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Hydrogen and Fuel Cells: From Materials to Systems

A special issue of Materials (ISSN 1996-1944). This special issue belongs to the section "Energy Materials".

Deadline for manuscript submissions: closed (30 June 2018) | Viewed by 38714

Special Issue Editors


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Guest Editor
Istituto di Tecnologie Avanzate per l'Energia, Consiglio Nazionale delle Ricerche, 98126 Messina, Italy
Interests: materials for energy, electrochemistry, systems, fuel cells, electrolysis, photo-electrochemical cells, batteries, physico-chemical characterisation
Special Issues, Collections and Topics in MDPI journals

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Guest Editor
CNR-ITAE Institute for Advanced Energy Technologies “N. Giordano”, Via Salita S. Lucia sopra Contesse 5, 98126 Messina, Italy
Interests: polymer electrolyte fuel cells; direct alcohol fuel cells; water electrolysis; metal–air batteries; dye-sensitized solar cells; photo-electrolysis; carbon dioxide electro-reduction
Special Issues, Collections and Topics in MDPI journals

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Guest Editor
CNR—ITAE, Istituto di Tecnologie Avanzate per l’Energia “Nicola Giordano”, Via Salita S. Lucia sopra Contesse n. 5, 98126 S. Lucia-Messina, Italy
Interests: polymers, membranes, nano carbon materials, metal oxides and hybrid materials, fuel cells, supercapacitors, electrochemistry
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

The Special Issue, “Hydrogen and Fuel Cells: From Materials to Systems”, will address advances in materials science, processing, characterization, technology development and system testing of various types of fuel cells and hydrogen processes. The introduction of efficient and sustainable energy conversion technologies and zero-emission vehicles is strongly required worldwide to address urgent environmental issues. Fuel cell technology represents one of the most appropriate approaches to address these problems, and hydrogen can become an important energy vector in future energy systems. These technologies comply with the requirement of a low carbon economy by 2050, where both hydrogen and a highly efficiency distributed power generation using fuel cells, providing both electrical power and heat, can significantly reduce the emission of green-house gases. Original papers are solicited on all types of fuel cells and hydrogen production technologies. Of particular interest are recent developments in advanced materials, processes, characterization, stack designs, and systems. Articles and reviews dealing with fuel cells and hydrogen for different market applications, including zero-emission vehicles, grid-balancing service, power-to-gas, portable power systems, combined heat and power (CHP) production, consumer devices and distributed energy systems are very welcome.

Dr. Antonino Salvatore Aricò
Dr. Vincenzo Baglio
Dr. Francesco Lufrano
Guest Editors

Manuscript Submission Information

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Keywords

  • Fuel cells and Hydrogen
  • Proton-conducting and Alkaline Polymer Electrolyte Fuel Cells
  • Direct alcohol Fuel Cells
  • Solid Oxide Fuel Cells
  • Molten Carbonate Fuel Cells
  • Combined Heat and Power
  • Distributed Power Generation
  • Transportation
  • Portable power
  • Electrolysis
  • Reforming

Published Papers (7 papers)

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Research

9 pages, 5126 KiB  
Communication
Annealing of Gadolinium-Doped Ceria (GDC) Films Produced by the Aerosol Deposition Method
by Jörg Exner, Hendrik Pöpke, Franz-Martin Fuchs, Jaroslaw Kita and Ralf Moos
Materials 2018, 11(11), 2072; https://0-doi-org.brum.beds.ac.uk/10.3390/ma11112072 - 23 Oct 2018
Cited by 12 | Viewed by 3601
Abstract
Solid oxide fuel cells need a diffusion barrier layer to protect the zirconia-based electrolyte if a cobalt-containing cathode material like lanthanum strontium cobalt ferrite (LSCF) is used. This protective layer must prevent the direct contact and interdiffusion of both components while still retaining [...] Read more.
Solid oxide fuel cells need a diffusion barrier layer to protect the zirconia-based electrolyte if a cobalt-containing cathode material like lanthanum strontium cobalt ferrite (LSCF) is used. This protective layer must prevent the direct contact and interdiffusion of both components while still retaining the oxygen ion transport. Gadolinium-doped ceria (GDC) meets these requirements. However, for a favorable cell performance, oxide ion conducting films that are thin yet dense are required. Films with a thickness in the sub-micrometer to micrometer range were produced by the dry room temperature spray-coating technique, aerosol deposition. Since commercially available GDC powders are usually optimized for the sintering of screen printed films or pressed bulk samples, their particle morphology is nanocrystalline with a high surface area that is not suitable for aerosol deposition. Therefore, different thermal and mechanical powder pretreatment procedures were investigated and linked to the morphology and integrity of the sprayed films. Only if a suitable pretreatment was conducted, dense and well-adhering GDC films were deposited. Otherwise, low-strength films were formed. The ionic conductivity of the resulting dense films was characterized by impedance spectroscopy between 300 °C and 1000 °C upon heating and cooling. A mild annealing occurred up to 900 °C during first heating that slightly increased the electric conductivity of GDC films formed by aerosol deposition. Full article
(This article belongs to the Special Issue Hydrogen and Fuel Cells: From Materials to Systems)
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11 pages, 2959 KiB  
Article
Reduced Graphene Oxide and Its Modifications as Catalyst Supports and Catalyst Layer Modifiers for PEMFC
by Sergey A. Grigoriev, Vladimir N. Fateev, Artem S. Pushkarev, Irina V. Pushkareva, Natalia A. Ivanova, Valery N. Kalinichenko, Mikhail Yu. Presnyakov and Xing Wei
Materials 2018, 11(8), 1405; https://0-doi-org.brum.beds.ac.uk/10.3390/ma11081405 - 10 Aug 2018
Cited by 42 | Viewed by 3766
Abstract
Reduced graphene oxide (RGO) and RGO modified by ozone (RGO-O) and fluorine (RGO-F) were synthesized. Pt nanoparticles were deposited on these materials and also on Vulcan XC-72 using the polyol method. The structural and electrochemical properties of the obtained catalysts were investigated in [...] Read more.
Reduced graphene oxide (RGO) and RGO modified by ozone (RGO-O) and fluorine (RGO-F) were synthesized. Pt nanoparticles were deposited on these materials and also on Vulcan XC-72 using the polyol method. The structural and electrochemical properties of the obtained catalysts were investigated in a model glass three-electrode electrochemical cell and in a laboratory PEM fuel cell. Among the RGO-based catalysts, the highest electrochemically active surface area (EASA) was obtained for the oxidized RGO supported catalyst. The EASA of the fluorine-modified RGO-supported catalyst was half as big. In the PEM fuel cell the performance of RGO-based catalysts did not exceed the activity of Vulcan XC-72-based catalysts. However, the addition of an RGO-O-based catalyst to Vulcan XC-72-based catalyst (in contrast to the RGO-F-based catalyst) allowed us to increase the catalyst layer activity and PEM fuel cell performance. Possible reasons for such an effect are discussed. Full article
(This article belongs to the Special Issue Hydrogen and Fuel Cells: From Materials to Systems)
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15 pages, 2999 KiB  
Article
Electrochemical Impedance Spectroscopy as a Diagnostic Tool in Polymer Electrolyte Membrane Electrolysis
by Stefania Siracusano, Stefano Trocino, Nicola Briguglio, Vincenzo Baglio and Antonino S. Aricò
Materials 2018, 11(8), 1368; https://0-doi-org.brum.beds.ac.uk/10.3390/ma11081368 - 07 Aug 2018
Cited by 93 | Viewed by 10256
Abstract
Membrane–electrode assemblies (MEAs) designed for a polymer electrolyte membrane (PEM) water electrolyser based on a short-side chain (SSC) perfluorosulfonic acid (PFSA) membrane, Aquivion®, and an advanced Ir-Ru oxide anode electro-catalyst, with various cathode and anode noble metal loadings, were investigated. Electrochemical [...] Read more.
Membrane–electrode assemblies (MEAs) designed for a polymer electrolyte membrane (PEM) water electrolyser based on a short-side chain (SSC) perfluorosulfonic acid (PFSA) membrane, Aquivion®, and an advanced Ir-Ru oxide anode electro-catalyst, with various cathode and anode noble metal loadings, were investigated. Electrochemical impedance spectroscopy (EIS), in combination with performance and durability tests, provided useful information to identify rate-determining steps and to quantify the impact of the different phenomena on the electrolysis efficiency and stability characteristics as a function of the MEA properties. This technique appears to be a useful diagnostic tool to individuate different phenomena and to quantify their effect on the performance and degradation of PEM electrolysis cells. Full article
(This article belongs to the Special Issue Hydrogen and Fuel Cells: From Materials to Systems)
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9 pages, 3045 KiB  
Article
N,P-Codoped Carbon Layer Coupled with MoP Nanoparticles as an Efficient Electrocatalyst for Hydrogen Evolution Reaction
by Shuai Wang, Jia Wang, Ping Li, Zexing Wu and Xien Liu
Materials 2018, 11(8), 1316; https://0-doi-org.brum.beds.ac.uk/10.3390/ma11081316 - 30 Jul 2018
Cited by 6 | Viewed by 3641
Abstract
Efficient electrocatalyst plays a significant role on the development of hydrogen energy. In this work, an N,P-codoped carbon layer coupled with MoP nanoparticles (MoP/NPCs) was prepared through a facile high-temperature pyrolysis treatment. The obtained MoP/NPCs presented efficient activity for hydrogen evolution reaction (HER), [...] Read more.
Efficient electrocatalyst plays a significant role on the development of hydrogen energy. In this work, an N,P-codoped carbon layer coupled with MoP nanoparticles (MoP/NPCs) was prepared through a facile high-temperature pyrolysis treatment. The obtained MoP/NPCs presented efficient activity for hydrogen evolution reaction (HER), with low onset potential of 90 mV, and a small Tafel slope (71 mV dec−1), as well as extraordinary stability in acidic electrolyte. This work provides a new facile strategy for the design and synthesis of sustainable and effective molybdenum-based electrocatalysts as alternatives to non-Pt catalysts for HER. Full article
(This article belongs to the Special Issue Hydrogen and Fuel Cells: From Materials to Systems)
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12 pages, 6751 KiB  
Article
Application of Low-Cost Me-N-C (Me = Fe or Co) Electrocatalysts Derived from EDTA in Direct Methanol Fuel Cells (DMFCs)
by Carmelo Lo Vecchio, Antonino Salvatore Aricò and Vincenzo Baglio
Materials 2018, 11(7), 1193; https://0-doi-org.brum.beds.ac.uk/10.3390/ma11071193 - 12 Jul 2018
Cited by 18 | Viewed by 3620
Abstract
Co-N-C and Fe-N-C electrocatalysts have been prepared by mixing Fe or Co precursors, ethylene diamine tetra acetic acid (EDTA) as a nitrogen source, and an oxidized carbon. These materials were thermally treated at 800 °C or 1000 °C under nitrogen flow to produce [...] Read more.
Co-N-C and Fe-N-C electrocatalysts have been prepared by mixing Fe or Co precursors, ethylene diamine tetra acetic acid (EDTA) as a nitrogen source, and an oxidized carbon. These materials were thermally treated at 800 °C or 1000 °C under nitrogen flow to produce four samples, named CoNC8, CoNC10, FeNC8, and FeNC10. They have been physicochemically characterized by X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM). Direct methanol fuel cell (DMFC) analyses have been carried out to investigate the performance of the nonprecious cathode catalysts, using a low amount of Pt (0.7 mg/cm2) at the anode side. It appears that FeNC8 is the best performing low-cost cathode catalyst in terms of higher oxygen reduction reaction activity and methanol tolerance. Full article
(This article belongs to the Special Issue Hydrogen and Fuel Cells: From Materials to Systems)
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10 pages, 3907 KiB  
Article
Graphitized Carbon: A Promising Stable Cathode Catalyst Support Material for Long Term PEMFC Applications
by Paritosh Kumar Mohanta, Fabian Regnet and Ludwig Jörissen
Materials 2018, 11(6), 907; https://0-doi-org.brum.beds.ac.uk/10.3390/ma11060907 - 28 May 2018
Cited by 23 | Viewed by 5171
Abstract
Stability of cathode catalyst support material is one of the big challenges of polymer electrolyte membrane fuel cells (PEMFC) for long term applications. Traditional carbon black (CB) supports are not stable enough to prevent oxidation to CO2 under fuel cell operating conditions. [...] Read more.
Stability of cathode catalyst support material is one of the big challenges of polymer electrolyte membrane fuel cells (PEMFC) for long term applications. Traditional carbon black (CB) supports are not stable enough to prevent oxidation to CO2 under fuel cell operating conditions. The feasibility of a graphitized carbon (GC) as a cathode catalyst support for low temperature PEMFC is investigated herein. GC and CB supported Pt electrocatalysts were prepared via an already developed polyol process. The physical characterization of the prepared catalysts was performed using transmission electron microscope (TEM), X-ray Powder Diffraction (XRD) and inductively coupled plasma optical emission spectrometry (ICP-OES) analysis, and their electrochemical characterizations were conducted via cyclic voltammetry(CV), rotating disk electrode (RDE) and potential cycling, and eventually, the catalysts were processed using membrane electrode assemblies (MEA) for single cell performance tests. Electrochemical impedance spectroscopy (EIS) and scanning electrochemical microscopy (SEM) have been used as MEA diagonostic tools. GC showed superior stability over CB in acid electrolyte under potential conditions. Single cell MEA performance of the GC-supported catalyst is comparable with the CB-supported catalyst. A correlation of MEA performance of the supported catalysts of different Brunauer–Emmett–Teller (BET) surface areas with the ionomer content was also established. GC was identified as a promising candidate for catalyst support in terms of both of the stability and the performance of fuel cell. Full article
(This article belongs to the Special Issue Hydrogen and Fuel Cells: From Materials to Systems)
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5806 KiB  
Article
Proton Conduction in Grain-Boundary-Free Oxygen-Deficient BaFeO2.5+δ Thin Films
by Alexander Benes, Alan Molinari, Ralf Witte, Robert Kruk, Joachim Brötz, Reda Chellali, Horst Hahn and Oliver Clemens
Materials 2018, 11(1), 52; https://0-doi-org.brum.beds.ac.uk/10.3390/ma11010052 - 29 Dec 2017
Cited by 20 | Viewed by 7400
Abstract
Reduction of the operating temperature to an intermediate temperature range between 350 °C and 600 °C is a necessity for Solid Oxide Fuel/Electrolysis Cells (SOFC/SOECs). In this respect the application of proton-conducting oxides has become a broad area of research. Materials that can [...] Read more.
Reduction of the operating temperature to an intermediate temperature range between 350 °C and 600 °C is a necessity for Solid Oxide Fuel/Electrolysis Cells (SOFC/SOECs). In this respect the application of proton-conducting oxides has become a broad area of research. Materials that can conduct protons and electrons at the same time, to be used as electrode catalysts on the air electrode, are especially rare. In this article we report on the proton conduction in expitaxially grown BaFeO2.5+δ (BFO) thin films deposited by pulsed laser deposition on Nb:SrTiO3 substrates. By using Electrochemical Impedance Spectroscopy (EIS) measurements under different wet and dry atmospheres, the bulk proton conductivity of BFO (between 200 °C and 300 °C) could be estimated for the first time (3.6 × 10−6 S cm−1 at 300 °C). The influence of oxidizing measurement atmosphere and hydration revealed a strong dependence of the conductivity, most notably at temperatures above 300 °C, which is in good agreement with the hydration behavior of BaFeO2.5 reported previously. Full article
(This article belongs to the Special Issue Hydrogen and Fuel Cells: From Materials to Systems)
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