Marielle Eyraud

Highly conformal electrodeposition of copolymer electrolytes into titania nanotubes for 3D Li-ion batteries

The highly conformal electrodeposition of a copolymer electrolyte (PMMA-PEO) into self-organized titania nanotubes (TiO2nt) is reported. The morphological analysis carried out by scanning electron microscopy and transmission electron microscopy evidenced the formation of a 3D nanostructure consisting of a copolymer-embedded TiO2nt. The thickness of the copolymer layer can be accurately controlled by monitoring the electropolymerization parameters. X-ray photoelectron spectroscopy measurements confirmed that bis(trifluoromethanesulfone)imide salt was successfully incorporated into the copolymer electrolyte during the deposition process. These results are crucial to fabricate a 3D Li-ion power source at the micrometer scale using TiO2nt as the negative electrode.

Simple approach for the fabrication of PEDOT-coated Si nanowires

Summary The synthesis of a conformal poly(3,4-ethylenedioxythiophene) (PEDOT) layer on Si nanowires was demonstrated using a pulsed electrodeposition technique. N-type Si nanowire (SiNWs) arrays were synthesized using an electroless metal-assisted chemical etching technique. The dependence of the SiNW reflection on the concentration of the AgNO3 solution was identified. A reflection of less than 2% over the entire visible spectral range was obtained for these structures, evidencing their excellent antireflective properties. The etched SiNWs nanostructures can be further modified by using a tapering technique, which further preserves the strong light trapping effect. P-type PEDOT was grown on these SiNWs using electrochemical methods. Since the polymerization reaction is a very fast process with regards to monomer diffusion along the SiNW, the conformal deposition by classical, fixed potential deposition was not favored. Instead, the core–shell heterojunction structure was finally achieved by a pulsed deposition method. An extremely large shunt resistance was exhibited and determined to be related to the diffusion conditions occurring during polymerization.

Electrochemical deposition of indium: nucleation mode and diffusional limitation

Abstractthe electrochemical deposition of indium metal from InCl3 solutions was investigated. Cyclovoltammetric experiments showed that the initial hydrogen evolution reaction, observed together with the metal deposition on Pt surface, is blocked when the surface is covered by In. At large cathodic potentials, the current is diffusion-limited. The scan rate dependence of cyclovoltammograms allowed the determination of the diffusion coefficient of In3+ ions, 8.18 × 10–6 cm2/s, using the Delahay equation. The activation energy of diffusion, determined from the temperature dependence of cyclovoltammograms, is about 0.3 eV (23 kJ/mol). Chrono-amperometric experiments are consistent with the cyclovoltammetry; the In3+ diffusion coefficient determined using the Cottrell law is in good agreement with the value determined by the Randles-Ševčik equation. Moreover the use of the nucleation models developed by Scharifker and Hills showed a progressive nucleation mode. Electron microscopy observations and X-ray diffraction patterns confirmed the formation of crystalline indium deposits.

Development and tribological characterisation of nanostructured Zn-Ni and Zn-Co coatings: a comparative study

ABSTRACT Zn-Ni and Zn-Co alloy coatings were electrodeposited on mild steel from sulphate-based baths. The morphology, microstructure, microhardness and tribological behaviours of the coatings have been studied and discussed. While the Zn-5wt-% Co layers presented a nanocrystalline simple nodular structure (45 ± 5 nm), the Zn-14wt-% Ni showed a particular structure called cauliflower morphology (30 ± 7 nm). The X-ray diffraction analysis showed that each of the electrodeposits was formed from zinc solid solution with a uniform zinc-cobalt intermetallic phase γ2 (CoZn13) for Zn-5wt-% Co alloy. However, a single γ-phase (intermetallic compound Ni5Zn21) was presented for the Zn-14wt-% Ni alloys. The Zn-14wt-% Ni films were found to be harder and rougher than the Zn-5wt-% Co layers. Plastic deformation and oxide layers production were the main wear mechanisms for the investigated coatings. The Zn-14wt-% Ni coatings were found to have the best wear resistance due to their microhardness and particular structure.

Structural, Micromechanical and Tribological Analyses of Electrodeposited Nickel–Graphite Coatings with Different Fractions of Graphite Microparticles

Nickel–graphite composite coatings were electrodeposited on a steel substrate from typical watts bath and with specific operating conditions for different weight fractions of graphite microparticles. The weight percentage of particles in coatings and the microstructure were studied, respectively, by atomic absorption, scanning electron microscope and X-ray diffraction. The influence of graphite fraction on roughness and microhardness were also investigated. It was found that roughness increases with the increase of particle content while microhardness decreases. The tribological response was examined against high chromium steel ball using linear reciprocating tribometer. The results indicated that the friction coefficient decreases when graphite content increases. This was ascribed to the development of tribo-layer on the wear track and transfer film on the counterface. However, it was found that the improvement of wear resistance was obtained until an optimal value of graphite concentration, which provided the best condition that promoted the tribo-layer stability and maintained the matrix integrity.