Publications by authors named "Suchithra Ashoka Sahadevan"

We recommend best practices for the recovery of cobalt from LiCoO (LCO) lithium-ion battery (LIB) cathodes by (i) leaching using green deep eutectic solvents (DES) and (ii) subsequent electrodeposition, through a case study of the choline chloride (ChCl):ethylene glycol (EG) DES. DES physical properties (conductivity, viscosity, and surface tension) were tailored by varying the composition between mole ratios of 1 : 2 and 1 : 5 (ChCl:EG). Examined along with leaching process parameters (temperature, duration), increasing the fraction of hydrogen bond donors (HBDs) decreased DES surface tension and enhanced leaching.

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The potential of silicon-based fluorescent platforms for the detection of trace toxic metal ions was investigated in an aqueous environment. To this aim, silicon chips were first functionalized with amino groups, and fluorescein organic dyes, used as sensing molecules, were then covalently linked to the surface formation of thiourea groups. The obtained hybrid heterostructures exhibited high sensitivity and selectivity towards copper(ii), a limit of detection compatible with the recommended upper limits for copper in drinking water, and good reversibility using a standard metal-chelating agent.

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The synthesis, structural and photophysical characterization, and theoretical studies on homo/heteroleptic neutral 2D-layered coordination polymers (CPs), obtained by combining the Er ion with chlorocyananilate (ClCNAn) and/or tetrafluoroterephthalate (FBDC) linkers, are herein reported. The structure of the heteroleptic Er-based CP, formulated as [Er(ClCNAn)(FBDC)(DMSO)] () is also reported. crystallizes in the triclinic 1̅ space group, and the structure consists of neutral 2D layers formed by Er ions linked through the two linkers oriented in such a way that the neighboring 2D layers are eclipsed along the axis, leading to parallelogram-like cavities.

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Achieving metal-organic frameworks (MOFs) in the form of nanoparticles (NanoMOFs) represents a recent challenge due to the possibility to combine the intrinsic porosity of these materials with the nanometric dimension, a fundamental requirement for strategic biomedical applications. In this outlook we envision the current/future opportunities of the NanoMOFs in the field of biomedicine, with particular emphasis on (i) biocompatible MOFs composition; (ii) MOFs miniaturization and (iii) nanoMOFs applications.

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Electrocrystallization of the bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF) organic donor in the presence of the [Fe(ClCNAn)] tris(chlorocyananilato)ferrate(III) paramagnetic anion in different stoichiometric ratios and solvent mixtures afforded two different hybrid systems formulated as [BEDT-TTF][Fe(ClCNAn)]·3HO () and [BEDT-TTF][Fe(ClCNAn)]·2CHCN () (An = anilato). Compounds and present unusual structures without the typical segregated organic and inorganic layers, where layers of are formed by Λ and Δ enantiomers of the anionic paramagnetic complex together with mixed-valence BEDT-TTF tetramers, while layers of are formed by Λ and Δ enantiomers of the paramagnetic complex together with dicationic BEDT-TTF dimers and monomers. Compounds and show semiconducting behaviors with room-temperature conductivities of ca.

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A series of two-dimensional (2D)-layered coordination polymers (CPs) based on the heterosubstituted anilate ligand ClCNAn derived from 3-chloro-6-cyano-2,5-dihydroxybenzoquinone and Dy are reported. By changes in the synthetic methods (layering technique, solvothermal or conventional one-pot reactions) and conditions (solvent, concentration, etc.), different types of 2D extended networks could be prepared and structurally characterized.

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A Raman study on Zinc-substituted Cobalt ferrites, with different Zn(II) contents in each sample of formula: CoFe₂O₄ (), ZnCoFeO₄ (), ZnCoFeO₄ (), ZnCoFeO₄ () is reported. These samples show the same crystallite size (∼6 nm), particle size (∼7 nm) and particle size distribution (∼20%) and they have been synthesized through heating up surfactant-assisted thermal decomposition of metalorganic precursors. The effect of Zn(II) substitution in the cationic distribution is investigated by using the known metal-oxygen vibrational modes in tetrahedral and octahedral sites.

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The mixed-valence FeFe 2D coordination polymer formulated as [TAG][FeFe(ClCNAn)]·(solvate) 1 (TAG = tris(amino)-guanidinium, ClCNAn = chlorocyanoanilate dianionic ligand) crystallized in the polar trigonal space group P3. In the solid-state structure, determined both at 150 and at 10 K, anionic 2D honeycomb layers [FeFe(ClCNAn)] establish in the ab plane, with an intralayer metal-metal distance of 7.860 Å, alternating with cationic layers of TAG.

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Radical cation salts composed of a bis(ethylenedithio)tetrathiafulvalene (ET) donor with homo-/heterosubstituted Cl/CN anilic acids as purely organic molecular conducting materials formulated as [BEDT-TTF][HClCNAn] (1) and [BEDT-TTF][HClAn] (2) have been prepared by electrocrystallization. Compounds 1 and 2 crystallized in the monoclinic space group P2/c for 1 and I2/a for 2, showing segregated donor-anion layers arranged in a α'-type donor packing pattern (1) and twisted parallel columns (2), respectively. Single-crystal conductivity measurements show that 1 is a semiconductor with room-temperature conductivity of 10 S cm and an activation energy E of 1900 K.

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