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Rewritable paper is meaningful to the recyclable and sustainable utilization of environmental resources and thus has been extensively investigated for several decades. In this work, we demonstrated an efficient and convenient strategy to fabricate rewritable paper based on reversible hydrochromism of donor-acceptor Stenhouse adducts (DASAs). The kinetics and efficiency of isomerization could be well-controlled by adjusting the surrounding temperature and humidity. Monocolored rewritable paper was prepared by coating cyclic DASA·xH2O on the paper surface. Writing, printing, stamping and patterning were realized on the rewritable paper. The information could be controllably erased by treatment in a humid atmosphere. More importantly, the rewritable paper was upgraded to multicolored by combination of two DASA materials. The color of chirography was switched by controlling the writing speed.

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.

The construction of flexible electrochemical devices for energy storage and generation is of utmost importance in modern society. In this article, we report on the synthesis of flexible MoS2-based composite paper by high-energy shear force milling and simple vacuum filtration. This composite material combines high flexibility, mechanical strength and good chemical stability. Chronopotentiometric charge–discharge measurements were used to determine the capacitance of our paper material. The highest capacitance achieved was 33 mF·cm−2 at a current density of 1 mA·cm−2, demonstrating potential application in supercapacitors. We further used the material as a cathode for the hydrogen evolution reaction (HER) with an onset potential of approximately −0.2 V vs RHE. The onset potential was even lower (approximately −0.1 V vs RHE) after treatment with n-butyllithium, suggesting the introduction of new active sites. Finally, a potential use in lithium ion batteries (LIB) was examined. Our material can be used directly without any binder, additive carbon or copper current collector and delivers specific capacity of 740 mA·h·g−1 at a current density of 0.1 A·g−1. After 40 cycles at this current density the material still reached a capacity retention of 91%. Our findings show that this composite material could find application in electrochemical energy storage and generation devices where high flexibility and mechanical strength are desired.Keywords: flexible composites; hydrogen evolution reaction (HER); lithium ion batteries (LIBs); molybdenum disulfide; nanoarchitectonics; supercapacitors

In this work, a novel holey graphene oxide bonded with sulfonic acid groups (S-HGO) was developed using a facile and eco-friendly strategy: erosion and oxidation of graphene oxide (GO) by H2O2 and sulfonation by 4-benzenediazoniumsulfonate. The freestanding paper fabricated by S-HGO shows a high proton conductivity of 4.97 × 10−2 S cm−1 at 60 °C and 100% relative humidity (RH), which is comparable to Nafion 115 (7.67 × 10−2 S cm−1) at the same condition. The holes on S-HGO provide shortcut channels for proton transfer across the GO nanosheet. The chemical-linked sulfonic acid groups afford additional hop sites for proton conduction and endow itself an enhanced thermostability. Under 100% RH and ambient pressure, the freestanding S-HGO deliver a peak power density of 103 mW cm−2 at a load current density of 273 mA cm−2, which is about three times more than that of GO at 35 °C. The results demonstrate that this S-HGO paper is a promising nanoscale inorganic material for proton exchange membranes.

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.

A free-standing palladium/reduced graphene oxide paper (Pd/rGOP) based on one-pot co-reduction was prepared. The as-prepared Pd/rGOPs contain evenly distributed Pd particles interposing between the rGOP layers. The structure and composition of Pd/rGOP were characterized by SEM, EDX, XRD and Raman spectra. We investigated the glucose sensing performance of Pd/rGOP by chronoamperometry, the sensitivity reach as high as 6.70 µA mM−1 cm−2 with the linear range between 0.5 mM and 8 mM. The sensor also exhibits a good anti-interference ability and detection selectivity toward the interference. The proposed sensor has great potential to become a reliable tool in point-of-care medical devices.

Raman spectroscopy has been widely used to measure thermophysical properties of 2D materials. The local intense photon heating induces strong thermal nonequilibrium between optical and acoustic phonons. Both first principle calculations and recent indirect Raman measurements prove this phenomenon. To date, no direct measurement of the thermal nonequilibrium between optical and acoustic phonons has been reported. Here, this physical phenomenon is directly characterized for the first time through a novel approach combining both electrothermal and optothermal techniques. While the optical phonon temperature is determined from Raman wavenumber, the acoustic phonon temperature is precisely determined using high‐precision thermal conductivity and laser power absorption that are measured with negligible nonequilibrium among energy carriers. For graphene paper, the energy coupling factor between in‐plane optical and overall acoustic phonons is found at (1.59–3.10) × 1015 W m−3 K−1, agreeing well with the quantum mechanical modeling result of 4.1 × 1015 W m−3 K−1. Under ≈1 µm diameter laser heating, the optical phonon temperature rise is over 80% higher than that of the acoustic phonons. This observation points out the importance of subtracting optical–acoustic phonon thermal nonequilibrium in Raman‐based thermal characterization., The optical–acoustic phonon thermal nonequilibrium is first probed through novel electrothermal and optothermal techniques. For graphene paper, the optical‐acoustic phonon energy coupling factor is found at (1.59–3.10) × 1015 W m−3 K−1, agreeing well with theoretical predictions. Under ≈1 µm laser heating, the optical phonon temperature rise is over 80% higher than that of the acoustic phonons.

Although Al-ion battery is attracting researchers’ attention worldwide, its volumetric energy density was not so promising due to low density of graphite-based positive electrodes in the current published literatures. Thus, defect-free yet densely packed graphene electrodes with high electronic conductivity and fast ionic diffusion are crucial to the realization of compacted Al-ion batteries with high volumetric energy density. In the present work, a self-supported and defect-free graphene-positive electrode (RHG-P-2850) was successfully produced by a hydriodic acid reduction of the graphene oxide (GO) method, followed by an ultrahigh temperature (2850 °C) annealing treatment. The density of the RHG-P-2850 (0.32 g cm−3) is currently the highest positive electrode material in the preparation of graphene-positive electrodes from GO. RHG-P-2850 positive electrode enables to deliver considerably high specific capacity 27.1 mAh cm−3 (85 mAh g−1) at the current density 2 A g−1. More importantly, a remarkably stable performance was achieved with 20% fading over 8000 cycles. The results enlighten and promote the design and preparation of densely packed graphene-positive electrode to develop high-performance Al/graphene battery.

Halide perovskite quantum dots (PQDs) are promising materials for diverse applications including displays, light‐emitting diodes, and solar cells due to their intriguing properties such as tunable bandgap, high photoluminescence quantum yield, high absorbance, and narrow emission peaks. Despite the prosperous achievements over the past several years, PQDs face severe challenges in terms of stability under different circumstances. Currently, researchers have overcome part of the stability problem, making PQDs sustainable in water, oxygen, and polar solvents for long‐term use. However, halide PQDs are easily degraded under continuous irradiation, which significantly limits their potential for conventional applications. In this study, an oleic acid/oleylamine (traditional surface ligands)‐free method to fabricate perovskite quantum dot papers (PQDP) is developed by adding cellulose nanocrystals as long‐chain binding ligands that stabilize the PQD structure. As a result, the relative photoluminescence intensity of PQDP remains over ≈90% under continuous ultraviolet (UV, 16 W) irradiation for 2 months, showing negligible photodegradation. This proposed method paves the way for the fabrication of ultrastable PQDs and the future development of related applications., Solid‐state perovskite quantum dot papers are fabricated using a unique vacuum filtration growth method without a purification process. The bonding between cellulose nanocrystals and perovskite quantum dots makes the hybrid structure stable, and record high UV stability and thermal stability are achieved for perovskite quantum dot papers.

Graphene has an extremely high in-plane strength yet considerable out-of-plane softness. High crystalline order of graphene assemblies is desired to utilize their in-plane properties, however, challenged by the easy formation of chaotic wrinkles for the intrinsic softness. Here, we find an intercalation modulated plasticization phenomenon, present a continuous plasticization stretching method to regulate spontaneous wrinkles of graphene sheets into crystalline orders, and fabricate continuous graphene papers with a high Hermans’ order of 0.93. The crystalline graphene paper exhibits superior mechanical (tensile strength of 1.1 GPa, stiffness of 62.8 GPa) and conductive properties (electrical conductivity of 1.1 × 105 S m−1, thermal conductivity of 109.11 W m−1 K−1). We extend the ultrastrong graphene papers to the realistic laminated composites and achieve high strength combining with attractive conductive and electromagnetic shielding performance. The intercalation modulated plasticity is revealed as a vital state of graphene assemblies, contributing to their industrial processing as metals and plastics., Strong but flexible graphene tends to wrinkle, which compromises some properties. Here the authors report a solid plasticization method to prepare continuous graphene papers with high crystalline order, achieving high strength, stiffness, electrical and thermal conductivities.

The core of decorative laminates is generally made of stacked Kraft paper sheets impregnated with a phenolic resin. As the impregnation process in industry is relatively fast, new methods need to be developed to characterize it for different paper-resin systems. Several phenolic resins were synthesized with the same Phenol:Formaldehyde ratio of 1:1.8 and characterized by Fourier Transform Infrared Spectrometry (FTIR) as well as Size-Exclusion Chromatography (SEC). In addition, their viscosities and surface tensions when diluted in methanol to 45% of solid content were measured. The capacity of each resin to penetrate a Kraft paper sheet was characterized using a new method, which measures the conductivities induced by the liquid resin crossing the paper substrate. With this method, crossing times could be measured with a good accuracy. Surprisingly, the results showed that the penetration time of the resin samples is not correlated to the viscosity values, but rather to the surface tension characteristics and the chemical characteristics of paper. Furthermore, some resins had a higher swelling effect on the fibers that delayed the crossing of the liquid through the paper.

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.

In this work, the commercial carbon paper was firstly peeled in K2CO3 solution and then was further treated in a KNO3 solution to form functional exfoliation graphene (FEG) on the commercial carbon paper. The FEG/carbon paper was characterized by Raman spectra and scanning electron microscopy, confirming that some typical layered fold graphenes were successfully peeled off and stood on the carbon paper matrix. Then, Fe3O4 nanoparticles (NPs) were grown on the surface of FEG/carbon paper and the as-prepared Fe3O4 NPs/FEG/carbon paper was directly used as supercapacitor electrode. The specific capacitance of Fe3O4 NPs/FEG/carbon paper was about 316.07 F g−1 at a current density of 1 A g−1. Furthermore, the FEG/carbon papers were also functionalized by benzene carboxylic acid to form FFEG/carbon papers, and then the Fe3O4 NPs were grown on the surface of FFEG/carbon paper. The specific capacitance of Fe3O4 NPs/FFEG/carbon paper was 470 F g−1 at a current density of 1 A g−1, superior to some previous reported results. This work might provide a new strategy to prepare various nanostructures on FFEG/carbon papers for future applications.

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.

Nanoparticles are used in several applications due to the unique properties they possess compared to bulk materials. Production techniques have continuously evolved over the years. Recently, there has been emphasis on environmentally friendly manufacturing processes. Substrate properties often limit the possible production techniques and, for example; until recently, it has been difficult to incorporate nanoparticles into paper. Chemical reduction of a precursor in the presence of paper changes the bulk properties of paper, which may limit intended end-use. In this study, we present a novel technique for incorporating silver nanoparticles into paper surface using a flame pyrolysis procedure known as Liquid Flame Spray. Papers precoated with mineral pigments and plastic are used as substrates. Silver nanoparticles were analyzed using SEM and XPS measurements. Results show a homogeneous monolayer of silver nanoparticles on the surface of paper, which demonstrated antibacterial properties against E. coli . Paper precoated with plastic showed more nanoparticles on the surface compared to pigment coated paper samples except for polyethylene-precoated paper. The results demonstrate a dry synthesis approach for depositing silver nanoparticles directly onto paper surface in a process which produces no effluents. The production technique used herein is up scalable for industrial production of antibacterial paper.

Demands for flexible electronic equipment such as wearable devices and wrap-round displays have motivated the development of flexible energy storage devices. Although cellulose paper is one of the most promising substrates for flexible devices, its intrinsic limitations, such as poor mechanical durability, hamper its practical use. In this study, we adopted the traditional Korean paper, Hanji, with superior mechanical robustness as a substrate for supercapacitor electrodes. The effective infiltration of activated carbons (ACs) as an electrode material into the dense network of Hanji cellulose fibers was performed by a simultaneous one-pot process of network formation and AC embedment. The fabricated symmetric supercapacitors based on the AC-embedded Hanji electrode exhibited a specific capacitance (Csp) of 16.0 F/g measured at a scan rate of 10 mV/s with excellent cycle stability, the Csp retention of 94.5%, over 1000 charge-discharge cycles.

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.

Cellulose fiber (CF) paper is a low-cost, sustainable, and flexible substrate, which has gained increasing interest recently. Before practical usage, the functionalization of the pristine CF paper is indispensable to meet requirements of specific applications. Different from conventional surface modification or physical mixing methods, we report in situ growth of ultralong hydroxyapatite nanowires (HAPNWs) with lengths larger than 10 μm on the CF paper. HAPNWs are radially aligned on the surface of CFs, creating a micro/nanoscale hierarchical structure. By means of the excellent ion exchange ability of HAP and the hierarchical structure, the functions of the CF paper can be easily customized. As a proof-of-concept, we demonstrate two kinds of functional CF paper: (1) the photoluminescent CF paper by doping Eu3+ and Tb3+ ions into the crystal lattice of HAPNWs and (2) the superhydrophobic CF paper by coating poly(dimethylsiloxane) on the HAPNW hierarchical structure, which can be applied for self-cleaning and oil/water separation. It is expected that an in situ growth of ultralong HAPNWs will provide an instructive guideline for designing a CF paper with specific functions.

The effective implantation of conductive and charge storage materials into flexible frames has been strongly demanded for the development of flexible supercapacitors. Here, we introduce metallic cellulose paper-based supercapacitor electrodes with excellent energy storage performance by minimizing the contact resistance between neighboring metal and/or metal oxide nanoparticles using an assembly approach, called ligand-mediated layer-by-layer assembly. This approach can convert the insulating paper to the highly porous metallic paper with large surface areas that can function as current collectors and nanoparticle reservoirs for supercapacitor electrodes. Moreover, we demonstrate that the alternating structure design of the metal and pseudocapacitive nanoparticles on the metallic papers can remarkably increase the areal capacitance and rate capability with a notable decrease in the internal resistance. The maximum power and energy density of the metallic paper-based supercapacitors are estimated to be 15.1 mW cm−2 and 267.3 μWh cm−2, respectively, substantially outperforming the performance of conventional paper or textile-type supercapacitors., With ligand-mediated layer-by-layer assembly between metal nanoparticles and small organic molecules, the authors prepare metallic paper electrodes for supercapacitors with high power and energy densities. This approach could be extended to various electrodes for portable/wearable electronics.

Understanding and modulating the conformation of graphene are pivotal in designing graphene macroscopic materials. Here, we revealed the sheet collapsing behavior of graphene oxide (GO) sheets by poor solvents in an analogy with linear macromolecules. Triggered by poor solvents, extended GO sheets in good solvents can collapse to hierarchically wrinkled conformations. The collapsing behavior of GO enabled the fabrication of amorphous self-standing GO and graphene papers with rich hierarchical wrinkles and folds over mutliple size scales. The collapsed GO and graphene papers had a rubber-like mechanical behavior with viscoelasticity. By our collapsing method, GO and graphene self-standing papers were designed to be stiff with high modulus or to become soft with low modulus of 100 MPa at a remarkably large breakage elongation up to 23%. Our philosophy of treating graphene as a 2D polymer enables the efficient control of molecular conformations of graphene and other 2D polymers and the design of macroscopic materials of 2D nanomaterials as in the polymer industry.

Silver nanoparticles deposited on surfaces can provide an antibacterial effect with potential uses in, for example, healthcare settings. However, release of nanoparticles and their potential exposure to the environment is of concern. The current work demonstrates a continuous synthesis that simultaneously deposits silver nanoparticles onto plastic coated paper surface by utilizing the liquid flame spray (LFS) aerosol process. Heat from LFS is used to soften the thermoplastic paper surface, which enables partial and full embedding of the nanoparticles, thereby improving adhesion. The embedding is confirmed with atomic force and scanning electron microscopy, and the deposited silver amounts are quantified with X-ray photoelectron spectroscopy. The results suggest that embedding was more effective in PE-coated paper samples due to the lower glass transition temperature when compared to PET-coated paper samples. The antibacterial properties of the surfaces against E. coli and S. aureus were maintained and confirmed with a previously developed `Touch-Test Method'. The LFS process has the potential to be used for large-scale manufacturing of antibacterial surfaces with improved nanoparticle adhesion on appropriately chosen thermoplastic surfaces. publishedVersion

The colour of water-jet rewritable paper (WJRP) is difficult to be expanded via single hydrochromic molecule, especially black. Here, inspired by the amazing phenomenon of bound-water in cells enabling various biological transformations via facilitating synergistic inter-/intra-molecular proton transfer, we present a simple strategy toward WJRP based on binary systems containing less-sensitive acidochromic dyes and mild proton donors (or developers). With such a binary system containing commercial black dye as the colouring agent, benzyl 4-hydroxybenzoate as the developer, and biomimetic bound-water as proton-transferring medium, we successfully achieve the long-awaited black WJRP. Printed images on such WJRP have excellent performances and long retaining time (>1 month). In addition, the robustness, durability and reversibility of WJRP could be increased distinctly by using polyethylene terephthalate as substrate. This strategy significantly expands hydrochromic colours to entire visible range in an eco-friendly way, which opens an avenue of smart materials for practical needs and industrialization., Water based inks used for water-jet rewritable paper (WJRP) are an environmental friendly alternative to conventional printing, but black colour in WJRP could not be realized so far. Here the authors demonstrate black as well as other colour WJRP based on binary systems containing less-sensitive acidochromic dyes and mild proton donors.

Paper-based supercapacitors have attracted more and more attention for high electrochemical performance. However, most of them adopt sandwiched structure. Here, we prepared planar polypyrrole (PPy) coated paper-based supercapacitors by applying simple laser carving assisted method. The planar device showed a significant performance improvement (13.9 mF/cm2) compared to the sandwiched device (12.3 mF/cm2). In addition, by adjusting the polymerization time of pyrrole, the device capacity can be further increased to 87.4 mF/cm2. We firmly believed that the laser carving assisted method has a significant role in promoting the development of flexible planar electronic devices.

In this paper, using a low-cost paper fiber (PF) as a substrate, eigenstate polyaniline–coated PFs with graphene (GO/PANI/PF) ternary materials were synthesized by using the chemical oxidative polymerization method. Electrochemical measurements showed that the GO/PANI/PF electrode exhibited an excellent electrochemical performance compared with the PANI electrode. By adjusting the ratio of PANI and PF, the as-prepared GO/PANI/PF–2.5% electrode exhibited the highest specific capacitance 937 F g−1 at current density 1 A g−1 in a 0.5 M H2SO4 aqueous solution, and 74.5% retention of initial capacitance after 2000 charge–discharge cycles at 5 A g−1. The symmetric capacitor on the basis of GO/PANI/PF nanocomposite delivers a superior energy density of 10.12 Wh kg−1 at 456 W kg−1 at a current density of 1 A g−1.

Paper transistors have the advantages of recyclability, high abundance, low cost, disposability, and biodegradability. In this paper, a nonvolatile transistor fabricated on a paper substrate without protective layers by using solution-based methods is presented, and promising performance is reported. The memory window of ferroelectric field-effect transistors is approximately 16 V when the gate voltage is swept from +20 V to -20 V. The on/off ratio is 3.45 × 102, even on the paper substrate. Electrical characteristics of the memory device are not degraded, as compared with those of transistors on rigid substrates fabricated simultaneously.

Dendrite growth of metal anodes is one of the key hindrances for both secondary aqueous metal batteries and nonaqueous metal batteries. In this work, a freestanding Ti3C2Tx MXene@Zn paper is designed as both zinc metal anode and lithium metal anode host to address the issue. The binder-free Ti3C2Tx MXene@Zn paper exhibits merits of good mechanical flexibility, high electronic conductivity, hydrophilicity, and lithiophilicity. The crystal growth mechanism of Zn metal on common Zn foil and Ti3C2Tx MXene@Zn composite is also studied. It is found that the Ti3C2Tx MXene@Zn paper can effectively suppress the dendrite growth of Zn, enabling reversible and fast Zn plating/stripping kinetics in an aqueous electrolyte. Moreover, the Ti3C2Tx MXene@Zn paper can be used as a 3D host for a lithium metal anode. In this host, Zn is utilized as a nucleation agent to suppress the Li dendrite growth. The freestanding Ti3C2Tx MXene@Zn@Li anode exhibits superior reversibility with high Coulombic efficiency (97.69% over 600 cycles at 1.0 mA cm-2) and low polarization compared with the Cu@Li anode. These findings may be useful for the design of dendrite-free metal-based energy storage systems.

Metal oxides can deliver high capacity to Li-ion batteries, surpassing conventional graphite, but they suffer from a huge volume change during charging-discharging and poor cycle life. Herein, we merge the dual strategies of 3D-network support and sandwiching design to tackle such issue. We develop a skillful O2-NH3 reactive pyrolysis of cellulose, where the preoxidation and the aminolysis result in the spatially separated charring of cellulose chains. A cellulose fiber is wonderfully converted into several ultrathin twisted graphenic sheets instead of a dense carbon fiber, and consequently, a cellulose paper is directly transformed into a porous flexible carbon paper with high surface area and conductivity (denoted as CP). CP is further fabricated as a 3D-network support into the hybrid CP@Fe3O4@RGO, where RGO is reduced graphene oxide added for sandwiching Fe3O4 particles. As a binder-free free-standing anode, CP@Fe3O4@RGO effectively fastens Fe3O4 and buffers the volume changes on cycling, which stabilizes the passivating layer and lifts the Coulombic efficiency. The anode thus presents an ultralong cycle life of >2000 running at a high capacity level of 1160 mAh g-1. It additionally facilitates electron and ion transports, boosting the rate capability. CP and CP@Fe3O4@RGO represent a technological leap underpinning next-generation long-life high-capacity high-power batteries.

Целью данной работы является изучение состава и морфологии поверхностных слоев, создаваемых ионным пучком вспомогательного осаждения каталитических металлов (иридия и платины) на подложки электрокатализатора копировальной бумаги

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.

Made available in DSpace on 2018-12-11T17:16:11Z (GMT). No. of bitstreams: 0 Previous issue date: 2018-02-01 Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) The use of paper as a platform to manufacture organic electronic devices, electronic paper, has expanding potential for many applications because of several properties offered. In this work, we show a study of PEDOT:PSS printed by inkjet on bond paper, vegetal paper and sheets of PET. The relation between the surface density of the deposited material, morphology and resistivity was investigated for samples printed with a commercial Hewlett-Packard(HP)® printer and Microsoft Word® software. The amount of material deposited, i.e. surface density, was controlled using the print number in the same position and changing the gray scale used in the image formation. Changing the surface density of printed PEDOT:PSS, it is possible to produce a continuous film permeating the papers fibers. Sheet resistances obtained, when 7.0 mg cm−2 of PEDOT:PSS were deposited on the surfaces, were: (a) 413.2 kΩ/Sq for bond paper, (b) 5.6 kΩ/Sq for vegetable paper and (c) 2.3 kΩ/Sq for PET. The exponential dependence of sheet resistance with the surface density of printed material allows us to evaluate the strong influence of substrate roughness on PEDOT:PSS conductivity and to predict, for each one, conditions to minimize it. São Paulo State University (UNESP) School of Technology and Applied Sciences Campus Presidente Prudente São Paulo State University (UNESP) School of Technology and Applied Sciences Campus Presidente Prudente

Commercial carbon paper was coated with polyaniline (PANI) using in situ polymerization of aniline. Prior to the PANI coating, acid treatment was performed to carboxylate the surface of the carbon paper for enhancing PANI adhesion by sonication of the carbon paper in a mixture of concentrated sulfuric and nitric acids. The loading mass density of PANI on the acid-treated carbon paper increased more than three times compared to that on the carbon paper without acid treatment. The specific capacitance also increased from 112 to 174 F/g in a two-electrode system (calculated using a total mass of carbon paper and PANI) due to better PANI coating on the acid-treated carbon paper. The simple acid treatment provides good adhesion of PANI to the commercial carbon paper and can be applied to prepare supercapacitor electrodes., J. Pedrós acknowledges the support of the Moncloa Campus of International Excellence (UCM-UPM, ISOM)

Effect of ferric chloride concentration on micro-nano structure surface and superhydrophobic property of filter paper was investigated by adsorption and simple immersion process. The results showed that the concentration of ferric chloride solution had great impact on the superhydrophobic property of filter paper. When the concentration was 0 mol/L, filter paper presented hydrophilicity. When the concentration was bigger than 0 mol/L, it exhibited hydrophobicity. The modified filter paper’s surface displayed advancing contact angels of 167 ± 2°, which was attributed to its’ formed micro/nano structure. This may contribute to the development in production applications.

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.

Thermodynamic properties of cellulose insulation paper are vital factors affecting the life of a transformer; in order to obtain cellulose insulation paper with better thermodynamic properties, three types of silane coupling agents—3-aminopropyltriethoxy silane (KH550), 3-glycidoxypropyltrimethoxy silane (KH560), and 3-methacryloyloxypropyltrimethoxy silane (KH570)—were grafted on the surface of nano-SiO2, and thermodynamic properties of cellulose modified with nano-SiO2 were explored. The molecular dynamics method was used to establish a composite model of nano-SiO2/cellulose. Also, different silane coupling agent grafted nano-SiO2/cellulose models were established to explore the effect of mechanical properties, interaction energy, free volume, and hydrogen bonds on thermodynamic properties. The results showed that KH550 was the best modification of the nano-SiO2/cellulose system among the three grafted silane coupling agents because KH550 grafted on the surface of nano-SiO2 formed more hydrogen bonds in the cellulose system. The interfacial bonding strength between the nano-SiO2 and the cellulose chains can effectively improve the thermal stability of the cellulose insulating paper.

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.

Novel multiple emitting amphiphilic conjugated polythiophene‐coated CdTe quantum dots for picogram level determination of the 2,4,6‐trinitrophenol (TNP) explosive are developed. Four biocompatible sensors, cationic polythiophene nanohybrids (CPTQDs), nonionic polythiophene nanohybrids (NPTQDs), anionic polythiophene nanohybrids (APTQDs), and thiophene copolymer nanohybrids (TCPQDs), are designed using an in situ polymerization method, which shows highly enhanced fluorescence intensity and quantum yield (up to 78%). All sensors are investigated for nitroexplosive detection to provide a remarkable fluorescence quenching for TNP and the quenching efficiency reached 96% in the case of TCPQDs. The fluorescence of the sensors are quenched by TNP through inner filter effect, electrostatic, π−π, and hydrogen bonding interactions. Under optimal conditions, the detection limits of CPTQDs, NPTQDs, APTQDs, and TCPQDs are 2.56, 7.23, 4.12, and 0.56 × 10−9 m, respectively, within 60 s. More importantly, portable, cost effective, and simple to use paper strips and chitosan film are successfully applied to visually detect as little as 2.29 pg of TNP. The possibility of utilizing a smartphone with a color‐scanning APP in the determination of TNP is also established. Moreover, the practical application of the developed sensors for TNP detection in tap and river water samples is described with satisfactory recoveries of 98.02−107.50%.

The non-woven mat has a three-dimensionally distributed fiber structure, but because the randomly dispersed structure caused the pore diameter of the separator to enlarge, this may lead to a short circuit of the battery. In this work, organic polyethylene terephthalate (PET) was combined with inorganic zirconia (ZrO2) ceramic fiber using a low-cost papermaking method. The addition of PET blocked part of the macropores of the fiber separator, enabling the separator a suitable pore size. The PET connected the nodes of the zirconia fibers to provide mechanical support. At the same time, the ZrO2-PET composite separator inherited the excellent high temperature resistance of zirconia ceramic fiber and a maintained dimensional stability after heating at 300 °C for 1 h, providing a strong guarantee for the safe performance of the battery. We found that when the concentration of PET was 5%, the highest electrolyte uptake (301.83%) occurred as well as electrochemical performance. In addition, the ZrO2-PET composite separator achieved an excellent cycle performance at 60 °C compared with the polypropylene (PP) separator.

In view of a great demand for paper-based technologies, nonwettable fibrous substrates with excellent durability have drawn much attention in recent years. In this context, the use of cellulose nanofibers (CNFs), the smallest unit of cellulosic substrates (5-20 nm wide and 500 nm to several microns in length), to design waterproof paper can be an economical and smart approach. In this study, an eco-friendly and facile methodology to develop a multifunctional waterproof paper via the fabrication of fluoroalkyl functionalized CNFs in the aqueous medium is presented. This strategy avoids the need for organic solvents, thereby minimizing cost as well as reducing safety and environmental concerns. Besides, it widens the applicability of such materials as nanocellulose-based aqueous coatings on hard and soft substrates including paper, in large areas. Water droplets showed a contact angle of 160° (±2°) over these surfaces and rolled off easily. While native CNFs are extremely hydrophilic and can be dispersed in water easily, these waterborne fluorinated CNFs allow the fabrication of a superhydrophobic film that does not redisperse upon submersion in water. Incorporated chemical functionalities provide excellent durability toward mechanochemical damages of relevance to daily use such as knife scratch, sand abrasion, spillage of organic solvents, etc. Mechanical flexibility of the chemically modified CNF composed paper remains intact despite its enhanced mechanical strength, without additives. Superhydrophobicity induced excellent microbial resistance of the waterproof paper which expands its utility in various paper-based technologies. This includes waterproof electronics, currency, books, etc., where the integrity of the fibers, as demonstrated here, is a much-needed criterion.

High-performance electromagnetic interference (EMI) shielding materials with ultraflexibility, outstanding mechanical properties, and superior EMI shielding performances are highly desirable for mo...

Determination of the pH value of the paper is a very specific phenomenon, especially the surface pH measurement. In the case of heritage objects, such as archival documents, books, artworks on paper carriers, is a determination of real pH value in the whole structure (in cross section) of paper very important, because of the mechanism of degradation and thus the rate of degradation of the paper components at a given point in the paper structure depends on the pH value in the environment. This paper is aimed to show the possibilities of using modified papers by acid–base indicator, in the field of measurement of pH value of paper in the cross section of the paper. A calibration series of acidic samples neutralizing by magnesium bicarbonate of different concentrations was created. It was found that the indicator changed in the desired area, pH value 6–8, and it was observed gradual color change. The color parameters were measured and the most correlated parameter with pH value was found. The new method enables the observation of pH distribution in a critical cross section of modified paper after deacidification processes.

We have proposed and fabricated resistive-type flexible pressure sensors composed of multi-walled carbon nanotube thin films, liquid metal droplets, sponge rubber, and paper. The pressure sensor detects external pressure in the range of tens of kilopascals. The resistance change was found to be approximately 70% when a pressure of 100 kPa was applied. The sensor operation showed good reproducibility under cyclic applied pressure. The simple sensor structure and environment-friendly materials allow the sensor to be easily disassembled into its components, which are reusable and combustible.

A Li–O2 battery has been considered as one of the most promising energy storage systems owing to their ultrahigh theoretical energy densities. However, low energy efficiency (high polarization) during discharge/charge and resulting cycle stabilities have severely limited the development of this type of battery. Here, we demonstrate a simple preparation of NiO supported on carbon paper by dipping carbon paper in Ni acetate solution and heating it to apply NiO directly to the carbon as a cathode material for nonaqueous Li–O2 batteries. The prepared sample was confirmed as the structure of NiO-incorporated carbon using X-ray photoelectron spectroscopy (XPS), X-ray absorption spectroscopy (XAS), and high-resolution transmission electron microscopy (HR-TEM) analysis despite amorphous patterns seen in XRD (~ 10% NiO in NiO supported on carbon paper). A Li–O2 cell in which the NiO supported on carbon paper was applied as an electrocatalyst showing an initial ~ 6% increase in energy efficiency and a subsequent 50 cycle retention.

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).

Ag triangular nanoplates have been widely used as the SERS substrate due to their anisotropic morphology and sharp corners. In this work, SERS activity of Ag triangular nanoplates on glass and paper substrates was investigated with different concentration and size. A tiny triangular nuclei based synthesis method was employed to produce Ag triangular nanoplates with different size. And the extinction coefficients of Ag triangular nanoplates with different size were quantified by inductively coupled plasma mass spectrometry (ICP-MS) and transmission electron microscopy (TEM). With definite concentration, Ag triangular nanoplates with small size showed stronger SERS intensity on glass substrate at high concentrations, while large Ag triangular nanoplates exhibited better SERS effect on paper substrate at low concentrations. The possible reasons for distinct SERS activity of Ag triangular nanoplates on glass and paper were discussed with scanning electron microscope (SEM) characterization. These results exhibited important implications for fabricating Raman substrates using Ag triangular nanoplates and could be applied to the SERS sensing with flexile substrate.

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.

This paper presents the microdroplets electrowetting causing by the voltage actuation on the flexible lab on a chip. The electrode is made of a thin Aluminium (Al) film while the lab on a chip substrate is made from the cellulose paper, which is flexible. Consistently in this work the microdroplet samples of 5 µl from Potassium Chloride (KCl) is experimented on top of the electrodes. It is shown that the flexible paper-based lab on a EW chip has fulfilled the Lippmann’s equation where the higher the voltage supply, the lesser the interfacial tension of droplet. Moreover, the droplet has efficiently trailed along the track of activated electrodes when using the olive oil as the dielectric layer. The olive oil with dielectric permittivity of 3.2 has given the best displacement and high velocity of the droplet transportation. The best low voltage to move the microdroplet between the two planar electrodes is 12 Vpp under the frequency of 10 Hz. Keywords: Microdroplet, Electrowetting, Flexible device, Aluminium electrode, Paper-based chip

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 larger size of graphene sheets should intuitively generate higher overall properties of their macroscopic materials. However, this intuitive notion still remains ambiguous. Here, we uncover that the wrinkle formation causes the counterintuitive size predicament of graphene sheets in their macroscopic materials. In the model of graphene oxide assembled papers, we reveal that the giant size of graphene oxide sheets aggravates the formation of larger wrinkles and more microvoids, causing the negative size effect in mechanical strength. A major microscopic origin of the size predicament is the skin wrinkling in the drying process, and the wrinkling behavior follows a general rule of deformation of an elastic thin plate. We use a wrinkle-engineering strategy to depress the spontaneously formed large wrinkles and succeed in the resolution of the size predicament. After wrinkle modulation, an authentically positive size effect reversely appears in which giant graphene sheets generate ultrahigh mechanical strength and superior functionalities of graphene papers. The origin of the size predicament reminds us of the hidden importance of modulating wrinkles for graphene macroscopic materials and provides a guidance of wrinkle engineering for graphene materials with advanced performances.

Stretchable micropower sources with high energy density and stability under repeated tensile deformation are key components of flexible/wearable microelectronics. Herein, through the combination of strain engineering and modulation of the interlayer spacing, freestanding and lightweight MXene/bacterial cellulose (BC) composite papers with excellent mechanical stability and a high electrochemical performance are first designed and prepared via a facile all‐solution‐based paper‐making process. Following a simple laser‐cutting kirigami patterning process, bendable, twistable, and stretchable all‐solid‐state micro‐supercapacitor arrays (MSCAs) are further fabricated. As expected, benefiting from the high‐performance MXene/BC composite electrodes and rational sectional structural design, the resulting kirigami MSCAs exhibit a high areal capacitance of 111.5 mF cm−2, and are stable upon stretching of up to 100% elongation, and in bent or twisted states. The demonstrated combination of an all‐solution‐based MXene/BC composite paper‐making method and an easily manipulated laser‐cutting kirigami patterning technique enables the fabrication of MXene‐based deformable all‐solid‐state planar MSCAs in a simple and efficient manner while achieving excellent areal performance metrics and high stretchability, making them promising micropower sources that are compatible with flexible/wearable microelectronics.