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Bio-electroactive fuel cells are systems that produce useful products from renewable sources without causing environmental pollution and treating waste. In this study, general design properties, operation mechanisms, application areas, and historical advancement of the bio-electroactive fuel cell was reviewed. Electricity generating microbial fuel cells offer new opportunities as with hydrogen and methane-producing microbial electrolysis cells due to their attractive variety of electroactive microorganisms and operating situations. This article provides an up-to-date review for Bio-electroactive fuel cells and outlines instructions for future studies.

A modifiable, spontaneously formed and biocompatible polymer gel, composed of phosphorylcholine and N-hydroxysuccinimide ester, is reported, which can be subjected to postmodification by amine-cont...

This review deals with the use of the highly conductive polymer PEDOT:PSS in biomedical and bioelectrochemical systems. The examples of toxic effects on living cells, positive effects of PEDOT:PSS on the viability of cells and tissues are given. The properties of the polymer, methods of increasing its electrical conductivity by its modification with various nanoparticles and nanomaterials are discussed. Examples of using PEDOT and its composites in bioelectrochemical devices, such as biosensors and biofuel cells, are considered. Changes in the characteristics of biosensors and biofuel cells under the influence of PEDOT are discussed.

We report on a photobioelectrochemical fuel cell consisting of a glucose‐oxidase‐modified BiFeO3 photobiocathode and a quantum‐dot‐sensitized inverse opal TiO2 photobioanode linked to FAD glucose dehydrogenase via a redox polymer. Both photobioelectrodes are driven by enzymatic glucose conversion. Whereas the photobioanode can collect electrons from sugar oxidation at rather low potential, the photobiocathode shows reduction currents at rather high potential. The electrodes can be arranged in a sandwich‐like manner due to the semi‐transparent nature of BiFeO3, which also guarantees a simultaneous excitation of the photobioanode when illuminated via the cathode side. This tandem cell can generate electricity under illumination and in the presence of glucose and provides an exceptionally high OCV of about 1 V. The developed semi‐artificial system has significant implications for the integration of biocatalysts in photoactive entities for bioenergetic purposes, and it opens up a new path toward generation of electricity from sunlight and (bio)fuels., A photobioelectrochemical tandem cell is presented in which two photoelectrodes have been functionally coupled with two biocatalysts for supplying the light‐driven reaction with charge carriers from glucose conversion. The cell allows the generation of electricity from biofuels and light with a high open‐circuit voltage of 1 V.

Photoelectrochemical biofuel cells can convert light and chemical energy into electrical energy using a dye-sensitized titania (TiO2) fluorine-doped tin oxide photoanode and a platinum-coated fluorine-doped tin oxide cathode. TiO2 of the photoanode serves both as a support for dyes and as an electron-transporting medium, the structure of which can limit electron trapping and charge transporting and then affect the performance of the photoelectrochemical biofuel cells. TiO2 nanotube array films have been shown to enhance the efficiencies of both charge collection and electron injection, and hence a vertically aligned TiO2 nanotube array is investigated as a conductor for the tetrakis(4-carboxyphenyl)porphyrin dye to construct a new two-compartment photoelectrochemical biofuel cell. The photoelectrochemical biofuel cell containing the TiO2 nanotube array photoanode yields a short-circuit (Isc) current of 110 μA and an open-circuit (Voc) potential of 1010 mV. In contrast, the photovoltaic parameters, Isc and Voc of the photoelectrochemical biofuel cell with the mesoporous TiO2 nanocrystal fluorine-doped tin oxide photoanode, are 96.96 μA and 740 mV, respectively. Photovoltaic measurements show that the maximum incident photon-to-collected electron conversion efficiency was 58% at 430 nm through the spectral range (400–800 nm) for the photoelectrochemical biofuel cell with the TiO2 nanotube array fluorine-doped tin oxide photoanode. These results revealed that the TiO2 nanotube array had great potential for the photoelectrochemical biofuel cells.

Black phosphorus (BP) has attracted tremendous attention as a new two-dimensional semiconductor material with excellent optical and electrical properties. Unfortunately, the mimicking enzyme charac...

Flexible enzymatic biofuel cell (EBFC) has been considered as an alternative power source for wearable devices, in which, the design of the substrate electrode is of significance for its mechanical...

Variants of the highly active [NiFeSe] hydrogenase from D. vulgaris Hildenborough that exhibit enhanced O2 tolerance were used as H2‐oxidation catalysts in H2/O2 biofuel cells. Two [NiFeSe] variants were electrically wired by means of low‐potential viologen‐modified redox polymers and evaluated with respect to H2‐oxidation and stability against O2 in the immobilized state. The two variants showed maximum current densities of (450±84) μA cm−2 for G491A and (476±172) μA cm−2 for variant G941S on glassy carbon electrodes and a higher O2 tolerance than the wild type. In addition, the polymer protected the enzyme from O2 damage and high‐potential inactivation, establishing a triple protection for the bioanode. The use of gas‐diffusion bioanodes provided current densities for H2‐oxidation of up to 6.3 mA cm−2. Combination of the gas‐diffusion bioanode with a bilirubin oxidase‐based gas‐diffusion O2‐reducing biocathode in a membrane‐free biofuel cell under anode‐limiting conditions showed unprecedented benchmark power densities of 4.4 mW cm−2 at 0.7 V and an open‐circuit voltage of 1.14 V even at moderate catalyst loadings, outperforming the previously reported system obtained with the [NiFeSe] wild type and the [NiFe] hydrogenase from D. vulgaris Miyazaki F., Triple protection: A stable, high‐current‐density‐based H2‐oxidation bioanode is presented. It is equipped with [NiFeSe] variants that show enhanced O2 tolerance, which are immobilized and wired to electrode surfaces with a low‐potential viologen‐modified polymer. The polymer acts simultaneously as a high‐potential and O2 shield. The triply protected bioanodes are incorporated in membrane‐free biofuel cells, which reveal benchmark performances at moderate catalyst loading.

Важным направлением в области медицинской техники является создание имплантируемых устройств, поддерживающих функционирование организма. Многие из таких устройств требуют энергоснабжения, причем желательно, чтобы такие источники работали весь период имплантации, даже если речь идет о пожизненной установке импланта. Представлен обзор литературных данных по источникам энергии для питания имплантируемых и носимых медицинских устройств. Приведена сравнительная оценка характеристик биотопливных элементов как наиболее проработанного варианта имплантируемого источника энергии с другими возобновляемыми источниками электрической энергии на основе термо-, пьезо-, электростатических, магнито- и фотопреобразователей. Особое внимание уделено применению имплантируемых устройств, которые могут служить источником энергии для маломощных потребителей – микропомп, кардиостимуляторов, нейроимплантов и т.д.

Glucose oxidase (GOx) is one of the most widely investigated enzymes in the field of bioelectrochemistry. It is mainly used for the detection of glucose in solutions and enzyme-based biofuel cells. On the basis of the combination of GOx with graphene, novel nanodevices exceeding conventional limits can be developed. To develop a hybrid enzyme-graphene nanodevice with a good performance, it is important that GOx is deposited well on the graphene surface while maintaining its structure and not impeding the oxidation activity of the GOx. In this study, we propose a method to improve the stability of GOx and secure its immobility on the graphene sheet and its glucose-binding affinity by single-point mutation of GOx using molecular dynamics simulations. We confirm that the structural stability, immobility, and substrate binding affinity of GOx can be modified by changing the hydrophobicity of a key residue. We demonstrate that biosensors or biofuel cells can be redesigned and their properties can be improved by using molecular dynamics simulation.

Transient energy supply remains one of the key challenges limiting the development of transient implantable medical devices for monitoring, diagnosis, and treatment of diseases within a predetermined time frame. A key feature of such devices is their controllable degradation during service life. An on-board transient energy supply with predictable performance over time is required to drive transient electronics. In this article, we present recent advances in the development of materials for biodegradable energy-storage devices (batteries and supercapacitors) and biodegradable energy-harvesting systems (enzymatic biofuel cells and triboelectric nanogenerators). Future perspectives, challenges, and opportunities related to energy materials for transient power sources will also be summarized.

Various methods of immobilizing enzymes on electrodes have been developed for the research of enzymatic biofuel cells (EBFCs). Among these methods, the layer-by-layer (LbL) assembly is a delicate technology that can form controllable enzyme layers and load a high density of enzyme molecules by electrostatic deposition, hydrogen bonding, or covalent bonding. In this paper, recent advancements of the LbL assembly for immobilizing enzymes in EBFCs are presented in detail. First, the LbL formation mechanism of a multilayer sensitive film on electrodes is analyzed, and the potential of the multilayer structure is also discussed. Then, the applications of enzyme immobilization by the LbL assembly in combination with various materials in EBFCs are investigated. The power density of LbL assembly-based EBFCs increases by several orders of magnitude with the widespread use of nanomaterials. As a convenient and efficient operation, the LbL assembly technology is expected to become a popular method for immobilizing enzymes in EBFCs.

Supercapacitive biofuel cells' (SBFCs) most recent advancements are herein disclosed. In conventional SBFCs the biocomponent is employed as the pseudocapacitive component, while in self-charging biodevices it also works as the biocatalyst. The performance of different types of SBFCs are summarized according to the categorization based on the biocatalyst employed: supercapacitive microbial fuel cells (sMFCs), supercapacitive biophotovoltaics (SBPV) and supercapacitive enzymatic fuel cells (s-EFCs). SBFCs could be considered as promising 'alternative' energy devices (low-cost, environmentally friendly, and technically undemanding electric power sources etc.) being suitable for powering a new generation of miniaturized electronic applications.

International audience; Metal organic frameworks (MOFs) with their high pore volumes and chemically-diverse pore environments have emerged as components of catalytic electrodes for biosensors, biofuel cells, and bioreactors. MOFs are widely exploited for gas capture, separations, and catalysis, but their integration at electrodes with biocatalysts for (bio)electrocatalysis is a niche topic that remains largely unexplored. This review focuses on recent advances in MOF and MOF-derived carbon electrodes for bioelectrochemical applications. A range of MOF materials and their integration into devices with enzymes and microbes are reported. Key properties and performance characteristics are considered and opportunities facing MOFs for (bio)electrochemical applications are discussed.

Electrically conductive polymers are promising materials for charge transfer from living cells to the anodes of electrochemical biosensors and biofuel cells. The modification of living cells by polypyrrole (PPy) causes shortened cell lifespan, burdens the replication process, and diminishes renewability in the long term. In this paper, the viability and morphology non-modified, inactivated, and PPy-modified yeasts were evaluated. The results displayed a reduction in cell size, an incremental increase in roughness parameters, and the formation of small structural clusters of polymers on the yeast cells with the increase in the pyrrole concentration used for modification. Yeast modified with the lowest pyrrole concentration showed minimal change; thus, a microbial fuel cell (MFC) was designed using yeast modified by a solution containing 0.05 M pyrrole and compared with the characteristics of an MFC based on non-modified yeast. The maximal generated power of the modified system was 47.12 mW/m2, which is 8.32 mW/m2 higher than that of the system based on non-modified yeast. The open-circuit potentials of the non-modified and PPy-modified yeast-based cells were 335 mV and 390 mV, respectively. Even though applying a PPy layer to yeast increases the charge-transfer efficiency towards the electrode, the damage done to the cells due to modification with a higher concentration of PPy diminishes the amount of charge transferred, as the current density drops by 846 μA/cm2. This decrease suggests that modification by PPy may have a cytotoxic effect that greatly hinders the metabolic activity of yeast.

Biofuel cells involving enzymes and whole cells of microorganisms are gaining interest with the increasing need for self-powered devices. Their nontoxic, pollution-free energy conversion technology has received tremendous attention in the last two decades, evidenced by the existing literature on this field. There are also various reviews explaining the developments of microbial fuel cells. Biofuel cells can convert a wide range of substrates from sustainable sources to electrical power and could have a promising prospect of contributing to future energy requirements. However, this technology needs steady exploration to lead it toward technology readiness. In this chapter, we focus on the recent developments in the area of biofuel cells with respect to enzymatic and microbial fuel cells, along with their future aspects leading to develop a promising technology for mankind.

This chapter introduces polymer membranes used in microbial fuel cells (MFCs), beginning with a brief introduction on biofuel cells. Following the same, it focuses on membrane properties and characterizations. Ion exchange membranes, particularly cation exchange membrane (CEM) used in MFC performance, are elucidated. Polymer membranes categorized into polymer-polymer composites, metal-based nano polymer composites and carbon-polymer composites including recent advances of the same are elaborated. A short review on membrane-free MFC is also discussed. The chapter concludes with other potential uses of MFC.

Polydopamine (PDA), formed by self-polymerizing dopamine, is coated over a lactate oxidase (LOx)- and 1,2-naphthoquinone-modified MgO-template carbon electrode to improve electrode stability. After...

With the rapid decline of fossil fuels, various types of biofuel cells (BFCs) are being developed as an alternative energy source. BFCs based on multi-enzyme cascade reactions are utilized to extract more electrons from substrates. Thus, more power density is obtained from a single molucule of substrate. In the present study, a bioanode that could extract six electrons from a single molecule of L-proline via a three-enzyme cascade reaction was developed and investigated for its possible use in BFCs. These enzymes were immobilized on the electrode to ensure highly efficient electron transfer. Then, oriented immobilization of enzymes was achieved using two types of self-assembled monolayers (SAMs). In addition, a microfluidic system was incorporated to achieve efficient electron transfer. The microfluidic system, in which the electrodes were arranged in a tooth-shaped comb, allowed for substrates to be supplied continuously to the cascade, which resulted in smooth electron transfer. Finally, we developed a high-performance bioanode which resulted in the accumulation of higher current density compared to that of a gold disc electrode (205.8 μA cm−2: approximately 187 times higher). This presents an opportunity for using the bioanode to develop high-performance BFCs in the future.

Fast and sensitive determination of biologically active compounds is very important in biomedical diagnostics, the food and beverage industry, and environmental analysis. In this review, the most promising directions in analytical application of conducting polymers (CPs) are outlined. Up to now polyaniline, polypyrrole, polythiophene, and poly(3,4-ethylenedioxythiophene) are the most frequently used CPs in the design of sensors and biosensors; therefore, in this review, main attention is paid to these conducting polymers. The most popular polymerization methods applied for the formation of conducting polymer layers are discussed. The applicability of polypyrrole-based functional layers in the design of electrochemical biosensors and biofuel cells is highlighted. Some signal transduction mechanisms in CP-based sensors and biosensors are discussed. Biocompatibility-related aspects of some conducting polymers are overviewed and some insights into the application of CP-based coatings for the design of implantable sensors and biofuel cells are addressed. New trends and perspectives in the development of sensors based on CPs and their composites with other materials are discussed.

An efficient immobilization of Glucose oxidase (GOx) on an appropriate substrate is one of the main challenges of developing fuel cells that allow energy to be obtained from renewable substrates such as carbohydrates in physiological environments. The research importance of biofuel cells relies on their experimental robustness and high compatibility with biological organisms such as tissues or the bloodstream with the aim of obtaining electrical energy even from living systems. In this work, we report the use of 5,10,15,20 tetrakis (1-methyl-4-pyridinium) porphyrin and glutathione capped CdTe Quantum dots (GSH-CdTeQD) as a support matrix for the immobilization of GOx on carbon surfaces. Fluorescent GSH-CdTeQD particles were synthesized and their characterization by UV-Vis spectrophotometry showed a particle size between 5–7 nm, which was confirmed by DLS and TEM measurements. Graphite and Toray paper electrodes were modified by a drop coating of porphyrin, GSH-CdTeQD and GOx, and their electrochemical activity toward glucose oxidation was evaluated by cyclic voltammetry, chronoamperometry and electrochemical impedance spectroscopy. Additionally, GOx modified electrode activity was explored by scanning electrochemical microscopy, finding that near to 70% of the surface was covered with active enzyme. The modified electrodes showed a glucose sensitivity of 0.58 ± 0.01 μA/mM and an apparent Michaelis constant of 7.8 mM. The addition of BSA blocking protein maintained the current response of common interferent molecules such as ascorbic acid (AA) with less than a 5% of interference percentage. Finally, the complex electrodes were employed as anodes in a microfluidic biofuel cell (μBFC) in order to evaluate the performance in energy production. The enzymatic anodes used in the μBFC allowed us to obtain a current density of 7.53 mAcm−2 at the maximum power density of 2.30 mWcm−2; an open circuit potential of 0.57 V was observed in the biofuel cell. The results obtained suggest that the support matrix porphyrin and GSH-CdTeQD is appropriate to immobilize GOx while preserving the enzyme’s catalytic activity. The reported electrode arrangement is a viable option for bioenergy production and/or glucose quantification.

This review article focusses on new advances in the field of enzyme fuel cells (EFCs), especially, on flexible materials which can be used to make flexible EFCs for wearable devices, three-dimensional (3D) printed structures to prepare electrodes for EFCs and micro/nano electromechanical structures (MEMS/NEMS) to fabricate micro-EFCs. Particular attention is given to newly developed approaches to obtain efficient electrodes for harvesting energy via EFCs. This review article explains the various attributes of these recently developing technologies and their ability to mitigate the energy requirements of flexible/wearable bioelectronic devices. Besides discussing key milestones achieved, this perspective review article also emphasizes the main hurdles that are currently impeding the realization of flexible/wearable EFCs. We have also emphasized on the major hurdles related to the flexible materials required to fabricate wearable EFCs, suitable 3D printing techniques required, and MEMS and NEMS to fabricate micro-EFCs. In all the recently developed techniques, there are some common issues like stability, low power output, mechanical strength and flexibility. This review article also provides various routes to mitigate these issues. The main aim of this perspective article is to develop curiosity among the researchers of various fields to team up in order to address the huge challenges that restrict the real-world application of flexible/wearable EFCs. Such collaboration is important to harness the full potential of EFCs. It is requested to read this review article with supporting information to get the complete essence.

Enzymatic biofuel cells are a promising source of alternative energy for small device applications, but still face the challenge of achieving direct electron transfer with high enzyme concentrations in a simple system. In this dissertation, methods of constructing electrodes consisting of enzymes attached to nanoparticle-enhanced substrates that serve as high surface area templates are evaluated. In the first method described, glucose oxidase is covalently attached to gold nanoparticles that are assembled onto genetically engineered M13 bacteriophage. The resulting anodes achieve a high peak current per area and a significant improvement in enzyme surface coverage. In the second system, fructose dehydrogenase, a membrane-bound enzyme that has the natural ability to achieve direct electron transfer, is immobilized into a matrix consisting of binders and carbon nanotubes to extend the lifetime of the anode. For the cathode, bilirubin oxidase is immobilized in a carbon nanotube and sol-gel matrix to achieve direct electron transfer. Finally, a full fuel cell consisting of both an anode and cathode is constructed and evaluated with each system described.

The continuous operation of wearable electronics demands reliable sources of energy, currently met through Li-ion batteries and various energy harvesters. These solutions are being used out of necessity despite potential safety issues and unsustainable environmental impact. Safe and sustainable energy sources can boost the use of wearables systems in diverse applications such as health monitoring, prosthetics, and sports. In this regard, sweat- and sweat-equivalent-based studies have attracted tremendous attention through the demonstration of energy-generating biofuel cells, promising power densities as high as 3.5 mW cm-2 , storage using sweat-electrolyte-based supercapacitors with energy and power densities of 1.36 Wh kg-1 and 329.70 W kg-1 , respectively, and sweat-activated batteries with an impressive energy density of 67 Ah kg-1 . A combination of these energy generating, and storage devices can lead to fully energy-autonomous wearables capable of providing sustainable power in the µW to mW range, which is sufficient to operate both sensing and communication devices. Here, a comprehensive review covering these advances, addressing future challenges and potential solutions related to fully energy-autonomous wearables is presented, with emphasis on sweat-based energy storage and energy generation elements along with sweat-based sensors as applications.

Protonic ceramic fuel cell (PCFC) is an all ceramic oxide fuel cell, but different from SOFC, protons rather than oxygen ions are going through the ceramic oxide electrolyte. Due to the high mobility of protons, PCFC offers promising potential as efficient fuel cells at low temperatures of 300–600 oC. This Chapter will give an overview of the principle, protonic ceramic electrolyte and electrode materials of PCFC. For highly efficient PCFCs, it is necessary to develop cathode materials with oxide ion, protonic and electronic conductivity, or triple conducting oxides (TCO) for oxygen reduction reaction. Finally some important and emerging fuel cells are briefly introduced, including microbial fuel cells (MFCs), and biofuel cells (BFCs).

The appearance and evolution of biofuel cells can be categorized into three groups: microbial biofuel cells (MBFCs), enzymatic biofuel cells (EBFCs), and enzyme-like nanomaterial (nanozyme)-based biofuel cells (NBFCs). MBFCs can produce electricity from waste; however, they have significantly low power output as well as difficulty in controlling electron transfer and microbial growth. EBFCs are more productive in generating electricity with the assistance of natural enzymes, but their vulnerability under diverse environmental conditions has critically hindered practical applications. In contrast, because of the intrinsic advantages of nanozymes, such as high stability and robustness even in harsh conditions, low synthesis cost through facile scale-up, and tunable catalytic activity, NBFCs have attracted attention, particularly for developing wearable and implantable devices to generate electricity from glucose in the physiological fluids of plants, animals, and humans. In this review, recent studies on NBFCs, including the synthetic strategies and catalytic activities of metal and metal oxide-based nanozymes, the mechanism of electricity generation from glucose, and representative studies are reviewed and discussed. Current challenges and prospects for the utilization of nanozymes in glucose biofuel cells are also discussed.

Enzymes have been incorporated into a wide variety of fields and industries as they catalyze many biochemical and chemical reactions. The immobilization of enzymes on carbon nanotubes (CNTs) for generating nano biocatalysts with high stability and reusability is gaining great attention among researchers. Functionalized CNTs act as excellent support for effective enzyme immobilization. Depending on the application, the enzymes can be tailored using the various surface functionalization techniques on the CNTs to extricate the desirable characteristics. Aiming at the preparation of efficient, stable, and recyclable nanobiocatalysts, this review provides an overview of the methods developed to immobilize the various enzymes. Various applications of carbon nanotube-based biocatalysts in water purification, bioremediation, biosensors, and biofuel cells have been comprehensively reviewed.