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Electrochem, Volume 2, Issue 4 (December 2021) – 9 articles

Cover Story (view full-size image): Measured DLCs were neither satisfied with the Stern model nor the Gouy–Chapman theory. Our model assumes that salts destroy hydrogen bonds at the electrode|solution interface to orient water dipoles toward the external electric field. A degree of orientation depends on the interaction energy between the salt ion and a water dipole. The observed DLC took the Langmuir-type in relation with concentration. The interaction energy for eight kinds of salts showed a linear relation with the energy of ion-solvent for viscosity, called the B-coefficient. View this paper.
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12 pages, 3735 KiB  
Review
Doped Polythiophene Chiral Electrodes as Electrochemical Biosensors
by M’hamed Chahma
Electrochem 2021, 2(4), 677-688; https://doi.org/10.3390/electrochem2040042 - 20 Dec 2021
Cited by 4 | Viewed by 3202
Abstract
π-conducting materials such as chiral polythiophenes exhibit excellent electrochemical stability in doped and undoped states on electrode surfaces (chiral electrodes), which help tune their physical and electronic properties for a wide range of uses. To overcome the limitations of traditional surface immobilization methods, [...] Read more.
π-conducting materials such as chiral polythiophenes exhibit excellent electrochemical stability in doped and undoped states on electrode surfaces (chiral electrodes), which help tune their physical and electronic properties for a wide range of uses. To overcome the limitations of traditional surface immobilization methods, an alternative pathway for the detection of organic and bioorganic targets using chiral electrodes has been developed. Moreover, chiral electrodes have the ability to carry functionalities, which helps the immobilization and recognition of bioorganic molecules. In this review, we describe the use of polythiophenes for the design of chiral electrodes and their applications as electrochemical biosensors. Full article
(This article belongs to the Special Issue Surface Modification by Conductive Materials)
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13 pages, 2177 KiB  
Review
Recent Applications of Molecular Structures at Silicon Anode Interfaces
by Chen Fang and Gao Liu
Electrochem 2021, 2(4), 664-676; https://doi.org/10.3390/electrochem2040041 - 18 Dec 2021
Viewed by 3669
Abstract
Silicon (Si) is a promising anode material to realize many-fold higher anode capacity in next-generation lithium-ion batteries (LIBs). Si electrochemistry has strong dependence on the property of the Si interface, and therefore, Si surface engineering has attracted considerable research interest to address the [...] Read more.
Silicon (Si) is a promising anode material to realize many-fold higher anode capacity in next-generation lithium-ion batteries (LIBs). Si electrochemistry has strong dependence on the property of the Si interface, and therefore, Si surface engineering has attracted considerable research interest to address the challenges of Si electrodes such as dramatic volume changes and the high reactivity of Si surface. Molecular nanostructures, including metal–organic frameworks (MOFs), covalent–organic frameworks (COFs) and monolayers, have been employed in recent years to decorate or functionalize Si anode surfaces to improve their electrochemical performance. These materials have the advantages of facile preparation, nanoscale controllability and structural diversity, and thus could be utilized as versatile platforms for Si surface modification. This review aims to summarize the recent applications of MOFs, COFs and monolayers for Si anode development. The functionalities and common design strategies of these molecular structures are demonstrated. Full article
(This article belongs to the Collection Feature Papers in Electrochemistry)
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21 pages, 8855 KiB  
Article
Coupled Electrochemical-Thermal Simulations and Validation of Minichannel Cold-Plate Water-Cooled Prismatic 20 Ah LiFePO4 Battery
by Chaithanya Akkaldevi, Sandeep Dattu Chitta, Jeevan Jaidi, Satyam Panchal, Michael Fowler and Roydon Fraser
Electrochem 2021, 2(4), 643-663; https://doi.org/10.3390/electrochem2040040 - 22 Nov 2021
Cited by 88 | Viewed by 5144
Abstract
This paper discusses the quantitative validation carried out on a prismatic 20 Ah LiFePO4 battery sandwiched between two minichannel cold-plates with distributed flow having a single U-turn. A two-way coupled electrochemical-thermal simulations are performed at different discharge rates (1–4 C) and coolant [...] Read more.
This paper discusses the quantitative validation carried out on a prismatic 20 Ah LiFePO4 battery sandwiched between two minichannel cold-plates with distributed flow having a single U-turn. A two-way coupled electrochemical-thermal simulations are performed at different discharge rates (1–4 C) and coolant inlet temperatures (15–35 °C). The predicted battery voltage response at room temperature (22 °C) and the performance of the Battery Thermal Management System (BTMS) in terms of the battery surface temperatures (maximum temperature, Tmax and temperature difference, ΔT) have been analyzed. Additionally, temperature variation at ten different locations on the battery surface is studied during the discharge process. The predicted temperatures are compared with the measured data and found to be in close agreement. Differences between the predicted and measured temperatures are attributed to the assumption of uniform heat generation by the Li-ion model (P2D), the accuracy of electrochemical property input data, and the accuracy of the measuring tools used. Overall, it is suggested that the Li-ion model can be used to design the efficient BTMS at the cell level. Full article
(This article belongs to the Collection Feature Papers in Electrochemistry)
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12 pages, 2474 KiB  
Article
Double-Layer Capacitances Caused by Ion–Solvent Interaction in the Form of Langmuir-Typed Concentration Dependence
by Koichi Jeremiah Aoki, Ridong He and Jingyuan Chen
Electrochem 2021, 2(4), 631-642; https://doi.org/10.3390/electrochem2040039 - 18 Nov 2021
Cited by 3 | Viewed by 2990
Abstract
Variations of the double layer capacitances (DLCs) at a platinum electrode with concentrations and kinds of salts in aqueous solutions were examined in the context of facilitating orientation of solvent dipoles. With an increase in ionic concentrations, the DLCs increased by ca. a [...] Read more.
Variations of the double layer capacitances (DLCs) at a platinum electrode with concentrations and kinds of salts in aqueous solutions were examined in the context of facilitating orientation of solvent dipoles. With an increase in ionic concentrations, the DLCs increased by ca. a half and then kept constant at concentrations over 1 mol dm−3. This increase was classically explained in terms of the Gouy–Chapman (GC) equation combined with the Stern model. Unfortunately, measured DLCs were neither satisfied with the Stern model nor the GC theory. Our model suggests that salts destroy hydrogen bonds at the electrode–solution interface to orient water dipoles toward the external electric field. A degree of the orientation depends on the interaction energy between the salt ion and a water dipole. The statistical mechanic calculation allowed us to derive an equation for the DLC as a function of salt concentration and the interaction energy. The equation took the Langmuir-type in the relation with the concentration. The interaction energy was obtained for eight kinds of salts. The energy showed a linear relation with the interaction energy of ion–solvent for viscosity, called the B-coefficient. Full article
(This article belongs to the Collection Feature Papers in Electrochemistry)
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27 pages, 29273 KiB  
Article
Fault Structural Analysis Applied to Proton Exchange Membrane Fuel Cell Water Management Issues
by Etienne Dijoux, Nadia Yousfi Steiner, Michel Benne, Marie-Cécile Péra and Brigitte Grondin-Perez
Electrochem 2021, 2(4), 604-630; https://doi.org/10.3390/electrochem2040038 - 1 Nov 2021
Cited by 5 | Viewed by 3107
Abstract
Proton exchange membrane fuel cells are relevant systems for power generation. However, they suffer from a lack of reliability, mainly due to their structural complexity. Indeed, their operation involves electrochemical, thermal, and electrical phenomena that imply a strong coupling, making it harder to [...] Read more.
Proton exchange membrane fuel cells are relevant systems for power generation. However, they suffer from a lack of reliability, mainly due to their structural complexity. Indeed, their operation involves electrochemical, thermal, and electrical phenomena that imply a strong coupling, making it harder to maintain nominal operation. This complexity causes several issues for the design of appropriate control, diagnosis, or fault-tolerant control strategies. It is therefore mandatory to understand the fuel cell structure for a relevant design of these kinds of strategies. This paper proposes a fuel cell fault structural analysis approach that leads to the proposition of a structural graph. This graph will then be used to highlight the interactions between the control variables and the functionalities of a fuel cell, and therefore to emphasize how changing a parameter to mitigate a fault can influence the fuel cell state and eventually cause another fault. The final aim of this work is to allow an easier implementation of an efficient and fault-tolerant control strategy on the basis of the proposed graphical representation. Full article
(This article belongs to the Topic Electromaterials for Environment & Energy)
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14 pages, 6855 KiB  
Review
Catalysts for Oxygen Reduction Reaction in the Polymer Electrolyte Membrane Fuel Cells: A Brief Review
by Martin Tomas, Fatemeh Gholami, Zahra Gholami and Jan Sedlacek
Electrochem 2021, 2(4), 590-603; https://doi.org/10.3390/electrochem2040037 - 22 Oct 2021
Cited by 4 | Viewed by 4085
Abstract
This mini-review presents a short account of materials with exceptional activity towards oxygen reduction reaction. Two main classes of catalytic materials are described, namely platinum group metal (PGM) catalyst and Non-precious metal catalyst. The classes are discussed in terms of possible application in [...] Read more.
This mini-review presents a short account of materials with exceptional activity towards oxygen reduction reaction. Two main classes of catalytic materials are described, namely platinum group metal (PGM) catalyst and Non-precious metal catalyst. The classes are discussed in terms of possible application in low-temperature hydrogen fuel cells with proton exchange membrane and further commercialization of these devices. A short description of perspective approaches is provided and challenging issues associated with developed catalytic materials are discussed. Full article
(This article belongs to the Collection Feature Papers in Electrochemistry)
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27 pages, 6941 KiB  
Review
Fabrication of Metal/Carbon Nanotube Composites by Electrochemical Deposition
by Susumu Arai
Electrochem 2021, 2(4), 563-589; https://doi.org/10.3390/electrochem2040036 - 21 Oct 2021
Cited by 11 | Viewed by 5256
Abstract
Metal/carbon nanotube (CNT) composites are promising functional materials due to the various superior properties of CNTs in addition to the characteristics of metals, and consequently, many fabrication processes of these composites have been vigorously researched. In this paper, the fabrication process of metal/CNT [...] Read more.
Metal/carbon nanotube (CNT) composites are promising functional materials due to the various superior properties of CNTs in addition to the characteristics of metals, and consequently, many fabrication processes of these composites have been vigorously researched. In this paper, the fabrication process of metal/CNT composites by electrochemical deposition, including electrodeposition and electroless deposition, are comprehensively reviewed. A general introduction for fabrication of metal/CNT composites using the electrochemical deposition is carried out. The fabrication methods can be classified into three types: (1) composite plating by electrodeposition or electroless deposition, (2) metal coating on CNT by electroless deposition, and (3) electrodeposition using CNT templates, such as CNT sheets and CNT yarns. The performances of each type have been compared and explained especially from the view point of preparation methods. In the cases of (1) composite plating and (2) metal coating on CNTs, homogeneous dispersion of CNTs in electrochemical deposition baths is essential for the formation of metal/CNT composites with homogeneous distribution of CNTs, which leads to high performance composites. In the case of (3) electrodeposition using CNT templates, the electrodeposition of metals not only on the surfaces but also interior of the CNT templates is the key process to fabricate high performance metal/CNT composites. Full article
(This article belongs to the Collection Feature Papers in Electrochemistry)
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17 pages, 4943 KiB  
Article
Effect of Cr Content on Corrosion Resistance of Low-Cr Alloy Steels Studied by Surface and Electrochemical Techniques
by Alicja Łukaszczyk, Jacek Banaś, Marcin Pisarek, Antoine Seyeux, Philippe Marcus and Jolanta Światowska
Electrochem 2021, 2(4), 546-562; https://doi.org/10.3390/electrochem2040035 - 18 Oct 2021
Cited by 8 | Viewed by 3425
Abstract
The electrochemical behavior of low alloyed Fe-Cr steels with 3 and 5% wt. of Cr in neutral Na2SO4 electrolyte combined with a detailed chemical and morphological characterization of these alloys performed by Auger electron spectroscopy, X-ray photoelectron spectroscopy, time-of-flight secondary [...] Read more.
The electrochemical behavior of low alloyed Fe-Cr steels with 3 and 5% wt. of Cr in neutral Na2SO4 electrolyte combined with a detailed chemical and morphological characterization of these alloys performed by Auger electron spectroscopy, X-ray photoelectron spectroscopy, time-of-flight secondary ion mass spectrometry and scanning electron microscopy are presented here. The corrosion of low alloyed Fe-Cr steels proceeds in the prepassive range, with the formation of corrosion surface films having a duplex structure with outer iron oxide/hydroxide layer and inner Cr oxide-rich layer. The thickness, composition, and the morphology of the surface films vary as a function of chromium content in the alloy as well as conditions of electrochemical tests (temperature). Even a low chromium content shows a beneficial effect on the corrosion performances of the Fe-Cr steels. The chromium as a more active component than iron of ferrite increases the anodic activity of this phase, which results in a rapid saturation of the surface with the anodic reaction products forming a fine crystalline-like and compact layer of corrosion products. In this way, the chromium acts as a modifier of formation/crystallization of the iron-rich surface film (mainly magnetite) in the prepassive range. Full article
(This article belongs to the Collection Feature Papers in Electrochemistry)
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12 pages, 9609 KiB  
Article
Synthesis and Characterization of Supercapacitor Materials from Soy
by Iris Denmark, Amna Khan, Taylor Scifres, Tito Viswanathan, Fumiya Watanabe and Noureen Siraj
Electrochem 2021, 2(4), 534-545; https://doi.org/10.3390/electrochem2040034 - 14 Oct 2021
Cited by 4 | Viewed by 3339
Abstract
Renewable resources and their byproducts are becoming of growing interest for alternative energy. Here, we have demonstrated the use of Arkansas’ most important crop, soy, as a carbon precursor for the synthesis of carbonized activated materials for supercapacitor applications. Different soy products (soymeal, [...] Read more.
Renewable resources and their byproducts are becoming of growing interest for alternative energy. Here, we have demonstrated the use of Arkansas’ most important crop, soy, as a carbon precursor for the synthesis of carbonized activated materials for supercapacitor applications. Different soy products (soymeal, defatted soymeal, soy flour and soy protein isolate) were converted into carbonized carbon and co-doped with phosphorus and nitrogen simultaneously, using a facile and time-effective microwave synthesis method. Ammonium polyphosphate was used as a doping agent which also absorbs microwave radiation. The surface morphology of the resulting carbonized materials was characterized in detail using scanning electron microscopy. X-ray photoelectron spectroscopy was also performed, which revealed the presence of a heteroelemental composition, along with different functional groups at the surface of the carbonized materials. Raman spectroscopy results depicted the presence of both a graphitic and defect carbon peak, with defect ratios of over one. The electrochemical performance of the materials was recorded using cyclic voltammetry in various electrolytes including acids, bases and salts. Among all the other materials, soymeal exhibited the highest specific capacitance value of 127 F/g in acidic electrolytes. These economic materials can be further tuned by changing the doping elements and their mole ratios to attain exceptional surface characteristics with improved specific capacitance values, in order to boost the economy of Arkansas, USA. Full article
(This article belongs to the Collection Feature Papers in Electrochemistry)
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