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The present work is aimed at demonstrating the potentiality of lithium ion batteries recycling through the production of high added value nanostructured material. Nanostructured electrodic materials were synthesized starting from waste lithium ion batteries (LIBs). Firstly, the metals contained in the electrodic powder of exhausted LIBs were extracted by acid-reducing leaching. After filtration, metals rich solution was separated from graphite. Nanoparticles- based electrodes were produced by controlled precipitation and subsequent calcination of metals in order to obtain nanoparticles of LiNi1/3Co1/3Mn1/3O2, one of the most employed LIBs cathodic material. Cathodic materials synthesized starting from waste LIBs and from high grade synthetic reagents were compared after their characterization by SEM, EDX and XRD. The electrochemical performance of the electrodes was evaluated by galvanostatic cycling the electrodes in a lithium half-cell. Remarkably, the electrochemical performances obtained with the electrodes produced by the recovery of metals are close to those recorded using electrodes produced by synthetic reagents.

In this contribution we report on electrochemical approaches in TiO2 based electrodes synthesis. TiO2 nanotubes (NTs) were synthesized following a facile anodization of titanium sheets. Optimizing the experimental conditions two electrodes with NTs lengths of ∼10 μm (Long) and ∼2 μm (Short), were obtained. At the end of the anodization the amorphous TiO2 (a-TiO2) was thermally treated to promote the conversion in the anatase crystal phase (c-TiO2). Both the Long and Short NTs electrodes were tested for their applications as anodes in lithium-ion batteries (LIBs). A preliminary comparison was performed to evaluate the role of a-TiO2 and c-TiO2 phases. Here, Short a-TiO2 NTs exhibited a fast storage rate respect to Short c-TiO2. Comparing the NTs length, Long a-TiO2 electrodes exhibited the highest specific capacity, close to the theoretical value. Furthermore, all the electrodes tested showed an excellent capacity retention proceeding with Discharge/Charge cycles.

In order to characterize magnetic properties of cobalt-based nanoparticles synthesized through electrodeposition on metal substrates, methods must be employed which enable the imaging of sample surface, the selection of a specific nanoparticle, and the accurate evaluation of local magnetic parameters, such as magnetic moment or saturation magnetization. Due to the combination of imaging capability and quantitative probing of ultra-low magnetic field through the use of a nanometer sized tip with a magnetic coating, magnetic force microscopy (MFM) is a promising tool to characterize Co-based nanoparticles directly on substrates. In this work, the report the preliminary results of the use of MFM to analyze Co nanoparticles electrodeposited on an Al substrate. The aim wa to assess the effective capability of this technique to investigate this kind of nanomaterials, foresee offered possibilities, and highlight current limitations to overcome.