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Sökning: L773:2050 7488

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1.
  • Abazari, R., et al. (författare)
  • High specific capacitance of a 3D-metal-organic framework-confined growth in CoMn2O4nanostars as advanced supercapacitor electrode materials
  • 2021
  • Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry. - 2050-7488 .- 2050-7496. ; 9:17, s. 11001-11012
  • Tidskriftsartikel (refereegranskat)abstract
    • In the presence of fossil fuels, several environmental concerns, such as energy shortage, environmental pollution, and global warming may occur in the present century. In this respect, supercapacitors have been introduced as green energy storage systems playing a central role in providing a sustainable human society. In this work, an advanced strategy was initially demonstrated through various synergistic effects to synthesize cobalt(ii) metal-organic framework#CoMn2O4nanocomposites (Co(ii)-TMU-63#CoMn2O4NCPs) having interfaces adapted at tunable chemical nanocomposites for hybrid supercapacitors. The given NCPs showed excellent electrochemical performance at 7 A g−1current density endowed with a specific capacity of 156 mA h g−1(1420 F g−1) and good cycling stability at 10 A g−1current density, following 7000 cycles with 93.3% capacity retention. The hybrid supercapacitor was assembled using activated carbon (AC) as negative and NCPs as positive electrodes, which delivered specific energy of 38.54 W h kg−1and maximum-specific power of 2312.4 W kg−1with 89.5% capacity retention over 7000 cycles. The enhanced electrochemical performances of Co(ii)-TMU-63#CoMn2O4NCPs can be attributed to the high surface area, porous structure, open metal sites functioning as electron collectors to enhance electron transfer as well as unique morphology and synergistic effect between Co(ii)-TMU-63 and CoMn2O4. This work may inspire a new development of interface-adapted nanocomposite for advanced energy storage applications. © The Royal Society of Chemistry 2021.
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2.
  • Abrashev, Miroslav V., et al. (författare)
  • Origin of the heat-induced improvement of catalytic activity and stability of MnOx electrocatalysts for water oxidation
  • 2019
  • Ingår i: Journal of Materials Chemistry A. - : ROYAL SOC CHEMISTRY. - 2050-7488 .- 2050-7496. ; 7:28, s. 17022-17036
  • Tidskriftsartikel (refereegranskat)abstract
    • Catalysis of the oxygen evolution reaction (OER) by earth-abundant materials in the near-neutral pH regime is of great interest as it is the key reaction for non-fossil fuel production. To address the pertinent stability problems and insufficiently understood structure-activity relations, we investigate the influence of moderate annealing (100-300 degrees C for 20 min) for two types of electrodeposited Mn oxide films with contrasting properties. Upon annealing, the originally inactive and structurally well-ordered Oxide 1 of birnessite type became as OER active as the non-heated Oxide 2, which has a highly disordered atomic structure. Oxide 2 also improved its activity upon heating, but more important is the stability improvement: the operation time increased by about two orders of magnitude (in 0.1 M KPi at pH 7). Aiming at atomistic understanding, electrochemical methods including quantitative analysis of impedance spectra, X-ray spectroscopy (XANES and EXAFS), and adapted optical spectroscopies (infrared, UV-vis and Raman) identified structure-reactivity relations. Oxide structures featuring both di-mu-oxo bridged Mn ions and (close to) linear mono-mu-oxo Mn3+-O-Mn4+ connectivity seem to be a prerequisite for OER activity. The latter motif likely stabilizes Mn3+ ions at higher potentials and promotes electron/hole hopping, a feature related to electrical conductivity and reflected in the strongly accelerated rates of Mn oxidation and O-2 formation. Poor charge mobility, which may result from a low level of Mn3+ ions at high potentials, likely promotes inactivation after prolonged operation. Oxide structures related to the perovskite-like zeta-Mn2O3 were formed after the heating of Oxide 2 and could favour stabilization of Mn ions in oxidation states lower than +4. This rare phase was previously found only at high pressure (20 GPa) and temperature (1200 degrees C) and this is the first report where it was stable under ambient conditions.
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3.
  • Admassie, Shimelis, et al. (författare)
  • A renewable biopolymer cathode with multivalent metal ions for enhanced charge storage
  • 2014
  • Ingår i: JOURNAL OF MATERIALS CHEMISTRY A. - : Royal Society of Chemistry. - 2050-7488. ; 2:6, s. 1974-1979
  • Tidskriftsartikel (refereegranskat)abstract
    • A ternary composite supercapacitor electrode consisting of phosphomolybdic acid (HMA), a renewable biopolymer, lignin, and polypyrrole was synthesized by a simple one-step simultaneous electrochemical deposition and characterized by electrochemical methods. It was found that the addition of HMA increased the specific capacitance of the polypyrrole-lignin composite from 477 to 682 F g(-1) ( at a discharge current of 1 A g(-1)) and also significantly improved the charge storage capacity from 6(to 128 mA h g(-1).
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4.
  • Aguirre, Miren, et al. (författare)
  • Hybrid acrylic/CeO2 nanocomposites using hydrophilic, spherical and high aspect ratio CeO2 nanoparticles
  • 2014
  • Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry (RSC). - 2050-7488 .- 2050-7496. ; 2:47, s. 20280-20287
  • Tidskriftsartikel (refereegranskat)abstract
    • A dispersion of CeO2 nanoparticles and nanorods stabilized with nitrilotriacetic acid (NTA) and a 4,4'-azobis(4-cyanovaleric acid) (V-501) initiator has been used to initiate the emulsion polymerization of acrylic monomers, yielding stable hybrid CeO2 nanoparticle-nanorod/polyacrylate latexes for the first time. Films cast from these hybrid latexes are transparent due to the very homogenous distribution of the polymer compatibilized CeO2. Furthermore, it has been proven that the UV-Vis absorption capacity of the hybrid latexes is enhanced with the incorporation of the nanorods.
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5.
  • Ajjan, Fátima, et al. (författare)
  • High performance PEDOT/lignin biopolymer composites for electrochemical supercapacitors
  • 2016
  • Ingår i: Journal of Materials Chemistry A. - : ROYAL SOC CHEMISTRY. - 2050-7488 .- 2050-7496. ; 4:5, s. 1838-1847
  • Tidskriftsartikel (refereegranskat)abstract
    • Developing sustainable organic electrode materials for energy storage applications is an urgent task. We present a promising candidate based on the use of lignin, the second most abundant biopolymer in nature. This polymer is combined with a conducting polymer, where lignin as a polyanion can behave both as a dopant and surfactant. The synthesis of PEDOT/Lig biocomposites by both oxidative chemical and electrochemical polymerization of EDOT in the presence of lignin sulfonate is presented. The characterization of PEDOT/Lig was performed by UV-Vis-NIR spectroscopy, FTIR infrared spectroscopy, thermogravimetric analysis, scanning electron microscopy, cyclic voltammetry and galvanostatic charge-discharge. PEDOT doped with lignin doubles the specific capacitance (170.4 F g(-1)) compared to reference PEDOT electrodes (80.4 F g(-1)). The enhanced energy storage performance is a consequence of the additional pseudocapacitance generated by the quinone moieties in lignin, which give rise to faradaic reactions. Furthermore PEDOT/Lig is a highly stable biocomposite, retaining about 83% of its electroactivity after 1000 charge/discharge cycles. These results illustrate that the redox doping strategy is a facile and straightforward approach to improve the electroactive performance of PEDOT.
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6.
  • Ajjan, Fátima, et al. (författare)
  • Spectroelectrochemical investigation of redox states in a polypyrrole/lignin composite electrode material
  • 2015
  • Ingår i: Journal of Materials Chemistry A. - : ROYAL SOC CHEMISTRY. - 2050-7488 .- 2050-7496. ; 3:24, s. 12927-12937
  • Tidskriftsartikel (refereegranskat)abstract
    • We report spectroelectrochemical studies to investigate the charge storage mechanism of composite polypyrrole/lignin electrodes. Renewable bioorganic electrode materials were produced by electropolymerization of pyrrole in the presence of a water-soluble lignin derivative acting as a dopant. The resulting composite exhibited enhanced charge storage abilities due to a lignin-based faradaic process, which was expressed after repeated electrochemical redox of the material. The in situ FTIR spectroelectrochemistry results show the formation of quinone groups, and reversible oxidation-reduction of these groups during charge-discharge experiments in the electrode materials. The most significant IR bands include carbonyl absorption near 1705 cm(-1), which is attributed to the creation of quinone moieties during oxidation, and absorption at 1045 cm(-1) which is due to hydroquinone moieties.
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7.
  • Alkadir Abdulahi, Birhan, 1985, et al. (författare)
  • Structural engineering of pyrrolo[3,4-: F] benzotriazole-5,7(2 H,6 H)-dione-based polymers for non-fullerene organic solar cells with an efficiency over 12%
  • 2019
  • Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry (RSC). - 2050-7488 .- 2050-7496. ; 7:33, s. 19522-19530
  • Tidskriftsartikel (refereegranskat)abstract
    • In this work, we have synthesized two wide band gap donor polymers based on benzo[1,2-b:4,5-b′]dithiophene (BDT) and pyrrolo[3,4-f]benzotriazole-5,7(2H,6H)-dione (TzBI), namely, PBDT-TzBI and PBDT-F-TzBI and studied their photovoltaic properties by blending them with ITIC as an acceptor. Polymer solar cell devices made from PBDT-TzBI:ITIC and PBDT-F-TzBI:ITIC exhibited power conversion efficiencies (PCEs) of 9.22% and 11.02% and while annealing at 160 °C, improved the device performances to 10.24% and 11.98%, respectively. Upon solvent annealing with diphenyl ether (DPE) (0.5%) and chlorobenzene (CB), the PCE of the PBDT-F-TzBI-based device increased to 12.12%. The introduction of the fluorinated benzodithiophene (BDT-F) moiety on the backbone of PBDT-F-TzBI improved the open circuit voltage, short circuit current and fill factor simultaneously. The high PCEs of the PBDT-F-TzBI:ITIC-based devices were supported by comparison and analysis of the optical and electronic properties, the charge carrier mobilities, exciton dissociation probabilities, and charge recombination behaviors of the devices.
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8.
  • An, J., et al. (författare)
  • Supramolecular Co-adsorption on TiO2to enhance the efficiency of dye-sensitized solar cells
  • 2021
  • Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry (RSC). - 2050-7488 .- 2050-7496. ; 9:23, s. 13697-13703
  • Tidskriftsartikel (refereegranskat)abstract
    • Three novel push-pull dyes, with carbazole donors, codedAJ502,TZ101andTZ102are synthesized and applied as co-sensitizers in dye-sensitized solar cells (DSSCs).TZ101andTZ102have similar structures except for two fluorine atoms introduced on the benzotriazole (BTZ) unit.AJ502shows a near-IR absorption spectrum that is suitable for co-sensitization withTZ101andTZ102. The co-sensitized DSSC device based onCO-1(AJ502 : TZ101= 3 : 4 (0.075 mM : 0.1 mM)) achieves a power conversion efficiency (PCE) of 10.3% under AM 1.5G irradiation, with 1.06 V open-circuit voltage (Voc), 13.75 mA cm−2short-circuit photocurrent density (Jsc), and 70.8% fill factor (FF), a significant improvement compared to the single dye, 6.0% forAJ502and 5.1% forTZ101with a copper(i/ii)-based redox electrolyte. A PCE of 8.9% is also obtained by devices based onCO-2(AJ502 : TZ102= 3 : 4). ForCO-1, the fluorine atoms inTZ101play a critical role by widening the active light capturing bands of bothTZ101andAJ502on the TiO2film whileTZ102andAJ502show weaker interaction under the same conditions. The UV-vis spectrum and Raman spectrum revealed thatAJ502can form supramolecules withTZ101andTZ102formed on the TiO2film. 
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9.
  • Anil, Athira, et al. (författare)
  • Effect of pore mesostructure on the electrooxidation of glycerol on Pt mesoporous catalysts
  • 2023
  • Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry (RSC). - 2050-7488 .- 2050-7496. ; 11:31, s. 16570-16577
  • Tidskriftsartikel (refereegranskat)abstract
    • Glycerol is a renewable chemical that has become widely available and inexpensive due to the increased production of biodiesel. Noble metal materials have shown to be effective catalysts for the production of hydrogen and value-added products through the electrooxidation of glycerol. In this work we develop three platinum systems with distinct pore mesostructures, e.g., hierarchical pores (HP), cubic pores (CP) and linear pores (LP); all with high electrochemically active surface area (ECSA). The ECSA-normalized GEOR catalytic activity of the systems follows HPC > LPC > CPC > commercial Pt/C. Regarding the oxidation products, we observe glyceric acid as the main three-carbon product (3C), with oxalic acids as the main two-carbon oxidation product. DFT-based theoretical calculations support the glyceraldehyde route going through tartronic acid towards oxalic acid and also help understanding why the dihydroxyacetone (DHA) route is active despite the absence of DHA amongst the observed oxidation products.
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10.
  • Araujo, Rafael B., et al. (författare)
  • Designing strategies to tune reduction potential of organic molecules for sustainable high capacity batteries application
  • 2017
  • Ingår i: Journal of Materials Chemistry A. - 2050-7488 .- 2050-7496. ; 5:9, s. 4430-4454
  • Tidskriftsartikel (refereegranskat)abstract
    • Organic compounds evolve as a promising alternative to the currently used inorganic materials in rechargeable batteries due to their low-cost, environmentally friendliness and flexibility. One of the strategies to reach acceptable energy densities and to deal with the high solubility of known organic compounds is to combine small redox active molecules, acting as capacity carrying centres, with conducting polymers. Following this strategy, it is important to achieve redox matching between the chosen molecule and the polymer backbone. Here, a synergetic approach combining theory and experiment has been employed to investigate this strategy. The framework of density functional theory connected with the reaction field method has been applied to predict the formal potential of 137 molecules and identify promising candidates for the referent application. The effects of including different ring types, e.g. fused rings or bonded rings, heteroatoms, [small pi] bonds, as well as carboxyl groups on the formal potential, has been rationalized. Finally, we have identified a number of molecules with acceptable theoretical capacities that show redox matching with thiophene-based conducting polymers which, hence, are suggested as pendent groups for the development of conducting redox polymer based electrode materials.
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