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A facile and feasible method for decoration of iron oxide (Fe3O4) submicron-sized particles on carbon paper at room temperature in a short time of 10 min is demonstrated in this work. The Fe3O4-particles decorated carbon papers were used as the negative electrode for an Fe-air rechargeable battery in both an alkaline aqueous solution system and an all-solid-state system. As for the all-solid-state Fe-air rechargeable battery, KOH-ZrO2 electrolyte powder developed by our group was used in the battery fabrication. In the alkaline aqueous solution based Fe-air rechargeable battery, a high initial discharge capacity of 460 mAh g−1(Fe) was achieved. Meanwhile, in the novel all-solid-state Fe-air rechargeable battery system, an initial discharge capacity of 70 mAh g−1(Fe) was obtained demonstrating the feasibility of this system that could be further developed towards a practical Fe-air rechargeable battery for portable and lightweight device application.

Here we report the construction of CoFe2O4 coating on carbon fiber and the coated paper was used as the interlayer between the separator and cathode of Li-S batteries. The amorphous CoFe2O4 coating was deposited by the industry-oriented spray pyrolysis technique and carbon fiber was completely enwrapped by the coating. Compared to the non-coated carbon fiber, the coated carbon fiber as the interlayer exhibits a superior reversible capacity of 1086 mA h g−1 at moderate current of 0.1C and a low decay rate in the capacity of 0.043% per cycle after 1000 cycles at 1C. Excellent long-term cycling life and rate capacity were also achieved through the coated interlayer. The specially designed interlayer showed remarkable capability to trap effectively the intermediate LPS (lithium polysulfide). The significantly inhibited “shuttle effect” of LPS would give insight into designing and making the interlayer by using new coating materials for enhanced performances of the Li-S batteries.

paper-like films of reduced graphene oxide with controllable shapes and thickness were prepared via funnel filtration and thermal reduction of graphene oxide (GO), which could work as flexible surface-enhanced Raman scattering (SERS) substrates to detect Rhodamine 6G (R6G) molecules. The SERS signal intensity of R6G on annealed films was found to be related with the annealling temperature. The most intense signal was observed for the film obtained at 800 °C. While for the sample annealed at 1000 °C, no SERS signal could be detected. The underlying mechanism for the difference was discussed. The reported preparation process of flexible rGO paper is simple and cost-effective, which shows great potential in rapid biochemical analysis of agricultural products with irregular surfaces.

As a typical membrane matrix with attractive flexibility, paper has exhibited great feasibility to serve as surface-enhanced Raman scattering (SERS) substrate in the environmental monitoring and surveillance. In this research, we have designed and fabricated a distinctive hydrophilic-hydrophobic SERS substrate utilizing several ordinary papers loaded with Ag nanowires (Ag NWs). Remarkable SERS activities with an enhancement factor (EF) up to 2.63 × 106 was successfully achieved in the assembly Ag NWs with the optimal amount of nanotips and overlaps. The hydrophilic-hydrophobic strategy could contribute to anchoring microdroplets and thus enrich analytes to improve the homogeneity of substrate with a low relative standard deviation of 10.6%. Furthermore, the sophisticated SERS substrate was also applied in the in-situ detection of trace furazolidone on fish under the interference of malachite green and the reliable recovery rates were demonstrated as well.

We presented a three-step method for the preparation of superhydrophobic cellulose filter paper. It involved ZnCl2 pre-treatment to activate the cellulose fibers, a SiO2 sol-gel process to increase surface roughness and grafting of hexadecyl trimethoxysilane groups to chemically enhance the water repellency. The water contact angle of the modified paper reached 154.8°. XRD analysis confirmed silica as the product from the sol-gel process. EDS and SEM analysis showed that pre-treatment results in greater silica adhesion and retention on the paper surface. The modified paper proved to be self-cleaning and resistant to staining. Further tests under various conditions showed that ZnCl2 pre-treatment improved the durability of the superhydrophobic paper. It was concluded that pre-treatment of the filter paper prior to superhydrophobic coating results in a disruption in the cellulose crystalline structure that favours greater silica adhesion and retention.

In this work, a facile method was developed to prepare reactive superhydrophobic paper by the attachment of 10-undecylenoyl chloride onto homogenized α-cellulose followed by one-step spray-coating of the resulting cellulose derivative (α-cellulose 10-undecylenoyl ester, CUE) onto filter paper. By spray-coating a CUE suspension with a concentration of 1.04 wt% for at least 6 mL, the paper surface became superhydrophobic, which had a water contact angle of 152 ± 2° with the advancing and receding angles of 165 ± 2° and 144 ± 2° and the slide angle of 6°. Additionally, the resulting surface showed a good durable stability, acid-base stability and thermal stability. More interestingly, an obvious photoclick thiol-ene reaction could be conducted on such superhydrophobic paper, which would further enlarge the application fields of superhydrophobic surfaces.

In this paper, an effective strategy using potassium dichromate lotion to activate surfaces of commercial carbon papers leading to enhanced electrochemical capacitances was reported. It is revealed that surfaces of activated carbon papers became rougher and their specific surface areas enlarged after treatment. Further, surface hydrophilicity of the treated carbon papers enhanced due to the generation of hydrophilic groups such as hydroxyl (–OH), carbonyl (〉C O) and carboxyl (–COOH) and they act as strong polar sites to absorb water molecules. With the synergistic effect of enlarged specific surface area and enhanced surface hydrophilicity, the activated carbon papers provide high areal capacitances. In general, this strategy offers a feasible pathway to make commercial carbon paper a promising candidate for practical supercapacitors and is expected to extend to other carbon based electrode materials.

In the current efficient energy focused society, metal–air batteries (MAB), which have high theoretical energy densities in comparison with other batteries have attracted tremendous attention for electronics and electric vehicle applications. Efficient utilization of the active material in the negative electrode with oxygen from air as the positive electrode could enable the development of a lightweight and portable metal-air battery with large energy density. Zinc (Zn), which is an abundant and inexpensive material that exhibits small voltage fluctuation during discharge as well as large discharge capacity in a liquid electrolyte-based battery system, is a good candidate as the active material in a MAB. Therefore, in this work, a Zn-air battery is fabricated and characterized using electroplated metallic Zn on carbon paper in order to increase the working contact area between Zn and the carbon paper which serves as the current collector. A near theoretical discharge capacity of 814 mAh g−1 (Zn) was achieved in an aqueous KOH liquid electrolyte system. Meanwhile, an all-solid-state Zn-air battery using a sol-gel-derived KOH-ZrO2 solid electrolyte was also fabricated which demonstrated an initial discharge capacity of 30 mAh g−1 (Zn).

Flexible nanohybrid paper electrode (termed as C-I) consisting of multi-walled carbon nanotubes (MWCNTs) and indium sulfide (In2S3) nanoplates is formed via a simple vacuum-assisted assembly and used as an anode for sodium-ion batteries (SIBs). In2S3 nanoplates which are well distributed on and bound to the MWCNTs provide a high Na storage capacity of the nanohybrid electrode as high as 410 mAh g−1 at a specific current of 50 mA g−1 over 100 charge/discharge cycles and ∼97% of rate-retention capability over the specific currents of 50 mA g−1 to 1 A g−1 for at least 50 charge/discharge cycles. Particularly, when In2S3 in the form of nanoplates was added to MWCNTs, the electrochemical performances are considerable as compared to those of bulk In2S3 or MWCNTs film electrodes. This highlights the importance of nanohybrid approach in overcoming the intrinsic complication of In2S3, i.e., the agglomeration of In2S3 into bulk form during assembly, followed by annealing. For C-I nanohybrid electrode, capacitive contribution (∼95%) rather than insertion contribution (∼5%) is predominant during charge/discharge process. The nanohybrid paper electrode is robust and thus retains capacity even under repeated mechanical deformation (flat-bent-flat cycles), demonstrating the potential of the electrode being used for flexible and wearable energy storage.

Here, a novel, simple, cost-effective, environment-friendly, non-invasive and mediator free, reduced graphene oxide (RGO) modified paper-based biosensing platform was reported. A conductive platform was generated over the ivory paper sheet via in-situ reduction of graphene oxide. The conductivity of the RGO paper was found as 0.86 S cm−1. This substrate was used for deposition of cysteine capped gold nanoparticles (Cys-AuNPs) using electrophoretic deposition technique at 60 V for biosensing application. Scanning electron microscopic images show the deposition of Cys-AuNPs in the spherical bunch on the RGO paper. The Cys-AuNPs deposition on RGO paper was confirmed by energy-dispersive x-ray spectroscopy and X-ray photoelectron spectroscopy and used for immobilization of monoclonal antibodies. This paper-based immunosensor based on chronoamperometry technique has the ability of direct electron transfer without using any mediator. This platform can replace commercially available electrodes [Indium Tin Oxide (ITO) and fluorine-doped tin oxide (FTO)] coated glass substrate, glassy carbon and gold] for electronic and electrochemical applications including point-of-care (POC) devices.

Owing to the high specific surface area and easy accessability to targeting biomolecules, emerging non-noble-metal networks are developed as an ultra-active catalyst for molecular detection. In this work, a facile flexible enzyme-free glucose sensor with superior sensing performance has been successfully constructed by integrating laser-scribed carbon paper (LSCP) with copper network (CN). Remarkably, operation parameters are modeled and optimized by Central Composite Design (CCD) to obtain an optimal conductivity of 4.783 × 107 S·m−1 for CN. Due to the great electronic/ionic pathway between LSCP of ample active sites and CN of excellent conductivity, the disposable biosensor exhibits fast electron transfer kinetics. For glucose detection, LSCP/CN exhibits an excellent sensitivity of 3626.6 μA mM−1 cm−2, a wide linear range from 1 μM to 7.96 mM, an ultra-low detection limit of 30 nM (S/N = 3) as well as favorable reusability. Satisfactory anti-interference capacity to electro-active oxides and selectivity against carbohydrates studied for concentrations up to normal physiologic levels and higher concentrations are systematically investigated. The applications of glucose determination in human serum and perspiration samples are also successful, with recoveries of 100.8% (± 2.28%) and 92.1% (±3.61%), respectively. Experimentally, the current response of the LSCP/CN biosensor is resilient to mechanical deformation with less than 8% decay even after 1000 cycles of 1 mm repeated bending and 180° cyclical folding tests. As such, LSCP/CN can be applicable for flexible, attachable and potentially wearable biosensors to attain real-time physiological monitoring.

For lipid–hydrocolloid emulsion based film, the increase of lipid amount would improve its water vapor barrier property, but also reduce the mechanical strength of the film in the meantime thus leading to a compromised lipid content in the film. However, when the emulsion is coated on paper surface, more lipid could be used for emulsion preparation to enhance the moisture resistance without considering the weakened strength of the film induced by lipid, because the mechanical properties of emulsion coated paper is mainly governed by the strength of base paper instead of the coating layer. In this study, beeswax–chitosan emulsion was first prepared and then coated on paper surface to improve paper's water vapor barrier and water resistance properties. The range and variance analysis of orthogonal test design showed that the order of priorities of the factors accordingly was beeswax solid content, drying temperature and chitosan concentration. The effect of drying temperature on water vapor transmission rate (WVTR) and water contact angle of coated paper was further investigated using 1.2 wt% chitosan and 96% beeswax solid content in the coating layer. The results indicated that water vapor barrier property was in accordance with the density of the coating layer. Atomic force microscope (AFM) was also used to characterize the surface morphology and explain the hydrophobicity of beeswax–chitosan coated paper. It was found that surface beeswax particles melted to wrinkle at high drying temperatures, while roughness values maintained at micro-scale over the temperature range investigated.

A facile and cost-effective method was developed to create superhydrophobic surfaces onto a superhydrophilic commercial paper for the application of droplet splitting of microliter droplets into nano and sub-nano-liter droplets. The high wettability contrast of nearly 180° between the superhydrophobic region created via candle soot coated onto the patterned poly (dimethylsiloxane) and the paper causes the self-partitioning of a 1 µl droplet while sliding through the surface with a speed ranging from 0.001 to 7.3 mm/s. Additionally, the splitting of the droplet demonstrated for µl droplets of surface tension ranging from 72 mN/m to 38.5 mN/m. The plasmonic droplet assay for surface-enhanced Raman spectroscopy was fabricated via in-situ reduction of Ag nanoparticles onto the superhydrophilic region. The Raman scattering studies of methyl orange using the prepared substrates exhibit a limit of detection of 670 pM. Further, by using methyl orange as a probe molecule, selective detection of Hg2+ ions up to a concentration of 100 pM in nanoliter droplet volume is demonstrated. It is envisaged that these cost-effective plasmonic nanoliter droplet assays created via patterned superhydrophilic-superhydrophobic can find applications in high throughput screening, microfluidic bioassays, medical diagnosis.

For the important applications of gas identification related to specific diseases in healthcare, flexible gas sensors have attracted more attention. Among them, two-dimensional transition metal dichalcogenides (2D TMDs) have been known as good promising flexible gas-sensitive materials. While how to tightly attach 2D materials on flexible substrates is still challenging. Here, we propose an enhanced room-temperature flexible paper-substrate sensors based on 2D tungsten disulfide (WS2) with S defects, which are facilely synthesized by chemical exfoliation and vacuum filtration method. Structure characterization shows that most of the as-prepared 2D WS2 are within 3 layers. Spectroscopic characterization proves the existence of S defects on the surface of 2D WS2 produced by chemical exfoliation. The room-temperature (25 °C) NH3 gas sensitivity results show that the response intensity of 2D WS2 with rich S defects is nearly three times higher than the highly crystalline 2D WS2. The results of the flexible gas sensitivity indicate the fast response and high stability of our devices in breathing detection and bending experiments. Furthermore, the devices can effectively distinguish bending stress changes and gas-sensitive response signals at the same time, realizing multifunctional sensing detection. Our work will be a reference for fabricating flexible sensors based on 2D materials.

Lithium-sulfur (Li-S) batteries have remarkably high theoretical specific capacity as promising candidates for next-generation energy storage. However, the “polysulfides shuttle” effect hampers its commercial application. Here, we use a kind of rice paper as a raw material to get inorganic oxides doping carbon felt by the facile carbonization method, and then modified by a simple coating process using poly (fluorenyl ether ketone) and Super P slurry. The special structure of the carbon felt derived from rice paper and its modified layer endow the final electronic conductive interlayer with inherent polysulfides absorbents and ion Coulombic repulsion functions, respectively, which show synergistic effect for trapping polysulfides. As an interlayer of Li-S batteries, the obtained carbon felt/poly (fluorenyl ether ketone)& Super P (CFSS) interlayer shows excellent electrochemical performance in improving specific capacity and decreasing polarization. The batteries with CFSS interlayer exhibit a high capacity of 837 mA h g−1 at 2.0 C and a high initial capacity of 1073.4 mA h g−1 and good capacity retention of 824.5 mA h g−1 after 500 cycles at 0.5 C. CFSS interlayer also shows excellent anti-self-discharge performance. Therefore, the simple and economical CFSS interlayer can be considered as a promising component for high performance Li-S batteries.

Mechanically robust graphene papers with both high gravimetric and volumetric capacitances are desired for high-performance energy storages. However, it’s still a challenge to tailor the structure of graphene papers in order to meet this requirement. In this work, a kind of chemical-reduction-tailored mechanically-robust reduced graphene oxide/carbon nanotube hybrid paper has been reported for high-performance electrochemical capacitive energy storages. Gallic acid (GA), as an excellent reducing agent, was used to reduce graphene oxide. Through vacuum filtration of gallic acid reduced graphene oxide (GA-rGO) and carboxylic multiwalled carbon nanotubes (MWCNTs) aqueous suspensions, mechanically robust GA-rGO/MWCNTs hybrid papers were obtained. The resultant hybrid papers showed high gravimetric capacitance of 337.6 F g−1 (0.5 A g−1) and volumetric capacitance of 151.2 F cm−3 (0.25 A cm−3). In addition, the assembled symmetric device based on the hybrid papers exhibited high gravimetric capacitance of 291.6 F g−1 (0.5 A g−1) and volumetric capacitance of 136.6 F cm−3 (0.25 A cm−3). Meanwhile, it exhibited excellent rate capability and cycling stability. Above all, this chemical reduction tailoring technique and the resultant high-performance GA-rGO/MWCNTs hybrid papers give an insight for designing high-performance electrodes and hold a great potential in the field of energy storages.

Paper sheets are economic and sustainable materials alleviating the world’s reliance on petroleum plastics, yet the facile preparation of water-proof paper combing high strength with tunable surface properties is difficult. This work exploited a self-crosslinkable polyelectrolyte (poly[1-cyanomethyl-3-vinylimidazolium], PCMVIm) to circumvent this problem. The PCMVIm solution was filled into paper sheets, dried, and treated by mild ammonia (NH3) vapor at 25 °C. Paper sheets incorporated with 0.6 wt% PCMVIm were rendered water-proof (80 °C, 1 week) and acid-resistant (6 M HCl), exhibiting a wet strength that is 6 times higher than pristine paper without PCMVIm. In addition, the hydrophilicity and oleophilicity of NH3-treated paper were easily tuned by modulating the counter anions of PCMVIm. The modified paper sheets show high permeability, selectivity and stability in separating water/oil emulsions containing toluene, petroleum ether, hexane and chloroform, respectively. The facile method of NH3 vapor treatment confers wet-resistance, high strength, and tunable surface properties to paper valorization, leading to sustainable paper sheets for efficient oil/water separation.

Two organic–inorganic hybrid sol–gel coatings were developed in order to modify the surface energy and moisture behaviour of the commercial impregnated paper. The surface characteristics of the paper samples were studied by scanning electron microscopy (SEM), confocal laser scanning microscopy (CLSM), atomic force microscopy (AFM), attenuated total reflectance Fourier transform infrared spectrometry (ATR-FTIR), X-ray photoelectron spectroscopy (XPS) and time of flight secondary ion mass spectroscopy (ToF-SIMS). It was found that the applied sol–gel coatings as well as the curing process changed the surface structural and chemical properties of the impregnated paper. The chemical bonding between the hydroxyl groups present on paper surface and silanol groups from sol–gel coatings was confirmed by the FTIR spectra. The measured surface energies divided into polar and dispersive components indicated that the coating B resulted in less polar surface than did the coating A which was more polar than the reference (the impregnated paper with water and heat treatment). Coating B brought about the lowest total surface energy. It was obtained that the water repellence of the impregnated paper was improved by both coatings and the curing process.

Graphene oxide (GO) paper was treated in supercritical ethanol as a green route for its reduction, which was confirmed by Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis and conductivity measurements. The reduced GO paper showed good electrochemical properties. As a sole component of the anode in lithium ion batteries, its specific capacity was comparable to those of free standing GO papers reduced by hydrazine or carbon nanotube paper. The GO paper reduced by supercritical ethanol can be a potential candidate for a binder-free anode in high performance lithium batteries.

Tin-based compounds are potential anode materials for high performance lithium-ion batteries (LIBs). Due to the low melting point of metallic Sn, it is hard to maintain the crystal morphology of Sn during the as-follow process of carbon coating for high performance anode. In this work, the core@shell composite of SnOx@carbon (SnOx@C) is successfully fabricated on the substrate of carbon paper (CP) through electrodeposition and carbonization based on the precursor of Sn nanoparticles. A passivation shell is essentially grown onto Sn particles to obtain a stable structure of SnOx@C, otherwise the Sn particles will be pulverized and fell off the substrate of CP during the subsequent process of carbonization. The as-produced CP/SnOx@C film has excellent flexibility and mechanical stability to be directly served as electrode for LIBs. Carbon shell prevents the detachment and agglomeration of the active particles during lithiation/delithiation processes and maintains the stability of the conductive network. After 100th cycles, CP/SnOx@C electrode delivers 0.8 mAh cm−2, much higher than the capacity 0.37 mAh cm−2 of CP/Sn electrode operated at the current density of 0.1 mA cm−2. These features enable the flexible film of CP/SnOx@C to be attractive applications in energy storage devices.

Novel sensors based on fluorescent carbon dots were developed for a rapid, selective, and sensitive detection of pyrimethanil, a fungicide widely used in many agricultural crops. The carbon dots were synthesized from maleic anhydride and triethylenetetramine via a facile one-pot pyrolysis. A quenched fluorescence intensity of carbon dots in the presence of pyrimethanil occurred via inner filter effect and strong π-π interaction. The carbon dots were sensitive to pyrimethanil across a linear range from 0.5 to 75 µM with a low detection limit of 14 nM. The sensing results could be generated in 30 s. The fluorescent carbon dots showed excellent stability and selectivity to pyrimethanil in the presence of interferences, including fungicides and metal ions. They were also successfully employed for pyrimethanil detection in apples, cucumbers, and drinking water, yielding 98.6–107.1% recovery. The practical, portable, and reusable paper-based sensor was also developed. The cytotoxicity of carbon dots was tested to demonstrate that they are sufficiently safe to use. The novel pyrimethanil sensor based on fluorescent carbon dots developed in this work can be used as a high-performance sensor and a rapid tool for quality control in food, agricultural, and environmental monitoring.

Pigment-coated, surface-sized, and surface-sized copy papers were treated with conventional corona, experimental pilot-scale plasma and laboratory-scale plasma. All the treatments increased the surface energy and oxidized the surface. The changes in the surface chemistry depended on treatment time and composition of the substrate surface. It seems that plasma especially oxidizes the long polymer chains, such as surfactants and other paper chemicals, on the surface of the paper. The ToF-SIMS distribution maps indicated that the pilot-scale treatment led to an uneven CO+ group distribution, whereas laboratory scale treatment gave a more even distribution of CO+ groups. In addition to chemical changes, topographical changes due to plasma treatment were detected. The RMS roughness increased for pigment-coated paper, whereas plasma treatment induced small nodules between the paper pigment particles with pigmented and surface-sized paper. The increase in roughness was also found to increase the wettability. This serves as a demonstration of roughness-induced increase of surface energy of the samples.

Superhydrophobic paper with remarkable durability is of considerable interest for its practical applications. In this study, a scalable, inexpensive, and universal surface sizing technique was implemented to prepare superhydrophobic paper with enhanced durability. A thin layer of starch-based composite, acting as a bio-binder, was first coated onto the paper surface by a sophisticated manufacturing technique called surface sizing, immediately followed by a spray coating of hexamethyl disilazane treated silica nanoparticles (HMDS-SiNPs) dispersed in ethanol on the surface of the wet starch-coated sheet, and the dual layers dried at the same time. Consequently, durable superhydrophobic paper with bi-layer structure was obtained after air drying. The as-prepared superhydrophobic paper not only exhibited a self-cleaning behavior, but also presented an enhanced durability against scratching, bending/deformation, as well as moisture. The universal surface sizing of starch-based composites may pave the way for the up-scaled and cost-effective production of durable superhydrophobic paper.

Paper-based surface-enhanced Raman scattering (SERS) substrates receive a great deal of attention due to low cost and high flexibility. Herein, we developed an efficient SERS substrate by gravure printing of sulfonated reduced graphene-oxide (S-RGO) thin film and inkjet printing of silver nanoparticles (AgNPs) on weighing paper successively. Malachite green (MG) and rhodamine 6G (R6G) were chosen as probe molecules to evaluate the enhanced performance of the fabricated SERS-active substrates. It was found that the S-RGO/AgNPs composite structure possessed higher enhancement ability than the pure AgNPs. The Raman enhancement factor of S-RGO/AgNPs was calculated to be as large as 109. The minimum detection limit for MG and R6G was down to 10−7 M with good linear responses (R2 = 0.9996, 0.9983) range from 10−4 M to 10−7 M. In addition, the S-RGO/AgNPs exhibited good uniformity with a relative standard deviation (RSD) of 7.90% measured by 572 points, excellent reproducibility with RSD smaller than 3.36%, and long-term stability with RSD less than 7.19%.

Graphene-based all-solid-state supercapacitors (ASSSCs) have received increasing attention. It’s a great challenge to fabricate high-performance flexible solid-state supercapacitors with high areal and volumetric energy storage capability, superior electron and ion conductivity, robust mechanical flexibility, as well as long term stability. Herein, we report a facile method to fabricate flexible ASSSCs based on densely-packed reduced graphene oxide (rGO)/polypyrrole nanoparticle (PPy NP) hybrid papers with a sandwich framework, which consists of well-separated and continuously-aligned rGO sheets. The incorporation of PPy NPs not only provides pseudocapacitance but also facilitates the infiltration of gel electrolyte. The assembled ASSSCs possess maximum areal and volumetric specific capacitances of 477 mF/cm 2 and 94.9 F/cm 3 at 0.5 mA/cm 2 . They also exhibit little capacitance deviation under different bending states, excellent cycling stability, small leakage current and low self-discharge characteristics. Additionally, the maximum areal and volumetric energy densities of 132.5 μWh/cm 2 and 26.4 mWh/cm 3 are achieved, which indicate that this hybrid paper is a promising candidate for high-performance flexible energy storage devices.

The study reports on the preparation of polyacrylonitrile fiber paper (PANFP) functionalized with polydopamine (PD) and silver nanoparticles (Ag NPs), named as Ag NPs/PD/PANFP. The composite material was obtained via a simple two-step chemical process. First, a thin polydopamine layer was coated onto the PANFP surface through immersion into an alkaline dopamine (pH 8.5) aqueous solution at room temperature. The reductive properties of polydopamine were further exploited for the deposition of Ag NPs. The morphology and chemical composition of the composite material were characterized using scanning electron microscopy (SEM), X-ray diffraction pattern (XRD) and X-ray photoelectron spectroscopy (XPS). The catalytic activity of the nanocomposite was evaluated for the reduction of 4-nitrophenol using sodium borohydride (NaBH 4 ) at room temperature. The Ag NPs/PD/PANFP displayed good catalytic performance with a full reduction of 4-nitrophenol into the corresponding 4-aminophenol within 30 min. Moreover, the composite material exhibited a good stability up to 4 cycles without a significant loss of its catalytic activity.

A controlled monolayer-by-monolayer deposition process has been developed to fabricate Pt coating on carbon fiber paper with complex network structures using a dual buffer (Au/Ni) strategy. The X-ray diffraction, electrochemical quartz crystal microbalance, current density analyses, and X-ray photoelectron spectroscopy results conclude that the monolayer deposition process accomplishes full coverage on the substrate and that the thickness of the deposition layer can be controlled on a single atom scale. This development may pave a way to fabricate superior Pt catalysts with the minimal Pt usage. In fact, the present Pt group metal loading is 25 times lower than the U.S. DOE 2017 target value. (C) 2017 Elsevier B.V. All rights reserved.

Herein, we proposed a facile strategy for preparing well-distributed Sb-doped SnO2 nanoparticles on carbon paper (CP) via electrodeposition and in-situ oxidation as bifunctional electrodes for vanadium redox flow batteries. SnO2 and Sb-doped SnO2 modified carbon paper (CP-SnO2 and CP-SnO2/Sb) was respectively obtained by electrodepositing metals (Sn and Sn/Sb) nanoparticles, followed by a conversion to metal oxides with in-situ oxidation. CP-SnO2 exhibited better electrochemical performance toward V3+/V2+ and VO2+/VO2+ redox reactions than CP. This is because SnO2 increases active sites and hydrophilicity, which accelerates electrochemical kinetic and mass transfer for vanadium redox reactions. CP-SnO2/Sb had better electrochemical activity than CP-SnO2, because smaller Sb-doped SnO2 nanoparticles more effectively disperse through carbon fibers, producing more active sites. Furthermore, Sb doping improved conductivity of SnO2. Briefly, CP-SnO2/Sb exhibited excellent hydrophilicity, abundant active sites, and good conductivity, resulting in superior electrochemical activity. We next employed CP-SnO2/Sb as bifunctional electrodes in cell. The cell using CP-SnO2/Sb had better cycling stability and more capacity retention during a 50-cycle charge–discharge test at 50 mA cm−2. CP-SnO2/Sb reduced the electrochemical polarization of cell at higher current density. Overall, the cell using CP-SnO2/Sb showed a 9% increase in energy efficiency compared to pristine cell (64.5%) at 150 mA cm−2.

Graphene-based all-solid-state supercapacitors (ASSSCs) are one of the most ideal candidates for high-performance flexible power sources. The achievement of high volumetric energy density is highly desired for practical application of this type of ASSSCs. Here, we present a facile method to boost volumetric performances of graphene-based flexible ASSSCs through incorporation of ultrafine polyaniline-poly(4-styrenesulfonate) (PANI-PSS) nanoparticles in reduced graphene oxide (rGO) papers. A compact structure is obtained via intimate contact and π–π interaction between PANI-PSS nanoparticles and rGO sheets. The hybrid paper electrode with the film thickness of 13.5 μm, shows an extremely high volumetric specific capacitance of 272 F/cm3 (0.37 A/cm3 in a three-electrode cell). The assembled ASSSCs show a large volumetric specific capacitance of 217 F/cm3 (0.37 A/cm3 in a two-electrode cell), high volumetric energy and power density, excellent capacitance stability, small leakage current as well as low self-discharge characteristics, revealing the usefulness of this robust hybrid paper for high-performance flexible energy storage devices.

In this study, we report the simple fabrication of an active substrate assisted by gold nanostructures (AuNS) for application in surface-enhanced Raman scattering (SERS) using copier paper, which is a biodegradable and cost-effective material. As cellulose is the main component of paper, it can behave as a reducing agent and as a capping molecule for the synthesis of AuNS on the paper substrate. AuNS can be directly generated on the surface of the copier paper by addition of halides. The AuNS thus synthesized were characterized by ultraviolet–visible spectroscopy, SEM, XRD, and XPS. In addition, the SERS effect of the AuNS–paper substrates synthesized by using various halides was investigated by using rhodamine 6G and melamine as probe molecules.

In this work, a novel polymeric fluorescent brightener based on coumarin (PFBC) was synthesized, using three-step synthetic route, from 7-amino-4-methylcoumarin, coumarin monomer (FBC), Acrylamide (AM) and methacrylatoethyl trimethyl ammonium chloride (DMC). The structure of PFBC was characterized by FT-IR, 1HNMR and GPC. PFBC was applied to paper fiber as light stabilizer, fluorescent brightener and surface sizing agent and its performances were evaluated by measuring the UV–vis, fluorescence, thermal stability, the cationic degree, surface strength and smoothness of paper, the brightness degree of paper and the PC value of paper. Results showed that PFBC had better solubility in water than that of FBC, by measuring the optical properties. Through the surface sizing experiment and UV aging experiment, PFBC not only enhanced the surface strength and smoothness of paper as a surface sizing agent, but also had better effect on anti-UV aging than that of FBC as light stabilizer and fluorescent brightener.

The integration of flexible electronic sensors in clinical diagnostics is visioned to significantly reduce the cost of many diagnostic tests and ultimately make healthcare more accessible. This study concentrates on the characterisation of inkjet-printed bio-functionalised polythiophene films on paper-based ultrathin gold film (UTGF) electrodes and their possible application as biorecognition layers. Physicochemical surface properties (topography, chemistry, and wetting) and electrochemical characteristics of water-soluble regioirregular tetraethylene-glycol polythiophene (TEGPT) and biotin-functionalised TEGPT (b-TEGPT) films were examined and compared. In addition, their specificity towards streptavidin protein was tested. The results show that stable supramolecular biorecognition layers of insulating b-TEGPT and streptavidin were successfully fabricated on a paper-based UTGF by inkjet-printing. Good adhesion of thiophene to UTGF can be attributed to covalent linkage between sulphur and gold, whereas the stability of the streptavidin layer is due to the high affinity between biotin and streptavidin. The device introduced can be utilised in the development of biosensors for clinically relevant analytes e.g. for detecting complementary DNA oligomers or antibody–antigen complexes.

Lithium-sulfur (Li-S) battery is next generation battery technology but it’s commercialization is obstructed primarily due to the shuttling effect of lithium polysulfides (LiPSs). Herein, we report an effective approach using pencil coated pyrolyzed cellulose filter paper as an interlayer to suppress the LiPSs dissolution into the electrolyte and thus allowing effective utilization of active sulfur cathode. Here, the binder clay particles (mainly SiO2) of pencil graphite facilitate the adsorption of LiPSs, whereas graphite increases the electrical conductivity and acts as a physical barrier to LiPSs. To investigate further, we utilize three different grades of pencil (4B, HB, 5H) which vary in terms of clay (SiO2) composition. It is observed that the HB pencil coated interlayer has the right balance of silica and graphite, which results in an impressive initial capacity of 1352 and 995 mAh g−1 at the current density of 0.1 and 0.5 A g−1, respectively. The cell exhibit high cycling stability of 900 mAh g−1 at 1 A g−1 (3.0 C) for 350 cycles with a slow capacity decay of 0.07% per cycle. The phenomenon of LiPSs adsorption is further understood using post-cycling analysis, H-cell adsorption testing, and shuttle factor calculation for the development of commercial Li-S batteries.

The portable, low-cost and sensitive biosensors are essential for in vitro diagnostics. Here, with a highly porous poly( l -lactic) acid nanofiber membrane (p-PLLA), an efficient and sensitive bioassay is created for biomarker detection, giving out colorimetric and fluorescence dual signals. A sensitivity-enhancing strategy is achieved based on the high porosity, loading capacity of p-PLLA and gold nanoparticles-based signal amplification. Through a sandwich immunoreaction strategy, the gold nanoparticle-labeled detector antibodies accumulate on the p-PLLA membrane and show a naked-eye-readable red spot starting from a cut-off value of the target biomarker. After adding goat anti-mouse IgG/FITC antibody (IgG-FITC), which is bound to the detector antibody, the concentration of the target biomarker can be accurately calculated by the differences in fluorescence intensity of IgG-FITC solution before and after the immunoreaction. When the liver cancer marker (α-fetoprotein) is used as a model analyte, this bioassay performs with excellent convenience and a high level of sensitivity. The preset visual color mutation point is 10 ng mL−1 (cut-off value) and the limit of detection is 0.17 pg mL−1. It shows good prospects of screening cancer biomarkers and point-of-care diagnostics applications.

Visible laser cleaning of charcoal particulates from yellow acid mechanical ground wood cellulose paper was compared with that from bleached sulphite softwood cellulose paper. About one order of magnitude of fluence range is available for a cleaning dynamics between the cleaning threshold and the destruction threshold for two laser pulses. Wood cellulose paper exhibited a higher destruction threshold of the original paper than that of the contaminated specimen because of heat transfer from the hot or evaporating charcoal particulates. In contrast, the contaminated bleached cellulose paper exhibited a higher destruction threshold due to shading by the particulates. The graphite particles are not only detached thermo-mechanically, but also by evaporation or combustion. A cleaning effect was found also outside the illuminated areas due to lateral blasting. Infrared measurements revealed dehydration/dehydrogenation reactions and cross-links by ether bonds together with structural changes of the cellulose chain arrangement and the degree of crystallinity.

A superhydrophobic and superoleophilic coating for oil filter paper was synthesized based on waterborne bisphenol-A novolac epoxy emulsion. The benzoic acid (BA) and maleic anhydride (MA) were used as modification agents to give the epoxy resin hydrophilic groups (carboxyl) and C C double bonds. And the fluorinated waterborne epoxy emulsion was prepared by free radical solution polymerization of dodecafluoroheptyl methacrylate (DFMA) monomer. The covalent bound low free energy fluorinated chains in the monomer reduce the surface energy of solidification polymers sufficiently to give rise to superhydrophobic behavior while conserving superoleophilicity. Surfaces prepared show a sticky property, which exhibits a static water contact angle of 152° for a 5 μL droplet that does not slid off even when the sample is held upside down. This synthetic emulsion is simple and convenient as impregnating agent for filter paper, which can be considered as a suitable candidate for various substrates such as cotton textiles, E-glass and artificial fiber, and so on.

Red sealing-ink samples are frequently submitted to forensic laboratories for identification and comparison in a wide variety of criminal and civil cases. The non-destructive identification of sealing-inks on paper is of important to preserve as large an amount of a fraudulent check, forged document, or other such evidence as possible for use in legal proceedings. Time-of-flight secondary ion mass spectrometry (TOF-SIMS) for the analysis of red sealing-inks on paper surfaces was investigated. TOF-SIMS spectra were employed to identify elements and organic compounds in red sealing-inks. An analysis was performed on five sealing-inks of red color manufactured in Korea, Japan, and China. Several fibers from specific sealing-ink sample on paper can be removed leaving little evidence of tampering and can be distinguished from other sealing-inks. Overlapped area of sealing-ink and ballpoint pen in the document was also investigated in order to identify the sequence of recording. Therefore, this study shows that TOF-SIMS is a useful technique for the non-destructive analysis of red sealing-inks on paper.

Surface products of oil-impregnated insulation paper during the damage process caused by partial discharge (PD), as well as gas within the cavity, were studied. An optical microscope and a scanning electron microscope (SEM) were used to investigate surface morphology, while an infrared spectroscopy (IR) and an X-ray photoelectron spectroscopy (XPS) were used to study surface products and their components. The volume variation in cavity gas was also analyzed. Furthermore, gas constituents and their relevant contents were studied using a gas chromatography–mass spectrometer (GC–MS). The study results reveal the following: during the PD damage process, the total gas volume and the content of electronegative gasses alternately decline and increase, while discharge types alternate between pulse type and pseudo-glow type (or glow type); “surface droplets” and “crystalline solids” appear on the insulation surface one after another; surface droplets mainly consist of (C O)-group-containing compounds, whereas crystalline solids are mainly carboxylic acids, with carboxyl groups also found in cellulose chains; and the discharge type related to the oxidization of decomposition products is the main factor that determines the state (liquid or solid) of the surface products.

In thin film electronic applications, the limiting factor, in terms of cost and usability, is generally the substrate material. As a consequence, different materials are being investigated as potential lightweight, inexpensive and flexible substrates. In this respect, we have been the first research collaboration to produce silicon-based electronics on paper substrates. Here we present structural characterisation of hydrogenated amorphous silicon (a-Si:H) layers deposited on 80 g m −2 wood-free paper, with and without an intermediate metallic interlayer, using low temperature hot wire chemical vapour deposition (HW-CVD). Both pulsed positron beam profiling and X-ray diffraction studies indicate that the growth rate on the uncoated substrate is slightly higher than with prior metallization. There is no evidence of a crystalline phase or voids in the a-Si:H layers. The internal defect structure is similar, with a dominant dangling bond complex of similar size, which has a slightly longer lifetime than in layers grown at higher temperatures on conventional substrates.

Using a molecular fluorine laser at 157 nm foxing stains were removed successfully from a 16th century old paper. Laser cleaning of stains and foxing from old paper manuscripts is far more effective at 157 nm in comparison to different wavelengths without leaving any yellowish after-effect on the paper. This is because at 157 nm illumination of old paper, complete bond breaking of all the organic molecules of the paper is taking place. Mass spectroscopy at 157 nm and for moderate laser intensities up to 1 mJ/cm 2 of old paper suffering from foxing indicate organic matter disintegration to small photofragments atomic, diatomic or triatomic, which are flying apart with supersonic speed. In addition high spatial resolution energy dispersive X-ray system (EDXS) analysis over the effected areas indicate the presence of iron, suggesting that biological activity is taking place preferentially in paper areas containing iron.

The interactions of SO 2 and O 3 with fresh or aged bleached softwood pulp have been investigated using two techniques. The dry deposition of SO 2 (g) on paper was studied using on-line gas analysis. Diffuse Reflectance Infrared Fourier Transform (DRIFT) spectrometry was applied in situ to characterise the paper surface during exposure to the pollutants. The DRIFT technique is shown to be sensitive enough to measure very small changes on the paper surface. The initial reaction on paper subjected to SO 2 and O 3 is shown to be the protonation of carboxylate groups present on the fibre, the hydrogen ions being added through the interaction of SO 2 with the moisture present in the paper. Results supportive of the protonation are produced by exposure of the aged paper to NH 3 (g). The results show that the combination of these techniques has a potential to show the degradation chemistry of paper under ambient conditions.

Honeycomb-like zinc oxide structures were prepared on the surface of cellulosic materials including cotton fabric fiber and filter paper fiber through plasma treatment followed by wet chemical reaction, the effect of plasma treatment is to increase the wettability and reactivity of cellulosic materials, so that the zinc oxide can nucleate and grow into a honeycomb-like structure on the cellulose fibers. The superhydrophobic surface was then obtained by modifying stearic acid on the zinc oxide structure. The microstructure, chemical composition and state, and wettability of the cellulosic materials were studied in detail. After the modification, the water contact angle and water sliding angle of the modified cotton fabric were 151° and 3.4°, respectively, and those of the modified filter paper is 154° and 4.5°, which indicates super-hydrophobicity. Due to the structural characteristics of zinc oxide-stearic acid structure, the superhydrophobic structure can maintain superhydrophobic performance in strong acidic or strong alkaline environments or after ultrasonic vibration treatment. Further, superhydrophobic modified cotton fabric and filter paper can be used for oil–water separation and adsorption of oil droplets in aqueous solution, and the oil–water separation efficiency is greater than 90%. This method of superhydrophobic modification of cellulosic materials has broad application prospects.

Room-temperature phosphorescence (RTP) materials have harvested enormous attention owing to their advanced optical properties, providing their possibility of the wider applications. Here, we designed a facile strategy to synthesize phosphorus and nitrogen co-doped carbon dots, while creatine provided the carbon and nitrogen source (CDs@creatine). Meanwhile, the as-prepared CDs@creatine exhibited the bright blue fluorescence in aqueous suspension, and showed the green RTP while being fixed on the filter paper. Significantly, the fluorescence of CDs@creatine was quenched by the introduction of warfarin, whereas their RTP was simultaneously enhanced. Specifically, their fluorescence reduction was mainly ascribed to static quenching effect (SQE) and inner filter effect (IFE). In addition, the abundant hydroxyl groups on the surface of CDs@creatine interacted with the carbonyl groups of warfarin to form hydrogen bonds which rigidified the excited triplet against the non-radiative transition, and thus leading to their enhanced phosphorescence. Therefore, a dual-channel detecting strategy of warfarin has been successfully proposed with the fluorescent linear range from 8 × 10−3 to 8 × 10−7 M and phosphorescent linear range of 2 × 10−5 to 1 × 10−8 M, which established a new way of assaying warfarin. Besides, CDs@creatine served as both fluorescent and phosphorescent ink, and were applied for painting and information encryption.

Inkjet-printing of metal nanoparticles is a particularly promising technique for the fabrication and modification of surfaces with a multifunctional nature. Recently copper sulfide nanoparticles (CuS NPs) have attracted wide interest due to a range of valuable properties including long term stability, photo-thermal activity, ease of synthesis and low cost. In the present study, printed CuS patterns were successfully fabricated on latex coated paper substrates and characterized by means of atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS), UV–Vis-NIR spectroscopy, and grazing incidence X-ray diffraction (GID). The resulted patterns displayed pronounced photo-thermal effect under Near Infrared Irradiation (NIR) even with relatively low laser power. Finally, by utilizing an automated real-time imaging platform it was possible to verify that the CuS printed film was not cytotoxic to human dermal fibroblast cells (HDF). The pronounced photo-thermal properties and nontoxic nature of these printed low-cost flexible CuS films make them promising candidates for fabrication of devices with localized photo-thermal effect suitable for biomedical applications.

Fe3O4 nanoparticles were modified by tetraethoxysilane and different amounts of trimethoxy (1H,1H,2H,2H-heptadecafluorodecyl) silane in sequence to obtain the magnetic nanoparticles with low surface energy, which could be used to construct the superhydrophobic surfaces for PU sponge, cotton fabric, and filter paper by a simple drop-coating method. Particularly, all the resultant Fe3O4/PU sponges containing different fluoroalkylsilane-modified Fe3O4 nanoparticles possessed both high water repellency with contact angle in the range of 150.2–154.7° and good oil affinity, which could not only effectively remove oil from water followed by convenient magnetic recovery but also easily realize the oil-water separation as a filter only driven by gravity. The Fe3O4/PU sponges showed high absorption capability of peanut oil, pump oil, and silicone oil with the maximum absorptive capacities of 40.3, 39.3, and 46.3 g/g, respectively. Such novel sponges might be a potential candidate for oil-water separation as well as oil absorption and transportation accompanied by the advantages of simple process, remote control by magnetic field, and low energy consumption.

Reduced graphene oxide (RGO), a two-dimensional (2D) system, has attracted much interest in photonic applications owing to its ability to absorb light over a broad wavelength. This leads to several studies on RGO-based photosensors. In this paper, chemical oxidation of graphite was carried out at room temperature for the preparation of large area reduced graphene oxide using a modified Hummer’s method. The as-prepared reduced graphene oxide was characterized by XRD, Raman spectroscopy, FESEM, and TEM to confirm the absence of impurities and to ascertain their morphology. In addition, the as-prepared reduced graphene oxide for its possible application as UV photosensor is reported. The electric and optoelectronic properties of RGO based UV photosensor shows a fast response and recovery time of 1 s and 3 s; high photoresponsitivity (3.74 AW −1 ) and quantum efficiency (1274%) indicating that the graphene oxide is an important material for high performance photosensor. This work demonstrates the ultrafast photoresponse with high photoresponsivity, proving its potential as a promising material for optoelectronic devices.

Graphene oxide (GO) synthesized from a flake-type of graphite powder, which was oxidized by various oxidizing agents, temperature control and two sets of drying processes, was electrophoresed on steel substrate for corrosion protection evaluation. The surface morphology, phase crystallization and defect states were determined by Electron microscopy equipped with an Energy dispersion spectrometry, X-ray diffraction and Raman and infrared spectra. The degrees of graphene oxide formation, intercalated defects and crystalline were observed by the impurities’ changes and extending d-spacing. Besides, the BET, Zeta potential and electrochemical impedance spectra were measured to evaluate corrosion protection performance of GO electrophoresis deposition on steel. A strong oxidizing agent (NaNO3) with freeze drying provides high oxygenated functional groups in GO, thus, providing good corrosion protection against hydrochloric acid aqueous due to dense electrophoresis deposition, a lower corrosive current and high resistance of the carrier pathway.

In this study, the surface characteristics, water vapor interactions, and state of water adsorbed on unmodified and coated paper samples were investigated in an attempt to obtain a better understanding of the fundamental principles related to thermodynamics of this process, as well as to provide essential insight that could be used for further improvement of the papers’ barrier properties. Based on the BET measurement, the coated paper samples showed higher specific surface areas than unmodified paper; however, their mean pore diameters are smaller. The BJH method was used for pore size distribution analysis. Hydrophobic properties of the paper samples were determined from experimental isotherms, e.g., monolayer moisture content, and these results have been related to the water vapor transfer rates (WVTRs) showing a complex nature of these relations. The highest peak corresponding to the modified samples with smaller pore sizes was found to be in the range of 1–30 nm, while it was in the 30–100 nm pore size range for unmodified paper. The net isosteric heats of sorption for different unmodified and modified paper samples were determined from water vapor adsorption isotherms measured at 15, 25, and 35 °C. The net isosteric heats of sorption decreased with an increase of moisture content after reaching the maximum values at 12.53, 15.25, 14.71, 23.2, and 22.77 kJ/mol for unmodified, zein grafted, calendered coated, PLA, and PHBV coated papers, respectively. The state of adsorbed water and water-vapor interaction on paper surface were also studied by TGA–DSC and FT-IR spectroscopic techniques. The FT-IR results revealed the formation of water vapor clusters due to poly-layer formation at the higher relative humidity. This has a profound effect on the equilibrium properties, e.g., the intensity of interactions between water molecules and the paper surface decreases as the relative humidity (moisture content) increases. Percentage of bound and unbound water formation and also the dehydration energy at various relative humidities were determined for the paper samples using the TGA–DSC technique.