Woosung Choi, Heon-Cheol Shin, Ji Man Kim et al.

Journal of Electrochemical Science and Technology • 2020

As research on secondary batteries becomes important, interest in analytical methods to examine the condition of secondary batteries is also increasing. Among these methods, the electrochemical impedance spectroscopy (EIS) method is one of the most attractive diagnostic techniques due to its convenience, quickness, accuracy, and low cost. However, since the obtained spectra are complicated signals representing several impedance elements, it is necessary to understand the whole electrochemical environment for a meaningful analysis. Based on the understanding of the whole system, the circuit elements constituting the cell can be obtained through construction of a physically sound circuit model. Therefore, this mini-review will explain how to construct a physically sound circuit model according to the characteristics of the battery cell system and then introduce the relationship between the obtained resistances of the bulk (Rb), charge transfer reaction (Rct), interface layer (RSEI), diffusion process (W) and battery characteristics, such as the state of charge (SOC), temperature, and state of health (SOH).

Xiaojia Zhao, Pradip Pachfule, Arne Thomas

Chemical Society Reviews • 2021

Covalent organic frameworks are a class of extended crystalline organic materials that possess unique architectures with high surface areas and tuneable pore sizes. Since the first discovery of the topological frameworks in 2005, COFs have been applied as promising materials in diverse areas such as separation and purification, sensing or catalysis. Considering the need for renewable and clean energy production, many research efforts have recently focused on the application of porous materials for electrochemical energy storage and conversion. In this respect, considerable efforts have been devoted to the design and synthesis of COF-based materials for electrochemical applications, including electrodes and membranes for fuel cells, supercapacitors and batteries. This review article highlights the design principles and strategies for the synthesis of COFs with a special focus on their potential for electrochemical applications. Recently suggested hybrid COF materials or COFs with hierarchical porosity will be discussed, which can alleviate the most challenging drawback of COFs for these applications. Finally, the major challenges and future trends of COF materials in electrochemical applications are outlined.

C. Zhong, Yida Deng, Wenbin Hu et al.

Chemical Society Reviews • 2015

Electrolytes have been identified as some of the most influential components in the performance of electrochemical supercapacitors (ESs), which include: electrical double-layer capacitors, pseudocapacitors and hybrid supercapacitors. This paper reviews recent progress in the research and development of ES electrolytes. The electrolytes are classified into several categories, including: aqueous, organic, ionic liquids, solid-state or quasi-solid-state, as well as redox-active electrolytes. Effects of electrolyte properties on ES performance are discussed in detail. The principles and methods of designing and optimizing electrolytes for ES performance and application are highlighted through a comprehensive analysis of the literature. Interaction among the electrolytes, electro-active materials and inactive components (current collectors, binders, and separators) is discussed. The challenges in producing high-performing electrolytes are analyzed. Several possible research directions to overcome these challenges are proposed for future efforts, with the main aim of improving ESs' energy density without sacrificing existing advantages (e.g., a high power density and a long cycle-life) (507 references).

Anoop Singh, Asha Sharma, Aamir Ahmed et al.

Biosensors • 2021

The electrochemical biosensors are a class of biosensors which convert biological information such as analyte concentration that is a biological recognition element (biochemical receptor) into current or voltage. Electrochemical biosensors depict propitious diagnostic technology which can detect biomarkers in body fluids such as sweat, blood, feces, or urine. Combinations of suitable immobilization techniques with effective transducers give rise to an efficient biosensor. They have been employed in the food industry, medical sciences, defense, studying plant biology, etc. While sensing complex structures and entities, a large data is obtained, and it becomes difficult to manually interpret all the data. Machine learning helps in interpreting large sensing data. In the case of biosensors, the presence of impurity affects the performance of the sensor and machine learning helps in removing signals obtained from the contaminants to obtain a high sensitivity. In this review, we discuss different types of biosensors along with their applications and the benefits of machine learning. This is followed by a discussion on the challenges, missing gaps in the knowledge, and solutions in the field of electrochemical biosensors. This review aims to serve as a valuable resource for scientists and engineers entering the interdisciplinary field of electrochemical biosensors. Furthermore, this review provides insight into the type of electrochemical biosensors, their applications, the importance of machine learning (ML) in biosensing, and challenges and future outlook.

Ben Zhang, Yijuan Zheng, Tian-Yi Ma et al.

Advanced Materials • 2021

Electrochemical water splitting has attracted significant attention as a key pathway for the development of renewable energy systems. Fabricating efficient electrocatalysts for these processes is intensely desired to reduce their overpotentials and facilitate practical applications. Recently, metal–organic framework (MOF) nanoarchitectures featuring ultrahigh surface areas, tunable nanostructures, and excellent porosities have emerged as promising materials for the development of highly active catalysts for electrochemical water splitting. Herein, the most pivotal advances in recent research on engineering MOF nanoarchitectures for efficient electrochemical water splitting are presented. First, the design of catalytic centers for MOF‐based/derived electrocatalysts is summarized and compared from the aspects of chemical composition optimization and structural functionalization at the atomic and molecular levels. Subsequently, the fast‐growing breakthroughs in catalytic activities, identification of highly active sites, and fundamental mechanisms are thoroughly discussed. Finally, a comprehensive commentary on the current primary challenges and future perspectives in water splitting and its commercialization for hydrogen production is provided. Hereby, new insights into the synthetic principles and electrocatalysis for designing MOF nanoarchitectures for the practical utilization of water splitting are offered, thus further promoting their future prosperity for a wide range of applications.

Song Jin, Zhimeng Hao, Kai Zhang et al.

Angewandte Chemie International Edition • 2021

Electrochemical carbon dioxide reduction reaction (CO2RR) provides an attractive approach to convert renewable electricity into fuels and feedstocks in the form of chemical bonds. Among the different CO2RR pathways, CO2 conversion to carbon monoxide (CO) is considered as one of the most promising candidate reactions in the chemical industry due to its high technologically and economically feasibility. Integrating catalyst and electrolyte design with understanding of catalytic mechanism will yield scientific insights and promote this technology towards industrial implementation. Herein, we review recent advances and challenges for selective CO2 conversion to CO. The intelligent multidimensional catalyst and electrolyte engineering for CO2RR are comprehensively summarized. Furthermore, recent efforts on large-scale production of CO are provided so as to facilitate the industrialization of electrochemical CO2 reduction. To conclude, the remaining technological challenges and future direction of industrialized application of CO2RR to CO are put forward.

Hend S. Magar, Rabeay Y. A. Hassan, A. Mulchandani

Sensors • 2021

Electrochemical impedance spectroscopy (EIS) is a powerful technique used for the analysis of interfacial properties related to bio-recognition events occurring at the electrode surface, such as antibody–antigen recognition, substrate–enzyme interaction, or whole cell capturing. Thus, EIS could be exploited in several important biomedical diagnosis and environmental applications. However, the EIS is one of the most complex electrochemical methods, therefore, this review introduced the basic concepts and the theoretical background of the impedimetric technique along with the state of the art of the impedimetric biosensors and the impact of nanomaterials on the EIS performance. The use of nanomaterials such as nanoparticles, nanotubes, nanowires, and nanocomposites provided catalytic activity, enhanced sensing elements immobilization, promoted faster electron transfer, and increased reliability and accuracy of the reported EIS sensors. Thus, the EIS was used for the effective quantitative and qualitative detections of pathogens, DNA, cancer-associated biomarkers, etc. Through this review article, intensive literature review is provided to highlight the impact of nanomaterials on enhancing the analytical features of impedimetric biosensors.

Z. Yang, Jianlu Zhang, M. Kintner-Meyer et al.

Chemical Reviews • 2011

The is a comprehensive review on the needs and potential storage technologies for electrical grid that is expected to integrate significant levels of renewables. This review offers details of the technologies, in terms of needs, status, challenges and future R&d directions.

Mohammad A. Alkhadra, Xiao Su, M. Suss et al.

Chemical Reviews • 2022

Agricultural development, extensive industrialization, and rapid growth of the global population have inadvertently been accompanied by environmental pollution. Water pollution is exacerbated by the decreasing ability of traditional treatment methods to comply with tightening environmental standards. This review provides a comprehensive description of the principles and applications of electrochemical methods for water purification, ion separations, and energy conversion. Electrochemical methods have attractive features such as compact size, chemical selectivity, broad applicability, and reduced generation of secondary waste. Perhaps the greatest advantage of electrochemical methods, however, is that they remove contaminants directly from the water, while other technologies extract the water from the contaminants, which enables efficient removal of trace pollutants. The review begins with an overview of conventional electrochemical methods, which drive chemical or physical transformations via Faradaic reactions at electrodes, and proceeds to a detailed examination of the two primary mechanisms by which contaminants are separated in nondestructive electrochemical processes, namely electrokinetics and electrosorption. In these sections, special attention is given to emerging methods, such as shock electrodialysis and Faradaic electrosorption. Given the importance of generating clean, renewable energy, which may sometimes be combined with water purification, the review also discusses inverse methods of electrochemical energy conversion based on reverse electrosorption, electrowetting, and electrokinetic phenomena. The review concludes with a discussion of technology comparisons, remaining challenges, and potential innovations for the field such as process intensification and technoeconomic optimization.

Kui Fan, Wenfu Xie, Jinze Li et al.

Nature Communications • 2022

Electrochemical nitrate reduction to ammonia is a promising alternative strategy to the traditional Haber-Bosch process but suffers from a low Faradaic efficiency and limited ammonia yield due to the sluggish multi-electron/proton-involved steps. Herein, we report a typical hollow cobalt phosphide nanosphere electrocatalyst assembled on a self-supported carbon nanosheet array synthesized with a confinement strategy that exhibits an extremely high ammonia yield rate of 8.47 mmol h−1 cm−2 through nitrate reduction reaction, which is highly superior to previously reported values to our knowledge. In situ experiments and theoretical investigations reveal that the dynamic equilibrium between the generation of active hydrogen on cobalt phosphide and its timely consumption by nitrogen intermediates leads to a superior ammonia yield with a high Faradaic efficiency. This unique insight based on active hydrogen equilibrium provides new opportunities for large-scale ammonia production through electrochemical techniques and can be further used for carbon dioxide capture. While electrochemical conversion of nitrate to ammonia offers a renewable means to remediate waste compounds, it is challenging to achieve selective catalysis. Here, authors demonstrate a strategy to improve electrocatalytic ammonia production using cobalt phosphide on carbon nanosheet arrays.

Jaya Baranwal, Brajesh Barse, G. Gatto et al.

Chemosensors • 2022

The world of sensors is diverse and is advancing at a rapid pace due to the fact of its high demand and constant technological improvements. Electrochemical sensors provide a low-cost and convenient solution for the detection of variable analytes and are widely utilized in agriculture, food, and oil industries as well as in environmental and biomedical applications. The popularity of electrochemical sensing stems from two main advantages: the variability of the reporting signals, such as the voltage, current, overall power output, or electrochemical impedance, and the low theoretical detection limits that originate from the differences in the Faradaic and nonFaradaic currents. This review article attempts to cover the latest advances and applications of electrochemical sensors in different industries. The role of nanomaterials in electrochemical sensor research and advancements is also examined. We believe the information presented here will encourage further efforts on the understanding and progress of electrochemical sensors.

John Wang, J. Polleux, James Lim et al.

The Journal of Physical Chemistry C • 2007

The advantages in using nanostructured materials for electrochemical energy storage have largely focused on the benefits associated with short path lengths. In this paper, we consider another contribution, that of the capacitive effects, which become increasingly important at nanoscale dimensions. Nanocrystalline TiO2 (anatase) was studied over a dimensional regime where both capacitive and lithium intercalation processes contribute to the total stored charge. An analysis of the voltammetric sweep data was used to distinguish between the amount of charge stored by these two processes. At particle sizes below 10 nm, capacitive contributions became increasingly important, leading to greater amounts of total stored charge (gravimetrically normalized) with decreasing TiO2 particle size. The area normalized capacitance was determined to be well above 100 μF/cm2, confirming that the capacitive contribution was pseudocapacitive in nature. Moreover, reducing the particle size to the nanoscale regime led to faster...

H. M. Saleh, Amal I. Hassan

Sustainability • 2023

Nanomaterials have gained significant attention as a remarkable class of materials due to their unique properties and the fact that they encompass a wide range of samples with at least one dimension ranging from 1 to 100 nm. The deliberate design of nanoparticles enables the achievement of extremely large surface areas. In the field of cost-effective electrochemical devices for energy storage and conversion applications, nanomaterials have emerged as a key area of research. Their exceptional physical and chemical properties have led to extensive investigations aimed at improving the performance and cost-effectiveness of electrochemical devices, including batteries, supercapacitors, and fuel cells. The continuous development and enhancement of these high-performance materials are driven by the demand for enhanced productivity, connectivity, and sustainability at a reduced cost. This review focuses on the electrochemical performance of electrodes, energy storage, and electrochemical sensors (ES) based on nanotechnology. It discusses the application of nanotechnology in electrochemistry for water purification and the fate of substances in water, while also introducing green nanotechnology and cost-effective, high-fidelity product creation through electrochemical methods. The study emphasizes the synthesis of novel nanomaterials, such as metal–organic frameworks (MOFs), covalent organic frameworks (COFs), and MXenes, with applications in electrochemical devices. Furthermore, it explores the integration of nanostructures with electrochemical systems in economically significant and future applications, along with the challenges faced by nanotechnology-based industries. The paper also explores the interplay between nanomaterials and biosensors, which play a vital role in electrochemical devices. Overall, this review provides a comprehensive overview of the significance of nanomaterials in the development of cost-effective electrochemical devices for energy storage and conversion. It highlights the need for further research in this rapidly evolving field and serves as a valuable resource for researchers and engineers interested in the latest advancements in nanomaterials for electrochemical devices.

L. Canham

Applied Physics Letters • 1990

Indirect evidence is presented that free‐standing Si quantum wires can be fabricated without the use of epitaxial deposition or lithography. The novel approach uses electrochemical and chemical dissolution steps to define networks of isolated wires out of bulk wafers. Mesoporous Si layers of high porosity exhibit visible (red) photoluminescence at room temperature, observable with the naked eye under <1 mW unfocused (<0.1 W cm−2) green or blue laser line excitation. This is attributed to dramatic two‐dimensional quantum size effects which can produce emission far above the band gap of bulk crystalline Si.

Yonggang Wang, Yanfang Song, Yongyao Xia

Chemical Society Reviews • 2016

Electrochemical capacitors (i.e. supercapacitors) include electrochemical double-layer capacitors that depend on the charge storage of ion adsorption and pseudo-capacitors that are based on charge storage involving fast surface redox reactions. The energy storage capacities of supercapacitors are several orders of magnitude higher than those of conventional dielectric capacitors, but are much lower than those of secondary batteries. They typically have high power density, long cyclic stability and high safety, and thus can be considered as an alternative or complement to rechargeable batteries in applications that require high power delivery or fast energy harvesting. This article reviews the latest progress in supercapacitors in charge storage mechanisms, electrode materials, electrolyte materials, systems, characterization methods, and applications. In particular, the newly developed charge storage mechanism for intercalative pseudocapacitive behaviour, which bridges the gap between battery behaviour and conventional pseudocapacitive behaviour, is also clarified for comparison. Finally, the prospects and challenges associated with supercapacitors in practical applications are also discussed.

Lei Zhao, Yuan Li, Meimei Yu et al.

Advanced Science • 2023

The electrolyte‐wettability of electrode materials in liquid electrolytes plays a crucial role in electrochemical energy storage, conversion systems, and beyond relied on interface electrochemical process. However, most electrode materials do not have satisfactory electrolyte‐wettability for possibly electrochemical reaction. In the last 30 years, there are a lot of literature have directed at exploiting methods to improve electrolyte‐wettability of electrodes, understanding basic electrolyte‐wettability mechanisms of electrode materials, exploring the effect of electrolyte‐wettability on its electrochemical energy storage, conversion, and beyond performance. This review systematically and comprehensively evaluates the effect of electrolyte‐wettability on electrochemical energy storage performance of the electrode materials used in supercapacitors, metal ion batteries, and metal‐based batteries, electrochemical energy conversion performance of the electrode materials used in fuel cells and electrochemical water splitting systems, as well as capacitive deionization performance of the electrode materials used in capacitive deionization systems. Finally, the challenges in approaches for improving electrolyte‐wettability of electrode materials, characterization techniques of electrolyte‐wettability, as well as electrolyte‐wettability of electrode materials applied in special environment and other electrochemical systems with electrodes and liquid electrolytes, which gives future possible directions for constructing interesting electrolyte‐wettability to meet the demand of high electrochemical performance, are also discussed.

Guoping Wang, Lei Zhang, Jiujun Zhang

Chem. Soc. Rev. • 2012

In this critical review, metal oxides-based materials for electrochemical supercapacitor (ES) electrodes are reviewed in detail together with a brief review of carbon materials and conducting polymers. Their advantages, disadvantages, and performance in ES electrodes are discussed through extensive analysis of the literature, and new trends in material development are also reviewed. Two important future research directions are indicated and summarized, based on results published in the literature: the development of composite and nanostructured ES materials to overcome the major challenge posed by the low energy density of ES (476 references).

Jie Wu, Hong Liu, Weiwei Chen et al.

Nature Reviews Bioengineering • 2023

Electrochemical biosensors incorporate a recognition element and an electronic transducer for the highly sensitive detection of analytes in body fluids. Importantly, they can provide rapid readouts and they can be integrated into portable, wearable and implantable devices for point-of-care diagnostics; for example, the personal glucose meter enables at-home assessment of blood glucose levels, greatly improving the management of diabetes. In this Review, we discuss the principles of electrochemical biosensing and the design of electrochemical biosensor devices for health monitoring and disease diagnostics, with a particular focus on device integration into wearable, portable and implantable systems. Finally, we outline the key engineering challenges that need to be addressed to improve sensing accuracy, enable multiplexing and one-step processes, and integrate electrochemical biosensing devices in digital health-care pathways. Electrochemical biosensors can be integrated into wearable, portable and implantable devices for health monitoring and disease diagnosis. This Review discusses the design and integration of different types of electrochemical biosensors for the detection of analytes related to health and disease, and outlines engineering challenges that need to be addressed to enable clinical translation of electrochemical biosensor-based point-of-care devices. Electrochemical biosensors are self-contained, analytical devices, in which a biological recognition element is in direct contact with an electrochemcial transduction element to allow the sensitive and specific detection of analytes. Depending on the design and sensor type, health-related and disease-related biomarkers, such as carbohydrates, proteins, nucleic acids and cells, can be rapidly analysed in different body fluids, including blood, saliva and tears. Electrochemical biosensors, including amperometric, voltammetric, potentiometric, organic electrochemical transistor, photoelectrochemical and electrochemiluminescent sensors, can be integrated into wearable, portable and implantable devices to enable point-of-care diagnostics and health monitoring. Commercialization and broad point-of-care applicability of integrated electrochemical biosensors will require improvements in stability, sensitivity, reproducibility, multiplexing, and digitalization and, importantly, low-cost materials and easy fabrication methods. Electrochemical biosensors are self-contained, analytical devices, in which a biological recognition element is in direct contact with an electrochemcial transduction element to allow the sensitive and specific detection of analytes. Depending on the design and sensor type, health-related and disease-related biomarkers, such as carbohydrates, proteins, nucleic acids and cells, can be rapidly analysed in different body fluids, including blood, saliva and tears. Electrochemical biosensors, including amperometric, voltammetric, potentiometric, organic electrochemical transistor, photoelectrochemical and electrochemiluminescent sensors, can be integrated into wearable, portable and implantable devices to enable point-of-care diagnostics and health monitoring. Commercialization and broad point-of-care applicability of integrated electrochemical biosensors will require improvements in stability, sensitivity, reproducibility, multiplexing, and digitalization and, importantly, low-cost materials and easy fabrication methods.

A. Lazanas, M. Prodromidis

ACS Measurement Science Au • 2023

This tutorial provides the theoretical background, the principles, and applications of Electrochemical Impedance Spectroscopy (EIS) in various research and technological sectors. The text has been organized in 17 sections starting with basic knowledge on sinusoidal signals, complex numbers, phasor notation, and transfer functions, continuing with the definition of impedance in electrical circuits, the principles of EIS, the validation of the experimental data, their simulation to equivalent electrical circuits, and ending with practical considerations and selected examples on the utility of EIS to corrosion, energy related applications, and biosensing. A user interactive excel file showing the Nyquist and Bode plots of some model circuits is provided in the Supporting Information. This tutorial aspires to provide the essential background to graduate students working on EIS, as well as to endow the knowledge of senior researchers on various fields where EIS is involved. We also believe that the content of this tutorial will be a useful educational tool for EIS instructors.

V. Augustyn, P. Simon, B. Dunn

Energy &amp; Environmental Science • 2014

Electrochemical energy storage technology is based on devices capable of exhibiting high energy density (batteries) or high power density (electrochemical capacitors). There is a growing need, for current and near-future applications, where both high energy and high power densities are required in the same material. Pseudocapacitance, a faradaic process involving surface or near surface redox reactions, offers a means of achieving high energy density at high charge–discharge rates. Here, we focus on the pseudocapacitive properties of transition metal oxides. First, we introduce pseudocapacitance and describe its electrochemical features. Then, we review the most relevant pseudocapacitive materials in aqueous and non-aqueous electrolytes. The major challenges for pseudocapacitive materials along with a future outlook are detailed at the end.

Shuang Guo, Wan Qian Guo, Yuan Yuan et al.

Advanced Materials Research • 2013

Anaerobic biological technology and bioelectrochemical technology are regarded as promising sustainable wastes treatment processes. With biocatalysis in BESs anode or cathode, various pollutants can be removed. The pollutants range from nitrogen and sulfur to complex compounds. However, the investigation on recalcitrant wastes removal with biocathode has only been reported recently. Recalcitrant wastes, especially chlorinated nitroaromatic compounds, are highly persistent and toxic environmental pollutions which should be removed before discharging to environment. This paper provides a review on anaerobic biocathode BESs for recalcitrant wastes treatment and the feasibility of this system for CANs transformation. It is expected that anaerobic biocathode BESs can provide an appropriate condition for these compounds to transform to easily degradable forms. The technical challenges for future research are also discussed.

O. Lefebvre, A. Al-Mamun, H. Y. Ng

Water Science and Technology • 2008

Microbial fuel cells (MFCs) are a promising anaerobic technology but they are limited by the high cost of the catalyst used at the cathode (typically platinum). In this study, we designed a novel type of two-chambered MFC wherein an autoheterotrophic denitrifying biofilm replaced the costly catalyst on the cathode surface. Micro-organisms performed denitrification by using electrons supplied by bacteria oxidizing domestic wastewater and acetate as substrates in the anode chamber. This two-chambered MFC equipped with a biocathode generated during more than 1.5 month up to 9.4 mW m−2 of anode surface or 0.19 W m−3 of anode chamber volume, while removing over 65% of COD, 84% of total nitrogen and nearly 30% of suspended solids with domestic wastewater as a substrate, and nearly 95% of acetate in the subsequent experiments.

Varun Srinivasan, Jacob Weinrich, Caitlyn Butler

Environmental Science: Water Research &amp; Technology • 2016

This study presents the conditions of nitrite accumulation in MFC biocathodes through batch experiments and derives kinetic parameters with an Activated Sludge Model with an integration of the Nernst–Monod model and Indirect Coupling of Electrons (ASM–NICE).

Mohita Sharma, Priyangshu M. Sarma, Deepak Pant et al.

RSC Advances • 2015

This study focuses on the effect of operational and physiochemical factors on a stable sulfate reducing bacteria biocathode and their effect on the electrochemical response thereof.

Caitlyn Shea, Peter Clauwaert, Willy Verstraete et al.

Water Science and Technology • 2008

Perchlorate is widely used as a propellant in the aerospace and defense industries, and is of environmental concern due to its high mobility and inhibiting effect on thyroid function. An ideal treatment approach is bioreduction to chloride via dissimilatory perchlorate-reducing bacteria (PCRB). PCRB are ubiquitous in the environment, and are mainly facultative anaerobes and denitrifiers. Previous research suggests that PCRB may grow using a cathode as an electron donor, although this research was performed in a half cell with exogenous electron shuttles. We investigated a functioning MFC with a denitrifying biocathode for perchlorate reduction, as a means to confirm the existence of biocathode-utilizing PCRB and the possibility of perchlorate remediation without added shuttles. The biocathode was initially run with 20 mgN/L nitrate. The perchlorate concentration was increased stepwise from 0.1 mg/L to 20 mg/L, while the nitrate concentration was decreased from 20 mgN/L to 5 mgN/L. The maximum perchlorate removal was 12 mg/L-d, contributing 64% to the 0.28 mA produced by the cell. Given the lack of soluble electron donor in the medium, the extent of perchlorate reduction, and the improvement of perchlorate reduction over time, these tests strongly suggest PCRB are utilizing the cathode as an electron donor without exogenous electron shuttles.

Yue Du, Youpeng Qu, Xiangtong Zhou et al.

RSC Advances • 2015

Biocathode coupled photoelectrochemical cells (Bio-PEC) have the potential for electricity generation and pollutant removal, with the simultaneous utilization of both solar energy and bioenergy.

Moustafa Almunla, Yudum Tepeli Büyüksünetçi, Oğuz Akpolat et al.

Electroanalysis • 2021

Abstract A biofuel cell (BFC) was fabricated by combining multiwalled carbon nanotube ‐platinum‐gold (MWCNT−Pt−Au) hybrid nanomaterial, glucose oxidase (GOx) and benzoquinone included carbon felt electrode (CFE) bioanode with apple tissue included CFE biocathode. The working parameters of bioanode were optimized both experimentally and chemometrically. For the biocathode, apple, banana and pear tissues were tried and best power output was obtained with apple tissue. By combining MWCNT−Pt−Au/GOx/CFE bioanode with apple tissue based biocathode, single cell, double cell with membrane and with salt‐bridge BFCs were formed. The best power output with highest current density were obtained with single cell BFC.

Tahsin Bahar

Asia-Pacific Journal of Chemical Engineering • 2016

Abstract Ferrocene groups introduced polyethylenimine was adsorbed onto multi‐wall carbon nanotubes attached carbon cloth before crosslinking via glutaraldehyde to develop an enzyme electrode (anode) for biofuel cell applications. Glucose oxidase was covalently immobilized onto this electrode by leftover aldehyde groups on the surface. The apparent Michaelis constant of immobilized enzyme was measured as approximately fivefold higher than that of the free enzyme. Thermal stability of immobilized enzyme was improved as estimated. Activity half‐life of the immobilized glucose oxidase was determined as approximately 8 times longer than that of the free one; 2.4 mA/cm 2 electrical current was obtained by using this electrode by forming a basic biofuel half‐cell. Copyright © 2016 Curtin University of Technology and John Wiley &amp; Sons, Ltd.

Aya Kontani, Miyuki Masuda, Hirotoshi Matsumura et al.

Electroanalysis • 2014

Abstract To extend the range of biofuel cell applications, we wish to increase their maximum operational temperatures. Using a thermostable alcohol dehydrogenase as a biocatalyst, we prepared an enzyme‐immobilized bioanode that can operate at high temperatures. The catalytic current for ethanol oxidation was increased using this electrode at temperatures up to 80 °C.

Jérémie-Luc Sanchez, Christel Laberty-Robert

Journal of Materials Chemistry B • 2021

A microbial fuel cell bioanode encapsulating electroactive bacteria in core–shell fibers mixed with a conductive scaffold was electrospun. This new design opens up perspectives of storable ready-to-use anodes for portable applications.

Yuhe Shi, Lin Li, Ling Zhang

Electroanalysis • 2022

Abstract Herein, we successfully construct the 3D biocompatible graphene through crosslinking 2D graphene nanosheet onto carbon fiber paper with poly(diallyldimethylammonium chloride) (PDDA) as anode of the alcohol biofuel cell. Compared with the bioanode without 3D graphene, the current density and output power of PDDA‐graphene‐ADH bioanode is increased by 23 % and 41 % at a high concentration of ethanol at pH 8.9, suggesting the stabilization role of graphene in enzyme loading. The study provides us a deep analysis on structures and performances of the bioanode incl. electrochemistry, X‐ray photoelectron spectra, and atomic force microscopy images, which is significant to develop the new methods to construct 3D porous electrodes in energy conversion device.

Yuki Sakurada, Kouta Takeda, Hiroyuki Ohno et al.

Catalysts • 2017

A bioanode for ethanol oxidation was prepared by immobilizing the recombinant pyrroloquinoline quinone (PQQ)-dependent alcohol dehydrogenase from Pseudomonas putida KT 2440 (PpADH) with polyion complex (PIC) and redox polymer. The PIC based on poly-l-lysine (PLL) and poly-l-glutamic acid (PGA) was suitable for immobilizing PpADH on the electrode. PpADH was immobilized using only one redox polymer, aminoferrocene, which was attached to the PGA backbone (PGA-AmFc) on the electrode. The anodic current density at 0.6 V (vs. Ag/AgCl) was 22.6 μA·cm−2. However, when the number of the cycles was increased, the catalytic current drastically decreased. PpADH was immobilized using PGA-AmFc and PIC on the electrode. The anodic current density at 0.5 V (vs. Ag/AgCl) was 47.3 μA·cm−2, and the performance maintained 74% of the initial value after five cycles. This result indicated that the combination of PIC and PGA-AmFc was suitable for the immobilization of PpADH on the electrode. In addition, the long-term stability and catalytic current density were improved by using the large surface area afforded by the gold nanoparticles.

Tomohiro Komatsu, Kazuki Hishii, Michiko Kimura et al.

International Journal of Molecular Sciences • 2021

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.

Bongkyu Kim, Junyeong An, In Seop Chang

ChemSusChem • 2017

Abstract The power overshoot generated by electron depletion in microbial fuel cells (MFCs) was characterized in this study. Various causes of power overshoot, identified in previous studies, are discussed in terms of their plausible contributions to electron depletion. We found that power overshoot occurred if the anodic overpotential generated by electron depletion exceeded the cathodic overpotential. The introduction of assistance current from anode connections, which ameliorated the electron depletion in the MFCs, immediately eliminated the power overshoot. As a result, if the electron production at the anode exceeded electron reduction at the cathode, a power overshoot was not generated. The results revealed that introducing assistance current supplied from an additional anode to the limited anode eliminated power overshoot. The power overshoot is not generated by kinetic limitation at the cathode; it is only generated by the kinetic limitation at the anode. The mechanism underlying power overshoot should be considered in the design of MFCs to improve reliability, particularly in scaled‐up plant applications. The proposed technique is more practical than previously proposed methods.

Yuanyuan Zhang, Mary Arugula, Shannon Williams et al.

ECS Transactions • 2015

We report here a novel layer-by-layer (LbL) assembled enzyme cascade bioanode incorporated with CNT-invertase and CNT-glucose dehydrogenase for sucrose oxidation in a biofuel cell. Methylene green (MG) was used as redox mediator for electrocatalytic oxidation of NADH at reduced overpotentials on screen printed electrode (SPE). The LbL architecture showed advantages for sequential enzymatic reaction that favored the efficient penetration of substrate and products in a cascade system. The maximum current density and power density achieved were 412 ± 36 μA/cm 2 and 85±6μW/cm 2 .The high current density/power density obtained showed LbL assembly is of great advantage and can be employed as a simple and efficient way to construct enzyme cascade bioanode for biofuel cell applications.

T. Matsumoto, S. Shimada, K. Yamamoto et al.

Fuel Cells • 2013

Abstract The present study reports the design of a novel bioanode to deeply oxidize glucose in an enzymatic biofuel cell (EFC). This enzymatic glucose cell utilizes three co‐immobilized enzymes: NAD‐dependent glucose dehydrogenase (GDH), NAD(P) + ‐dependent gluconate‐5‐dehydrogenase (Ga5DH), and diaphorase (DI). Glucose is oxidized to gluconate by NAD‐dependent GDH, gaining two electrons per glucose; the gluconate obtained as a by‐product is oxidized at the C5 carbon to 5‐keto‐gluconate by Ga5DH. Operation of our bioanode enabled the oxidation of glucose in two stages, resulting in the gain of four electrons. The three‐enzyme EFC provides a maximum power density of 10.51 ± 1.72 μW cm –2 , which is about 1.6 times higher than the maximum power density of an EFC using a bioanode based on the co‐immobilization of two enzymes (GDH and DI). Our results hold promise for increasing the current density of EFCs, and for application in glucose biosensor.

Roman Chomicz, Michał Bystrzejewski, Krzysztof Stolarczyk

Catalysts • 2021

This work demonstrates the application of magnetic carbon-encapsulated iron nanoparticles (CEINs) for the construction of bioelectrodes in a biobattery and a biofuel cell. It has been shown that carbon-encapsulated iron nanoparticles are a suitable material for the immobilization of laccase (Lc) and 1,4-naphthoquinone (NQ) and fructose dehydrogenase (FDH). The system is stable; no leaching of the enzyme and mediator from the surface of the modified electrode was observed. The onset of the catalytic reduction of oxygen to water was at 0.55 V, and catalytic fructose oxidation started at −0.15 V. A biobattery was developed in which a zinc plate served as the anode, and the cathode was a glassy carbon electrode modified with carbon-encapsulated iron nanoparticles, laccase in the Nafion (Nf) layer. The maximum power of the cell was ca. 7 mW/cm2 at 0.71 V and under external resistance of 1 kΩ. The open-circuit voltage (OCV) for this system was 1.51 V. In the biofuel cell, magnetic nanoparticles were used both on the bioanode and biocathode to immobilize the enzymes. The glassy carbon bioanode was coated with carbon-encapsulated iron nanoparticles, 1,4-naphthoquinone, fructose dehydrogenase, and Nafion. The cathode was modified with carbon-encapsulated magnetic nanoparticles and laccase in the Nafion layer. The biofuel cell parameters were as follows: maximum power of 78 µW/cm2 at the voltage of 0.33 V and under 20 kΩ resistance, and the open-circuit voltage was 0.49 V. These enzymes worked effectively in the biofuel cell, and laccase also effectively worked in the biobattery.

Longfei Sun, Xiaohua Zhang, Wenyang Wang et al.

Analytical Methods • 2015

An easy-operation and high-performance bioanode based on a composite gel of ferrocenecarboxaldehyde modified CNTs and an ionic liquid was successfully developed.

Zonghua Wang, Lin Xia, Jianfei Xia et al.

RSC Advances • 2016

A hybrid anode integrating enzymatic hydrolysis of starch by glucoamylase and non-enzymatic oxidation of glucose by gold nanoparticles is presented to achieve an efficient cascade energy conversion from starch.

Ting‐Ting Zhu, Zhou‐Hua Cheng, Sheng‐Song Yu et al.

Environmental Microbiology • 2022

Summary Exoelectrogenic bacteria (EEB) are capable of anaerobic respiration with diverse extracellular electron acceptors including insoluble minerals, electrodes and flavins, but the detailed electron transfer pathways and reaction mechanisms remain elusive. Here, we discover that CymA, which is usually considered to solely serve as an inner‐membrane electron transfer hub in Shewanella oneidensis MR‐1 (a model EEB), might also function as a reductase for direct reducing diverse nitroaromatic compounds (e.g. 2,4‐dichloronitrobenzene) and azo dyes. Such a process can be accelerated by dosing anthraquinone‐2,6‐disulfonate. The CymA‐based reduction pathways in S . oneidensis MR‐1 for different contaminants could be functionally reconstructed and strengthened in Escherichia coli . The direct reduction of lowly polar contaminants by quinol oxidases like CymA homologues might be universal in diverse microbes. This work offers new insights into the pollutant reduction mechanisms of EEB and unveils a new function of CymA to act as a terminal reductase.