Microbial Fuel Cell Stack Performance Enhancement Through

Total Page:16

File Type:pdf, Size:1020Kb

Microbial Fuel Cell Stack Performance Enhancement Through Applied Energy 262 (2020) 114475 Contents lists available at ScienceDirect Applied Energy journal homepage: www.elsevier.com/locate/apenergy Microbial Fuel Cell stack performance enhancement through carbon veil T anode modification with activated carbon powder ⁎ ⁎ Iwona Gajdaa, , John Greenmana,b, Ioannis Ieropoulosa, a Bristol BioEnergy Centre, Bristol Robotics Laboratory, University of the West of England, Bristol BS16 1QY, UK b Department of Applied Sciences, University of the West of England, Bristol BS16 1QY, UK HIGHLIGHTS GRAPHICAL ABSTRACT Novel modification of carbon veil • anode with activated carbon in urine fed MFC stack. • Modified microstructure enhanced surface area and power performance up to 21.1 W m−3. • The modification exhibited 77% in- crease in power output of the MFC stack. • It improved COD reduction by 13.5% in comparison to control stack. • It exhibited a stable performance after 500 days and resilience to prolonged starvation. ARTICLE INFO ABSTRACT Keywords: The chemical energy contained in urine can be efficiently extracted into direct electricity by Microbial FuelCell Activated carbon stacks to reach usable power levels for practical implementation and a decentralised power source in remote Ceramic locations. Herein, a novel type of the anode electrode was developed using powdered activated carbon (PAC) Long-term operation applied onto the carbon fibre scaffold in the ceramic MFC stack to achieve superior electrochemical performance Microbial Fuel Cell during 500 days of operation. The stack equipped with modified anodes (MF-CV) produced up to 37.9 mW Urine (21.1 W m−3) in comparison to the control (CV) that reached 21.4 mW (11.9 W m−3) showing 77% increase in Stacking power production. The novel combination of highly porous activated carbon particles applied onto the con- ductive network of carbon fibres promoted simultaneously electrocatalytic activity and increased surface area, resulting in excellent power output from the MFC stack as well as higher treatment rate. Considering the low cost and simplicity of the material preparation, as well as the outstanding electrochemical activity during long term operation, the resulting modification provides a promising anode electrocatalyst for high-performance MFC stacks to enhance urine and waste treatment for the purpose of future scale-up and technology implementation as an applied off-grid energy source. ⁎ Corresponding authors. E-mail addresses: [email protected] (I. Gajda), [email protected] (I. Ieropoulos). https://doi.org/10.1016/j.apenergy.2019.114475 Received 2 September 2019; Received in revised form 26 December 2019; Accepted 28 December 2019 0306-2619/ © 2020 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/BY/4.0/). I. Gajda, et al. Applied Energy 262 (2020) 114475 1. Introduction activated carbon derived from the chestnut shell was proven suitable in the MFC anode [34] or as an addition to the constructed wetland MFC Microbial Fuel Cell is a type of bioelectrochemical device that em- [35]. Further development of new, efficient and cost effective materials ploys electroactive microorganisms to transform chemical energy into is needed for construction of sustainable bioelectrochemical technolo- direct electricity by means of a combination of microbial metabolic and gies, which can be deployed in wastewater treatment plants and in electrochemical reactions from a variety of substrates [1] including remote locations as the decentralised power sources. This work aims to wastewater [2] and urine [3]. In the anode of the MFCs, microbial explore for the first time, simple and inexpensive modification ofthe consortia break down organic “fuel” into electrons and protons. Elec- anodic carbon veil scaffold with the addition of powdered activated trons derived from the anaerobic oxidation by the microbial consortia carbon onto the fibres to produce a three-dimensional (3D) structure in are transported to the anodic electrode and travel through the external order to improve the output of a MFC stack. It aims to test the MFC circuit to the cathode electrode, while protons and other cations pass performance, as a result of this modification, over a long term period through a membrane, which separates both chambers. Urine is a va- (500 days) under feeding and starvation regimes and discusses scale-up luable “waste” that could potentially be used to off-set the need to mine challenges for wider implementation. This is in order to aid the de- and produce synthetic fertilisers [4]. It is also an energy-rich substrate velopment of an affordable system that is designed for the ease ofmass possessing good electrical conductivity due to high ionic content, which production of future urine-powered systems deployed as decentralised makes it an ideal substrate for the production of direct electric current energy sources in a wide range of real world environments. In order for as well as nutrient recovery [5] both in MFCs [6] and Microbial Elec- MFCs to be fully realised as off-the-grid power sources, research must trolysis Cells (MECs) [7]. Urine operated MFCs have the ability to focus on producing low cost and easy to manufacture electrode and generate electricity in remote locations as the off- grid energy source membrane materials, which have been tested in realistic environments. and can thus be used in areas of poor energy infrastructure. There are however major limiting factors that hinder the practical implementa- 2. Materials and methods tion of MFCs at larger scale, which are low power output, material cost and difficulties in the scale-up process as well as system longevity. 2.1. Experimental set-up Multiple findings suggest that the viability of the urine-operated sys- tems is directly correlated with its use [8,9] and its suitability for Individual MFCs were assembled using terracotta cylinders (Jain generating enough power to directly light an LED [10] or charge a Scientific Suppliers, India) as previously described [36]. The cylinder mobile phone [11]. Technology scale-up is of enormous importance as dimensions were 50 mm (h), 22 mm inside and 30 mm outside dia- it brings the bioelectrochemical technology innovations into real world meter. The cathodes were made of activated carbon (G Baldwins and environments, where it is tested in practice for electricity production Co., UK) and 20% PTFE blend applied onto the hydrophobic carbon veil [8,9], treatment [12] and hydrogen generation [13]. One approach into as previously described [31]. The cathodes (22.5 cm2) were placed in scale-up is through stacking and multiplication of MFC units [14] where the inner chamber of the cylinder, with the activated carbon layer ex- the miniaturisation of stacked [15] reactors achieves higher energy posed to the ceramic wall using stainless steel crocodile clips as con- efficiency through lower ohmic losses [14]. To improve the MFC nectors to the external circuit and data acquisition hardware. Blocks of output, efforts have been made into the reactor design focusing ona activated carbon foam (Finest Filters, UK) were inserted into the cy- membrane-based [15] or membrane-less configuration [9,16], anodic linders to maintain good electrical contact between the cathode and the [17] and cathodic modifications [18,19] as well as achieving low-cost ceramic membrane. and low-tech production procedures for materials including ceramic For the test, two types of anode materials were prepared: carbon [20] and cardboard [21]. Numerous anode modifications have been veil fibre (CV) as the control and modified carbon veil (MF-CV) with pursued over the past decades looking into the metallic [22], carbon activated carbon powder. The preparation is described as follows: [23], composite [24] and chemical modifications [25] that aim to in- CV- Carbon veil fibre was purchased from PRF Composites, UKwith crease its specific surface area as well as to increase electron transfer the carbon loading of 20 g/m−2 and cut to the dimensions of rates, however in light of the practical application of the technology, 200 × 140 mm. It was folded and wrapped around the terracotta cy- selected materials and methodology of their synthesis/preparation linder and tightened with stainless steel wire to hold the electrode in should take cost and ease of assembly into account [26] in order to place and to maintain an electrical connection for the external circuit. allow for the electrode materials to be mass produced in a cost-effective MF-CV- identical piece of carbon veil used as the control was coated way. However, the vast majority of electrode modification strategies with activated carbon ink. For the preparation of the ink, food-grade are unsuitable for practical applications due to complex manufacturing powdered activated carbon originating from coconut shells, was pur- processes and high costs, and their long-term stability is rarely tested chased from a health store (G Baldwins and Co., UK) and had a typical [27]. One of the most promising, readily available and affordable ma- surface area of 1 g between 800–1000 m2 and size: approx 100 µm. It terials is activated carbon [28] typically used in granular (GAC) form in was blended with 5% PTFE (60% water dispersion in H2O, Sigma the anodic half-cell [29] and powdered form (PAC) for the fabrication Aldrich) and 300 mL of deionised water. The mixture was stirred for of the cathode when applied onto stainless steel mesh [9,30] or carbon 2 min -in order to obtain a slurry and applied onto both sides of carbon matrix [10,31]. PAC-based cathodes are widely applied in MFC studies veil using a paintbrush. The sheets of such prepared material were then including field trials and prototypes of the membrane-based [8] and heat treated at 250 °C for 30 min. The final loading of the activated membrane-less systems [9] and its properties suggest it would be an carbon was 5 mg/cm−2.
Recommended publications
  • Towards the Hydrogen Economy—A Review of the Parameters That Influence the Efficiency of Alkaline Water Electrolyzers
    energies Review Towards the Hydrogen Economy—A Review of the Parameters That Influence the Efficiency of Alkaline Water Electrolyzers Ana L. Santos 1,2, Maria-João Cebola 3,4,5 and Diogo M. F. Santos 2,* 1 TecnoVeritas—Serviços de Engenharia e Sistemas Tecnológicos, Lda, 2640-486 Mafra, Portugal; [email protected] 2 Center of Physics and Engineering of Advanced Materials (CeFEMA), Instituto Superior Técnico, Universidade de Lisboa, 1049-001 Lisbon, Portugal 3 CBIOS—Center for Research in Biosciences & Health Technologies, Universidade Lusófona de Humanidades e Tecnologias, Campo Grande 376, 1749-024 Lisbon, Portugal; [email protected] 4 CERENA—Centre for Natural Resources and the Environment, Instituto Superior Técnico, Universidade de Lisboa, Av. Rovisco Pais, 1049-001 Lisbon, Portugal 5 Escola Superior Náutica Infante D. Henrique, 2770-058 Paço de Arcos, Portugal * Correspondence: [email protected] Abstract: Environmental issues make the quest for better and cleaner energy sources a priority. Worldwide, researchers and companies are continuously working on this matter, taking one of two approaches: either finding new energy sources or improving the efficiency of existing ones. Hydrogen is a well-known energy carrier due to its high energy content, but a somewhat elusive one for being a gas with low molecular weight. This review examines the current electrolysis processes for obtaining hydrogen, with an emphasis on alkaline water electrolysis. This process is far from being new, but research shows that there is still plenty of room for improvement. The efficiency of an electrolyzer mainly relates to the overpotential and resistances in the cell. This work shows that the path to better Citation: Santos, A.L.; Cebola, M.-J.; electrolyzer efficiency is through the optimization of the cell components and operating conditions.
    [Show full text]
  • Nitrogen-Rich Graphitic-Carbon@Graphene As A
    www.nature.com/scientificreports OPEN Nitrogen‑rich graphitic‑carbon@ graphene as a metal‑free electrocatalyst for oxygen reduction reaction Halima Begum, Mohammad Shamsuddin Ahmed & Young‑Bae Kim* The metal‑free nitrogen‑doped graphitic‑carbon@graphene (Ng‑c@G) is prepared from a composite of polyaniline and graphene by a facile polymerization following by pyrolysis for electrochemical oxygen reduction reaction (ORR). Pyrolysis creates a sponge‑like with ant‑cave‑architecture in the polyaniline derived nitrogenous graphitic‑carbon on graphene. The nitrogenous carbon is highly graphitized and most of the nitrogen atoms are in graphitic and pyridinic forms with less oxygenated is found when pyrolyzed at 800 °C. The electrocatalytic activity of Ng-C@G-800 is even better than the benchmarked Pt/C catalyst resulting in the higher half-wave potential (8 mV) and limiting current density (0.74 mA cm−2) for ORR in alkaline medium. Higher catalytic performance is originated from the special porous structure at microscale level and the abundant graphitic‑ and pyridinic‑n active sites at the nanoscale level on carbon-graphene matrix which are benefcial to the high O2‑mass transportation to those accessible sites. Also, it possesses a higher cycle stability resulting in the negligible potential shift and slight oxidation of pyridinic‑n with better tolerance to the methanol. To save the world from day-by-day increasing energy demands and environmental concerns, the clean, highly efcient and renewable energy technologies are immediately required to be implemented 1. Among various renewable energy technologies, fuel cells (FCs) and metal-air batteries are regarded as the promising clean energy sources because of their high energy conversion efciency and emission-free power generation 2,3.
    [Show full text]
  • Recent Technologies of Electrode and System in the Enzymatic Biofuel Cell (EBFC)
    applied sciences Review Mini-Review: Recent Technologies of Electrode and System in the Enzymatic Biofuel Cell (EBFC) Nabila A. Karim 1,* and Hsiharng Yang 2,3,* 1 Fuel Cell Institute, Universiti Kebangsaan Malaysia, Bangi 43600, Selangor, Malaysia 2 Graduate Institute of Precision Engineering, National Chung Hsing University, 145 Xingda Road, South District, Taichung City 402, Taiwan 3 Innovation and Development Center of Sustainable Agriculture (IDCSA), National Chung Hsing University, 145 Xingda Road, South District, Taichung City 402, Taiwan * Correspondence: [email protected] (N.A.K.); [email protected] (H.Y.) Abstract: Enzymatic biofuel cells (EBFCs) is one of the branches of fuel cells that can provide high potential for various applications. However, EBFC has challenges in improving the performance power output. Exploring electrode materials is one way to increase enzyme utilization and lead to a high conversion rate so that efficient enzyme loading on the electrode surface can function correctly. This paper briefly presents recent technologies developed to improve bio-catalytic proper- ties, biocompatibility, biodegradability, implantability, and mechanical flexibility in EBFCs. Among the combinations of materials that can be studied and are interesting because of their properties, there are various nanoparticles, carbon-based materials, and conductive polymers; all three have the advantages of chemical stability and enhanced electron transfer. The methods to immobilize enzymes, and support and substrate issues are also covered in this paper. In addition, the EBFC system is also explored and developed as suitable for applications such as self-pumping and microfluidic EBFC. Citation: A. Karim, N.; Yang, H. Keywords: electrode; support; immobilization; enzyme; EBFC Mini-Review: Recent Technologies of Electrode and System in the Enzymatic Biofuel Cell (EBFC).
    [Show full text]
  • Steering CO2 Electroreduction Toward Ethanol Production by a Surface-Bound Ru Polypyridyl Carbene Catalyst on N-Doped Porous Carbon
    Steering CO2 electroreduction toward ethanol production by a surface-bound Ru polypyridyl carbene catalyst on N-doped porous carbon Yanming Liua,b, Xinfei Fanc, Animesh Nayakb, Ying Wangb, Bing Shanb, Xie Quana, and Thomas J. Meyerb,1 aKey Laboratory of Industrial Ecology and Environmental Engineering, Ministry of Education, School of Environmental Science and Technology, Dalian University of Technology, Dalian 116024, China; bDepartment of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599; and cCollege of Environmental Science and Engineering, Dalian Maritime University, Dalian 116024, China Contributed by Thomas J. Meyer, November 10, 2019 (sent for review May 6, 2019; reviewed by Andrew B. Bocarsly and Clifford P. Kubiak) Electrochemical reduction of CO2 to multicarbon products is a sig- necessitates coupling reactions between a CO intermediate and/or nificant challenge, especially for molecular complexes. We report intermediates from CO protonation (29–31). Assembling the Ru(II) here CO2 reduction to multicarbon products based on a Ru(II) poly- polypyridyl carbene on an electrode surface that is capable of pyridyl carbene complex that is immobilized on an N-doped porous C–C dimerization offers an attractive strategy for reducing CO2 carbon (RuPC/NPC) electrode. The catalyst utilizes the synergistic to multicarbon products. effects of the Ru(II) polypyridyl carbene complex and the NPC N-doped carbon nanomaterials have been widely used for interface to steer CO2 reduction toward C2 production at low electroreduction due to their electrocatalytic activity and low cost. overpotentials. In 0.5 M KHCO3/CO2 aqueous solutions, Faradaic N-doped carbon electrodes have been shown to be capable of C–C efficiencies of 31.0 to 38.4% have been obtained for C2 production dimerization (6, 32).
    [Show full text]
  • Electrocatalyst Development for PEM Water Electrolysis and DMFC: Towards the Methanol Economy
    Electrocatalyst development for PEM water electrolysis and DMFC: towards the methanol economy Radostina Vasileva Genova-Koleva ADVERTIMENT. La consulta d’aquesta tesi queda condicionada a l’acceptació de les següents condicions d'ús: La difusió d’aquesta tesi per mitjà del servei TDX (www.tdx.cat) i a través del Dipòsit Digital de la UB (diposit.ub.edu) ha estat autoritzada pels titulars dels drets de propietat intel·lectual únicament per a usos privats emmarcats en activitats d’investigació i docència. No s’autoritza la seva reproducció amb finalitats de lucre ni la seva difusió i posada a disposició des d’un lloc aliè al servei TDX ni al Dipòsit Digital de la UB. No s’autoritza la presentació del seu contingut en una finestra o marc aliè a TDX o al Dipòsit Digital de la UB (framing). Aquesta reserva de drets afecta tant al resum de presentació de la tesi com als seus continguts. En la utilització o cita de parts de la tesi és obligat indicar el nom de la persona autora. ADVERTENCIA. La consulta de esta tesis queda condicionada a la aceptación de las siguientes condiciones de uso: La difusión de esta tesis por medio del servicio TDR (www.tdx.cat) y a través del Repositorio Digital de la UB (diposit.ub.edu) ha sido autorizada por los titulares de los derechos de propiedad intelectual únicamente para usos privados enmarcados en actividades de investigación y docencia. No se autoriza su reproducción con finalidades de lucro ni su difusión y puesta a disposición desde un sitio ajeno al servicio TDR o al Repositorio Digital de la UB.
    [Show full text]
  • Polymer Electrolyte Fuel Cell Lifetime Limitations: the Role of Electrocatalyst Degradation
    V.H.1 Polymer Electrolyte Fuel Cell Lifetime Limitations: The Role of Electrocatalyst Degradation (A) Durability Deborah J. Myers (Primary Contact) and (B) Cost Xiaoping Wang (C) Performance Argonne National Laboratory 9700 S. Cass Avenue Lemont, IL 60439 Technical Targets Phone: (630) 252-4261 E-mail: [email protected] This project is conducting fundamental studies of platinum-based PEMFC cathode electrocatalyst DOE Technology Development Manager: degradation mechanisms. Insights gained from these Nancy Garland studies can be applied toward the definition of operating Phone: (202) 586-5673 conditions to extend PEMFC lifetimes and to the E-mail: [email protected] development of cathode electrocatalyst materials that meet the following DOE 2015 electrocatalyst durability Subcontractors: targets with voltage cycling: • Johnson Matthey Fuel Cells, Sonning Commons, United Kingdom • 5,000 hours (<80ºC) and 2,000 hours (>80°C), • United Technologies Research Center, • <40% loss of initial catalytic mass activity, and East Hartford, CT • Massachusetts Institute of Technology, Boston, MA • <30 mV loss at 0.8 A/cm² • University of Texas at Austin, Austin, TX • University of Wisconsin-Madison, Madison, WI Accomplishments Project Start Date: October 1, 2009 • Prepared Ketjen carbon-supported Pt nano-particle Project End Date: September 30, 2012 electrocatalysts (Pt/C) of varying particle size and incorporated these electrocatalysts into the cathodes of membrane-electrode assemblies (MEAs). • Quantified Pt/C catalyst oxygen reduction reaction Objectives (ORR) activity, electrochemically-active surface • Understand the role of cathode electrocatalyst area (ECA), and performance losses in a fuel cell degradation in the long-term loss of polymer as a function of initial Pt particle size and cell electrolyte membrane fuel cell (PEMFC) parameters (relative humidity, temperature, upper performance, potential limit, and cycling protocol).
    [Show full text]
  • Direct Enzymatic Glucose/O2 Biofuel Cell Based on Poly-Thiophene Carboxylic Acid Alongside Gold Nanostructures Substrates Derive
    www.nature.com/scientificreports OPEN Direct Enzymatic Glucose/O2 Biofuel Cell based on Poly- Thiophene Carboxylic Acid Received: 16 April 2018 Accepted: 18 September 2018 alongside Gold Nanostructures Published: xx xx xxxx Substrates Derived through Bipolar Electrochemistry Fereshte Gholami1, Aso Navaee1, Abdollah Salimi1,2, Rezgar Ahmadi2, Azam Korani1,3 & Rahman Hallaj1,2 Bipolar electrochemistry (BPE) has been lately explored as a simple, reliable and novel electrochemical technique for the adjustment of various conductive substrates. Herein, BPE is performed to derive both of cathode and anode electrodes for the development of mediatorless/membraneless biofuel cell (BFC). On one hand, a preferable substrate for immobilization of bilirubin oxidase enzyme is prepared based on the electropolymerization of thiophene-3-carboxcylic acid (TCA) on an Au microflm as a bipolar electrode. The resulted biocathode as novel bioelectrocatalyst ofers a high electrocatalytic activity toward direct oxygen reduction reaction (ORR) with onset potential and current density of 0.55 V (vs. Ag/AgCl) and 867 μA cm−2, respectively. On the other hand, another analogous Au bipolar electrode is electroplated through BPE to derive Au nanostructures (AuNSs). This modifed Au electrode is utilized as an anodic platform for immobilization of favin adenine dinucleotide-dependent glucose dehydrogenase (FAD-GDH) enzyme aimed at electrocatalytic glucose oxidation. The prepared bioanode displays a current density of 2.7 mA cm−2 with onset potential of −0.03 V. Finally, the proposed bioanode and biocacthode in an assembled membraneless glucose/O2 BFC ofers a power output of 146 μW cm−2 with open circuit voltage of 0.54 V. This novel BPE method provides disposable electrochemical platforms for design of novel sensors, biosensors or other devices.
    [Show full text]
  • A Novel Non-Platinum Group Electrocatalyst for PEM Fuel Cell Application
    ARTICLE IN PRESS international journal of hydrogen energy xxx (2010) 1e8 Available at www.sciencedirect.com journal homepage: www.elsevier.com/locate/he A novel non-platinum group electrocatalyst for PEM fuel cell application Jin Yong Kim*, Tak-Keun Oh, Yongsoon Shin, Jeff Bonnett, K. Scott Weil Pacific Northwest National Laboratory, Richland, WA 99352, USA article info abstract Article history: Precious-metal catalysts (predominantly Pt or Pt-based alloys supported on carbon) have Received 21 December 2009 traditionally been used to catalyze the electrode reactions in polymer electrolyte Received in revised form membrane (PEM) fuel cells. However as PEM fuel systems begin to approach commercial 19 April 2010 reality, there is an impending need to replace Pt with a lower cost alternative. The present Accepted 5 May 2010 study investigates the performance of a carbon-supported tantalum oxide material as Available online xxx a potential oxygen reduction reaction (ORR) catalyst for use on the cathode side of the PEM fuel cell membrane electrode assembly. Although bulk tantalum oxide tends to exhibit Keywords: poor electrochemical performance due to limited electrical conductivity, it displays a high Nanoscale tantaulum oxide oxygen reduction potential; one that is comparable to Pt. Analysis of the Pourbaix elec- PEM catalyst trochemical equilibrium database also indicates that tantalum oxide (Ta2O5) is chemically Oxygen reduction stable under the pH and applied potential conditions to which the cathode catalyst is typically exposed during stack operation. Nanoscale tantalum oxide catalysts were fabri- cated using two approaches, by reactive oxidation sputtering and by direct chemical synthesis, each carried out on a carbon support material.
    [Show full text]
  • Metal-Organic Framework and Carbon Black Supported Mofs As Dynamic Electrocatalyst for Oxygen Reduction Reaction in an Alkaline Electrolyte
    J. Chem. Sci. Ó (2021) 133:34 Indian Academy of Sciences https://doi.org/10.1007/s12039-021-01900-xSadhana(0123456789().,-volV)FT3](0123456789().,-volV) REGULAR ARTICLE Metal-Organic Framework and Carbon Black supported MOFs as dynamic electrocatalyst for oxygen reduction reaction in an alkaline electrolyte VRUSHALI RAUTa, BAPI BERAb, MANOJ NEERGATb and DIPANWITA DASa,* aDepartment of Chemistry, Institute of Chemical Technology, Matunga, Mumbai 400 019, India bDepartment of Energy Science and Engineering, Indian Institute of Technology Bombay (IITB), Powai, Mumbai 400 076, India E-mail: [email protected] MS received 15 October 2020; revised 18 January 2021; accepted 25 February 2021 Abstract. The Pt-based expensive catalysts and sluggish kinetics at cathode in oxygen reduction reaction (ORR) hinder the rapid commercialization of fuel cells. The quest for cheap, non-noble metal catalysts to replace Pt-based catalysts has thus become a critical issue in the field of fuel cells. The carbon black (CB) and CB supported catalyst have been explored with the ultimate goal of finding a substitute for Pt-based catalysts in fuel cells. In the present work, we synthesized Zn-based MOF (1), 1 selectivity gives H2O2 followed by two-electron pathways. However, sample 1 modification might be needed to enhance its selectivity for the generation of H2O. Two composites of MOFs with carbon black and 1 were prepared to increase the H2O yield, called 1.CB and 1.SCB. The electrochemical generation of H2O2 was analyzed by the rotating ring disk electrode (RRDE) using catalyst 1. Following the addition of CB, H2O2 yields decreased from above 93% (1) to 59% and 75% for 1.CB and 1.SCB, respectively.
    [Show full text]
  • Manganese Acting As a High-Performance Heterogeneous Electrocatalyst in Carbon Dioxide Reduction
    ARTICLE https://doi.org/10.1038/s41467-019-10854-1 OPEN Manganese acting as a high-performance heterogeneous electrocatalyst in carbon dioxide reduction Bingxing Zhang1,2, Jianling Zhang1,2, Jinbiao Shi1,2, Dongxing Tan1,2, Lifei Liu1,2, Fanyu Zhang1,2, Cheng Lu1,2, Zhuizhui Su1,2, Xiuniang Tan1,2, Xiuyan Cheng1,2, Buxing Han1,2, Lirong Zheng3 & Jing Zhang3 fi 1234567890():,; Developing highly ef cient electrocatalysts based on cheap and earth-abundant metals for CO2 reduction is of great importance. Here we demonstrate that the electrocatalytic activity of manganese-based heterogeneous catalyst can be significantly improved through halogen and nitrogen dual-coordination to modulate the electronic structure of manganese atom. Such an electrocatalyst for CO2 reduction exhibits a maximum CO faradaic efficiency of 97% and high current density of ~10 mA cm−2 at a low overpotential of 0.49 V. Moreover, the turnover frequency can reach 38347 h−1 at overpotential of 0.49 V, which is the highest among the reported heterogeneous electrocatalysts for CO2 reduction. In situ X-ray absorption experiment and density-functional theory calculation reveal the modified electronic structure of the active manganese site, on which the free energy barrier for intermediate formation is greatly reduced, thus resulting in a great improvement of CO2 reduction performance. 1 Beijing National Laboratory for Molecular Sciences (BNLMS), CAS Key Laboratory of Colloid, Interface and Chemical Thermodynamics, CAS Research/ Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P. R. China. 2 School of Chemical Sciences, University of Chinese Academy of Sciences, Beijing 100049, P.
    [Show full text]
  • ETHANOL ELECTRO-OXIDATION in ALKALINE MEDIUM USING Pd/MWCNT and Pdausn/MWCNT ELECTROCATALYSTS PREPARED by ELECTRON BEAM IRRADIATION
    2015 International Nuclear Atlantic Conference - INAC 2015 São Paulo, SP, Brazil, October 4-9, 2015 ASSOCIAÇÃO BRASILEIRA DE ENERGIA NUCLEAR - ABEN ISBN: 978-85-99141-06-9 ETHANOL ELECTRO-OXIDATION IN ALKALINE MEDIUM USING Pd/MWCNT AND PdAuSn/MWCNT ELECTROCATALYSTS PREPARED BY ELECTRON BEAM IRRADIATION Adriana Napoleão Geraldes (1), Dionisio Furtunato da Silva (1) , Leonardo Gondin de Andrade e Silva (1) , Estevam Vitório Spinacé (1) , Almir Oliveira Neto (1) , Mauro Coelho dos Santos (2) , 1. Instituto de Pesquisas Energéticas e Nucleares (IPEN/CNEN - SP) Av. Professor Lineu Prestes 2242 05508-000 - São Paulo, SP [email protected] ; [email protected] 2. LEMN – CCNH - Universidade Federal do ABC, Rua Santa Adélia, 166 09210-170 - Santo André, SP. ABSTRACT Environmental problems and the world growing demand for energy has mobilized the scientific community in finding of clean and renewable energy sources. In this context, fuel cells appear as appropriate technology for generating electricity through alcohols electro-oxidation. Multi Wall Carbon Nanotubes (MWCNT)-supported Pd and trimetallic PdAuSn (Pd:Au:Sn 50:10:40 atomic ratio) electrocatalysts were prepared using electron beam irradiation. The obtained materials were characterized by VC, Chronoamperometry, EDX, TEM and XRD. The catalytic activities of electrocatalysts toward ethanol electro-oxidation were evaluated in alkaline medium in a single alkaline direct ethanol fuel cell (ADEFC) in a range temperature 60 to 90 oC. The best performances were obtained at 85 oC: 33 mW.cm -2 and 31 mW.cm -2 for Pd/ MWCNT and PdAuSn/MWCNT electrocatalysts, respectively. X-ray diffractograms of electrocatalysts showed the presence of Pd-rich (fcc) and Au-rich (fcc) phases.
    [Show full text]
  • Earth-Abundant Electrocatalysts for Water Splitting: Current and Future Directions
    catalysts Review Earth-Abundant Electrocatalysts for Water Splitting: Current and Future Directions Sami M. Ibn Shamsah Department of Mechanical Engineering, College of Engineering, University of Hafr Al Batin, P.O. Box 1803, Hafr Al Batin 31991, Saudi Arabia; [email protected] Abstract: Of all the available resources given to mankind, the sunlight is perhaps the most abundant renewable energy resource, providing more than enough energy on earth to satisfy all the needs of humanity for several hundred years. Therefore, it is transient and sporadic that poses issues with how the energy can be harvested and processed when the sun does not shine. Scientists assume that electro/photoelectrochemical devices used for water splitting into hydrogen and oxygen may have one solution to solve this hindrance. Water electrolysis-generated hydrogen is an optimal energy carrier to store these forms of energy on scalable levels because the energy density is high, and no air pollution or toxic gas is released into the environment after combustion. However, in order to adopt these devices for readily use, they have to be low-cost for manufacturing and operation. It is thus crucial to develop electrocatalysts for water splitting based on low-cost and land-rich elements. In this review, I will summarize current advances in the synthesis of low-cost earth-abundant electrocatalysts for overall water splitting, with a particular focus on how to be linked with photoelectrocatalytic water splitting devices. The major obstacles that persist in designing these devices. The potential future developments in the production of efficient electrocatalysts for water electrolysis are also described.
    [Show full text]