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Copyright of China Pulp & Paper is the property of China Pulp & Paper Magazines Publisher 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.)

This work demonstrates the application of urea-powered paper-based fuel cells (PFCs) with Hydrogen Peroxide (H2O2) as the oxidant to drive a flexible electronic circuit (ring oscillator (RO)), for the first time. Herein, the electrochemical performance of four different PFCs has been studied by employing non-precious electrodes as the anode and cathode. These are the membraneless PFC with (i) Toray carbon paper (CP) (ii) Nickel (Ni)-mesh (iii) Nickel Cobalt nanoparticles supported on reduced Graphene Oxide loaded on the CP (Ni Co@rGo@CP) and (iv) membrane-based PFC with Ni Co@rGo@CP as the electrodes. In each PFC the same electrode is employed on both the sides. A single membraneless-PFC with Ni-Co@rGo@CP as electrodes delivered a peak power density (Pmax) of 55 µW cm−2, maximum current density (Jmax) of 371 µA cm−2 and an open-circuit voltage (OCV) of 0.7 V at 3 M urea. While, a single membrane-based PFC assembled on an anion exchange membrane with Ni-Co@rGo@CP electrodes, delivered a Pmax of ≈70 µW cm−2 and Jmax of ≈500 µA cm−2 at an OCV of 0.7 V with 3 M urea. Subsequently, a stack of two membrane-based PFCs delivered an OCV of ≈1.4 V for 400 s. Finally, this stack is employed as a power source to drive a RO. The measured frequency and peak-to-peak voltage are 37.52 kHz and 1.04 V, respectively. This demonstration opens a window to implement self-contained flexible electronic system using PFCs as the power source with minimal e-waste. [ABSTRACT FROM AUTHOR]

We developed an integrated gas diffusion layer (GDL) for proton exchange membrane (PEM) fuel cells by growing carbon nanofibers (CNFs) in situ on carbon paper via the electro-polymerization of polyaniline (PANI) on carbon paper followed by a subsequent carbonization treatment process. The CNF/carbon paper showed a microporous structure and a significantly increased pore volume compared to commercial carbon paper. By utilizing this CNF/carbon paper in a PEM fuel cell, it was found that the cell with CNF/carbon paper had superior performance compared to the commercial GDL at both high and low humidity conditions, and its power density was as high as 1.21 W cm−2 at 100% relative humidity, which is 26% higher than that of a conventional gas diffusion layer (0.9 W cm−2). The significant performance enhancement was attributed to a higher pore volume and porosity of the CNF/carbon paper, which improved gas diffusion in the GDL. In addition, the superior performance of the cell with CNF/carbon paper at low relative humidity demonstrated that it had better water retention than the commercial GDL. This study provides a novel and facile method for the surface modification of GDLs to improve the performance of PEM fuel cells. The CNF/carbon paper with a microporous structure has suitable hydrophobicity and lower through-plane resistance, which makes it promising as an advanced substrate for GDLs in fuel cell applications. [ABSTRACT FROM AUTHOR]

Persulfate is a potential oxidant in direct liquid fuel cells (DLFCs), and the commercial carbon paper (CP) can directly serve as the cathode due to strong oxidizability of persulfate. However, the poor catalytic activity and low specific surface area of CP limit the electrode performance. Herein, a defect-enriched, pyridine-N-dominated and self-standing carbon paper electrode with abundant carbon nanosheets is successfully prepared by hydrothermal treatment combined with in-situ electrochemical exfoliation. Benefitting from the integrated structure, plentiful defects and high-content pyridine-N dopants of the prepared electrode result in the superior electrocatalytic activity and long-term stability in persulfate reduction reaction. Remarkably, a membraneless DLFC with the prepared electrode as cathode and persulfate as the oxidant acquires prominent cell performance and extremely high open circuit voltage of 2.13 V. The maximum power density of the DLFC achieves 241.0 mW cm−2, far higher than those of the previously reported similar membraneless DLFCs. A three-dimensional computational model for the DLFC is developed, which is help to reveal the importance of improving the reaction kinetics and electrical conductivity for the cathode with persulfate as oxidant. A facile approach for in-situ preparation of highly N-doped CP electrode is provided to yield outstanding cell performance for low-cost DLFCs. [Display omitted] • A facile way to introduce high-content nitrogen on carbon paper is proposed. • Massive defective sites, carbon nanosheets and pyridine-N dopants are introduced. • N doping enhances charge transfer and electrocatalytic activity of the electrode. • Effects of hydrothermal duration and precursor concentration are discussed. • The N-doped cathode yields the outstanding cell performance for low-cost DLFC. [ABSTRACT FROM AUTHOR]

Microfluidic fuel cells (MFCs) are potential micro power sources for portable electronics. MFCs utilize the co‐laminar flowing of the solutions in the microchannel and remove the membranes in the traditional fuel cells. Flow‐through electrodes exploit the internal electrode surfaces and improve the MFC performance. Carbon paper (CP) has been widely used as a flow‐through electrode with a limited specific surface area. We have also used graphite felt (GF) with a high specific surface area as the electrode and then compared the performance of the MFCs with the CP and GF as the electrodes, respectively. Firstly, we showed the SEM surface morphologies of the two electrodes with or without the Pd catalysts. Secondly, we compared the electrochemical activities of the two electrodes in the solutions, respectively. The GF electrode always showed higher electrochemical activities than the CP electrode, since the GF electrode owned its larger accessible electrochemical surface area and less electrode resistance than the CP electrode. Thirdly, we compared the performance of the MFCs with the two electrodes. The results showed that the performance of the MFC with the GF electrodes electrodes was optimum, with the peak power density of 175.60 mW cm−2 and limiting current density of 616.53 mA cm−2. Finally, we conducted the discharge performance of the MFCs with the two electrodes. There existed a minor variation in the discharge current densities of the MFCs with the CP cathodes. [ABSTRACT FROM AUTHOR]

Micro Fuel cells or microfluidic fuel cells (μMFCs) are one of the most promising power supplies for portable electronics. However, the necessary electrode spacing is required to prevent fuel-crossover and maintain the stable operation, introducing the unavoidable ohmic resistance and retarding the miniaturization. Herein, we propose a novel μMFC device combining the cellulose paper as separator, with selective catalysts at the cathode side to eliminate the unwanted side reactions and increase the system compactness. One single reactant solution containing fuel and electrolyte is applied to keep the device stable operation. The power-generation properties are evaluated in typical alkaline conditions. A great construction simplification makes the device a substantial high-power density of 2.14 W cm−3 and maximum current density of 15.82 A cm−3. The μMFC stacks are arranged in series and parallel manners, which delivers a maximum power output of 23.6 mW and current of 194.6 mA. It is expected that innovative and customizable performance from commercial paper and low-cost carbonaceous catalysts can provide a forum for future advancement in chip-based electrochemical energy generation and storage devices. • Filter paper served as a membrane for μMFC is proposed. • The electrode-pair distance is greatly minimized (∼140 μm). • The optimized μMFC delivers an ultrahigh power density of 2.14 W cm−3. • The μMFC stacks power output of 23.6 mW and current output of 194.6 mA are achievable. [ABSTRACT FROM AUTHOR]

A facile and scalable approach to modify electrodes with achieving excellent performance and low-cost is urgently needed for direct liquid fuel cells (DLFCs). A carbon paper (CP) electrode with porous carbon nanosheets is successfully fabricated by electrochemical exfoliation to enhance the charge transfer and increase reaction sites in DLFCs. After in-situ electrochemical exfoliation for 4 min, the carbon fiber surface becomes porous and rough to enlarge specific surface area and produce abundant defects for the electrode, greatly increasing reaction active sites. In addition, massive oxygen functional groups are introduced to significantly improve the reaction kinetics and wettability of the electrode. The exfoliated CP shows superior electrocatalytic activity with minimum overpotential and highest reduction reaction rate, benefitting from the larger specific surface area, abundant defects, and superhydrophilic property. Moreover, the exfoliated CP without catalysts is directly used as the cathode for a membraneless DLFC with sodium persulfate as an oxidant to yield outstanding performance. The peak power density of the DLFC with the exfoliated CP is 188.6 mW cm−2, 93.4% higher than that with the pristine CP. Results show that a feasible way to acquire excellent cell performance and low cost is obtained by electrochemically exfoliated CP electrode for DLFCs. [Display omitted] • An effective method to modify cathode is proposed for low-cost DLFCs. • Carbon fiber surface becomes porous and rough to enlarge specific surface area. • Abundant defects and oxygen functional groups are introduced. • Electrochemical exfoliation enhances charge transfer and increases active sites. • The exfoliated cathode without catalysts yield the outstanding cell performance. [ABSTRACT FROM AUTHOR]

Due to the control of porosity and pore size on mass transfer, the structure of the gas diffusion layer (GDL) has a critical impact on the performance of fuel cells. The bucky paper has high conductivity and abundant pores, which has potential to be used as GDL in fuel cells. Herein, a whole‐process solid template method is used to prepare the bucky paper with microcrystalline cellulose (MCC), whose porosity and pore size can be regulated quantitatively. The bucky paper with MCC as a pore‐forming agent has more larger pores, and these pores are mostly connected, which meet the needs of fuel cell application. The result of gas flux shows that the permeability of the bucky paper increases from the initial 12 to 240 mL min−1 kPa−1 cm−2 with MCC. The pore structure of bucky paper are significantly improved, so that the bucky paper with MCC leads to a higher fuel cell power density. Furthermore, the impedance result presents that with the addition of MCC, the mass transfer resistance of the fuel cells decreases significantly. It is fully supported in these results that MCC can modify the pores of the bucky paper and applied in proton exchange membrane fuel cells well. [ABSTRACT FROM AUTHOR]

Summary: Microfluidic fuel cell (MFC) stacking is a prerequisite to enhance its power output for practical applications. However, most MFC stacks reported in the present literature require external pumps to maintain the co‐laminar flow and complex fluidic management networks for homogeneous flow and reactant distributions. To address these issues, a novel paper‐based self‐pumping MFC stack with potassium formate as the fuel and hydrogen peroxide as the oxidant is proposed in this study. The capillary action is employed to achieve passive liquid flow. A vertical stack structure with the unit cells piled one above another compactly is adopted to reduce the volumetric costs. The experimental results show that the maximum power outputs of the two‐cell and three‐cell stack prototypes are 4.01 and 7.26 mW cm−2, outperforming the MFC unit by 5.81 and 10.52 times, respectively. The superior performance is attributed to its distinct vertical stacking structure, which brings the enhanced capillary flows in the paper wicks and reduced ohmic losses in comparison with the unit cell. Further, effects of the filter paper and reactant concentrations on the stack performance were examined, and mass transfer of the fuel and/or oxidant to the electrode/electrolyte interface was identified as the main limiting factor. A loose microstructure of the paper wick was found beneficial in enhancing the mass transfer. The potential applications of the MFC stack in a variety of portable electronics are broad. [ABSTRACT FROM AUTHOR]

In this era, research and development are becoming a continuous and accelerating process because technology changes rapidly with a short lifecycle. As a result, various methodologies are being developed to monitor these rapidly changing research trends; In particular, clustering method-related studies in science and technology documents are being developed with a variety of approaches. However, previous studies on document clustering methods focus on a specific field or language but do not take into consideration certain important pieces of information in science and technology documents. Therefore, this study proposes an embedding methodology that uses important content from scientific and technical documents. We took into consideration the importance of information containing core structures in science and technology documents and proposed a clustering methodology that analyzes structured and unstructured data, such as textual information, author information, and citation information. The proposed method combines both textual and structural data from the paper, using a method that focuses on screening important information by sections in science and technology documents. Then, Girvan-Newman clustering and Louvain clustering models are applied to generate embedding vectors and show evaluation results through the clustering indices. As a practical example, we applied the proposed methodology using paper data from the field of hydrogen cell vehicles. The results of this study will be effective in identifying gaps in technology for new technological development, identifying technology trends, and presenting directional information for future technology development.

The use of microfluidic fuel cells (μFCs) as power sources in the development of non-implantable biomedical devices, such as patch sensors, could be broadened with the use of physiological fluids as fuels and the use of low-cost materials. In this work, we report the evaluation of a paper-based photo-μFC working with human blood as fuel, and we implement a nanocomposite as anode that presents photoactivity under visible light. The electrocatalyst was synthesized using Zn(NO3)2 and TiCl4 as precursors of the ZnO and the TiO2, respectively, which were coated with Au nanoparticles. It was demonstrated that ZnO and TiO2 nanoparticles consisted of crystals with wurtzite and anatase phases, with average sizes of 26.6 and 19.5 nm, respectively, and the TiO2/ZnO/Au nanocomposite presents 2.62 eV of band gap energy, demonstrating its photoactivity under visible light irradiation. The photocatalyst was tested as photoanode in half-cell for glucose oxidation in aqueous solutions, under illumination and dark conditions, showing characteristics peaks of glucose oxidation in both cases, but higher current was generated under illumination. Finally, we present the implementation of this anode and the construction of a paper-based photo-μFC using human blood as fuel; its performance was evaluated under visible light irradiations and in the dark. The results show a better performance under illumination with voltage, current, and power density values of 0.95 V, 1.2 mA cm−2, and 0.458 mW/cm2, respectively, compared to the corresponding values of 0.8 V, 0.96 mA cm−2, and 0.274 mW/cm2 in dark conditions. [ABSTRACT FROM AUTHOR]

The regenerative hydrogen/vanadium fuel cell (RHVFC) is investigated with Freudenberg carbon paper electrodes (CPs). Along with thermal treatment, the Freudenberg CPs are also treated with reduced graphene oxide (rGO) using electrophoretic deposition at 300 V. The rGO modified CP results in 25% higher power density than its untreated counterpart under the same operating conditions. In comparison to the first preliminary study, the power density reported herein is more than four times higher. Additionally, the Freudenberg CPs modified with heat treatment followed by rGO deposition facing the membrane (rGOHTFM) provide the best electrolyte discharge utilization (UE) of 99%, followed by untreated (98%) and heat treated samples (97%) at 50 mA cm−2. The rGOHTFM also record high charge and discharge energy efficiencies (η E) of 93% at the same current density, which is slightly higher than untreated CPs (η E = 91%). Cycling the system 10 times also results in higher η E and UE for rGOHTFM CP (η E = 92% and UE = 99% on average) in comparison to untreated electrodes (η E = 86% and UE = 97% on average). In comparison the widely investigated SGL 10AA CP has lower efficiencies and utilization as expected (η E = 74% and UE = 83% on average). Image 1 • Freudenberg carbon paper electrodes are studied in hydrogen/vanadium fuel cell. • Freudenberg electrodes give much better charge/discharge response to SGL 10AA. • Untreated samples have similar performance to rGO modified ones at 50 mA cm−2. • Reduced graphene oxide modification of heat treated samples gave best results. • High cycling efficiencies (92%) and electrolyte utilization (99%) are reported. [ABSTRACT FROM AUTHOR]

This paper focuses on proton exchange membrane fuel cell (PEMFC) operation at current densities in the order of 6 A/cm2. Such high current densities are conceivable when the traditional carbon fiber papers are replaced with perforated metal plates as the gas diffusion layer to enhance waste heat removal, and at the same time the relative humidity inside the fuel cell is kept below 100% by applying appropriate operating conditions as was found in previous one-dimensional modeling work. In the current paper, we applied a three-dimensional, multi-phase computational fluid dynamics model based on Ansys-CFX to obtain additional insight into the underlying physics. The calculated pressure drops are in very good agreement with previous one-dimensional modeling work, and the current densities in all case studies are in the order of 5–6 A/cm2, but different from the previous one-dimensional study, the results suggest that the relative humidity is very close to 100% throughout the entire channel length when the inlet relative humidity is 100%, ensuring best hydration cell conditions and hence best performance. Importantly, the model results suggest that fuel cell performance at a high current density in conjunction with relatively low stoichiometric flow ratios around 1.5–2 is possible. [ABSTRACT FROM AUTHOR]

Paper‐based microfluidics emerges as an innovative platform for constructing miniaturized electrochemical devices, which mainly benefit from the spontaneous capillary action of paper. Nevertheless, the capillary‐driven flow dynamics on paper are determined exclusively by the intrinsic properties of paper and fluidics, thus lacking the controllability that conventional pump‐based microfluidics can provide. Herein, an approach to regulating the capillary flow on paper is introduced by conjugating the outlets of microfluidic channels with a photothermal module for water evaporation. The capillary flow rate on paper can be handily regulated from 4 to 37 µL min−1 under controllable illumination conditions. As a proof‐of‐concept, prototypical paper‐based microfluidic fuel cells integrated with the photothermal module are constructed. Their peak power density can be boosted from 0.3 up to 2.1 mW cm−2 under the simulated sunlight irradiation. The influence of capillary flow rate on the fuel cell performance is further validated using multiphysics simulations. The present work not only provides a practically feasible method to boost the performance of paper‐based microfluidic fuel cells using solar energy, but also opens a new avenue for modulating the performance of paper‐based microfluidics, which has long been a challenge in this field. [ABSTRACT FROM AUTHOR]

Copyright of China Pulp & Paper is the property of China Pulp & Paper Magazines Publisher 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.)

Herein, a membraneless paper based co‐laminar microfluidic Hydrazine‐Hydrogen peroxide fuel cell, employing graphite pencil electrode, is presented. Hydrogen peroxide has been used as oxidant while sulphuric acid and sodium hydroxide have been employed as electrolytes. The electrodes were formed by manual stroking of graphite pencils. Maximum power output was achieved by examining various combinations of different grades of graphite electrodes on a suitable filter paper with 100 pencil strokes. Here, maximum current density and power density of 14.43 μA/cm2 and 1.30 μW/cm2 respectively were achieved at a stable open circuit potential of 410 mV for 40 mM of hydrazine concentration. [ABSTRACT FROM AUTHOR]

Microfluidic fuel cells that use microorganisms to oxidize different organic substances to generate electricity are gaining importance due to their versatility to use different fuels. Saccharomyces cerevisiae has used for various purposes due to its capacity to ferment broad spectrum of carbohydrates. In this research, the development of bioanodes based on the immobilization of this yeast was carried out to apply them in the evaluation of a paper lateral-flow microfluidic fuel cell. Immobilization was performed using two different supports, Vulcan carbon and graphene oxide, and four carbohydrates as fuel (saccharose, glucose, fructose, and maltose). The results indicated that the yeast is better distributed and reaches a higher capacity to oxidize carbohydrates when is immobilized on graphene oxide, this bioanode shows better performance in the microfluidic device, reaching a potential above 0.9V when saccharose are used as fuel, representing a promising approach to use microbial bioanodes in small energy conversion devices. • Electrodes based on the Saccharomyces cerevisiae immobilization were used to make paper lateral-flow microfluidic fuel cells. • Immobilization was performed using Vulcan carbon (VC) and graphene oxide (GO) as supports. • Saccharose, glucose, fructose, and maltose were used as fuel in the microfluidic device. • The GO-based bioanode shows better performance, reaching a potential greater than 0.9V when saccharose is supplied. [ABSTRACT FROM AUTHOR]

[Display omitted] • A two-phase mass transfer model of paper-based microfluidic fuel cell is proposed. • The coupling characteristics of capillary action and two-phase flow are revealed. • The fluctuation mechanism of cell performance and gas distribution is explored. • Gas removal strategies are summarized, with a maximum gas removal rate of 42.30%. Paper-based microfluidic fuel cell powered by capillary force has the advantages of compactness, low cost, and high sensitivity, presenting broad application prospects in portable electronic devices. However, the gas-liquid mass transfer mechanism within the porous medium remains unclear, with a lack of two-phase flow theories adapted to the unique paper-based system. In this study, a two-dimensional two-phase numerical model of a Y-shaped paper-based microfluidic fuel cell is developed to reveal the two-phase flow characteristics under capillary action and explore gas removal strategies. The reliability of the model is validated by real experimental data. By coupling multiple physical fields, the study elucidates the working principle and gas-liquid flow phenomena within the cell. Then, the effects of contact angle, inlet fuel concentration, and paper type on output performance, gas distribution, parasitic effect, and fuel utilization are discussed. The results indicate that increasing the contact angle and using paper with a larger average pore size and porosity as the channel substrate are ideal for promoting gas discharge. The optimal gas removal rate reached 42.30 %, with a favorable power density of 33.92 mW/cm2. This study provides a theoretical basis for a deeper understanding of the two-phase mass transfer process in paper-based microfluidic fuel cell. [ABSTRACT FROM AUTHOR]

The direct integration of paper-based microfluidic fuel cells (μFC's) toward creating autonomous lateral flow assays has attracted attention. Here, we show that an air-breathing paper-based μFC could be used as a power supply in pregnancy tests by oxidizing the human urine used for the diagnosis. We present an air-breathing paper-based μFC connected to a pregnancy test, and for the first time, as far as we know, it is powered by human urine without needing any external electrolyte. It uses TiO 2 -Ni as anode and Pt/C as cathode; the performance shows a maximum value of voltage and current and power densities of ∼0.96 V, 1.00 mA cm − 2 , and 0.23 mW cm − 2 , respectively. Furthermore, we present a simple design of a paper-based μFC's stack powered with urine that shows a maximum voltage and maximum current and power densities of ∼1.89 V, 2.77 mA cm − 2 and 1.38 mW cm − 2 , respectively, which powers the display of a pregnancy test allowing to see the analysis results. [ABSTRACT FROM AUTHOR]

In a proton exchange membrane fuel cell (FC), the gas diffusion layer (GDL) is identified as the component that is most affected by mechanical compression. In this article, a particular focus is provided on the methods to measure the three main electrical parameters—contact resistance, through‐plane resistance, and in‐plane resistance—of the GDL under compression. A nonlinear decrease of these resistances under compression is typically observed. In particular, an important decrease is observed from 0 to 2 MPa, then a lower one above 2 MPa. The smallest contact and in‐plane resistances are measured for the graphitized straight carbon papers analyzing GDL resistances under compression gives a first approach to explaining ohmic losses in FCs as a large part of these losses is related to the GDL. This review would be helpful for researchers in better understanding ohmic losses and establishing a database of main GDL electrical resistances and their variations according to several operating parameters. These data could be used in design models to optimize GDL properties. [ABSTRACT FROM AUTHOR]

High-performance carbon fiber paper (CFP) is usually an important part of the fuel cell gas diffusion layer (GDL). However, the preparation of CFP for GDL is still a challenge due to its arduous preparation process. Here, inspired by the structure of bird's nest in nature, we present the original design of PPS spherical sites welding three-dimensional (3D) carbon fiber network to produce high-performance CFP by facile wet papermaking and heat treatment. With a 3D CF network as the skeleton and PPS spherical sites as the welding points, CFs/PPS composite paper exhibits good mechanical strength and outstanding flexibility. Meanwhile, the excellent conductivity (6.8 S/cm) is integrated with super-hydrophobic performance, electrothermal performance (T max = 365 °C), heat resistance (DTG max >575 °C), and corrosion resistance, becoming a high-performance multifunctional CFP. The mythical combination of these properties makes CFs/PPS composite paper an ideal candidate in the field of fuel cell GDL. In addition, the evolution of chemical structure of CF/PPS during carbonization is emphasized, which is of great significance for the properties of composite paper. This work presents a leap forward in the preparation of multi-property high-performance CFP in a simple method and is a key step toward exploring how the structural changes of CFs/PPS composite paper can be understood during carbonization. [Display omitted] • Inspired by the structure of bird's nest in nature. • High-performance carbon paper prepared without graphitization. • The fabulous multi-performance combination makes composite paper an ideal candidate for the fuel cell gas diffusion layer. [ABSTRACT FROM AUTHOR]

Copyright of China Pulp & Paper is the property of China Pulp & Paper Magazines Publisher 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.)

Summary: Paper microfluidic devices are innovative platforms for building miniaturized devices for energy harvesting, energy storage, and sensing applications. Such devices are reported to be used as membraneless microfluidic fuel cells to power portable electronic in a pump‐less manner by leveraging the embedded capillaries and co‐laminar flow. This paper demonstrates fabrication and characterization of the high‐performance metal‐free aluminum‐air microfluidic paper fuel cell (AAMPFC). Herein, aluminum foil acts as an anode, buckypaper with built‐in multiwalled carbon nanotubes (MWCNTs) acts as a cathode and sodium hydroxide (NaOH) works as an electrolyte. The novel AAMPFC is analyzed with various electrolyte concentrations, and maximum output voltage, current density, and power density are recorded. This easy‐to‐fabricate AAMPFC platform, costing less than US$ 0.5, is further optimized to achieve peak energies by stacking four AAMPFCs (in series and parallel) with various concentrations of electrolyte (NaOH). With parallel configuration, maximum open‐circuit potential (OCP), peak current (mA/cm2), and power density (mW/cm2) of 1.32 V, 50.67 mA/cm2 and 22.80 mW/cm2, respectively, are observed with optimized electrolyte, while with series stacked configuration, a stable OCP of 4.10 V is measured. In a series configuration, AAMPFC generated sufficient power to powering a scientific calculator with LCD display for 3 days and 11 LEDs for 10 hours continuously. This research work provides a significant method to enhance the output power with inexpensive parameters (buckypaper, single paper microchannel) to power portable electronic devices. Further, the performance can be enhanced by investigating AAMPFC with various grades of aluminum foil in combination with different grades of porous cellulose papers. [ABSTRACT FROM AUTHOR]

Hydrogen peroxide (H2O2) is identified as a promising reagent for fuel cells, reducing the dependency on carbon‐based fuels. In this work, electrochemically synthesized polymers are employed to improve the efficiency of the oxygen (O2) reduction reaction, thus producing H2O2 in an environmentally friendly way. Two aminoanthraquinones, as well as riboflavin (vitamin B2), are successfully immobilized via oxidative electropolymerization onto both glassy carbon and carbon paper. Of the investigated compounds, polyriboflavin shows a high Faradaic efficiency toward O2 reduction, even at a very low potential of only −0.1 V versus SHE. This catalytic effect is present in neutral and alkaline conditions, using both glassy carbon and carbon paper, but highly pronounced in neutral, aqueous solutions. [ABSTRACT FROM AUTHOR]

Smaller volume/weight and higher output power/energy density are always the goals of electrochemistry energy devices. Here, a simple strategy is proposed to prepare an integrated gas diffusion electrode (GDE) with high conductivity through skin electroplating. The skin electroplating is the combination of magnetron sputtering and spatial confinement electroplating. The electroplated metal obtained by skin electroplating is uniformly, continuously, and tightly attached to the surface of carbon paper like a layer of skin. Uniform and continuous electroplating metal layer endows the integrated electrode excellent conductivity with the square resistance as low as 27 mΩ sq−1. In application, the self‐breathing fuel cell with 1 cm2 active area can harvest ultrahigh volume specific power density (20.9 kW L−1). Additionally, the weight of the fuel cell stack (23 W) with the integrated electrode is only 20 g, which is only 7% of the commercial stack with the same power. The mass specific power density reaches 1150 W kg−1, which is 15 times of the commercial stack. Outstandingly, the stack can charge 4 mobile phones at the same time. More importantly, the skin electroplating provides an effective strategy to improve the specific power density of other energy devices including Zn‐air batteries, Li‐air batteries, and so on. [ABSTRACT FROM AUTHOR]

Summary: Miniaturization of devices, combined with other features such as portability, proneness to automation, rapid performance, amenability to integration, multiplexing, and cost‐effectiveness, is rapidly increasing for various sensing and energy harvesting applications. One such emerging area is the development of microfluidic fuel cell on cellulose papers, which has enormous scope to optimize its performance. This is primarily because such devices eliminate the need for membranes as well as external pumps since they have built‐in colaminar flow embedded capillaries. Such peripherals are usually used in conventional microfluidic fuel cells, which are fabricated using methods like photolithography, PDMS lithography, and 3D printing. This paper presents investigations on microfluidic paper–based fuel cells (MPFCs) with different cellulose absorbent pads for their performance optimization. Herein, the MPFC utilizes formic acid as fuel, oxygen from quiescent air as oxidant, and sulfuric acid as electrolyte for conducting ionic exchange under colaminar flow. The electrodes are realized through simple pencil strokes depositing a thin layer of graphite. The porous graphite electrodes act as diffusion agents breathing oxygen directly from the atmospheric air. Such an MPFC configuration, costing less than US $1, was optimized to achieve maximum energy density by examining various combinations of absorbent pads with different grades of cellulose papers. It is seen that the maximum open circuit potential is 0.46 V, while the maximum current and power densities are 1505.66 μAcm−2 and 173.97 μWcm−2, respectively, with a grade 6 absorbent pad. Such performance can be further enhanced by investigating MPFCs with various graphite pencils with a diverse number of strokes at different concentration levels. [ABSTRACT FROM AUTHOR]

We described a new concept, carbon paper-free membrane electrode assembly (MEA) fabricated from Nafion membrane and multi-walled carbon nanotubes-based electrocatalyst, in which platinum nanoparticles were deposited on carbon nanotubes after coating with pyridine-polybenzimidazole (PyPBI). Polymer-coated carbon nanotubes served as platinum nanoparticles support and current collector in carbon paper-free MEA. The fabricated carbon paper-free MEA was systematically studied by in situ cyclic voltammetry, SEM and fuel cell test. Pt utilization efficiency of carbon paper-free MEA improved with decreasing in Pt loading and reached 62% with 0.1 mg cm. Meanwhile, the mass power density reached 1.1 W mg, which was comparable to that of MEA with carbon paper. Fuel cell performance maintained 50% after 100000 startup-shutdown cycles, suggesting that carbon paper-free MEA was applicable in real fuel cell operation. To the best of our knowledge, this is the first study of carbon paper-free MEA in polymer electrolyte fuel cells. [ABSTRACT FROM AUTHOR]

This paper presents the fabrication and characterization of a 'T'-shaped methanol-based fuel cell supported on paper. Methanol is used as the fuel and potassium permanganate is used as the oxidant. A polyacrylamide based gel, impregnated with H2SO4 limits the fuel and oxidant cross over and serves as the membrane/electrolyte to facilitate the ion transport between anode and cathode. Composite of nitrogen doped graphene oxide and NiCo2O4 micro-spheres, having flower-like structure, is used as the catalyst on both the electrodes to improve the cell performance. The use of catalyst has led to 5 times increase in the peak power density. The catalysts are characterized using XRD, SEM, EDX and TEM. A stack of two paper cells could illuminate an LED for 30 minutes. A simple mathematical model based on Butler-Volmer kinetics is used to predict the cell performance and predictions are compared with experimental measurements. [ABSTRACT FROM AUTHOR]

Paper-based self-pumping microfluidic fuel cells (PMFCs) typically exploit the wicking effects in porous papers to enable passive reactant delivery and co-laminar flow, eliminating micro pumps and physical membranes. PMFCs have been regarded as promising micro-power sources for next-generation paper-based electrochemical microfluidic assays for biomedical applications. However, the PMFC performance is fundamentally limited by the low capillary flow velocity and ineffective diffusive fuel transport. In this study, a novel PMFC with an anodic wedge-shaped channel is developed. The anodic wedge-shaped channel enables reactant convection at improved fuel flow velocity. Visualization experiments suggest that the fuel flow velocity can be improved by about 23 times in this anodic wedge-shaped channel configuration as compared to that in conventional single-layer paper-based flow channel. In addition, favorable features like localized enhancement of fuel transport and reduced fuel crossover are also observed in this novel configuration. Due to enhanced convective-diffusive fuel transport, the cell performance can be improved 245.8 % as compared to the single-layer case. The peak power density reaches 59.9 mW cm−2 and the limiting current density achieves 305.9 mA cm−2, outperforming most of the previous PMFCs. This anodic wedge-shaped channel configuration can also be potentially used in paper-based assays to enhance reactant delivery. • Wedge-shaped channel is formed by inserting anode between two-layer flow channel. • The anodic wedge-shaped channel can significantly increase fuel flow velocity. • The anodic wedge-shaped channel also helps to reduce fuel crossover. • Anodic fuel transport is enhanced by convection and diffusion. • The peak power density is increased 245.8 % by using wedge-shaped channel. [ABSTRACT FROM AUTHOR]

As a mainstream power storage and supply device, batteries are continuously upgraded. The microfluidic fuel cell has great development potential, and the paper-based microfluidic fuel cell is the latest achievement of its lightweight, which can be applied in the field of medical and biological detection. In this work, the cell models with various folding forms and unconventional absorption pads are creatively constructed, then the influence mechanism on cell performance is revealed by numerical simulation. Both transient and steady-state simulation methods are employed to monitor the whole process of paper-based microfluidic fuel cell. Conclusions show that the cell performance decreases with the increase of folding angle, the peak power density is as low as 1.71 mW/cm2, and the corresponding fuel utilization is only 2.73%. The changes in the absorbent pad shapes have little improvement on cell performance, thus the most direct way is increasing the absorbent pad volume. Moreover, materials with better water absorption capacity can increase the maximum current density to 28.70 mA/cm2, and the appropriate increase of operating temperature can also increase the peak power density to 2.36 mW/cm2, but the effect on the cell is significantly weakened if the temperature exceeds a certain limit. [ABSTRACT FROM AUTHOR]

Microfluidic fuel cells (μFCs) offer a promising avenue for generating energy from glycerol, utilizing flow‐through electrodes to enhance reactant utilization. However, the cathodic reaction must efficiently consume the electrons harvested at the anode side to unlock its full potential. Here, we explore the feasibility of employing liquid oxidants as an alternative to O2 reduction on metal‐free carbon paper (CP) cathodes. We investigated the half‐cell reactions and the energy conversion in a new reusable 3D‐printed μFC. Half‐cell reactions predict spontaneous reactions by coupling glycerol electrooxidation in an alkaline medium with O2, Na2S2O8, and HClO from commercial bleach in an acidic medium. The μFC printed using the stereolithography apparatus technique build microchannels to place the Pt/C/CP anode and CP cathodes. The glycerol/Na2S2O8 μFC delivered a maximum of 32.4 mW cm−2, while glycerol/HClO μFC displayed 55.9 mW cm−2. This research sheds light on the potential of liquid oxidants as effective alternatives to O2 reduction, presenting a pathway toward optimizing μFCs and their practical applications in energy conversion from glycerol. [ABSTRACT FROM AUTHOR]

Paper-based microfluidics is characteristic of fluid transportation through spontaneous capillary action of paper and has exhibited great promise for a variety of applications especially for sensing. Furthermore, paper-based microfluidics enables the design of miniaturized electrochemical devices to be applied in the energy sector, which is especially attractive for the rapid growing market of small size disposable electronics. This review gives a brief summary on the basics of paper chemistry and capillary-driven microfluidic behavior, and highlights recent advances of paper-based microfluidics in developing electrochemical sensing devices and miniaturized energy storage/conversion devices. Their structural features, working principles and exemplary applications are comprehensively elaborated and discussed. Additionally, this review also points out the existing challenges and future opportunities of paper-based microfluidic electronics. [ABSTRACT FROM AUTHOR]

Owing to the challenge of irregular morphology, the impact of compressed carbon fiber paper (CFP) on fuel cell performance and durability is intricate. As a carbon-carbon composite, the internal contact state of CFP directly determines its mechanical and physical properties. In this paper, fiber distribution and intersection of uncompressed CFP are achieved by X-ray computed tomography. Then we established an analytical model of bulk resistance based on the electron transfer path and provided a function to describe the internal contact state with strain. The results imply that the increasing number of electron paths and the variation of the contact state are the main factors for the decrease in bulk resistance under compression. The turning points in the contact state curve divide the range of pressure into fiber contact, elastic-plastic deformation and fiber fracture region, which can be used to assess the mechanical properties of CFP and determine the optimal pressure for fuel cell assembly. [Display omitted] • Fiber distribution and intersection of uncompressed CFP is given. • The effect of contact resistance between fibers on bulk resistance is evaluated. • The structural information to electric and mechanical properties is connected. [ABSTRACT FROM AUTHOR]

The purpose of this study is to identify the indicators needed to analyze the competitiveness of major countries' energy technologies and to conduct empirical analysis accordingly. In this paper, nine measurement variables were derived as an index centered on patents and papers for energy technology competitiveness analysis. For each of the nine set measurement variables, the index for each of the major energy technologies (photovoltaics, fuel cells, and secondary batteries) was calculated, compared, and analyzed for each of the eight major countries. [ABSTRACT FROM AUTHOR]

Herein, we develop a facile and efficient Thermal-Vaporization-Transformation (TVT) approach to prepare a highly active BP directly grown on carbon paper as the electrode for Oxygen evolution reaction (OER), showing a low onset potential of 1.45 V versus RHE. Simultaneously, the current density of BP-CP illustrates the excellent electro-catalysis stability only decreases by 3.4% after continuous operation for 10,000 s. [Display omitted] • BP-CP for OER is successfully synthesized by a novel efficient TVT approach. • The raw materials of the reaction are only the red phosphorus and carbon. • BP-CP exhibits a low onset potential and excellent electro-catalysis stability. • Electrocatalytic performance is fully demonstrated by DFT calculation in details. Black phosphorus (BP), as a new 2D material, is normally synthesized by a high-pressure and high-temperature (HPHT) method from white and red phosphorus, which severely hinders the further development of BP for any potential applications and leads to search for other potential applications of BP with big challenge. Herein, we develop a facile and efficient Thermal-Vaporization-Transformation (TVT) approach to prepare a highly active BP directly grown on carbon paper as the electrode for Oxygen evolution reaction (OER), showing a low onset potential of 1.45 V versus RHE. Simultaneously, the current density of BP-CP illustrates the excellent electro-catalysis stability only decreases by 3.4% after continuous operation for 10000 s. Meanwhile, the density functional theory (DFT) calculations further illustrates the P-doped carbon layer in the upper side of BP layer is actually responsible for its enhanced OER property, and the adjacent carbon atoms of the embedded P atoms are actually the active sites due to the induced local change distribution by intramolecular change transfer. Considering the facile, but efficient and scalable, TVT approach can directly synthesize BP-CP with excellent OER performance, which is promising for BP electrocatalysts used for OER in metal-air batteries, fuel cells, water-splitting devices, even other key renewable energy. [ABSTRACT FROM AUTHOR]

• Efforts to enhance PMFC performance are reviewed. • Both exciting advancements and current limitations are discussed. • An innovative strategy of multi-scale simultaneous optimization is proposed. Paper-based microfluidic fuel cell (PMFC) has attracted great attention in the microfluidic fuel cell field in recent years. It utilizes the spontaneous capillary flow of reactant solutions in paper-based porous substrate to achieve passive transportations of fuel and oxidant, solving the fluid driving issue encountered in traditional microfluidic fuel cells and thus having broad application prospects in medical detection, wearable devices, micro sensors, environmental monitoring, and many other fields. However, the commercialization of this technology is impeded by the low output performance caused by the limited mass and energy transfer in PMFCs. To enhance the mass and energy transfer in PMFCs, numerous research studies have been conducted via experimental optimization of the cell materials and structures. Numerical analyses focusing on the structure–activity relationship of PMFCs were also performed recently. To provide a comprehensive and thorough review about the efforts devoted to improving performance of PMFC, research papers relevant to PMFC since its invention in 2014 have been extracted in this work and significant works were filtered to highlight the exciting advancements. The experimental studies were classified and discussed based on the key components involved in the PMFC system, followed by a critical review of the limited computational models. Potential directions for future research were also provided, aimed at overcoming the current technological challenges in PMFCs. Importantly, an innovative strategy of multi-scale simultaneous optimization of the cell properties is proposed considering the typical multi-scale feature of the PMFC system, which could inspire the designing of advanced cell materials with optimal multi-scale structures for applications of PMFCs. [ABSTRACT FROM AUTHOR]

Microfluidic paper based microbial fuel cells (μP-MFCs) have gained considerable popularity due to their compact, quick and low-cost fluid manipulation paradigm. Compared to conventional technologies, paper as a substrate with advanced nanomaterial electrode material has many distinct advantages from point-of-care monitoring to energy harvesting. As a result, these have been used and are more popular in a variety of fields, such as health diagnostics, environmental and food quality management. By this encouragement, herein a portable microbial fuel cell as an origami array has been demonstrated using custom carbon electrodes with a modified the transition metal oxide MnO 2 nanomaterial. This customized electrode design was first printed using a tabletop PCB inkjet printer where the anode was further modified with synthesized MnO 2 nanoparticles. The entire cell was formed by folding the paper along predefined edges where the fuel, Shewanella putrefaciens , was streamed continuously via inherent capillary cation. Various studies, such as morphological, surface catalyst coating, amount loading and volumetric culture optimization experiments, have also been accomplished to find the most appropriate optimum parameter to enhance power conversion efficiency. The developed origami arrayed microbial fuel generated an open-circuit potential (OCP) for two parallel connected MFCs of 0.534 V and a maximum power density of 15.9 μW/cm2 with a maximum current density of 130 μA/cm2. In the end, the harvested power was used by powering the digital watch circuit through the ultra-low DC-DC booster board. Such an MFC origami array, with simple electrode manufacturing and modification process, has a great potential and bright future in Internet of Things (IoT) applications by making multiple stacks where the data can be monitored. [Display omitted] • Origami array-type MFC with printed electrode was fabricated by a PCB inkjet printer. • Several surface modification and loading (MnO 2 and bacteria) optimizations were done. • The developed device generates a maximum power density of 17.5 μW/cm2. • The device was used to power a digital watch using DC-DC booster. [ABSTRACT FROM AUTHOR]