Search

This paper systematically studies the effect of Fe 3 O 4 nanoparticle size on the insulation performance of nanofluid impregnated paper. Three kinds of Fe 3 O 4 nanoparticles with different sizes and their nanofluid impregnated papers were prepared. Environmental scanning electron microscopy (ESEM) and infrared spectroscopy were used to analyze the combination of Fe 3 O 4 nanoparticles and nanofluid impregnated paper. The effect of nanoparticle size on breakdown voltage and several dielectric characteristics, e.g., permittivity, dielectric loss, of the nanofluid impregnated paper were comparatively investigated. Studies show that the Fe 3 O 4 nanoparticles were bound to impregnated paper fibers by O-H bonds, while the relative permittivity and dielectric loss of the nanofluid impregnated papers were increased. Meanwhile, the increase of trap depth, caused by the nanoparticles, can trap the electric charge and improve the breakdown strength. The test results show that the direct current (DC) and alternating current (AC) breakdown voltages of nanofluid impregnated paper increased by 9.1% and 10.0% compared to FR3 nanofluid impregnated paper, respectively.

This study aims to explore the channel patterns and the characteristic parameters of the zigzag microchannel based on microfluidic paper-based analytical devices (μPADs), in which the mixing efficiency and speed can be greatly enhanced. Better mixing of the solutions was obtained by adding a simple directing electric field to the optimized structure of the zigzag microchannel on paper-based chips instead of the traditional complex devices. A higher mixing efficiency was reached when the direct-current (DC) power supply reached 20 V. Meanwhile, a piezoelectric transducer (PZT) driver was used in the mixing experiment with the paper-based zigzag microchannel. The results show that the mixing efficiency reached a maximum value when the input voltage and frequency were 30 V and 150 Hz, respectively. These paper-based devices meet the requirements of the biochemical analysis field because they are low cost, easy to operate, and have high efficiencies, giving them good prospects for future applications. Graphical Abstract.

Hybrid nanomaterials fabricated by the heterogeneous integration of 1D (carbon nanotubes) and 2D (graphene oxide) nanomaterials showed synergy in electrical and mechanical properties. Here, we reported the infiltration of carboxylic functionalized single-walled carbon nanotubes (C-SWNT) into free-standing graphene oxide (GO) paper for better electrical and mechanical properties than native GO. The stacking arrangement of GO sheets and its alteration in the presence of C-SWNT were comprehensively explored through scanning electron microscopy, X-ray photoelectron spectroscopy (XPS) and X-ray diffraction. The C-SWNTs bridges between different GO sheets produce a pathway for the flow of electrical charges and provide a tougher hybrid system. The nanoscopic surface potential map reveals a higher work function of the individual functionalised SWNTs than surrounded GO sheets showing efficient charge exchange. We observed the enhanced conductivity up to 50 times and capacitance up to 3.5 times of the hybrid structure than the GO-paper. The laminate of polystyrene composites provided higher elastic modulus and mechanical strength when hybrid paper is used, thus paving the way for the exploitation of hybrid filler formulation in designing polymer composites.

Highlights: The large-scale, high-strength, super-tough, and multifunctional nacre-like heterocyclic aramid (HA)/MXene@polypyrrole (PPy) (HMP) nanocomposite papers were fabricated using the in-situ assembly of PPy onto the HA/MXene hydrogel template. The "brick-and-mortar" layered structure and abundant hydrogen-bonding interactions among MXene, PPy, and HA respond cooperatively to external stress and effectively increase the mechanical properties of HMP nanocomposite papers. The templating effect from HA/MXene was utilized to guide the assembly of conducting polymers, leading to high electrical conductivity and outstanding electromagnetic interference shielding performance. Robust, ultra-flexible, and multifunctional MXene-based electromagnetic interference (EMI) shielding nanocomposite films exhibit enormous potential for applications in artificial intelligence, wireless telecommunication, and portable/wearable electronic equipment. In this work, a nacre-inspired multifunctional heterocyclic aramid (HA)/MXene@polypyrrole (PPy) (HMP) nanocomposite paper with large-scale, high strength, super toughness, and excellent tolerance to complex conditions is fabricated through the strategy of HA/MXene hydrogel template-assisted in-situ assembly of PPy. Benefiting from the "brick-and-mortar" layered structure and the strong hydrogen-bonding interactions among MXene, HA, and PPy, the paper exhibits remarkable mechanical performances, including high tensile strength (309.7 MPa), outstanding toughness (57.6 MJ m−3), exceptional foldability, and structural stability against ultrasonication. By using the template effect of HA/MXene to guide the assembly of conductive polymers, the synthesized paper obtains excellent electronic conductivity. More importantly, the highly continuous conductive path enables the nanocomposite paper to achieve a splendid EMI shielding effectiveness (EMI SE) of 54.1 dB at an ultra-thin thickness (25.4 μm) and a high specific EMI SE of 17,204.7 dB cm2 g−1. In addition, the papers also have excellent applications in electromagnetic protection, electro-/photothermal de-icing, thermal therapy, and fire safety. These findings broaden the ideas for developing high-performance and multifunctional MXene-based films with enormous application potential in EMI shielding and thermal management. [ABSTRACT FROM AUTHOR]

Carbon paper is one of the most widely used gas diffusion layer substrate materials due to its stable performance, relatively low cost, and easy for subsequent processing. Water-soluble phenolic resin, which is more ecologically friendly than alcohol-soluble phenolic resin, was used to prepare carbon paper as the precursor of the carbon matrix. And the effect of different resin solution concentrations on the properties of carbon paper was explored. The results showed that the graphitization, electrical conductivity and mechanical properties of carbon paper increased with the increase of resin solution concentration. When the concentration of resin solution was 20 wt%, the performance of carbon paper was relatively optimal. The graphitization of the carbon paper reached 65.45%, the porosity reached 80.74%, the resistance value at 1 MPa pressure was only 7.61 mΩ cm2, the tensile strength was 1.57 MPa, and the elastic modulus was 1210.98 MPa. [ABSTRACT FROM AUTHOR]

A facile method is proposed in this work to prepare a carbon paper (CP) with outstanding properties by doping boron to catalyze graphitization at lower temperature. Boron was introduced into CP by impregnating carbon fiber preform into a boron/phenolic resin/ethanol solution, and then CP was obtained after the consecutive procedures of hot pressing, carbonization, and graphitization. Morphology, microstructure, composition, and physical properties of the doped and undoped CPs were thoroughly investigated via various techniques to exam the effects of boron concentration and graphitization temperature. Furthermore, the boron doped CP was fabricated into fuel cell gas diffusion layer (GDL) and membrane electrode assembly (MEA) to evaluate its performance through the single cell performance. The findings indicated CP doping with 2 wt% boron could lower the graphitization temperature by at least 200 °C. The B-doped GDL had a higher power density in comparison with the undoped GDLs made in our lab or from the commercial brands. • The innovative preparation method for carbon paper with high conductivity. • The effect of boron concentration and graphitization temperature on carbon paper. • The single cell performance of B-doped gas diffusion layer. [ABSTRACT FROM AUTHOR]

Polyaniline (PANI) with/without polystyrene (PS), was successfully manufactured in the occurrence of dispersed pulp fibers via the oxidative polymerization reaction of aniline monomer to produce conductive paper sheets containing PANI, PANI/PS composites. Additionally, sliver nitrate (Ag-NO3) was added by varied loadings to the oxidative polymerization of aniline monomer to provide sliver nanoparticles (Ag-NPs) emptied into the prepared paper sheets. The prepared paper sheets were examined using scanning electron microscopy (SEM), X-ray diffraction (XRD) and infrared spectroscopy (IR), the mechanical properties of the prepared paper sheets were evaluated. Moreover, the electrical conductivity and biological studies such as cellulases assay, Microorganism & culture condition and detection of the released of Ag-NPs were evaluated. Furthermore, the prepared paper sheets were displayed good antibacterial properties contrary to gram positive and gram negative bacteria. Consequently, the prepared paper sheet may be used as novel materials for packaging applications., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

Materials that provide dynamically tunable infrared (IR) response are important for many applications, including active camouflage and thermal management. However, current IR-tunable systems often exhibit limitations in mechanical properties or practicality of their tuning modalities, or require complex and costly fabrication methods. An additional challenge relates to providing compatibility between different spectral channels, such as allowing an object to be reversibly concealed in the IR without making it appear in the visible range. Here, we demonstrate that conducting polymer-cellulose papers, fabricated through a simple and cheap approach, can overcome such challenges. The papers exhibit IR properties that can be electrochemically tuned with large modulation (absolute emissivity modulation of 0.4) while maintaining largely constant response in the visible range. Owing to high ionic and electrical conductivity, the tuning of the top surface can be performed electrochemically from the other side of the paper even at tens of micrometer thicknesses, removing the need for overlaying electrode and electrolyte in the optical beam path. These features enabled a series of electrically tunable IR devices, where we focus on demonstrating dynamic radiative coolers, thermal camouflage, anti-counterfeiting tags, and grayscale IR displays. The conducting polymer-cellulose papers are sustainable, cheap, flexible and mechanically robust, providing a versatile materials platform for active and adaptive IR optoelectronic devices. [ABSTRACT FROM AUTHOR]

We present a new paper-based isotachophoresis (ITP) device design for focusing DNA samples having lengths ranging from 23 to at least 1517 bp. DNA is concentrated by more than two orders of magnitude within 4 min. The key component of this device is a 2 mm-long, 2 mm-wide circular paper channel formed by concertina folding a paper strip and aligning the circular paper zones on each layer. Due to the short channel length, a high electric field of ~16 kV m(-1) is easily generated in the paper channel using two 9 V batteries. The multilayer architecture also enables convenient reclamation and analysis of the sample after ITP focusing by simply opening the origami paper and cutting out the desired layers. We profiled the electric field in the origami paper channel during ITP experiments using a nonfocusing fluorescent tracer. The result showed that focusing relied on formation and subsequent movement of a sharp electric field boundary between the leading and trailing electrolyte.

The intrinsic properties of paper, such as its light weight, flexibility, foldability, portability and degradability, have led to increasing interest in fabricating flexible energy storage devices and power supply devices on paper-based substrates. Hereby, a robust honeycomb-like thermoelectric generator (TEG) inspired by the origami and kirigami techniques was established in the present study. A thermoelectric ink with the properties of high electrical conductivity and low thermal conductivity was formulated by Bi2Te3 and bacterial cellulose (BC). The formulated ink was printed on a paper surface using a facile processing method. The manufactured paper was further folded and bonded to fabricate a honeycomb-like TEG. This honeycomb-like paper-based TEG exhibited 96 p-n junctions, achieving a maximum voltage and output power of ∼70.5 mV and ∼596 nW, respectively, at a 55 K temperature difference. Moreover, the honeycomb structure was able to withstand a large number of bending and stretching cycles while maintaining its pristine structure. This unique honeycomb structure thus provides a new strategy for future development of paper-based TEGs.

Highly porous polypyrrole (PPy)-nanocellulose paper sheets have been evaluated as inexpensive and disposable electrochemically controlled three-dimensional solid phase extraction materials. The composites, which had a total anion exchange capacity of about 1.1 mol kg(-1), were used for extraction and subsequent release of negatively charged fluorophore tagged DNA oligomers via galvanostatic oxidation and reduction of a 30-50 nm conformal PPy layer on the cellulose substrate. The ion exchange capacity, which was, at least, two orders of magnitude higher than those previously reached in electrochemically controlled extraction, originated from the high surface area (i.e. 80 m(2) g(-1)) of the porous composites and the thin PPy layer which ensured excellent access to the ion exchange material. This enabled the extractions to be carried out faster and with better control of the PPy charge than with previously employed approaches. Experiments in equimolar mixtures of (dT)(6), (dT)(20), and (dT)(40) DNA oligomers showed that all oligomers could be extracted, and that the smallest oligomer was preferentially released with an efficiency of up to 40% during the reduction of the PPy layer. These results indicate that the present material is very promising for the development of inexpensive and efficient electrochemically controlled ion-exchange membranes for batch-wise extraction of biomolecules.

In this study, a novel, cost-effective, and environmental-friendly acetylcholinesterase (AChE)-based electrochemical biosensor was developed and utilized for paraoxon-ethyl (PE) detection. In this biosensor, cerium oxide (CeO2) and poly(3,4 ethylenedioxythiophene):poly(styrenesulfonate) (PESOT:PSS) modified paper electrode was fabricated by a simple dip-coating method. The synergistic effect of CeO2 and PEDOT:PSS enhance the performance of AChE-based biosensor in terms of sensitivity and selectivity. The electrical conductivity and stability of the fabricated electrode are further improved with the treatment of ethylene glycol (EG). EG decreases the coulombic interactions between PEDOT and PSS molecules, causes polymer chain reorientation, and improves the non-covalent interaction between cellulose molecules and PEDOT, which further leads to higher conductivity. All electrochemical results validate that the biosensor shows good selectivity (Kselectivity < 1), high sensitivity of 52.10 µA/nM, and a low detection limit of 0.12 nM. The accuracy and applicability of the proposed biosensor were also checked with two real samples. All results validate that the fabricated paper electrode can be a promising alternative to other conventional electrodes. [ABSTRACT FROM AUTHOR]

As power sources for Internet-of-Things sensors, thermoelectric generators must exhibit compactness, flexibility, and low manufacturing costs. Stretchable and flexible painted thermoelectric generators were fabricated on Japanese paper using inks with dispersed p- and n-type single-walled carbon nanotubes (SWCNTs). The p- and n-type SWCNT inks were dispersed using the anionic surfactant of sodium dodecylbenzene sulfonate and the cationic surfactant of dimethyldioctadecylammonium chloride, respectively. The bundle diameters of the p- and n-type SWCNT layers painted on Japanese paper differed significantly; however, the crystallinities of both types of layers were almost the same. The thermoelectric properties of both types of layers exhibited mostly the same values at 30 °C; however, the properties, particularly the electrical conductivity, of the n-type layer increased linearly, and of the p-type layer decreased as the temperature increased. The p- and n-type SWCNT inks were used to paint striped patterns on Japanese paper. By folding at the boundaries of the patterns, painted generators can shrink and expand, even on curved surfaces. The painted generator (length: 145 mm, height: 13 mm) exhibited an output voltage of 10.4 mV and a maximum power of 0.21 μW with a temperature difference of 64 K at 120 °C on the hot side. [ABSTRACT FROM AUTHOR]

Highlights: m-BN/PNF nanocomposite paper with nacre-mimetic layered structures prepared via sol–gel film transformation approach presents excellent thermal conductivity, incredible electrical insulation, outstanding mechanical property and thermal stability. When the mass fraction of m-BN is 50 wt%, m-BN/PNF nanocomposite paper exhibits excellent thermal conductivity and electrical insulation. The λ∥ and λ⊥ are 9.68 and 0.84 W m−1 K−1, and the volume resistivity and breakdown strength are as high as 2.3 × 1015 Ω cm and 324.2 kV mm−1, respectively. The m-BN/PNF nanocomposite paper with 50 wt% m-BN also presents outstanding mechanical properties (tensile strength of 193.6 MPa) and thermal stability (thermal decomposition temperature of 640 °C). With the rapid development of 5G information technology, thermal conductivity/dissipation problems of highly integrated electronic devices and electrical equipment are becoming prominent. In this work, "high-temperature solid-phase & diazonium salt decomposition" method is carried out to prepare benzidine-functionalized boron nitride (m-BN). Subsequently, m-BN/poly(p-phenylene benzobisoxazole) nanofiber (PNF) nanocomposite paper with nacre-mimetic layered structures is prepared via sol–gel film transformation approach. The obtained m-BN/PNF nanocomposite paper with 50 wt% m-BN presents excellent thermal conductivity, incredible electrical insulation, outstanding mechanical properties and thermal stability, due to the construction of extensive hydrogen bonds and π–π interactions between m-BN and PNF, and stable nacre-mimetic layered structures. Its λ∥ and λ⊥ are 9.68 and 0.84 W m−1 K−1, and the volume resistivity and breakdown strength are as high as 2.3 × 1015 Ω cm and 324.2 kV mm−1, respectively. Besides, it also presents extremely high tensile strength of 193.6 MPa and thermal decomposition temperature of 640 °C, showing a broad application prospect in high-end thermal management fields such as electronic devices and electrical equipment. [ABSTRACT FROM AUTHOR]

To study the current response to space charge in oil–paper insulation, a simultaneous space charge and external current measurement system are developed for a solid–liquid sample. The space charge and external current of oil-immersed paper are tested under different applied voltages. In the oil–paper sample, it accumulates heterocharge at 0.25 kV and homocharge at a higher voltage. The external currents first decrease and then increase with time. The changing timepoint decreases with the applied voltage. It shows that dynamic space charge evolution influences external current development. An unusual phenomenon is observed that the charge on both electrodes increases without heterocharge accumulation in a certain time range after voltage application, resulting in an increase in the average electric field. The transient electric field and displacement current at the cathode are calculated according to the amount of surface charge at the cathode. It indicates that displacement current takes up the main part of external current and decreases to zero when the surface charge amount stops increasing. After this stage, the conduction current is almost equal to the external current. The correlation between conduction current and electric field is analyzed. It reveals that when the electric field is lower than 5 kV/mm, the conduction current of oil–paper seems to be linear to the electric field strength, following Ohm's law. When the electric field is higher than 5 kV/mm, the conduction current of oil–paper follows the Fowler–Nordheim law that the ln(jc/E2) is linear to 1/E. The transient external current has great potential in diagnosing electrical equipment. [ABSTRACT FROM AUTHOR]

Aging behavior occurs in the storage process of paper archives, which accelerates the aging process of the paper. Therefore, it is important for paper archives management to explore the aging behavior of acidified paper (AP) and to delay or prevent its further aging. The aging behavior of the commonly used university archives paper with artificial acidification were studied by measuring pH value, electrical conductivity, mechanical properties and whiteness. The results show that the pH value, conductivity, mechanical properties and whiteness of AP change significantly compared with the non-acidified raw paper (P). After dry-heat aging treatment, the pH value of AP decreased more obviously than P, which shows more obvious aging degradation and further acidification of AP. During the aging process of AP, the molecular and structural degradation are promoted by the presence of acidic substances, which increase the electrical conductivity of the system. The microstructures of the paper are changed by acidification and aging treatment, and more fiber fracture, etching and microscopic holes are found in the surface SEM images. The reductions of the tensile index and whiteness of AP are also more significant because of the degradation acceleration of the acid. [ABSTRACT FROM AUTHOR]

Polyacrylonitrile (PAN) carbon fibers are often used to prepare high-performance paper-based materials owing to their high strength, good electrical and thermal conductivity, and superior comprehensive properties. In this study, a novel method for preparing PAN-based carbon fibers by centrifugal spinning was developed, and a stable and homogeneous PAN carbon fiber paper was successfully obtained. Subsequently, the formation process, microscopic morphology, electrical conductivity, electrochemical performance and hydrophobicity of the PAN carbon fiber paper were studied and evaluated. The results showed that the electrical conductivity of the PAN carbon fiber paper prepared via this method reached 43.250 s·cm−1, resistivity was as low as 0.023–0.033 Ω·cm, and contact angle exceeded 140°. This study adopted a new method to prepare PAN carbon fiber paper, which provided another method for the preparation of high-performance fiber paper. [ABSTRACT FROM AUTHOR]

Polyacrylonitrile (PAN) carbon fibers are often used to prepare high-performance paperbased materials owing to their high strength, good electrical and thermal conductivity, and superior comprehensive properties. In this study, a novel method for preparing PANbased carbon fibers by centrifugal spinning was developed, and a stable and homogeneous PAN carbon fiber paper was successfully obtained. Subsequently, the formation process, microscopic morphology, electrical conductivity, electrochemical performance and hydrophobicity of the PAN carbon fiber paper were studied and evaluated. The results showed that the electrical conductivity of the PAN carbon fiber paper prepared via this method reached 43.250 s.cm-1, resistivity was as low as 0.023-0.033 Omega.cm, and contact angle exceeded 140°. This study adopted a new method to prepare PAN carbon fiber paper, which provided another method for the preparation of high-performance fiber paper. [ABSTRACT FROM AUTHOR]

The aging and acidification behavior of paper archives affect their long-term preservation. Therefore, delaying or preventing aging and acidification has become an important topic in the field of paper archives management. the aging and acidification behavior of commercial archival paper were studied by measuring pH value, electrical conductivity, mechanical properties and whiteness in this work. The results show that the aging and acidification phenomena are obvious after dry-heat aging treatment. The molecular degradation of cellulose, hemicellulose, lignin and other components results in the decrease of pH value of the system, which decrease with the increase of the treatment temperature and time. The electrical conductivity of the system increases because of the molecular degradation and structural degradation, and with the increase of the treatment temperature and time, the electrical conductivity increases more significantly. After aging treatment, the paper appears etching and increasing microcosmic pores. With the occurrence of molecular degradation and structural degradation, the tensile index and whiteness of the paper decrease, and with the increase of the treatment temperature and time, the tensile index and whiteness decrease more significantly. [ABSTRACT FROM AUTHOR]

A thin, lightweight and flexible electromagnetic interference (EMI) shielding paper composite is an urgent need for modern military confrontations. Herein, a sandwich-structured EMI shielding paper composite with an easy pavement consisting of a filter paper layer, middle AgNWs/MXene layer, and polyvinyl butyral (PVB) layer was constructed by vacuum-assisted filtration, spraying and air-drying. The middle AgNWs/MXene compound endowed the filter paper with excellent electrical conductivity (166 S cm−1) and the fabricated filter paper–AgNWs/MXene–PVB composite exhibits superior EMI shielding (30 dB) with a 141 μm thickness. Remarkably, the specific EMI shielding effectiveness (SSE/t) of the filter paper–AgNWs/MXene–PVB composite reached 13,000 dB cm2 g−1 within the X-band frequency range. This value represents one of the highest reported for cellulose-based EMI shielding materials. Therefore, our sandwich-structured filter paper composite with superior EMI shielding performance can be used in the medical and military fields. [ABSTRACT FROM AUTHOR]

Free-standing reduced graphene oxide (rGO) papers were prepared by chemical reduction, thermal reduction and combined chemical-thermal reduction, respectively. Four-point probe and nanoindentation experiments were conducted to investigate the electrical and mechanical properties of rGO papers. The rGO paper prepared by soaking in L-ascorbic acid and thermal annealing in argon at 1000 °C (labeled rGO-AsA-T) showed superior electrical and mechanical properties when compared with rGO papers prepared merely by chemical reduction or thermal reduction. The as-prepared rGO-AsA-T paper exhibited an electrical conductivity of 5.7 × 104 S/m, showing an increase of 90% compared to that in the thermally annealed rGO paper and nearly 40 times that of rGO paper reduced by L-ascorbic acid. It was also found that the rGO-AsA-T paper had the lowest elastic modulus of 288 MPa, showing enhanced flexibility. The nearly free voids in rGO-AsA-T paper proved by scanning electron microscopy (SEM) were due to the capillary action in chemical reduction and were significant in improving the electrical conductivity and flexibility of the paper. The rGO-AsA-T paper with high conductivity and flexibility has a promising application in flexible electronics. [ABSTRACT FROM AUTHOR]

• Preparation of ZIF-67/PEDOT/CP self-supporting electrodes using simple in situ hydrothermal. • The addition of PEDOT to ZIF-67 helps to achieve high electrical conductivity and large specific surface area. • The sensor has a high detection performance for CGA. • ZIF-67/PEDOT/CP provided a new sensor for the detection of CGA in real sample. The design of efficient electrocatalysts for the determination of chlorogenic acids (CGA) is crucial in the biological and medical fields. In this paper, ZIF-67/poly(3,4-ethylenedioxythiophene) (PEDOT) nanocomposites were synthesised. The introduction of PEDOT increased the electrical conductivity of the ZIF-67/PEDOT composites, inhibited the Co atom agglomeration, led to the exposure of more active sites and increased the transport channels. An ultrasensitive CGA sensor based on ZIF-67/PEDOT nanocomposite modified carbon paper (CP) electrode was developed. The nanomaterials were characterised using scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction spectroscopy (XRD). Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were used to study the electrochemical properties of the modified CP electrode. In addition, the effects of different experimental conditions such as pH, scan rate and concentration on the peak current of CGA were investigated. Under the optimised conditions, the linear range of ZIF-67/PEDOT/CP for the determination of CGA was 0.1 ∼ 40 μM, and the limit of detection (LOD) was as low as 0.003 μM (S/N = 3). Furthermore, the sensor was successfully used for the quantitative analysis of CGA in real samples. [ABSTRACT FROM AUTHOR]

In this paper, a MnO2 nanowire (MnO2-NW) modified carbon paper electrode (CP) was developed as a novel electrochemical sensor for the sensitive determination of tetrabromobisphenol A (TBBPA). The MnO2 nanowire was prepared by a hydrothermal synthesis method, and the morphology and structure of MnO2 were characterized using scanning electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy. The electrochemical performance of TBBPA on MnO2-NW/CP was investigated by cyclic voltammetry, and the result confirmed that MnO2-NW/CP exhibited excellent sensitivity for the determination of TBBPA due to the high specific surface area and good electrical conductivity of the nanowire-like MnO2. Moreover, the important electrochemical factors such as pH value, incubation time and modified material proportion were systematically studied to improve the determination sensitivity. The interferences from similar structure compounds on TBBPA have also been investigated. Under the optimal conditions, MnO2-NW/CP displayed a linear range of 70~500 nM for TBBPA with a detection limit of 3.1 nM. This was superior to some electrochemical methods in reference. The work presents a novel and simple method for the determination of TBBPA. [ABSTRACT FROM AUTHOR]

Recently, mulberry paper has attracted much attention as a substrate for paper-based energy storage and conversion systems due to the excellent mechanical and chemical stability arising from its holocellulose-based structure and low lignin content, which overcome the limitations of typical cellulose-based paper. The formation of an electrically conducting layer on the mulberry paper is a key step in fabricating the mulberry paper-based energy storage and conversion system. Various methods such as coating, printing, composite formation, and carbonization have been used to provide mulberry paper with electrical conductivity. The properties of mulberry paper electrodes largely depend on the choice of fabrication method, with each method having distinct advantages and disadvantages. Despite of the importance of the processing technology for forming the conducting layer, no comprehensive review on the topic exists to-date, especially with respect to mulberry paper. Hence, the present review introduces the research trends on mulberry paper-based energy storage and conversion devices, and focuses on the technology for fabricating the conducting layer. The advantages and disadvantages of the various fabrication methods are discussed in order to provide a future research direction for mulberry paper-based electrode fabrication, and for its application to the energy storage and conversion system. [ABSTRACT FROM AUTHOR]

A simple approach was developed to fabricate high‐performance MXene/cellulose (MC)‐based electromagnetic interference (EMI) shielding papers. The oriented MXene sheets located on one side of cellulose filter paper construct a continuous conductive layer, endowing the MC paper with high electrical conductivity (240.1 S/m) and excellent EMI shielding effectiveness (29.3 dB for 0.192‐mm thickness) at an MXene content of 0.72 vol%. Moreover, the EMI shielding effectiveness of four stacked MC papers reached 40.5 dB. This result means that 99.9911% of the microwave radiation is attenuated, and 0.0089% is transmitted, through the four‐piece MXene/cellulose filter papers. Therefore, MC paper has promising properties for excellent EMI shielding materials in current electronic devices. [ABSTRACT FROM AUTHOR]

Transition metal (Fe, Ni, Co)-based hydroxides, especially nickel hydroxide (Ni(OH)2), have been considered as promising candidate for hydrogen evolution reaction (HER) because of their low cost, natural abundance and high catalytic performance. However, the catalytic performance of Ni(OH)2 is still unsatisfactory for practical application due to its relatively low electrical conductivity. Here, a highly conductive silver nanowires (AgNWs) network is prepared on filter paper, followed by the electrodeposition of Ni(OH)2 on the surface of AgNWs to form AgNWs@Ni(OH)2 core-shell structure. In comparison with pure Ni(OH)2 (376 mV at −10 mA cm−2), the optimized AgNWs@Ni(OH)2 electrode can exhibit about 3-fold enhanced HER performance, which achieves a lower overpotential of 123 mV at the current density of −10 mA cm−2, and a small Tafel slope of 76 mV dec−1 in 1 M KOH electrolyte. Besides the superior activity, the AgNWs@Ni(OH)2 electrode also shows a better durability. Such enhanced catalytic performance benefits from the high conductivity of AgNWs network to facilitate electron transfer, and the synergistic interaction between AgNWs and Ni(OH)2. This work also provides general strategies to design highly active HER electrocatalysts by utilizing highly conductive AgNWs to form core-shell architecture. [ABSTRACT FROM AUTHOR]

At present, the self-supporting paper-based electrode has some problems, such as low mechanical strength and insufficient flexibility, which restrict its application in flexible electronics. In this paper, FWF is used as the skeleton fiber, and the contact area and the number of hydrogen bonds of the fiber are increased by grinding the fiber and adding nanofibers to bridge it, and a level three gradient enhanced skeleton support network structure is constructed, which effectively improves the mechanical strength and foldability of the paper-based electrodes. The tensile strength of FWF15-BNF5 paper-based electrode is 7.4 MPa, the elongation at break is increased to 3.7%, the electrode thickness is as low as 66 μm, the electrical conductivities is 5.6 S cm−1, and the contact angle to electrolyte as low as 45°, which has excellent electrolyte wettability, flexibility, and foldability. After three-layer superimposed rolling, the discharge areal capacity reached 3.3 mAh cm−2 and 2.9 mAh cm−2 at the rate of 0.1 C and 1.5 C, respectively, which was superior to the commercial LFP electrode, it had good cycle stability, and the areal capacity was 3.0 mAh cm−2 and 2.8 mAh cm−2 after 100 cycles at the rate of 0.3 C and 1.5 C. [ABSTRACT FROM AUTHOR]

A theory of control of cellular proliferation and differentiation in the early development of metazoan systems, postulating a system of electrical controls "parallel" to the processes of molecular biochemistry, is presented. It is argued that the processes of molecular biochemistry alone cannot explain how a developing organism defies a stochastic universe. The demonstration of current flow (charge transfer) along the long axis of DNA through the base-pairs (the "pi-way) in vitro raises the question of whether nature may employ such current flows for biological purposes. Such currents might be too small to be accessible to direct measurement in vivo but conduction has been measured in vitro, and the methods might well be extended to living systems. This has not been done because there is no reasonable model which could stimulate experimentation. We suggest several related, but detachable or independent, models for the biological utility of charge transfer, whose scope admittedly outruns current concepts of thinking about organization, growth, and development in eukaryotic, metazoan systems. The ideas are related to explanations proposed to explain the effects demonstrated on tumors and normal tissues described in Article I (this issue). Microscopic and mesoscopic potential fields and currents are well known at sub-cellular, cellular, and organ systems levels. Not only are such phenomena associated with internal cellular membranes in bioenergetics and information flow, but remarkable long-range fields over tissue interfaces and organs appear to play a role in embryonic development (Nuccitelli, 1992 ). The origin of the fields remains unclear and is the subject of active investigation. We are proposing that similar processes could play a vital role at a "sub-microscopic level," at the level of the chromosomes themselves, and could play a role in organizing and directing fundamental processes of growth and development, in parallel with the more discernible fields and currents described.

Light‐weight, portability and miniaturization are important characteristics for the next generation of high‐performance electromagnetic interference (EMI) shielding equipment. To meet the current demand for high‐performance EMI shielding materials, this paper proposes a simple and reliable method for preparing multilayer paper‐based composites. Paper‐based composites exhibit light weight, flexibility, easy processing and high temperature resistance. A conductive metal–organic skeleton (Ni‐CAT) layer and polypyrrole (PPy) layer were deposited on a polyimide (PI) fiber surface with an in situ synthesis and gas aggregation method to prepare paper‐based electromagnetic shielding composites with good properties. The results showed that the electromagnetic shielding effect (SE) of the paper‐based composites reached 41.0 dB. After the paper‐based composites underwent multiple ultrasonic washing and bending tests, their electrical conductivity retention rate was as high as 90%. Furthermore, the introduction of PPy/Ni‐CAT enhanced the bonding strength of the PI fibers, which caused the tensile strength of the paper‐based composites to reach 22.3 MPa. Due to the good thermal stability of the composites, they can withstand an open flame and protect the equipment during a fire. Thus, these paper‐based EMI shielding composites hold great promise for flexible electromagnetic shielding materials, protection of smart wearable devices and other fields. [ABSTRACT FROM AUTHOR]

Copyright of Cotton Textile Technology is the property of Cotton Textile Technology Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Recently, the macroporous and free-shaped reduced graphene oxide paper (MFGP) has been considered a sensing medium due to its ultralightweight, flexibility and good electrical conductivity performance. Here, a highly sensitive MFGP-based strain and pressure sensor is fabricated based on the macroporous reduced graphene oxide (rGO) paper. The honeycomb-like macroporous structure was obtained using a confined space to constrain the expansion paper to a certain thickness. Due to the interlock and layer-by-layer macroporous structure, the strain and pressure sensor has an ultrahigh gauge factor of 143 in the strain range of 7.6–11% and 1.5 kPa–1 in the pressure range of 0–60 kPa. Moreover, the MFGP-based strain and pressure sensor can monitor human motions such as wrist pulse, speaking and tiny muscle movements with a very low operating voltage of 5 mV. Therefore, the high sensitivity, flexibility, low operating voltage and free-shaped of the MFGP-based strain and pressure sensors demonstrate potential applications as wearable devices. [ABSTRACT FROM AUTHOR]

Mass-impregnated (MI) cables have been used for many years as cables in high-voltage direct current (HVDC) systems. In line commutated converter (LCC) HVDC systems, polarity reversal for power flow control can induce significant electrical stress on MI cables. Furthermore, the mass oil and kraft paper comprising the impregnated insulation have significantly different coefficients of thermal expansion. Load fluctuations in the cable lead to expansion and contraction of the mass, creating pressure within the insulation and causing redistribution of the impregnant. During this process, shrinkage cavities can form within the butt gaps. Since the dielectric strength of the cavities is lower than that of the surrounding impregnation, cavitation phenomena in impregnated paper insulation are considered a factor in degrading insulation performance. Consequently, this study analyzes the electrical conductivity of thermally aged materials and investigates the transient electric field characteristics within the cable. Additionally, it closely analyzes the formation and dissolution of cavities in MI cables during polarity reversal based on a numerical model of pressure behavior in porous media. The conductivity of the impregnated paper indicates that it has excellent resistance to thermal degradation. Simulation results for various load conditions highlight that the interval of load-off time and the magnitude of internal pressure significantly influence the cavitation phenomenon. Lastly, the study proposes stable system operation methods to prevent cavitation in MI cables. [ABSTRACT FROM AUTHOR]

MXene-based nanocomposites are highly desirable for electromagnetic interference (EMI) shielding applications. However, it is crucial but challenging to obtain an excellent trade-off between mechanical properties and EMI performances. Herein, inspired by Janus structure, flexible cellulose nanofiber-assisted MXene/silver nanowires (CNF-MXene/AgNWs) papers (CMAPs) are developed by a scalable sequential self-assembly plus a hot-pressing strategy. The ingenious introduction of highly conductive AgNWs into MXene forms a complementary leaf-like nanostructure, synergistically constructing highly effective conductive frameworks. Contributed by the designed Janus architecture, high-performance CNF substrate, and extensive hydrogen-bonding interactions, the resultant Janus CMAPs (J-CMAPs) with a low MXene/AgNWs addition of 30 wt% possess a high electrical conductivity (1066.85 S/cm), excellent mechanical strength (224.04 MPa) and modulus (9.98 GPa), exceptional EMI shielding effectiveness of 43.65 dB, and record-high EMI SE/t of 16788.51 dB cm−1 and SSE/t of 10543.18 dB cm2 g−1 with a reflection-dominant shielding mechanism, successfully achieving an outstanding balance between mechanical properties and EMI shielding performances. More importantly, high frequency structure simulator (HFSS) simulation in the frequency domain is further conducted to intuitively comprehend the attenuation process of electromagnetic waves and shield mechanism, verifying fascinating EMI shielding performances. Besides, the Janus paper also presents desirable Joule heating performances at low input voltage, short response time (<10 s), and superb heating stability and long-term steady reliability. We believe that the J-CMAPs demonstrate the great potential and advantage for advanced EMI shielding and portable thermal management applications. SynopsisIn this paper, inspired by Janus structure, flexible CNF-assisted MXene/AgNWs nanopapers with both excellent mechanical properties and impressive EMI shielding performance are developed. The nanopapers exhibit a high electrical conductivity, superior mechanical properties, impressive EMI shielding effectiveness of 43.65 dB, and record-high EMI SE/t of 16788.51 dB cm−1 and SSE/t of 10543.18 dB cm2 g−1, suggesting the great potential for advanced EMI shielding applications. [Display omitted] [ABSTRACT FROM AUTHOR]

In order to solve the problems of high cost and high brittleness of commercial carbon fiber paper, a low-cost mass production method of carbon fiber paper for flexible super capacitor was proposed. The dispersant CMC-Na is utilized to achieve uniform dispersion of chopped carbon fiber in a water system through ultrasonic dispersion. Sheath-core composite (PE/PET) fiber not only enhances the tensile strength of CFP but also consolidates the electrode network structure formed based on carbon fiber structure. The CFP-3 electrode, impregnated with 3 % AC phenolic resin, exhibits excellent mechanical and electrochemical properties. SEM images reveal that AC is deposited on each carbon fiber and that the CFP-3 electrode retains its three-dimensional structure (with a porosity of 71.2 %), providing an effective permeation path for electrons (with an electrical conductivity of 0.871 S m−1). The CFP-3 electrode can restore its original shape after folding and bending without damage. Electrochemical tests demonstrate that the CFP-3 electrode has a high areal capacitance of 507.2 mF cm−2 at a current density of 0.5 mA cm−2. At a current density of 10 mA cm−2, the capacitance retention rate of the CFP-3 electrode is 96.1 % after 5000 charge-discharge cycles, owing to the well-interconnected structure of the carbon fiber paper. Furthermore, when used as a direct electrode, CFP exhibits excellent stability. Most notably, the cost of producing the CFP-3 electrode (0.0314 m2) is only $0.195, significantly lower than that of commercial products, excluding equipment, utilities, and labor costs. This research provides valuable insights for the low-cost, large-scale production of paper-based flexible supercapacitors. [Display omitted] • Carbon fiber, PE/PET fiber, AC, CMC-Na and ultrasonic dispersion were prepared by traditional wet-mold papermaking method. • The cost of producing each CFP-3 electrode (0.0314 m2) is only $0.195, excluding equipment, utilities, and labor costs. • The areal capacitance of the CFP-3 electrode can reach 507.2 mF cm-2 at 0.5 mF cm-2 and retains 98.2% after 5000 cycles. [ABSTRACT FROM AUTHOR]

Organic/inorganic thermoelectric hybrids demonstrate great potential for wearable applications. However, their scalability is hindered by an inferior power factor (S 2 σ). Nowadays, achieving deep optimization of S 2 σ necessitates a strategy to decouple the Seebeck coefficient (S) and electrical conductivity (σ). In this work, we propose a strategy to break the coupling between S and σ by constructing a Schottky interface that exhibits an energy-filtering effect. We validate the feasibility of this approach using a PANI/TiN–TiO2/carbon paper. The results demonstrate a 1.16-fold increase in σ and a 1.08-fold increase in S in PANI/TiN–TiO2/carbon paper achieved through the construction of a Schottky-type TiN/TiO2 interface. The separation of hole/electron at the TiN/TiO2 interface serves as the scattering center for ionized impurity scattering and facilitates the transport pathway for charge carriers. These factors are crucial in determining the simultaneous optimization of S and σ , respectively. Additionally, the energy-filtering effect of the TiN/TiO2 interface plays a positive role in the ionized impurity scattering mechanism by selectively filtering out low-energy carriers. This further strengthens decoupling of the thermoelectric properties. The 14.9% PANI/11.2% TiN–14.5% TiO2/59.44% carbon paper displays the highest S 2 σ and achieves a high ZT value of 223.6 μVm−1 K−2 and 0.31 at 300 K, highlighting the advantages of PANI-based thermoelectric hybrids. This work provides valuable guidance for the design of thermoelectric hybrids incorporating multi-interface morphology. [ABSTRACT FROM AUTHOR]

To stabilize the detection signal of palladium-based hydrogen sensors on paper substrates, a graphite intermediate layer was painted on the surface of paper. The graphite-on-paper (GOP) substrate offers advantages such as good thermo-electrical conductivity, low cost, and uncomplicated preparation technology. Quasi-1-dimensional palladium (Pd) thin films with 8 nm and 60 nm thicknesses were deposited on the GOP substrates using the vacuum evaporation technique. Thanks to the unique properties of the GOP substrate, a continuous Pd microfiber network structure appeared after deposition of the ultra-thin Pd film. Additionally, the sensing performance of the palladium-based hydrogen sensor was not affected, whether using GOP or paper substrate at 25 °C. Surprisingly, heating-induced loss of sensitivity was restrained due to the increased electrical conductivity of the GOP substrate at 50 °C. [ABSTRACT FROM AUTHOR]

Cu-benzene–1, 3, 5-tricarboxylate (Cu-BTC) coating on carbon fiber paper (CFP@Cu-BTC) is synthesized by using the seed-induced hydrothermal method to improve H 2 adsorption capacity, CO 2 /H 2 selectivity, thermal and electrical conductivity of pure Cu-BTC. The electrical conductivity, effective thermal conductivity (ETC), CO 2 and H 2 adsorption capacity of CFP@Cu-BTC composites synthesized for 3, 9, 18, and 24 h are investigated, respectively. Results show the H 2 adsorption capacity of CFP@Cu-BTC (9 h) is similar to that of pure Cu-BTC. The value of the selectivity of equimolar CO 2 /H 2 (18 h) is 58–209 at 0–100 kPa and 273.15 K. The ETC of CFP@Cu-BTC is 17–25 times higher than that of pure Cu-BTC. The electrical conductivity is 1.3 × 1011–1.6 × 1011 times higher compared to that of pure Cu-BTC. The CFP@Cu-BTC composite can be used as a promising material for H 2 storage and electrodes of ultra-capacitor. • Cu-BTC/CFP is obtained by the seeds induced hydrothermal method. • The selectivity of equimolar CO 2 /H 2 (18 h) can reach up to 58–209. • The thermal conductivity of Cu-BTC/CFP is much higher than that of pure Cu-BTC. • The electric conductivity of Cu-BTC/CFP is 1.3 × 105 S/m when loading 40 wt% Cu-BTC. [ABSTRACT FROM AUTHOR]

Commercial Chinese ink was employed to disperse pristine vapor-grown carbon nanofibers (VGCNFs) in aqueous suspensions via horizontal ball milling. The obtained suspension was used to fabricate conductive paper-based composites through filtration-deposition onto filter paper. It was found that the carbon black particles from the Chinese ink helped separate VGCNFs and acted as connection points between the VGCNFs, while the glue reinforced the conduction network. Thus, the VGCNF-ink/paper ternary composite showed sufficiently low sheet resistance. With merely 2.5 mg·cm−2 VGCNFs, the sheet resistance could be reduced to 4.5 Ω·sq−1. As a proof of concept, these paper-based composites were directly used as electrodes of solid-state symmetric electronic double-layer capacitors (EDLCs) and the substrate for the electrodeposition of MnO2 to achieve higher electrochemical performances. The EDLCs fabricated with 2.5 mg·cm−2 VGCNFs showed a specific capacitance of 224 mF·cm−2 at a current density of 1 mA·cm−2, which was retained by 86.4% after 10,000 charge-discharge cycles. Moreover, thanks to the high electrical conductivity and the porous structure, the MnO2 decorated paper-based composites exhibited dramatically enhanced specific capacitance. It is believed that our finding offers an idea to directly utilize commercial Chinese ink for the fabrication of electrode materials. [ABSTRACT FROM AUTHOR]

Commercial inkjet-printers from manufacturers like Epson or Brother can be used for rapid prototype printing conductive traces onto paper or flexible PET substrates by using nanoparticle based dispersions. The surface coating of the substrate influences the attainable electrical conductivity and dielectric permittivity as well as the loss tangent, which are important parameters for developing inkjet-printed microwave circuits on paper substrates. For characterizing the permittivity conventional methods are using microstrip ring or microstrip transmission line resonators that require the printing of two electrically conductive layers. In the proposed paper, a novel method is introduced to determine the relative permittivity and loss tangent via a coplanar waveguide resonator realized on a single layer. [ABSTRACT FROM AUTHOR]

Paper‐based electronics are emerging as a new class of technology with broad areas of application. Despite several efforts to fabricate new types of flexible electronic devices by screen printing of conductive paste, many of them are often nonbiodegradable, toxic, and expensive, limiting their practical use in bioresorbable paper‐based electronics. To address this need, a highly conductive and biodegradable bimodal conductive paste is developed using cost‐effective zinc‐based micro and nanoparticles with a facile low‐temperature sintering process compatible with paper substrates. The two‐step sintering process involves the removal of the insulating zinc oxide layer by spray coating acetic acid followed by a heat press sintering process to ensure the formation of highly packed and continuous metallic traces. The required conditions for the heat press sintering process are systematically studied using electrical, optical, and mechanical characterization techniques. The results of these investigations revealed an ultra‐packed microstructure with high electrical conductivity (0.5 × 105 S m−1) and low oxide content that is obtained with a heat press sintering setting of 220 °C for 60 s. Finally, as a proof of concept, the conductive paste with an optimized sintering process is used to fabricate a wearable wireless heater for remote‐controlled release of therapeutics. The controlled delivery of the system is validated in the practical and on‐demand delivery of antibiotics for eradicating commonly found bacteria such as Staphylococcus aureus in dermal wound infections. The biocompatibility of all the materials and manufacturing process is validated by NIH/3T3 fibroblast cells via MTT assay and live/dead staining. [ABSTRACT FROM AUTHOR]

Silver nanowires were successfully prepared by polyol method using silver nitrate as silver source, ethylene glycol as solvent and reducing agent, and ferric chloride as nucleating agent and polyvinylpyrrolidone (PVP) as structure directing agent and protective agent. The obtained silver nanowires were mixed with Kraft pulp fibers and bacterial cellulose to prepare conductive paper via simple filtration process. The results indicated that the size of silver nanowires can be regulated by the dosage of ferric chloride used. At optimal dosage of FeCl3, the prepared silver nanowires can reach 20 μm length, 100 nm width, and 200 of width/diameter ratio. The adding of bacterial cellulose in preparing the conductive paper greatly enhanced the retention ratio of silver nanowires as well as the stress and strain of the conductive paper. The stress and strain of the paper with bacterial cellulose were increased by 60% and 7%, respectively, compared with that of the paper without bacterial cellulose. The maximum retention ratio and the highest recovery ratio of silver nanowires in conductive paper reached 94% and 75%, respectively. The resistance of as-prepared conductive paper was only 0.9 Ω. In conductive paper, the silver nanowires attached to the paper-based materials with cellulose fibers as the substrate, which achieved the electrical conductivity of paper-based materials. This conductive paper can be applied as antistatic, antibacterial packaging and conductive material. [ABSTRACT FROM AUTHOR]

Free-standing flexible supercapacitive electrodes have practical application for wearable energy storage devices. In this paper, graphene paper (GP), a flexible electrode substrate, was prepared by one-step reduction of graphene oxide (GO) using HI solution. GP can be used independently as a flexible electrode with specific capacitance of 227 F/g. In order to make up for the shortage of GP specific capacitance storage, polyaniline (PANI) with high specific capacitance and good electrical conductivity was selected to composite with GP by electrochemical polymerization approach. This method to fabricate electrode material by direct electrochemical polymerization avoids the use of conductive binder and organic solvent. Owing to the specific capacitance contribution of PANI and GP, the PANI/GP composites exhibit higher specific capacitance when the polymerization time is 30 s and the polymerization voltage is 0.8 V. At 1 A/g current density, the specific capacitance of composite is up to 759 F/g, which is 3.34 times of neat GP. [ABSTRACT FROM AUTHOR]

The performance of supercapacitor degenerates at low temperature, even fails to work sometimes. Solar photothermal conversion provides a new direction for the performance improvement of supercapacitor. Manganese dioxide (MnO2) has a high specific capacity, while it should be compounded with other active materials due to its low electric conductivity. Therefore, this study aimed to improve the performance of MnO2-based supercapacitor using the photothermal effect of polypyrrole (PPy), which exhibited excellent light absorption ability and pseudocapacitance property. MnO2 and PPy were successively deposited on slow filter paper by wet chemistry method and low-temperature interfacial polymerization approach, and PPy/MnO2 paper-based composites with different PPy contents were prepared. The structures and properties of the composites were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, cyclic voltammetry, galvanostatic charge/discharge, and AC impedance spectroscopy. The results showed that the porous structure of filter paper was well preserved after PPy deposition, and MnO2 was covered to form a large active area. The specific capacitance of MnO2/PPy-400 single electrode reached 1 487.1 mF/cm2, 67% higher than that of pure PPy electrode. Under the simulated sunlight with the intensity of 1 kW/m2, the surface temperature of the assembled symmetrical supercapacitor increased from 21.2 °C to 46.7 °C after 10 min. The specific capacitance of the symmetrical supercapacitor assembled by the paper electrode with PPy of 400.0 μL was 52.9 mF/cm2 with illumination, five times that in dark, suggesting excellent photothermal effect to enhanced capacitor performance. [ABSTRACT FROM AUTHOR]

Lithium-ion batteries have received considerable attention as energy storage tool for modern-life equipments. However, drawbacks like low electric conductivity and volume expansion are the obstacles that hinder its application. To solve these problems, we developed a facile method using waste eggshell as hard template to reduce its particle size and change its morphology by simple hydrothermal process. Then, by utilizing waste paper, conductive paper (CP) current collector with graphene and multiwalled carbon nanotube implanted was prepared and combined with MnO2 anode material. The composite anode shows extraordinary electrochemical performances like much smaller impedance, high reversible capacity of 1767/1762 mAh/g even after 200 cycles at 100 mA/g, superior rate performance, etc. Compared with anode using metal current collectors, this composite anode will reduce weight and can be generalized to other high energy storage applications. Our environment-friendly method has far-reaching referential significance to other active materials and battery systems. A composite electrode, with δ -MnO2 as active material and conductive paper as current collector, has been synthesized and used in lithium-ion battery. Waste eggshell and waste paper were used in the synthetic process to protect environment. The electrode is much lighter and has much better electrochemical performances. This method can be generalized to other active materials and battery systems. [ABSTRACT FROM AUTHOR]

To further improve the electrical insulation properties of meta-aramid paper, polydimethyldiallyl ammonium chloride (PDDA) was used for the modification of nano-Al2O3 in this work. The modified products were characterized by means of transmission electron microscopy, Fourier transform infrared spectrometer and liquid Zeta potential. The original and PDDA-modified nano-Al2O3 was doped into the aramid fiber composite, and the effects of PDDA and filler mass fraction on several properties such as electrical conductivity, breakdown strength and surface charge dissipation rate of insulating paper were studied. Finally, the interfacial properties of the composites were investigated using molecular dynamics. The results showed that PDDA was successfully coated on the surface of nano-Al2O3, and its surface potential was changed from negative to positive, which could improve the interface characteristics between filler and matrix and enhance the dielectric strength of aramid paper. Besides, saturation effect of PDDA modification was observed, and when the amount of PDDA was 10% and the content of modified nano-Al2O3 was 3%, the breakdown strength of aramid paper was increased by 20%, and the volume conductivity was decreased by 68%. The simulation result revealed that PDDA could improve the insulation performance of aramid paper by reducing the interfacial binding energy between aramid and filler. [ABSTRACT FROM AUTHOR]

By continuously varying the structure of graphene oxide paper (PRGP) using Joule heating annealing, we are able to tune its electrical conductivity (σ) and thermal diffusivity (α) in a very wide range: more than three orders of magnitude for σ (186–503009 S/m) and 10-fold for α (8.31 × 10−7 m2/s to 9.31 × 10−6 m2/s). Excellent coherency-linear relationship between σ and α is discovered although they are sustained by different carriers: electrons and phonons. Such coherency exists over two sections: σ > 2 × 104 S/m, and 103< σ < 2 × 104 S/m. A two-component parallel structure is proposed to interpret the observed discovery. The slope of α∼σ relation reflects the ratio of difference in α between the two components over σ of the ordered structure. The intercept of α∼σ relation reflects the α of the disordered structure. It is found the α of disordered structure in our PRGP agrees well with that of amorphous carbon. Past work on carbon nanocoil, graphene paper, graphene oxide film, and graphene fiber also reveals linear coherency between α and σ. However, there are no uniform slope and intercept while they are close for similar materials. The parameters of the linear coherency strongly depend on the two structures in the material. [Display omitted] [ABSTRACT FROM AUTHOR]

Oil impregnated paper in power transformers deteriorates in long-term operation, which leads to the variations of its dielectric characteristics. This paper focuses on investigating the generation mechanism of the dielectric processes in oil impregnated paper and their variations with thermal aging. Firstly, a set of thermally stimulated current tests with bias-voltages were conducted in distinguishing the dielectric processes and revealing their generation mechanism. Secondly, the standard thermally stimulated current spectrum and the M″ spectrum of 0–1000 h aged samples were joint analyzed in investigating the variations of dielectric processes in thermal aging process. Finally, additional experiments of moisture, acidity and microscopic observation were conducted in explaining these variations. It is concluded that three dielectric processes can be found in oil impregnated paper, i.e. the dipole polarization, the interfacial polarization and the electric conduction. These processes are all strengthened with thermal aging. The generation of molecules with strong polarity, the structural changes in insulating paper, and the generation of hydrogen ions are responsible for the strengthening of these processes sequentially. This investigation on distinguishing dielectric processes and obtaining their mechanism can promote further understanding on oil impregnated paper and provide information for insulation design in power transformers. [ABSTRACT FROM PUBLISHER]