Publications by authors named "Liliane Guerlou-Demourgues"

Article Synopsis
  • A manganese-cobalt asbolane material was synthesized from birnessite using low-temperature cationic exchange with cobalt nitrate, enabling a high active mass loading for use in supercapacitors.
  • The material features a unique structure with MnO-type slabs and Co(OH) islands, confirmed through electronic transmission microscopy, showing two interlocking hexagonal sublattices.
  • Electrochemical tests demonstrated impressive capacitance of up to 180 F g, revealing effective charge storage mechanisms synergizing the properties of both components, along with promising long-term performance durability.
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High internal phase emulsions (HIPEs) have templated self-standing porous carbonaceous materials (carboHIPEs) while employing Kraft Black Liquor, a paper milling industry byproduct, as a carbon precursor source. As such, the starting emulsion has been prepared through a laboratory-made homogenizer, while native materials have been characterized at various length scales either with Raman spectrometry, X-ray diffraction (XRD), mercury intrusion porosimetry, and nitrogen absorption. After thermal carbonization, specific surface areas ranging from ∼600 m g to 1500 m g have been reached while maintaining a monolithic character.

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In the energy storage field, an electrode material must possess both good ionic and electronic conductivities to perform well, especially when high power is needed. In this context, the development of composite electrode materials combining an electrochemically active and good ionic conductor phase with an electronic conductor appears as a perfectly adapted approach to generate a synergetic effect and optimize the energy storage performance. In this work, three layered MnO phases with various morphologies (veils, nanoplatelets and microplatelets) were combined with electronic conductor cobalt oxyhydroxides with different platelet sizes (∼20 nm 70 nm wide), to synthesize 6 different composites by exfoliation and restacking processes.

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Nanostructuration is one of the most promising strategies to develop performant electrode materials for energy storage devices, such as hybrid supercapacitors. In this work, we studied the influence of precipitation medium and the use of a series of 1-alkyl-3-methylimidazolium bromide ionic liquids for the nanostructuration of β(III) cobalt oxyhydroxides. Then, the effect of the nanostructuration and the impact of the different ionic liquids used during synthesis were investigated in terms of energy storage performances.

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Decoupling energy supply from fossil fuels through electrification and sustainable energy management requires efficient and environmentally low-impact energy storage technologies. Potential candidates are charge storage electrodes that combine nickel and cobalt hydroxides with reduced graphene oxide (rGO) designed to achieve high-energy, high-power density and long cycling lifetimes. An early eco-efficiency analysis of these electrodes seeks to examine the impacts of materials and processes used in the synthesis, specifically while focusing on the use of rGO.

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This paper reports on an innovative and efficient approach based on the use of ionic liquids to govern the nano-structuration of HCoO, in order to optimize the porosity and enhance the ionic diffusion through the electrode materials. In this work, we show that (1-pentyl-3-methyl-imidazolium bromide (PMIMBr) and 1-ethyl-3-methylimidazolium tetrafluoroborate (EMIMBF)) ionic liquids (ILs) used as templates during the synthesis orientate the nanoparticle aggregation which leads to increase of the porosity and the average pore size of the electrode material. It is also demonstrated that the ILs are strongly bonded to the HCoO surface, leading to surface functionalized HCoO materials, also called nanohybrids.

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To design novel layered materials, bottom-up strategy is very promising. It consists of (1) synthesizing various layered oxides, (2) exfoliating them, then (3) restacking them in a controlled way. The last step is based on electrostatic interactions between different layered oxides and is difficult to control.

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