| 1. |
- Wolkeba, Zewdneh Genene, 1983, et al.
(författare)
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Recent Advances in the Synthesis of Conjugated Polymers for Supercapacitors
- 2024
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Ingår i: Advanced Materials Technologies. - 2365-709X. ; 9:9
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Forskningsöversikt (refereegranskat)abstract
- Conjugated polymers have attracted growing attention for versatile applications in energy storage due to their potential benefits including low-cost processing, molecular tunability, environmental benignity, and high mechanical flexibility. In particular, polymer-based organic electrode materials have shown significant progress in supercapacitor (SC) applications with superior electrochemical behaviors. The performances of SCs are closely related to the intrinsic characteristics of different polymers in the nanoscale and the morphological features of the polymer-based electrode materials obtained by different fabrication techniques in the macroscale. This review summarizes the design and synthesis of both p-type and n-type conjugated polymers, highlighting the pros and cons of three synthesis techniques: electrochemical polymerization, chemical polymerization, and in situ polymerization. The performances of conjugated polymers in SCs, their cycling stabilities, and structure-performance relationships are discussed. Moreover, the existing challenges and future directions of polymer-based SCs are considered with respect to energy density, stability, and large-scale production to promote commercialization.
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| 2. |
- Chaudhary, Richa, 1988, et al.
(författare)
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Structural Positive Electrodes Engineered for Multifunctionality
- 2024
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Ingår i: Advanced Science. - 2198-3844 .- 2198-3844. ; In Press
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Tidskriftsartikel (refereegranskat)abstract
- Multifunctional structural batteries are of high and emerging interest in a wide variety of high-strength and lightweight applications. Structural batteries typically use pristine carbon fiber as the negative electrode, functionalized carbon fiber as the positive electrode, and a mechanically robust lithium-ion transporting electrolyte. However, electrochemical cycling of carbon fibre-based positive electrodes is still limited to tests in liquid electrolytes, which does not allow for to introduction of multifunctionality in real terms. To overcome these limitations, structural batteries with a structural battery electrolyte (SBE) are developed. This approach offers massless energy storage. The electrodes are manufactured using economically friendly, abundant, cheap, and non-toxic iron-based materials like olivine LiFePO4. Reduced graphene oxide, renowned for its high surface area and electrical conductivity, is incorporated to enhance the ion transport mechanism. Furthermore, a vacuum-infused solid-liquid electrolyte is cured to bolster the mechanical strength of the carbon fibers and provide a medium for lithium-ion migration. Electrophoretic deposition is selected as a green process to manufacture the structural positive electrodes with homogeneous mass loading. A specific capacity of 112 mAh g−1 can be reached at C/20, allowing the smooth transport of Li-ion in the presence of SBE. The modulus of positive electrodes exceeded 80 GPa. Structural battery-positive half-cells are demonstrated across various mass-loadings, enabling them to be tailored for a diverse array of applications in consumer technology, electric vehicles, and aerospace sectors.
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| 3. |
- Chaudhary, Richa, 1988, et al.
(författare)
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Unveiling the Multifunctional Carbon Fiber Structural Battery
- 2024
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Ingår i: Advanced Materials. - 0935-9648 .- 1521-4095. ; In Press
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Tidskriftsartikel (refereegranskat)abstract
- Structural batteries refer to the multifunctional device capable of both storing electrical energy and bearing mechanical loads concurrently. In this context, carbon fibers emerge as a compelling choice of material and serve dual purpose by storing energy and providing stiffness and strength to the battery. Previous investigation has demonstrated proof-of-concept of functional positive electrodes against metallic lithium in structural battery electrolyte. Here, an all-carbon fiber-based structural battery is demonstrated utilizing the pristine carbon fiber as negative electrode, lithium iron phosphate (LFP)-coated carbon fiber as positive electrode, and a thin cellulose separator. All components are embedded in structural battery electrolyte and cured to provide rigidity to the battery. The energy density of structural battery is enhanced by use of the thin separator. The structural battery composite demonstrates an energy density of 30 Wh kg−1 and cyclic stability up to 1000 cycles with ≈100% of Coulombic efficiency. Remarkably, the elastic modulus of the all-fiber structural battery exceeds 76 GPa when tested in parallel to the fiber direction – by far highest till date reported in the literature. Structural batteries have immediate implication in replacing structural parts of electric vehicles while reducing the number of conventional batteries. Thus, offering mass savings to future electric vehicles.
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| 4. |
- Lancellotti, Lidia, et al.
(författare)
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Selective ion transport in large-area graphene oxide membrane filters driven by the ionic radius and electrostatic interactions
- 2024
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Ingår i: Nanoscale. - 2040-3372 .- 2040-3364. ; 16:14, s. 7123-7133
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Tidskriftsartikel (refereegranskat)abstract
- Filters made of graphene oxide (GO) are promising for purification of water and selective sieving of specific ions; while some results indicate the ionic radius as the discriminating factor in the sieving efficiency, the exact mechanism of sieving is still under debate. Furthermore, most of the reported GO filters are planar coatings with a simple geometry and an area much smaller than commercial water filters. Here, we show selective transport of different ions across GO coatings deposited on standard hollow fiber filters with an area >10 times larger than typical filters reported. Thanks to the fabrication procedure, we obtained a uniform coating on such complex geometry with no cracks or holes. Monovalent ions like Na+ and K+ can be transported through these filters by applying a low electric voltage, while divalent ions are blocked. By combining transport and adsorption measurements with molecular dynamics simulations and spectroscopic characterization, we unravel the ion sieving mechanism and demonstrate that it is mainly due to the interactions of the ions with the carboxylate groups present on the GO surface at neutral pH.
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| 5. |
- Sanchez, Jaime S., et al.
(författare)
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Versatile electrochemical manufacturing of mixed metal sulfide/N-doped rGO composites as bifunctional catalysts for high power rechargeable Zn–air batteries
- 2024
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Ingår i: Journal of Materials Chemistry A. - 2050-7488 .- 2050-7496. ; 12:20, s. 11945-11959
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Tidskriftsartikel (refereegranskat)abstract
- The development of rechargeable zinc–air batteries requires air cathodes capable of performing both the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) with high performance and an extended operational lifespan. Here, we present a cost-effective and versatile electrochemical method for the direct assembly of such electrocatalysts, consisting of nitrogen-doped reduced graphene oxide (NrGO) and mixed transition metal sulfides (NiCoMnSx or NCMS). To this end, we use a small electric bias to electro-deposit both NrGO and NCMS directly on conductive graphene foam, resulting in a perfect porous network and two interpenetrated paths for the easy transport of electrons and ions. The NCMS/ NrGO composite shows one of the highest limiting currents reported so far for a non-noble metal catalyst. Additionally, it exhibits outstanding bifunctional performance for the ORR/OER, superior to both mixed transition metal compounds and noble metals from previous reports. Thus, it serves as a highly efficient air cathode for practical zinc–air batteries featuring high power densities (124 mW cm−2) and long catalyst durability (1560 cycles, around 260 h). We attribute the excellent performance to the synergistic effect between hetero-structured metallic sites and nitrogen dopants. Our approach can be used for preparing efficient zinc–air cathodes on conductive 3D carbon substrates with arbitrary shapes and good performance.
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| 6. |
- Xia, Zhenyuan, 1983, et al.
(författare)
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Green synthesis of positive electrodes for high performance structural batteries - A study on graphene additives
- 2024
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Ingår i: Composites Science and Technology. - 0266-3538. ; 251
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Tidskriftsartikel (refereegranskat)abstract
- Carbon fibres (CF) have the potential to serve as versatile and multifunctional conductive electrodes within the concept of “structural batteries”. These batteries possess the unique ability to both store electrical energy and bear mechanical loads without requiring extra current collectors. However, numerous challenges remain on the path to commercializing structural batteries. One significant challenge lies in the fabrication process of CF-based cathode composites, including the poor adhesion of active materials to the CF surface and the use of hazardous organic solvents, such as N-methyl pyrrolidone (NMP) through traditional blade coating. In this study, we present a sustainable fabrication approach, using electrophoretic deposition (EPD) to construct positive electrode composites with lithium iron phosphate (LiFePO4) and graphene nanosheets. Especially, ethanol was used as a green solvent replacing NMP to minimize the environmental impact. Meanwhile, the influence of different types of graphene additives (three kinds of graphene nanoplatelets (GNP), four kinds of reduced graphene oxide (rGO) and one home-made graphene) to the relative battery performance were evaluated under a systematic comparative analysis. Among the tested graphene additives, LFP/rGO2 based positive electrode exhibits a desirable specific capacity of 126.2 mAhg−1, maintaining over 93% retention even under the demanding conditions of 2C over 500 cycles.
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| 7. |
- Zhang, Panpan, et al.
(författare)
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Hydrogen-Bond-Repairing Solar Evaporator with Reconstructed Large-Width Channels for Durable Solarizing Seawater
- 2024
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Ingår i: Nano Letters. - 1530-6992 .- 1530-6984. ; In Press
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Tidskriftsartikel (refereegranskat)abstract
- Conventional solarizing seawater suffers from inefficiency and space constraints. Interfacial solar vapor generation (ISVG) presents an energy-efficient alternative, yet the scalability, adaptability, and durability of a solar evaporator for practical use are remaining concerns. Herein, a hydrogen-bond-repairing solar evaporator featuring reconstructed large-width channels is proposed for ongoing solarization of seawater in ISVG. The polyacrylamide/trehalose/graphene hydrogel (PTGH) exhibits excellent mechanical properties and large-width salt discharge channels. PTGH achieves a notable water evaporation rate of 2.82 kg m-2 h-1 under 1 sun and remains effective even in low-temperature environments. The large-area PTGH is able to continuously operate for solarizing seawater under different conditions, until raw brine is highly concentrated, and eventually solid salt is separated from water. Compared to conventional solarizing seawater, PTGH can save 66.67%-75% of time or land to obtain the same amount of solid salt.
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