADs use capillary action in a gap between stacked layers of paper and transparency sheets to drive flow at higher velocities than traditional μPADs. The multi-layer ffPADs allow particles and cells to move through the gap without being trapped in the paper layers. We first demonstrate that ffPADs enable magnetic particle separations in a μPAD with a neodymium permanent magnet and study key factors that affect performance. To demonstrate utility, E. coli was used as a model analyte and was isolated from human urine before detection with a fluorescently labeled antibody. A capture efficiency of 61.5% was then obtained of E. coli labeled magnetic beads in human urine. Future studies will look at the improvement of the capture efficiency and to make this assay completely off-chip without the need of a fluorescent label. The assay and device described here demonstrate the first example of magnetophoresis in a paper based, pump free microfluidic device.

β-Agonists are illegal feed additives in the feed industries of many countries, especially China. Here, we report a microfluidic paper-based analytical device (μPAD) coupled with the chemiluminescence (CL) method to provide the sensitive, simple and rapid quantitative detection of β-agonists in swine hair samples. In this study, we found that the β-agonists diminished the CL generated by the reaction of K3[Fe(CN)6] and luminol on μPAD, which was different from that observed in the aqueous solution, and the degree of diminishment was proportional to the concentration of β-agonists. The possible mechanism was discussed as well. Also, this detection method showed a wide linear range (from 4.0 × 10-8 to 1.0 × 10-5 mol L-1) and low limit of detection (2.0 × 10-8 mol L-1) with a low consumption of samples and reagents. Satisfactory recovery values (from 78% to 95%) were achieved. Therefore, our μPAD CL sensor will be favorable to develop a miniaturized instrument for the on-site analysis of β-agonists in swine hair samples.

Caused by the tick-borne spirochete Borrelia burgdorferi, Lyme disease (LD) is the most common vector-borne infectious disease in North America and Europe. Though timely diagnosis and treatment are effective in preventing disease progression, current tests are insensitive in early stage LD, with a sensitivity of $400/test) and extended sample-to-answer timelines (>24 h). To address these challenges, we created a cost-effective and rapid point-of-care (POC) test for early-stage LD that assays for antibodies specific to seven Borrelia antigens and a synthetic peptide in a paper-based multiplexed vertical flow assay (xVFA). We trained a deep-learning-based diagnostic algorithm to select an optimal subset of antigen/peptide targets and then blindly tested our xVFA using human samples (N(+) = 42, N(-) = 54), achieving an area-under-the-curve (AUC), sensitivity, and specificity of 0.950, 90.5%, and 87.0%, respectively, outperforming previous LD POC tests. With batch-specific standardization and threshold tuning, the specificity of our blind-testing performance improved to 96.3%, with an AUC and sensitivity of 0.963 and 85.7%, respectively.

C.-Y.K. and C.-H.L. contributed equally to this work. This publication was financially supported by the Ministry of Science and Technology, Taiwan (MOST) (107-2221-E-009-113-MY3), the King Abdullah University of Science and Technology (KAUST) Office of Sponsored Research (OSR) (OSR-2016-CRG5-3005), the KAUST Solar Center, KAUST Catalysis Center, and KAUST baseline funding. The authors would like to thank Prof. Nakamura Shuji of University of California, Santa Barbara and Dr. Lin Chien-Chung of the Industrial Technology Research Institute, Taiwan for the helpful discussion, and express sincere gratitude to Everlight Electronics for helpful technical support with the LED devices.

We report the development of a surface-enhanced Raman spectroscopy sensor chip by decorating gold nanoparticles (AuNPs) on ZnO nanorod (ZnO NR) arrays vertically grown on cellulose paper (C). We show that these chips can enhance the Raman signal by 1.25 × 107 with an excellent reproducibility of 92% clinical sensitivity and specificity. Our technology has the potential to be used for the early detection of prenatal diseases and can be adapted for point-of-care applications.

An important step in the conservation of old paper documents is the analysis of both the medium and the ink, in an attempt first to determine the extent of deterioration and degradation and then to choose the best preservation and restoration solutions. Our paper focuses on the analysis of three old documents displayed at the ‘Poni-Cernătescu’ Museum in Iaşi City, Romania by optical microscopy (OM), scanning electron microscopy and energy dispersive X-ray spectroscopy (SEM-EDX), micro-FTIR spectroscopy and FT-Raman. Thus, the morphology and chemical composition of the paper media and the type of ink, as well as the cellulose crystallinity index were determined. PCA (Principal Component Analysis) was also used while relying on spectra collected by FTIR spectroscopy. We were able to determine the extent of degradation of the documents by corroborating all these findings.

This work presents a comprehensive study on the behaviour and operation of a vertical 1.2 kV 4H-SiC junctionless power FinFET. The increased bulk conduction in the channel of this topology may bring reductions in the channel resistance compared to trench MOSFETs, whose performance is limited by the high interface state density. For this purpose, finite element (FE) simulations are used to examine the operation of this device. It is hence demonstrated that the junctionless FinFET can attain a high average channel drift mobility well above 100 cm2/(Vs), leaving the resistance to be determined by the drift and substrate regions. This allows the FinFET to turn on and reach its steady state current using a much (> 3x) smaller gate overdrive than standard designs. On the other hand, however, the overly high field in the gate oxide, the lack of an efficient mechanism for hole extraction, and the low threshold voltage can cause significant reliability issues. Furthermore, it is shown that the high input capacitance of the FinFET can limit its switching speed to slower levels than in standard trench MOSFETs, which raises the need for further development of the original design proposed for vertical GaN devices. In this context, it is demonstrated that the addition of a p-shield below the trenches can alleviate the off-state reliability issues and increase the speed, while still maintaining a competitive R on ∼ 2mΩ cm2 even without the use of n-JFET enhancement doping.

This paper presents a Switch-Mode Assisted Linear Amplifier (SMALA) designed for use as a Frequency Domain Spectroscopy (FDS) excitation voltage source for the diagnostic testing of oil/paper insulation systems in large power transformers. The developed voltage source has a low output voltage noise level, low harmonic content and is capable of driving highly capacitive loads with a maximum output voltage of 800 Vp-p in the frequency range of DC to 100 Hz current limited to 20 mA. Disturbances in the output voltage associated with switching of the main switching amplifier are minimised through the control of the switching time, taking the slew rate of the correction amplifier into account. The switching time of the main switching amplifier can be effectively controlled using a combination of a simple RC filter on the output of the main switching amplifier and controlling the rise-time and fall-time of the MOSFET gate drive voltage. Using the developed SMALA unit, it was possible to perform FDS measurement on an oil/paper insulated transformer at elevated excitation voltage. This resulted in a non-linear response current manifesting as odd harmonics in the measured current.

Near Infrared Spectroscopy (NIRS), as one of analysis technologies, has shown promisingly industrial applications for significant properties for recent decades such as fast response, preciseness, non-intrusion etc. Here, the authors employed NIRS coupled with a series of physical and chemical tests to assess the ageing condition of oil-paper insulation, which is responsible for the main insulation type of high-voltage power transformer. Among these procedures, the data analytic algorithms are of utmost importance to determine the evaluation precision. After plenty of trial-and-error, Savitzky-Golay (S-G) convolution was finally utilised to de-noise samples and improve the spectral data quality. The competitive adaptive reweighted sampling (CARS) was used to select the optimal wavelength combination of NIRS, which is found able to fully extract the effectively spectral information and reduce dimensions of spectral data. Based on the above-mentioned techniques, the quantitative analysis model of NIRS was established by partial least squares (PLS), which could synthetically process the spectral data and the degree of polymerisation (DP) of paper samples. The results indicated that compared with the traditional detection methods, the NIRS analysis is a powerful and informative tool to characterise the condition of oil-paper insulation without intrusion or damage to transformers.

Alzheimer's disease is a devastating condition characterized by a progressive and slow brain decay in elders. Here, we developed a paper-based lateral flow immunoassay for simultaneous and fast determination of Alzheimer's blood biomarkers, fetuin B and clusterin. Selective antibodies to targeted biomarkers were immobilized on gold nanoparticles (AuNPs) and deposited on paper pads. After adding the sample on the paper-based device, the biofluid laterally flows toward the selective antibody, permitting AuNP-Ab accumulation on the test zone, which causes a color change from white to pink. Image analysis was performed using a customized algorithm for the automatic recognition of the area of analysis and color clustering. Colorimetric detection was compared to electrochemical methods for the precise quantification of biomarkers. The best performance was found for the color parameter "L*". Good linearity (R2 = 0.988 and 0.998) and reproducibility (%RSD = 2.79% and 1.82%, N = 3) were demonstrated for the quantification of fetuin B and clusterin, respectively. Furthermore, the specificity of the immunosensor was tested on mixtures of proteins, showing negligible cross-reactivity and good performance in complex environments. We believe that our biosensor has a potential for early-stage diagnosis of Alzheimer's disease and toward a better understanding of Alzheimer's developing mechanisms.

Perovskite quantum dots (PQDs) are a competitive candidate for next‐generation display technologies as a result of their superior photoluminescence, narrow emission, high quantum yield, and color tunability. However, due to poor thermal resistance and instability under high energy radiation, most PQD‐based white light‐emitting diodes (LEDs) show only modest luminous efficiency of ≈50 lm W−1 and a short lifetime of, Perovskite quantum dot paper, a new type of perovskite quantum dot film, is demonstrated. Using a simple, fast, scalable, and inexpensive paper fabrication process, the resulting perovskite quantum dot paper is uniform, of high quality, and very stable; it is able to bear high energy radiation and greatly improve the efficiency of perovskite quantum dot–based white light‐emitting diodes.

With a host of new materials being investigated as active layers in organic electrochemical transistors (OECTs), several advantageous characteristics can be utilized to improve transduction and circuit level performance for biosensing applications. Here, the subthreshold region of operation of one recently reported high performing OECT material, poly(2‐(3,3′‐bis(2‐(2‐(2‐methoxyethoxy)ethoxy)ethoxy)‐[2,2′‐bithiophen]‐5‐yl)thieno[3,2‐b]thiophene), p(g2T‐TT) is investigated. The material's high subthreshold slope (SS) is exploited for high voltage gain and low power consumption. An ≈5× improvement in voltage gain (A V) for devices engineered for equal output current and 370× lower power consumption in the subthreshold region, in comparison to operation in the higher transconductance (g m), superthreshold region usually reported in the literature, are reported. Electrophysiological sensing is demonstrated using the subthreshold regime of p(g2T‐TT) devices and it is suggested that operation in this regime enables low power, enhanced sensing for a broad range of bioelectronic applications. Finally, the accessibility of the subthreshold regime of p(g2T‐TT) is evaluated in comparison with the prototypical poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS), and the role of material design in achieving favorable properties for subthreshold operation is discussed.

Cellulose nanopapers have gained significant attention in recent years as large-scale reinforcement for high-loading cellulose nanocomposites, substrates for printed electronics and filter nanopapers for water treatment. The mechanical properties of nanopapers are of fundamental importance for all these applications. Cellulose nanopapers can simply be prepared by filtering a suspension of nanocellulose, followed by heat consolidation. It was already demonstrated that the mechanical properties of cellulose nanopapers can be tailored by the fineness of the fibrils used or by modifying nanocellulose fibrils for instance by polymer adsorption, but nanocellulose blends remain underexplored. In this work, we show that the mechanical and physical properties of cellulose nanopapers can be tuned by creating nanopapers from blends of various grades of nanocellulose, i.e. (mechanically refined) bacterial cellulose or cellulose nanofibrils extracted from never-dried bleached softwood pulp by chemical and mechanical pre-treatments. We found that nanopapers made from blends of two or three nanocellulose grades show synergistic effects resulting in improved stiffness, strength, ductility, toughness and physical properties. This article is part of a discussion meeting issue ‘New horizons for cellulose nanotechnology’.

A crucial requirement for most engineering materials is the excellent balance of strength and toughness. By mimicking the hybrid hierarchical structure in nacre, a kind of nacre-like paper based on binary hybrid graphene oxide (GO)/sodium alginate (SA) building blocks has been successfully fabricated. Systematic evaluation for the mechanical property in different (dry/wet) environment/after thermal annealing shows a perfect combination of high strength and toughness. Both of the parameters are nearly many-times higher than those of similar materials because of the synergistic strengthening/toughening enhancement from the binary GO/SA hybrids. The successful fabrication route offers an excellent approach to design advanced strong integrated nacre-like composite materials, which can be applied in tissue engineering, protection, aerospace, and permeable membranes for separation and delivery.

Q-switched and mode-locked erbium-doped fibre lasers (EDFLs) are demonstrated by using non-conductive graphene oxide (GO) paper as a saturable absorber (SA). A stable and self-starting Q-switched operation was achieved at 1534.4 nm by using a 0.8 m long erbium-doped fibre (EDF) as a gain medium. The pulse repetition rate changed from 14.3 to 31.5 kHz, whereas the corresponding pulse width decreased from 32.8 to 13.8 µs as the pump power increased from 22 to 50.5 mW. A narrow spacing dual-wavelength Q-switched EDFL could also be realised by including a photonics crystal fibre and a tunable Bragg filter in the setup. It can operate at a maximum repetition rate of 31 kHz, with a pulse duration of 7.04 µs and pulse energy of 2.8 nJ. Another GOSA was used to realise mode-locked EDFL in a different cavity consisting of a 1.6 m long EDF in conjunction with 1480 nm pumping. The laser generated a soliton pulse train with a repetition rate of 15.62 MHz and pulse width of 870 fs. It is observed that the proposed fibre lasers have a low pulsing threshold pump power as well as a low damage threshold.

In this work, we report transistors made of van der Waals materials on a mesoporous paper with a smooth nanoscale surface. The aqueous transistor has a novel planar structure with source, drain, and gate electrodes on the same surface of the paper, while the mesoporous paper is used as an electrolyte reservoir. These transistors are enabled by an all-cellulose paper with nanofibrillated cellulose (NFC) on the top surface that leads to an excellent surface smoothness, while the rest of the microsized cellulose fibers can absorb electrolyte effectively. Based on two-dimensional van der Waals materials, including MoS2 and graphene, we demonstrate high-performance transistors with a large on-off ratio and low subthreshold swing. Such planar transistors with absorbed electrolyte gating can be used as sensors integrated with other components to form paper microfluidic systems. This study is significant for future paper-based electronics and biosensors.

Pressure sensors should have an excellent sensitivity in the range of 0–20 kPa when applied in wearable applications. Traditional pressure sensors cannot achieve both a high sensitivity and a large working range simultaneously, which results in their limited applications in wearable fields. There is an urgent need to develop a pressure sensor to make a breakthrough in both sensitivity and working range. In this paper, a graphene-paper pressure sensor that shows excellent performance in the range of 0–20 kPa is proposed. Compared to most reported graphene pressure sensors, this work realizes the optimization of sensitivity and working range, which is especially suitable for wearable applications. We also demonstrate that the pressure sensor can be applied in pulse detection, respiratory detection, voice recognition, as well as various intense motion detections. This graphene-paper pressure sensor will have great potentials for smart wearable devices to achieve health monitoring and motion detection.

Assembly of electrochemically active materials into paper‐based electrodes opens up new opportunities for flexible energy storage devices. Yat Li and co‐workers review the recent advances in the synthesis of paper‐based electrodes, including paper‐supported electrodes and paper‐like electrodes in article 1700107. Their structural features, electrochemical performances and implementationas electrodes for flexible energy storage devices are highlighted and discussed.

The development of solid materials which are able to upconvert optical radiation into photons of higher energy is attractive for many applications such as photocatalytic cells and photovoltaic devices. However, to fully exploit triplet-triplet annihilation photon energy upconversion (TTA-UC), oxygen protection is imperative because molecular oxygen is an ultimate quencher of the photon upconversion process. So far, reported solid TTA-UC materials have focused mainly on elastomeric matrices with low barrier properties because the TTA-UC efficiency generally drops significantly in glassy and semicrystalline matrices. To overcome this limit, for example, combine effective and sustainable annihilation upconversion with exhaustive oxygen protection of dyes, we prepare a sustainable solid-state-like material based on nanocellulose. Inspired by the structural buildup of leaves in Nature, we compartmentalize the dyes in the liquid core of nanocellulose-based capsules which are then further embedded in a cellulose nanofibers (NFC) matrix. Using pristine cellulose nanofibers, a sustainable and environmentally friendly functional nanomaterial with ultrahigh barrier properties is achieved. Also, an ensemble of sensitizers and emitter compounds are encapsulated, which allow harvesting of the energy of the whole deep-red sunlight region. The films demonstrate excellent lifetime in synthetic air (20.5/79.5, O2/N2)-even after 1 h operation, the intensity of the TTA-UC signal decreased only 7.8% for the film with 8.8 μm thick NFC coating. The lifetime can be further modulated by the thickness of the protective NFC coating. For comparison, the lifetime of TTA-UC in liquids exposed to air is on the level of seconds to minutes due to fast oxygen quenching.

Ionic polymer actuators driven by electrical stimuli have been widely investigated for use in practical applications such as bioinspired robots, sensors, and biomedical devices. However, conventional ionic polymer-metal composite actuators have a serious drawback of poor durability under long-term actuation in open air, mainly because of the leakage of the inner electrolyte and hydrated cations through cracks in the metallic electrodes. Here, we developed a highly durable and water-floatable ionic polymer artificial muscle by employing hydrophobic and asymmetrically laser-scribed reduced graphene oxide paper electrodes (HLrGOP). The highly conductive, flexible, and cost-effective HLrGOP electrodes have asymmetrically smooth hydrophobic outer and rough inner surfaces, resulting in liquid-impermeable and water-floatable functionalities and strong bonding between an ionic polymer and the electrodes. More interestingly, the HLrGOP electrode, which has a unique functionality to prevent the leakage of the vaporized or liquid electrolyte and mobile ions during electrical stimuli, greatly contributes to an exceptionally durable ionic polymer-graphene composite actuator that is a prerequisite for practical applications in active biomedical devices, biomimetic robots, touch-feedback haptic systems, and flexible soft electronics.

Cellulose fibers with porous structure and electrolyte absorption properties are considered to be a good potential substrate for the deposition of energy material for energy storage devices. Unlike traditional substrates, such as gold or stainless steel, paper prepared from cellulose fibers in this study not only functions as a substrate with large surface area but also acts as an interior electrolyte reservoir, where electrolyte can be absorbed much in the cellulose fibers and is ready to diffuse into an energy storage material. We demonstrated the value of this internal electrolyte reservoir by comparing a series of hierarchical hybrid supercapacitor electrodes based on homemade cellulose paper or polyester textile integrated with carbon nanotubes (CNTs) by simple solution dip and electrodeposited with MnO2. Atomic layer deposition of Al2O3 onto the fiber surface was used to limit electrolyte absorption into the fibers for comparison. Configurations designed with different numbers of ion diffusion pathways were compared to show that cellulose fibers in paper can act as a good interior electrolyte reservoir and provide an effective pathway for ion transport facilitation. Further optimization using an additional CNT coating resulted in an electrode of paper/CNTs/MnO2/CNTs, which has dual ion diffusion and electron transfer pathways and demonstrated superior supercapacitive performance. This paper highlights the merits of the mesoporous cellulose fibers as substrates for supercapacitor electrodes, in which the water-swelling effect of the cellulose fibers can absorb electrolyte, and the mesoporous internal structure of the fibers can provide channels for ions to diffuse to the electrochemical energy storage materials.

Progress of carbon nanotube (CNT) research and development in terms of published papers and patents is reported. Developments concerning CNT structures, synthesis, and major parameters, in terms of the published documents are surveyed. Publication growth of CNTs and related fields are analyzed for the period of 2000–2010. From the explored search term, “carbon nanotubes”, the total number of papers containing the CNT concept is 52,224, and for patents is 5,746, with a patent/paper ratio of 0.11. For CNT research in the given period, an annual increase of 8.09% for paper and 8.68% for patents are resulted. Published papers for CNT, CVD and CCVD synthesis parameters for the period of 2000–2010 are compared. In other research, publications for CNT laser synthesis, for the period of 2000–2010, are reviewed. Publications for major laser parameters in CNT synthesis for the period of 2000–2010 are described. The role of language of the published references for CNT research for the period of 2000–2010 is also investigated. Published papers/patents in English, Japanese, Chinese, Russian, German, French, Polish, and Spanish languages are compared. As expected, the number of paper/patent publications in English dominates other languages.

High-performance graphene nanopapers are prepared from an aqueous solution of functional graphenes with benzenesulfonic acid groups via covalent bonds. The formed hydrophobic graphene nanopapers showed the highest tensile strength of 360 MPa and Young's modulus of 102 GPa for samples with 13.7 wt % functional group and annealed at 150 °C. These samples showed a high electrical conductivity of 4.45 × 10(4) S/m after being annealed at 250 °C. The aforementioned properties of graphene nanopapers are much higher than any previously reported data. The properties of nanopapers depend on the degree of functionality on graphenes and the annealing temperatures, which are further evidenced by X-ray photoelectron spectroscopy, FTIR, and X-ray diffraction patterns. Such unique nanopapers can be easily bounded and sandwiched onto any solid surface to give rise to great potentials in many applications such as gas diffusion barriers, EMI shielding, thermal management, and anticorrosion.

The self-assembled nanostructures of carbon nanomaterials possess a damage-tolerable architecture crucial for the inherent mechanical properties at both micro- and macroscopic levels. Bone, or "natural composite," has been known to have superior energy dissipation and fracture resistance abilities due to its unique load-bearing hybrid structure. However, few approaches have emulated the desirable structure using carbon nanomaterials. In this paper, we present an approach in fabricating a hybrid composite paper based on graphene oxide (GO) and carbon nanotube (CNT) that mimicks the natural bone structure. The size-tuning strategy enables smaller GO sheets to have more cross-linking reactions with CNTs and be homogeneously incorporated into CNT-assembled paper, which is advantageous for effective stress transfer. The resultant hybrid composite film has enhanced mechanical strength, modulus, toughness, and even electrical conductivity compared to previously reported CNT-GO based composites. We further demonstrate the usefulness of the size-tuned GOs as the "stress transfer medium" by performing in situ Raman spectroscopy during the tensile test.

The mechanical properties of pristine graphene oxide paper and paper-like films of polyvinyl alcohol (PVA)-graphene oxide nanocomposite are investigated in a joint experimental-theoretical and computational study. In combination, these studies reveal a delicate relationship between the stiffness of these papers and the water content in their lamellar structures. ReaxFF-based molecular dynamics (MD) simulations elucidate the role of water molecules in modifying the mechanical properties of both pristine and nanocomposite graphene oxide papers, as bridge-forming water molecules between adjacent layers in the paper structure enhance stress transfer by means of a cooperative hydrogen-bonding network. For graphene oxide paper at an optimal concentration of ~5 wt % water, the degree of cooperative hydrogen bonding within the network comprising adjacent nanosheets and water molecules was found to optimally enhance the modulus of the paper without saturating the gallery space. Introducing PVA chains into the gallery space further enhances the cooperativity of this hydrogen-bonding network, in a manner similar to that found in natural biomaterials, resulting in increased stiffness of the composite. No optimal water concentration could be found for the PVA-graphene oxide nanocomposite papers, as dehydration of these structures continually enhances stiffness until a final water content of ~7 wt % (additional water cannot be removed from the system even after 12 h of annealing).

Significant enhancement in mechanical stiffness (10-200%) and fracture strength (approximately 50%) of graphene oxide paper, a novel paperlike material made from individual graphene oxide sheets, can be achieved upon modification with a small amount (less than 1 wt %) of Mg(2+) and Ca(2+). These results can be readily rationalized in terms of the chemical interactions between the functional groups of the graphene oxide sheets and the divalent metals ions. While oxygen functional groups on the basal planes of the sheets and the carboxylate groups on the edges can both bond to Mg(2+) and Ca(2+), the main contribution to mechanical enhancement of the paper comes from the latter.

Self-powered human-interactive but invisible electronics have many applications in anti-theft and anti-fake systems for human society. In this work, for the first time, we demonstrate a transparent paper-based, self-powered, and human-interactive flexible system. The system is based on an electrostatic induction mechanism with no extra power system appended. The self-powered, transparent paper device can be used for a transparent paper-based art anti-theft system in museums or for a smart mapping anti-fake system in precious packaging and documents, by virtue of the advantages of adding/removing freely, having no impairment on the appearance of the protected objects, and being easily mass manufactured. This initial study bridges the transparent nanopaper with a self-powered and human-interactive electronic system, paving the way for the development of smart transparent paper electronics.

We consider the constitutive law of paper and its relation to a spatially inhomogeneous, random paper structure, the so-called formation. Under biaxial tensile loading, paper may be taken as an elastic-plastic hardening material, modelled here by a hyperbolic tangent law. The fact that paper is a quasi-two-dimensional solid offers a chance to inspect its formation via a basis-weight distribution (mass per unit area), and then carry out cross-correlations of two planar fields: the formation versus the strain (or stress) field resulting from a fine-mesh finite-element simulation of a sheet of paper subjected to a specified in-plane loading. The simulation requires an assumption of constitutive coefficients as a function of formation, and the higher the resultant cross-correlation, the better the assumed constitutive law. With this methodology we conclude that the higher the basis-weight, the higher the local stiffness and strength of the paper (on millimetre scales) in two very different cases: a Crayola sketch-paper and a paperboard. We next set up a Boolean model of paper formation, where each grain plays the role of a floc of cellulose fibres. First, we employ a computational-mechanics fibre-network model to demonstrate the effects of formation on non-uniform strain fields in the elastic regime. Moving on to the inelastic regime, we treat flocs as continuum ellipses, and, employing the resulting relation between formation and constitutive coefficients, we study scale-dependent homogenization of paper and establish that the representative volume element in the sense of Hill (1963 J. Mech. Phys. Solids 11, 357-372) is approximately reached on scales about 10 times larger than the floc size.

Paper‐based materials are emerging as a new category of advanced electrodes for flexible energy storage devices, including supercapacitors, Li‐ion batteries, Li‐S batteries, Li‐oxygen batteries. This review summarizes recent advances in the synthesis of paper‐based electrodes, including paper‐supported electrodes and paper‐like electrodes. Their structural features, electrochemical performances and implementation as electrodes for flexible energy storage devices including supercapacitors and batteries are highlighted and compared. Finally, we also discuss the challenges and opportunity of paper‐based electrodes and energy storage devices.

We report the memory device on paper by means of an all-printing approach. Using a sequence of inkjet and screen-printing techniques, a simple metal–insulator–metal device structure is fabricated on paper as a resistive random access memory with a potential to reach gigabyte capacities on an A4 paper. The printed-paper-based memory devices (PPMDs) exhibit reproducible switching endurance, reliable retention, tunable memory window, and the capability to operate under extreme bending conditions. In addition, the PBMD can be labeled on electronics or living objects for multifunctional, wearable, on-skin, and biocompatible applications. The disposability and the high-security data storage of the paper-based memory are also demonstrated to show the ease of data handling, which are not achievable for regular silicon-based electronic devices. We envision that the PPMDs manufactured by this cost-effective and time-efficient all-printing approach would be a key electronic component to fully activate a paper-based circuit and can be directly implemented in medical biosensors, multifunctional devices, and self-powered systems.

We present a sequential, two-step procedure based on machine vision for detecting and characterizing impurities in paper. The method is based on a preliminary classification step to differentiate defective paper patches (i.e., with impurities) from non-defective ones (i.e., with no impurities), followed by a thresholding step to separate the impurities from the background. This approach permits to avoid the artifacts which occur when thresholding is applied to paper samples that contain no impurities. We discuss and compare different solutions and methods to implement the procedure and experimentally validate it on a datasets of 11 paper classes. The results show that a marked increase in detection accuracy can be obtained with the two-step procedure in comparison with thresholding alone.

We demonstrate all-solid-state flexible supercapacitors with high physical flexibility, desirable electrochemical properties, and excellent mechanical integrity, which were realized by rationally exploiting unique properties of bacterial nanocellulose, carbon nanotubes, and ionic liquid based polymer gel electrolytes. This deliberate choice and design of main components led to excellent supercapacitor performance such as high tolerance against bending cycles and high capacitance retention over charge/discharge cycles. More specifically, the performance of our supercapacitors was highly retained through 200 bending cycles to a radius of 3 mm. In addition, the supercapacitors showed excellent cyclability with C(sp) (~20 mF/cm(2)) reduction of only0.5% over 5000 charge/discharge cycles at the current density of 10 A/g. Our demonstration could be an important basis for material design and development of flexible supercapacitors.

The development of flexible electrodes is of considerable current interest because of the increasing demand for modern electronics, portable medical products, and compact energy devices. We report a modular approach to fabricating high-performance flexible electrodes by structurally integrating 2D-assemblies of nanoparticles with freestanding graphene paper. We have shown that the 2D array of gold nanoparticles at oil-water interfaces can be transferred on freestanding graphene oxide paper, leading to a monolayer of densely packed gold nanoparticles of uniform sizes loaded on graphene oxide paper. One major finding is that the postassembly electrochemical reduction of graphene oxide paper restores the ordered structure and electron-transport properties of graphene, and gives rise to robust and biocompatible freestanding electrodes with outstanding electrocatalytic activities, which have been manifested by the sensitive and selective detection of two model analytes: glucose and hydrogen peroxide (H(2)O(2)) secreted by live cells. The modular nature of this approach coupled with recent progress in nanocrystal synthesis and surface engineering opens new possibilities to systematically study the dependence of catalytic performance on the structural parameters and chemical compositions of the nanocrystals.

The unique combination of high surface area, high electrical conductivity and robust mechanical integrity has attracted great interest in the use of graphene sheets for future electronics applications. Their potential applications for high-power energy storage devices, however, are restricted by the accessible volume, which may be only a fraction of the physical volume, a consequence of the compact geometry of the stack and the ion mobility. Here we demonstrated that remarkably enhanced power delivery can be realized in graphene papers for the use in Li-ion batteries by controlled generation of in-plane porosity via a mechanical cavitation-chemical oxidation approach. These flexible, holey graphene papers, created via facile microscopic engineering, possess abundant ion binding sites, enhanced ion diffusion kinetics, and excellent high-rate lithium-ion storage capabilities, and are suitable for high-performance energy storage devices.

We demonstrate an interesting phenomenon that graphene can emit sound. The application of graphene can be expanded in the acoustic field. Graphene-on-paper sound source devices are made by patterning graphene on paper substrates. Three graphene sheet samples with the thickness of 100, 60, and 20 nm were fabricated. Sound emission from graphene is measured as a function of power, distance, angle, and frequency in the far-field. The theoretical model of air/graphene/paper/PCB board multilayer structure is established to analyze the sound directivity, frequency response, and efficiency. Measured sound pressure level (SPL) and efficiency are in good agreement with theoretical results. It is found that graphene has a significant flat frequency response in the wide ultrasound range 20-50 kHz. In addition, the thinner graphene sheets can produce higher SPL due to its lower heat capacity per unit area (HCPUA). The infrared thermal images reveal that a thermoacoustic effect is the working principle. We find that the sound performance mainly depends on the HCPUA of the conductor and the thermal properties of the substrate. The paper-based graphene sound source devices have highly reliable, flexible, no mechanical vibration, simple structure and high performance characteristics. It could open wide applications in multimedia, consumer electronics, biological, medical, and many other areas.

High mechanical performances of macroscopic graphene oxide (GO) papers are attracting great interest owing to their merits of lightweight and multiple functionalities. However, the loading role of individual nanosheets and its effect on the mechanical properties of the macroscopic GO papers are not yet well understood. Herein, we effectively tailored the interlayer adhesions of the GO papers by introducing small molecules, that is, glutaraldehyde (GA) and water molecules, into the gallery regions. With the help of in situ Raman spectroscopy, we compared the varied load-reinforcing roles of nanosheets, and further predicted the Young's moduli of the GO papers. Systematic mechanical tests have proven that the enhancement of the tensile modulus and strength of the GA-treated GO paper arose from the improved load-bearing capability of the nanosheets. On the basis of Raman and macroscopic mechanical tests, the influences of interlayer adhesions on the fracture mechanisms of the strained GO papers were inferred.

Graphene is a monolayer of tightly packed carbon atoms that possesses many interesting properties and has numerous exciting applications. In this work, we report the antibacterial activity of two water-dispersible graphene derivatives, graphene oxide (GO) and reduced graphene oxide (rGO) nanosheets. Such graphene-based nanomaterials can effectively inhibit the growth of E. coli bacteria while showing minimal cytotoxicity. We have also demonstrated that macroscopic freestanding GO and rGO paper can be conveniently fabricated from their suspension via simple vacuum filtration. Given the superior antibacterial effect of GO and the fact that GO can be mass-produced and easily processed to make freestanding and flexible paper with low cost, we expect this new carbon nanomaterial may find important environmental and clinical applications.

Electrophoretic displays (EPDs) have made their way into consumer products. EPDs enable displays that offer the look and form of a printed page, often called "electronic paper". We will review recent apparatus and method patents for EPD devices and their fabrication. A brief introduction into the basic display operation and history of EPDs is given, while pointing out the technological challenges and difficulties for inventors. Recently, the majority of scientific publications and patenting activity has been directed to micro-segmented EPDs. These devices exhibit high optical reflectance and contrast, wide viewing angle, and high image resolution. Micro-segmented EPDs can also be integrated with flexible transistors technologies into flexible displays. Typical particles size ranges from 200 nm to 2 micrometer. Currently one very active area of patenting is the development of full-color EPDs. We summarize the recent patenting activity for EPDs and provide comments on perceiving factors driving intellectual property protection for EPD technologies.