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Background: Efficient monitoring of glucose concentration in the human body necessitates the utilization of electrochemically active sensing materials in nonenzymatic glucose sensors. However, prevailing limitations such as intricate fabrication processes, lower sensitivity, and instability impede their practical application. Herein, ternary Cu-Co-Ni-S sulfides nanoporous network structure was synthesized on carbon fiber paper (CP) by an ultrafast, facile, and controllable technique through on-step cyclic voltammetry, serving as a superior self-supporting catalytic electrode for the high-performance glucose sensor., Results: The direct growth of free-standing Cu-Co-Ni-S on the interconnected three-dimensional (3D) network of CP boosted the active site of the composites, improved ion diffusion kinetics, and significantly promoted the electron transfer rate. The multiple oxidation states and synergistic effects among Co, Ni, Cu, and S further promoted glucose electrooxidation. The well-architected Cu-Co-Ni-S/CP presented exceptional electrocatalytic properties for glucose with satisfied linearity of a broad range from 0.3 to 16,000 μM and high sensitivity of 6829 μA mM - 1 cm - 2 . Furthermore, the novel sensor demonstrated excellent selectivity and storage stability, which could successfully evaluate the glucose levels in human serum. Notably, the novel Cu-Co-Ni-S/CP showed favorable biocompatibility, proving its potential for in vivo glucose monitoring., Conclusion: The proposed 3D hierarchical morphology self-supported electrode sensor, which demonstrates appealing analysis behavior for glucose electrooxidation, holds great promise for the next generation of high-performance glucose sensors., (© 2024. The Author(s).)

Many studies have been conducted on measuring avian influenza viruses and their hemagglutinin (HA) antigens via electrochemical principles; most of these studies have used gold electrodes on ceramic, glass, or silicon substrates, and/or labeling for signal enhancement. Herein, we present a paper-based immunosensor for label-free measurement of multiple avian influenza virus (H5N1, H7N9, and H9N2) antigens using flexible screen-printed carbon nanotube-polydimethylsiloxane electrodes. These flexible electrodes on a paper substrate can complement the physical weakness of the paper-based sensors when wetted, without affecting flexibility. The relative standard deviation of the peak currents was 1.88% when the electrodes were repeatedly bent and unfolded twenty times with deionized water provided each cycle, showing the stability of the electrodes. For the detection of HA antigens, approximately 10-μl samples (concentration: 100 pg/ml-100 ng/ml) were needed to form the antigen-antibody complexes during 20-30 min incubation, and the immune responses were measured via differential pulse voltammetry. The limits of detections were 55.7 pg/ml (0.95 pM) for H5N1 HA, 99.6 pg/ml (1.69 pM) for H7N9 HA, and 54.0 pg/ml (0.72 pM) for H9N2 HA antigens in phosphate buffered saline, and the sensors showed good selectivity and reproducibility. Such paper-based sensors are economical, flexible, robust, and easy-to-manufacture, with the ability to detect several avian influenza viruses., (© 2022. The Author(s).)

Screen-printed technology has helped considerably to the development of portable electrochemical sensors since it provides miniaturized but robust and user-friendly electrodes. Moreover, this technology allows to obtain very versatile transducers, not only regarding their design, but also their ease of modification. Therefore, in the last decades, the use of screen-printed electrodes (SPEs) has exponentially increased, with ceramic as the main substrate. However, with the growing interest in the use of cheap and widely available materials as the basis of analytical devices, paper or other low-cost flat materials have become common substrates for SPEs. Thus, in this revision, a comprehensive overview on paper-based SPEs used for analytical proposes is provided. A great variety of designs is reported, together with several examples to illustrate the main applications.

The indiscriminate use of herbicides in agriculture contributes to soil and water pollution, with important endangering consequences on the ecosystems. Among the available analytical systems, algal biosensors have demonstrated to be valid tools thanks to their high sensitivity, cost-effectiveness, and eco-design. Herein, we report the development of a dual electro-optical biosensor for herbicide monitoring, based on Chlamydomonas reinhardtii whole cells immobilised on paper-based screen-printed electrodes modified with carbon black nanomaterials. To this aim, a systematic study was performed for the selection and characterisation of a collection among 28 different genetic variants of the alga with difference response behaviour towards diverse herbicide classes. Thus, CC125 strain was exploited as case study for the study of the analytical parameters. The biosensor was tested in standard solutions and real samples, providing high sensitivity (detection limit in the pico/nanomolar), high repeatability (RSD of 5% with n = 100), long lasting working (10 h) and storage stability (3 weeks), any interference in the presence of heavy metals and insecticides, and low matrix effect in drinking water and moderate effect in surface one.

A facile strategy, engineered for low-cost mass production, to synthesize biomass-derived activated carbon/reduced graphene oxide composite electrodes (GBPCs) by one-pot carbonization of blotting papers containing graphene oxide (GO) and zinc chloride (ZnCl 2 ) was proposed. Benefitting from the water absorption characteristic of blotting papers in which the voids between the celluloses can easily absorb the GO/ZnCl 2 solution, the chemical activation and reduction of GO can synchronously achieve via one-step carbonization process. As a result, the GBPCs deliver a large specific surface area to accumulate charge. Simultaneously, it provides high conductivity for electron transfer. The symmetric supercapacitor assembled with the optimal GBPCs in 6 M KOH electrolyte exhibits an excellent specific capacitance of 204 F g -1 (0.2 A g -1 ), outstanding rate capability of 100 F g -1 (20 A g -1 ). Meanwhile, it still keeps 90% of the initial specific capacitance over 10,000 cycles. The readily available raw material, effective chemical activation, simple rGO additive, and resulting electrochemical properties hold out the promise of hope to achieve low-cost, green, and large-scale production of practical activated carbon composite materials for high-efficiency energy storage applications.

Gold is among the highly conductive and stable materials, which are ideal anodes for microbial fuel cells (MFCs). However, previous studies have shown that bare gold surface is recalcitrant for the colonization of some exoelectrogens, e.g., Shewanella putrefacians. In this work, the problem regarding the poor bio-compatibility of gold as an anode material was sorted out through coupling it with carbon paper. A new composite anode material was fabricated through sputtering gold layer homogeneously on carbon paper matrix. Results of cyclic voltammetry and electrochemical impedance spectroscopy in Fe(CN)6(3-/4-) solution demonstrated better electrochemical performance of the carbon paper-gold (C-Au) composite than either carbon paper or bare gold, when they were used in MFCs. With Shewanella oneidensis MR-1 as the inoculum, the C-Au anode-based MFC produced total electric charges higher than the carbon-paper-anode-based MFC by 47%. The cyclic voltammetry analysis and the scanning electron microscopy observation showed that the MR-1 biofilm growth was accelerated when the carbon paper surface was sputtered with gold. Utilization of such a carbon paper-gold composite significantly enhanced the MFC performance., (Copyright © 2010 Elsevier B.V. All rights reserved.)

Severe vibration of the core of ultra-high voltage (UHV) shunt reactors under operating conditions often leads to the occurrence of suspension electrode, and such a suspended discharge defect will destroy the oil-paper insulation. It is necessary to investigate the influence of vibration on suspended discharge when determining the best operating condition of UHV shunt reactors. The vibration frequency of the suspension electrode and the phase difference between the applied voltage and the vibration are studied by simulation and experiment. The simulation results show that the phase difference between the voltage and the vibration parameters will lead to an increase in the surface maximum field strength. The distortion of the field intensity caused by several typical vibration frequencies of reactor vibration is ranked (in ascending order) thus: 100, 300, 50, and 200 Hz. There is a coupling relationship between the phase difference and the vibration frequency on the suspended discharge, which will lead to an inconsistency between the field intensity and each single factor. The partial discharge test results of the collision between the suspension electrode and the high-voltage electrode show that the discharge generated by vibration at 100 Hz is much higher than that at other frequencies, followed by those at 300 and 50 Hz, and the discharge generated by vibration at 200 Hz is very small. When the phase difference of voltage advance vibration is between 0° and 90°, the quantity of local discharge is large. When the phase difference is between 90° and 180°, the local discharge is small. [ABSTRACT FROM AUTHOR]

In this work, we demonstrate an effective anion capturing in an aqueous medium using a highly porous carbon paper decorated with ZnO nanorods. A sol–gel technique was first employed to form a thin and compact seed layer of ZnO nanoparticles on the dense network of carbon fibers in the carbon paper. Subsequently, ZnO nanorods were successfully grown on the pre-seeded carbon papers using inexpensive chemical bath deposition. The prepared porous electrodes were electrochemically investigated for improved charge storage and stability under long-term operational conditions. The results show effective capacitive deionization with a maximum areal capacitance of 2 mF/cm2, an energy consumption of 50 kJ per mole of chlorine ions, and an excellent long-term stability of the fabricated C-ZnO electrodes. The experimental results are supported by COMSOL simulations. Besides the demonstrated capacitive desalination application, our results can directly be used to realize suitable electrodes for energy storage in supercapacitors. [ABSTRACT FROM AUTHOR]

Given its superior structure, the abundance of surface functional groups, and low cost, cotton fiber filtration paper can be used as the support for hydrogen evolution reaction (HER) and oxygen evolution reaction catalysts (OER) instead of copper foam (CF), nickel foam (NF), or carbon cloth (CC). Herein, the chemical plating method was used to create thin self-supporting electrodes based on cotton fiber filtration paper (FP). The Co-Ni-P amorphous nanospheres can be uniformly dispersed on the self-supporting FP due to its porous structure and oxygen functional groups. The Co-Ni-P/FP electrode has an overpotential as low as 125 mV for HER and 320 mV for OER at the current density of 10 mA cm−2. Additionally, according to density functional theory (DFT) calculations, the Co atom added to the Ni-P nanosphere can lead to considerably more charge accumulation around the Co and Ni active sites, which greatly encourages the HER and OER processes. The novel porous support, FP, provides a fresh way the preparation of self-supporting electrodes. [Display omitted] • Filter paper is used to prepare the self-supporting electrode as the substrate. • The preparation method is simple and the properties are stable. • Rich oxygen-containing functional groups of FP promote deposition and dispersion. • Explore the excellent electrochemical performance of amorphous Co-Ni-P/FP by DFT. [ABSTRACT FROM AUTHOR]

In the first part of the review article "General considerations" we give information about conventional flexible platforms and consider the advantages and disadvantages of paper when used in humidity sensors, both as a substrate and as a humidity-sensitive material. This consideration shows that paper, especially nanopaper, is a very promising material for the development of low-cost flexible humidity sensors suitable for a wide range of applications. Various humidity-sensitive materials suitable for use in paper-based sensors are analyzed and the humidity-sensitive characteristics of paper and other humidity-sensitive materials are compared. Various configurations of humidity sensors that can be developed on the basis of paper are considered, and a description of the mechanisms of their operation is given. Next, we discuss the manufacturing features of paper-based humidity sensors. The main attention is paid to the consideration of such problems as patterning and electrode formation. It is shown that printing technologies are the most suitable for mass production of paper-based flexible humidity sensors. At the same time, these technologies are effective both in the formation of a humidity-sensitive layer and in the manufacture of electrodes. [ABSTRACT FROM AUTHOR]

Gas diffusion electrodes (GDEs) represent a fundamental element for the development of gaseous electrochemical cells like water electrolysis reactors and fuel cells. Various technologies and materials are employed in order to obtain a conductive, stable and gas permeable structure. Among them, carbon-based structures such as carbon paper are widely used: their composition allows the diffusion of gaseous reagents and products and simultaneously does not permit the flooding of the gas-diffusion structure by aqueous electrolytes. However, the hydrophobicity of this material may represent a drawback to water-based electrode synthesis like galvanic deposition, and various chemical or thermal pretreatments were developed in the last decades. A new kind of pre-treatment based on electrical oxidation of the carbon paper surface is here described and evaluated. The electro-oxidative method allows a rapid and localized pre-treatment of the carbon paper, avoiding the use of highly reactive chemicals or long thermal treatments, reducing treatment wastes, time loss and electrical consumption. Surface wettability of the carbon paper before and after pretreatment was compared by contact angle analysis. Pre-treated and virgin carbon paper were subsequently electroplated from a copper deposition bath and deposition morphologies were compared, in order to establish the effect of the pre-treatment. Electroplated supports were analyzed by scanning electron microscopy (SEM) in order to analyze both micro and nanomorphology of the metallic structure. [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]

Traditional slurry-based electrodes consist of heavy current collectors and electroactive materials with a low weight percentage, which inevitably increase the total weight and cost of lithium-ion batteries (LIBs). Consequently, the development of low-cost, lightweight, flexible and binder-free electrodes for LIBs is highly desirable but also greatly challenging. In this work, we report the synthesis of small ZnO nanoparticles uniformly embedded in N-doped carbon (NC) nanoplate arrays (NPAs) tightly grown on a N-doped carbon paper (NCP) substrate (ZnO/NC NPAs@NCP) through a facile metal-organic framework-engaged strategy. This electrode design not only avoids the utilisation of insulating polymer binders but also offers other advantages, including large electrode/electrolyte contact areas, abundant electroactive sites, good wettability of the electrolyte, fast electron/ion transport and efficient volume accommodation. Notably, the freestanding ZnO/NC NPAs@NCP electrode displays a high reversible capacity of 610 mA h g−1 (based on the mass of entire electrode) at a current density of 100 mA g−1 for 50 cycles and excellent long-term cycling stability (363 mA h g−1 at 500 mA g−1 for 200 cycles). Furthermore, a full cell employing ZnO/NC NPAs@NCP as the anode and commercial LiFePO 4 as the cathode is constructed, indicating the feasibility for practical application. Moreover, an analysis of the electrode kinetics confirms the favourable lithium-ion storage kinetics within the ZnO/NC NPAs@NCP electrode. The present work could provide a new approach to develop low-cost, lightweight and flexible electrodes for advanced energy storage. N-doped carbon nanoplate arrays (NPAs) embedded with small ZnO nanoparticles tightly grown on N-doped carbon paper (NCP) substrate is designed and exhibits excellent performance as a low-cost, lightweight, flexible and binder-free electrode for lithium-ion batteries. Image 1 [ABSTRACT FROM AUTHOR]

Paper has been increasingly used in recent years as a substrate in the structure of sensors to determine diverse biological and pharmaceutical molecules and ions. Potentiometric sensors built with paper offer certain improvements since they are cost–effective, portable, biodegradable, eco–friendly, disposable and easy to manufacture. Paper is also an ideal substrate to be used, considering that it is flexible, lightweight, mechanically–resistant, a good medium for immobilization and trapping, and that it can be easily chemically and physically modified for customized applications, it can adsorb and transport liquid via capillary forces, can close the electrical circuit between electrodes when wet, it can be produced in diverse geometrical dimensions and porosities. Due to these characteristics, paper–based potentiometric sensors are more eco–friendly, suitable to be used in resource–limited areas, can be used in remote locations or on–site settings with low–cost analytical instrumentation. To our knowledge, the most recent advancements in the field have not been collectively reviewed, and this is of high importance considering the rapid developments made in paper–based potentiometric sensors lately. In these review, we covered paper–based potentiometric devices developed in the very recent years, detailed their structures, and compared their certain performance parameters including detection limit, linear concentration range, response time and applicability. [ABSTRACT FROM AUTHOR]

Soil microbial fuel cells (SMFCs) are attractive for low-cost bioelectricity generation. In this study, a multiwalled carbon nanotube paper (MCNTP) was fabricated by a simple method for use as the anode and cathode electrodes in a stab-type membrane-less SMFC (SSMFC). Activated carbon powder, carbon fibers, and cellulose fibers were bound by multiwalled carbon nanotube paint to form the MCNTP. As a result, the MCNTP exhibited high conductivity, flexibility, and durability. In addition, the SSMFC was designed as a module mounted with three anodes in series and a floating air cathode. The SSMFC could be activated on demand by simply stabbing in the wet soil. Experimental results showed that the floating cathode outperformed the non-floating one. The SSMFC generated the output shortly after being plugged into the wet soil. The maximum power density was at the level of 60–70 mW/m2 for three separate experiment cycles. Additionally, a single SSMFC was used to power a clock as an example to demonstrate its practical use. [ABSTRACT FROM AUTHOR]

With the rapid development of society, it is of paramount importance to expeditiously assess environmental pollution and provide early warning of toxicity risks. Microbial fuel cell-based self-powered biosensors (MFC-SPBs) have emerged as a pivotal technology, obviating the necessity for external power sources and aligning with the prevailing trends toward miniaturization and simplification in biosensor development. In this case, vigorous advancements in MFC-SPBs have been acquired in past years, irrespective of whether the target identification event transpires at the anode or cathode. The present article undertakes a comprehensive review of developed MFC-SPBs, categorizing them into substrate effect and microbial activity effect based on the nature of the target identification event. Furthermore, various enhancement strategies to improve the analytical performance like accuracy and sensitivity are also outlined, along with a discussion of future research trends and application prospects of MFC-SPBs for their better developments., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature.)

The growth of liquid biopsy, i. e., the possibility of obtaining health information by analysing circulating species (nucleic acids, cells, proteins, and vesicles) in peripheric biofluids, is pushing the field of sensors and biosensors beyond the limit to provide decentralised solutions for nonspecialists. In particular, among all the circulating species that can be adopted in managing cancer evolution, both for diagnostic and prognostic applications, microRNAs have been highly studied and detected. The development of electrochemical devices is particularly relevant for liquid biopsy purposes, and the screen-printed electrodes (SPEs) represent one of the building blocks for producing novel portable devices. In this work, we have taken miR-2115-3p as model target (it is related to lung cancer), and we have developed a biosensor by exploiting the use of a complementary DNA probe modified with methylene blue as redox mediator. In particular, the chosen sensing architecture was applied to serum measurements of the selected miRNA, obtaining a detection limit within the low nanomolar range; in addition, various platforms were interrogated, namely commercial and hand-made SPEs, with the aim of providing the reader with some insights about the optimal platform to be used by considering both the cost and the analytical performance., (© 2024 The Authors. ChemistryOpen published by Wiley-VCH GmbH.)

Improving the performance of porous nickel-based material used widely in the energy field is necessary. Alloying and increasing the specific surface area are essential approaches. This study used rice paper (Chinese traditional calligraphy and painting paper) as biomass templates to prepare hierarchical porous Ni and Ni-Cu foils (Nip and NiCup) with a thickness of about 60 μm by impregnating and high-temperature reduction process. The Ni3S2/Nip electrodes were prepared by an in situ-grown Ni3S2 nanosheet array on the struts of Nip via a hydrothermal process. Two modification methods using Cu-added alloying and Ni-S nanosheet growing were compared to determine their effects on the microstructure, phase, and performance in methanol oxidation (MOR) and urea oxidation (UOR). The results showed that both alloying effects and morphology control can promote MOR and UOR. Compared to the current density value of Nip at 0.8 V, the values of the preferred Ni10Cup and nanosheet array Ni3S2/Nip increased by 24.5% and 27.3% for methanol oxidation and by 15.4% and 38.4% for urea oxidation, respectively. Adding Cu helped to improve electron transfer and facilitated the transition from Ni2+ to Ni3+. The large specific surface area of Ni3S2 nanosheets provided more active sites for the reaction. Compared to Ni10Cup, Ni3S2/Nip with a lower impedance value exhibits better electrocatalytic performance and stability, achieving peak current densities of 269.7 mA cm−2 (MOR) and 303.9 mA cm−2 (UOR) at 0.8 V, maintaining 91.2% (MOR) and 102.4% (UOR) of the initial peak current density after 2000 cycles. The foil electrodes obtained under both modification strategies can be used as anode material in portable cells, and might also be applied to the oxidation of other small organic molecules. [ABSTRACT FROM AUTHOR]

Paper-based digital microfluidic biochips (PB-DMFBs) have emerged as the most promising solution to biochemical applications in resource-limited regions. However, like silicon chips, the reliability of PB-DMFBs is affected by physical defects. Even worse, since electrodes, conductive wires, and droplet routings are entangled on the same layer, multiple faults may occur simultaneously. Such faults not only cause waste of samples and human resource but also affect the correctness of the diagnostics. In this paper, we propose a reliability scheme with emphasis on design-for-reliability (DfR) and probability-based fault tolerance to ensure the correct functionality of PB-DMFBs with multiple faults. • Multiple fault assumption is considered for electrode open fault and wire open fault models. • Design-for-Reliability design flow is proposed for alternative droplet paths to bypass the faulty electrodes. • On-the-fly fault tolerance procedure is proposed to tolerate the faulty electrodes. • The proposed procedure has the least dependence on sensors for fault tolerance automation. [ABSTRACT FROM AUTHOR]

Flexible paper electrodes for supercapacitors were prepared with partially-exfoliated graphite and polypyrrole as the active materials. Graphite was coated on paper with pencil drawing and then electrochemically exfoliated using the cyclic voltammetry (CV) technique to obtain the exfoliated graphite (EG)-coated paper (EG-paper). Polypyrrole (PPy) doped with β-naphthalene sulfonate anions was deposited on EG-paper through in-situ polymerization, leading to the formation of PPy-EG-paper. The as-prepared PPy-EG-paper showed a high electrical conductivity of 10.0 S·cm-1 and could be directly used as supercapacitor electrodes. The PPy-EG-paper electrodes gave a remarkably larger specific capacitance of 2148 F·g-1 at a current density of 0.8 mA.cm-2, compared to PPy-graphite-paper (848 F·g-1). The capacitance value of PPy-EG-paper could be preserved by 80.4% after 1000 charge/discharge cycles. In addition, the PPy-EG-paper electrodes demonstrated a good rate capability and a high energy density of 110.3 Wh·kg-1 at a power density of 121.9W·kg-1. This work will pave the way for the discovery of efficient paper-based electrode materials. [ABSTRACT FROM AUTHOR]

The long-term operation of dry-type transformer bushings at high temperatures can impact the performance of their primary insulation material. This article presents an experimental study of the effect of thermal aging time on electrical treeing in the epoxy resin-impregnated paper. The experimental results show that the electrical treeing pattern along the middle path of the electric field and the interlayer creepage along the average direction of the electric field are closely related to the aging time. Under the effect of thermal aging at 150 °C, the tree-starting voltage of epoxy resin-impregnated paper tends to increase and decrease as the aging time increases. An analysis and discussion of the test results in conjunction with scanning electron microscope (SEM) and energy dispersive spectroscopy (EDS) tests suggest that the destruction of the cross-linked network of the epoxy resin-impregnated paper at 150 °C is a fundamental reason for the significant decrease in the material’s tree-starting voltage and the change in electrical treeing morphology and interlayer creepage. Long-term operation at high temperatures can seriously impact the primary insulation performance of dry-type transformer bushings and requires attention. [ABSTRACT FROM AUTHOR]

Sodium‐carbon dioxide (Na‐CO2) batteries are regarded as promising energy storage technologies because of their impressive theoretical energy density and CO2 reutilization, but their practical applications are restricted by uncontrollable sodium dendrite growth and poor electrochemical kinetics of CO2 cathode. Constructing suitable multifunctional electrodes for dendrite‐free anodes and kinetics‐enhanced CO2 cathodes is considered one of the most important ways to advance the practical application of Na‐CO2 batteries. Herein, RuO2 nanoparticles encapsulated in carbon paper (RuCP) are rationally designed and employed as both Na anode host and CO2 cathode in Na‐CO2 batteries. The outstanding sodiophilicity and high catalytic activity of RuCP electrodes can simultaneously contribute to homogenous Na+ distribution and dendrite‐free sodium structure at the anode, as well as strengthen discharge and charge kinetics at the cathode. The morphological evolution confirmed the uniform deposition of Na on RuCP anode with dense and flat interfaces, delivering enhanced Coulombic efficiency of 99.5% and cycling stability near 1500 cycles. Meanwhile, Na‐CO2 batteries with RuCP cathode demonstrated excellent cycling stability (>350 cycles). Significantly, implementation of a dendrite‐free RuCP@Na anode and catalytic‐site‐rich RuCP cathode allowed for the construction of a symmetric Na‐CO2 battery with long‐duration cyclability, offering inspiration for extensive practical uses of Na‐CO2 batteries. [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]