| 11. |
- Gueskine, Viktor, et al.
(författare)
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Oxygen reduction reaction at conducting polymer electrodes in a wider context: Insights from modelling concerning outer and inner sphere mechanisms
- 2023
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Ingår i: ELECTROCHEMICAL SCIENCE ADVANCES. - : WILEY. - 2698-5977. ; 3:2
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Forskningsöversikt (refereegranskat)abstract
- Practical interest in oxygen reduction reaction (ORR) has traditionally been due to its application at fuel cells' cathode following its complete 4e route to the water. In search of new electrode materials, it was discovered that conducting polymers (CPs) also are capable of driving ORR, though predominantly halting the process at 2e reduction leading to hydrogen peroxide generation. As alternative ways to produce this "green oxidant" are attracting increasing attention, a detailed study of the ORR mechanism at CP electrodes gains importance. Here, we summarize our recent theoretical work on the topic, which underscores the fundamental difference between CP and electrocatalytic metal ORR electrodes. Our insights also bring to us the attention of outer-sphere electron transfer, not unknown but somewhat ignored in the field. We also put the action of CP electrodes in a more general context of chemical ORR and redox mediation responsible for the electrocatalytic ORR mechanism.
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| 12. |
- Kangkamano, Tawatchai, et al.
(författare)
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Product-to-intermediate relay achieving complete oxygen reduction reaction (cORR) with Prussian blue integrated nanoporous polymer cathode in fuel cells
- 2020
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Ingår i: Nano Energy. - : ELSEVIER. - 2211-2855 .- 2211-3282. ; 78
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Tidskriftsartikel (refereegranskat)abstract
- The oxygen reduction reaction (ORR) is an essential process in electrocatalysis limiting the commercialization of sustainable energy conversion technologies, such as fuel cells. The use of conducting polymers as molecular porous and conducting catalysts obtained from the high abundance elements enables the route towards low cost and high-throughput fabrication of disposable plastic electrodes of fuel cells. Poly(3,4-ethylenedioxythiophene) (PEDOT) is a 2-electron ORR electrocatalyst yielding specifically hydrogen peroxide that limits the full utilization of chemical energy of oxygen. Here, we demonstrated an innovative product-to-intermediate relay approach achieving complete oxygen reduction reaction (cORR) with Prussian blue (PB) integrated microporous PEDOT cathode in fuel cells. The microporous structured PEDOT electrode prepared via a simple cryosynthesis allows the bulk integration and stabilization of the poor conducting PB co-catalyst into the PEDOT ion-electron conductor, while the microporous PEDOT allows effective oxygen diffusion into the matrix. We evaluated systematically the effect of sequential PEDOT 2-electron ORR followed by PB co-catalysis launching hydrogen peroxide reduction reaction (HPRR) into H2O. This resulted in the establishment of electronic and ionic transport between PEDOT and PB catalyst enabling the combination of enhanced ORR electrocatalysis by means of the ORR course extension from 2to 4-electron reduction to achieve cORR. The cORR performance delivered by the product-to-intermediate relay between microporous PEDOT and PB co-catalysis led to a four times increase in power density of model proton-exchange membrane fuel cell (PEMFC) assembled from the polymer-based air breathing cathode.
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| 13. |
- Khan, Ziyauddin, et al.
(författare)
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Can Hybrid Na-Air Batteries Outperform Nonaqueous Na-O-2 Batteries?
- 2020
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Ingår i: Advanced Science. - : Wiley-VCH Verlagsgesellschaft. - 2198-3844. ; 7:5
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Tidskriftsartikel (refereegranskat)abstract
- In recent years, there has been an upsurge in the study of novel and alternative energy storage devices beyond lithium-based systems due to the exponential increase in price of lithium. Sodium (Na) metal-based batteries can be a possible alternative to lithium-based batteries due to the similar electrochemical voltage of Na and Li together with the thousand times higher natural abundance of Na compared to Li. Though two different kinds of Na-O-2 batteries have been studied specifically based on electrolytes until now, very recently, a hybrid Na-air cell has shown distinctive advantage over nonaqueous cell systems. Hybrid Na-air batteries provide a fundamental advantage due to the formation of highly soluble discharge product (sodium hydroxide) which leads to low overpotentials for charge and discharge processes, high electrical energy efficiency, and good cyclic stability. Herein, the current status and challenges associated with hybrid Na-air batteries are reported. Also, a brief description of nonaqueous Na-O-2 batteries and its close competition with hybrid Na-air batteries are provided.
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| 14. |
- Kim, Nara, et al.
(författare)
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An intrinsically stretchable symmetric organic battery based on plant-derived redox molecules
- 2023
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Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry. - 2050-7488 .- 2050-7496. ; 11:46, s. 25703-25714
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Tidskriftsartikel (refereegranskat)abstract
- Intrinsically stretchable energy storage devices are essential for the powering of imperceptible wearable electronics. Organic batteries based on plant-derived redox-active molecules can offer critical advantages from a safety, sustainability, and economic perspective, but such batteries are not yet available in soft and stretchable form factors. Here we report an intrinsically stretchable organic battery made of elastomeric composite electrodes formulated with alizarin, a natural dye derived from the plant Rubia tinctorum, whose two quinone motifs enable its uses in both positive and negative electrodes. The quaternary biocomposite electrodes possess excellent electron-ion conduction/coupling and superior stretchability (>300%) owing to self-organized hierarchical morphology. In a full-cell configuration, its energy density of 3.8 mW h cm−3 was preserved at 100% strain, and assembled modules on stretchy textiles and rubber gloves can power integrated LEDs during various deformations. This work paves the way for low-cost, eco-friendly, and deformable batteries for next generation wearable electronics.
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| 15. |
- Lander, Sanna, et al.
(författare)
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Controlling the rate of posolyte degradation in all-quinone aqueous organic redox flow batteries by sulfonated nanocellulose based membranes: The role of crossover and Michael addition
- 2024
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Ingår i: Journal of Energy Storage. - : Elsevier BV. - 2352-152X .- 2352-1538. ; 83
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Tidskriftsartikel (refereegranskat)abstract
- Aqueous organic redox flow battery (AORFB) is a technological route towards the large-scale sustainable energy storage. However, several factors need to be controlled to maintain the AORFB performance. Prevention of posolyte and negolyte cross-contamination in asymmetric AORFBs, one of the main causes of capacity decay, relies on their membranes' ability to prevent migration of the redox-active species between the two electrolytes. The barrier properties are often traded for a reduction in ionic conductivity which is crucial to enable the device operation. Another factor greatly affecting quinone-based AORFBs is the Michael addition reaction (MAR) on the charged posolyte, quinone, which has been identified as a major reason for all-quinone AORFBs performance deterioration. Herein, we investigate deterioration scenarios of an all-quinone AORFB using both experimental and computational methods. The study includes a series of membranes based on sulfonated cellulose nanofibrils and different membrane modifications. The layer-by-layer (LbL) surface modifications, i.e. the incorporation of inorganic materials and the reduction of the pore size of the sulfonated cellulose membranes, were all viable routes to reduce the passive diffusion permeability of membranes which correlated to an increased cycling stability of the battery. The kinetics of MAR on quinone was detected using NMR and its impact on the performance fading was modeled computationally. The localization of MAR close to the membrane, which can be assigned to the surface reactivity, affects the diffusion of MAR reagent and the deterioration dynamics of the present all-quinone AORFB.
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| 16. |
- Lander, Sanna, 1990-
(författare)
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Sulfonated Cellulose Membranes for Energy Storage Applications
- 2023
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- In the ongoing efforts to reduce the dependency of mankind on fossil fuels for the supply of energy, renewable energy sources such as solar cells and wind turbines are employed to an increasing extent. Transitioning a large portion of electrical grids to intermittent power sources come with several problems that need to be taken into account and handled, such as ensuring supply at peak power demand and considering frequency regulation and other issues related to the stability of the grid. One possible way to increase the amount of intermittent energy sources while maintaining a stable grid and power supply is to use large scale energy storage systems to store energy that can then be used as needed.One of the most promising energy storage systems for this purpose is the redox flow battery, an electrochemical energy storage system in which the power output and total energy storage capacity are decoupled, the former relating to the area of the electrochemical cell and the latter to the amount of electrolyte. This decoupling is a great advantage since large electrolyte tanks can be used to store huge amounts of energy in a stationary manner.Redox flow batteries and other devices such as fuel cells and certain types of batteries are dependent on a selective membrane for their function. The membrane needs to efficiently transport certain species while blocking others, and the function of the membrane is often greatly influencing the performance of the devices that employ them. Current state-of-the-art ion selective membranes are often produced from PFSA-based materials, which are problematic in terms of sustainability and cost. Finding ways to replace such membranes with equally functional components produced from bio-based materials would be a large step forward in terms of improving the sustainability and cost-efficiency of large scale electrochemical energy storage.In this work, functionalized cellulose nanofibrils are used as starting material to produce novel bio-based selective membranes aimed to be employed in electrochemical energy storage systems, in particular redox flow batteries. The possibility to precisely tune the properties of membranes via the degree of modification of the starting material is investigated, as well as some strategies to further improve the performance of membranes via additives and post-fabrication modifications.
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| 17. |
- Lander, Sanna, 1990-, et al.
(författare)
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Sulfonated Cellulose Membranes Improve the Stability of Aqueous Organic Redox Flow Batteries
- 2022
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Ingår i: Advanced Energy and Sustainability Research. - : Wiley. - 2699-9412. ; 3:9
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Tidskriftsartikel (refereegranskat)abstract
- The drawbacks of current state-of-the-art selective membranes, such as poor barrier properties, high cost, and poor recyclability, limit the large-scale deployment of electrochemical energy devices such as redox flow batteries (RFBs) and fuel cells. In recent years, cellulosic nanomaterials have been proposed as a low-cost and green raw material for such membranes, but their performance in RFBs and fuel cells is typically poorer than that of the sulfonated fluoropolymer ionomer membranes such as Nafion. Herein, sulfonated cellulose nanofibrils densely cross-linked to form a compact sulfonated cellulose membrane with limited swelling and good stability in water are used. The membranes possess low porosity and excellent ionic transport properties. A model aqueous organic redox flow battery (AORFB) with alizarin red S as negolyte and tiron as posolyte is assembled with the sulfonated cellulose membrane. The performance of the nanocellulose-based battery is superior in terms of cyclability in comparison to that displayed by the battery assembled with commercially available Nafion 115 due to the mitigation of crossover of the redox-active components. This finding paves the way to new green organic materials for fully sustainable AORFB solutions.
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| 18. |
- Lander, Sanna, 1990-, et al.
(författare)
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Sulfonated Cellulose Membranes: Physicochemical Properties and Ionic Transport versus Degree of Sulfonation
- 2022
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Ingår i: Advanced Sustainable Systems. - : Wiley. - 2366-7486. ; 6:11
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Tidskriftsartikel (refereegranskat)abstract
- The next generation of green ion selective membranes is foreseen to be based on cellulosic nanomaterials with controllable properties. The introduction of ionic groups into the cellulose structure via chemical modification is one strategy to obtain desired functionalities. In this work, bleached softwood fibers are oxidatively sulfonated and thereafter homogenized to liberate the cellulose nanofibrils (CNFs) from the fiber walls. The liberated CNFs are subsequently used to prepare and characterize novel cellulose membranes. It is found that the degree of sulfonation collectively affects several important properties of the membranes via the density of fixed charged groups on the surfaces of the CNFs, in particular the membrane morphology, water uptake and swelling, and correspondingly the ionic transport. Both ionic conductivity and cation transport increase with the increased level of sulfonation of the starting material. Thus, it is shown that the chemical modification of the CNFs can be used as a tool for precise and rational design of green ion selective membranes that can replace expensive conventional fluorinated ionomer membranes.
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| 19. |
- Méhes, Gábor, et al.
(författare)
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Solar Heat-Enhanced Energy Conversion in Devices Based on Photosynthetic Membranes and PEDOT:PSS-Nanocellulose Electrodes
- 2020
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Ingår i: Advanced Sustainable Systems. - : Wiley-VCH Verlag. - 2366-7486. ; 4:1
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Tidskriftsartikel (refereegranskat)abstract
- Energy harvesting from photosynthetic membranes, proteins, or bacteria through bio-photovoltaic or bio-electrochemical approaches has been proposed as a new route to clean energy. A major shortcoming of these and solar cell technologies is the underutilization of solar irradiation wavelengths in the IR region, especially those in the far IR region. Here, a biohybrid energy-harvesting device is demonstrated that exploits IR radiation, via convection and thermoelectric effects, to improve the resulting energy conversion performance. A composite of nanocellulose and the conducting polymer system poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) is used as the anode in biohybrid cells that includes thylakoid membranes (TMs) and redox mediators (RMs) in solution. By irradiating the conducting polymer electrode by an IR light-emitting diode, a sixfold enhancement in the harvested bio-photovoltaic power is achieved, without compromising stability of operation. Investigation of the output currents reveals that IR irradiation generates convective heat transfer in the electrolyte bulk, which enhances the redox reactions of RMs at the anode by suppressing diffusion limitations. In addition, a fast-transient thermoelectric component, originating from the PEDOT:PSS-nanocellulose-electrolyte interphase, further increases the bio-photocurrent. These results pave the way for the development of energy-harvesting biohybrids that make use of heat, via IR absorption, to enhance energy conversion efficiency.
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| 20. |
- Meng, Lingyin, 1991-
(författare)
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Tailoring Conducting Polymer Interface for Sensing and Biosensing
- 2020
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Konstnärligt arbete (övrigt vetenskapligt/konstnärligt)abstract
- The routine measurement of significant physiological and biochemical parameters has become increasingly important for health monitoring especially in the cases of elderly people, infants, patients with chronic diseases, athletes and soldiers etc. Monitoring is used to assess both physical fitness level and for disease diagnosis and treatment. Considerable attention has been paid to electrochemical sensors and biosensors as point-of-care diagnostic devices for healthcare management because of their fast response, low-cost, high specificity and ease of operation. The analytical performance of such devices is significantly driven by the high-quality sensing interface, involving signal transduction at the transducer interface and efficient coupling of biomolecules at the transducer bio-interface for specific analyte recognition. The discovery of functional and structured materials, such as metallic and carbon nanomaterials (e.g. gold and graphene), has facilitated the construction of high-performance transducer interfaces which benefit from their unique physicochemical properties. Further exploration of advanced materials remains highly attractive to achieve well-designed and tailored interfaces for electrochemical sensing and biosensing driven by the emerging needs and demands of the “Internet of Things” and wearable sensors.Conducting polymers (CPs) are emerging functional polymers with extraordinary redox reversibility, electronic/ionic conductivity and mechanical properties, and show considerable potential as a transducer material in sensing and biosensing. While the intrinsic electrocatalytic property of the CPs is limited, especially for the bulk polymer, tailoring of CPs with controlled structure and efficient dopants could improve the electrochemical performance of a transducer interface by delivering a larger surface area and enhanced electrocatalytic property. In addition, the rich synthetic chemistry of CPs endows them with versatile functional groups to modulate the interfacial properties of the polymer for effective biomolecule coupling, thus bridging organic electronics and bioelectrochemistry. Moreover, the soft-material characteristics of CPs enable their use for the development of flexible and wearable sensing platforms which are inexpensive and light-weight, compared to conventional rigid materials, such as carbons, metals and semiconductors.This thesis focuses on the exploration of CPs for electrochemical sensing and biosensing with improved sensitivity, selectivity and stability by tailoring CP interfaces at different levels, including the CP-based transduction interface, CP-based bio-interface and CP-based device interface.First, we demonstrate different strategies for tailoring the physicochemical properties of poly (3,4-ethylenedioxythiophene) (PEDOT) beyond its intrinsic properties, via charge effects, structural effects and by the use of hybrid materials, as a CP-based transduction interface to improve sensing performance of various analytes. 1) A positively-charged PEDOT interface, and a negatively-charged carboxylic-acid-functionalised PEDOT (PEDOT:COOH) interface were developed to modulate the electrode kinetics for oppositely-charged analytes, e.g. negatively-charged nicotinamide adenine dinucleotide (NADH) and positively-charged dopamine (DA), respectively. These interfaces displayed high sensitivity and wide linear range towards the analytes due to the electrostatic attraction effect. 2) Various structured PEDOT including porous microspheres and nanofibres were synthesised via hard-template and soft-template methods, respectively, and were employed as building blocks for a hierarchical PEDOT and 3D nanofibrous PEDOT transduction interface, that facilitated signal transduction for NADH. 3) A PEDOT hybrid material interface was developed via using a novel bi-functional graphene oxide derivative with high reduction degree and negatively-charged sulphonate terminal functionality (S-RGO) as dopant to create PEDOT:S-RGO which delivered an enhanced electrochemical performance for various analytes.Based on the established CP-based transduction interface, biomolecules (e.g. enzymes) could be coupled to the CP surface to create CP-based bio-interfaces for biosensing. The immobilisation of enzyme was realised via either covalent bonding to a PEDOT derivative bearing a -COOH group (PEDOT-COOH) through EDC/NHS chemistry, or by physical absorption into the 3D porous PEDOT structure. The CP-based bio-interfaces were used to demonstrate the stable immobilisation of two different types of enzymes, i.e. lactate dehydrogenase and lactate oxidase, achieving the biosensing of analytes by relay bioelectrochemical signal transduction.Together, CP was employed as the CP-based device interface for the fabrication of a flexible and wearable biosensing device. A 3D honeycomb-structured graphene network was generated in-situ on a flexible polyimide surface by mask-free patterning using laser irradiation. The substrate was then reinforced with PEDOT as a polymeric binder to stabilise the 3D porous network by adhesion and binding, thus minimising the delamination of the biosensing interface under deformation and enhancing the mechanical behaviours for use in flexible and wearable devices. The subsequent nanoscale-coating of Prussian blue and immobilisation of enzyme into the 3D porous network provided a flexible platform for wearable electrochemical biosensors to detect lactate in sweat.
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