Electrodeposition concentration

Mixed Sulfite-Thiosulfate Bath for Soft Gold Electrodeposition (Concentration in mol h unless Otherwise Noted)... 

Toxic substances adsorbed on resins are removed during a regeneration procedure. The resulting spent regeneration solution has a higher concentration of the toxic substance than the stream from which it was removed by the resin. Toxic material in the spent regenerating solution can usually be precipitated, electrodeposited as in an electrolytic ceU, or made insoluble by other acceptable procedures. 

Germanium In situ STM studies on Ge electrodeposition on gold from an ionic liquid have quite recently been started at our institute [59, 60]. In these studies we used dry [BMIM][PF<3] as a solvent and dissolved Gel4 at estimated concentrations of 0.1-1 mmol 1 the substrate being Au(lll). This ionic liquid has, in its dry state, an electrochemical window of a little more than 4 V on gold, and the bulk deposition of Ge started several hundreds of mV positive from the solvent decomposition. Furthermore, distinct underpotential phenomena were observed. Some insight into the nanoscale processes at the electrode surface is given in Section 6.2.2.3. 

If the electrolysis parameters (precursor concentrations, pH, temperature, cur-rent/potential, substrate) be defined in a precise manner, a self-regulated growth of the compound can be established, and highly (111 )-oriented zinc blende (ZB) deposits up to several p,m thickness are obtained at potentials lying at the anodic limit of the diffusion range (Fig. 3.3) [60]. Currently, the typical method of cathodic electrodeposition has been developed to yield quite compact and coherent, polycrystalline, ZB n-CdSe films of well-defined stoichiometry. The intensity of the preferred ZB(f 11) orientation obtained with as-deposited CdSe/Ni samples has been quite high [61]. 

Telluro-cyanide (presumably TeCN ) has been explored as a source of tellurium for electrodeposition of CdTe [14], on account of the possible advantage that this species is less likely than tellurium dioxide to oxidize the cathodically produced telluride ion. Bath solutions were prepared by dissolving powdered Te in a concentrated aqueous solution of KCN and adding CdCb and EDTA. Stoichiometric CdTe deposits, free of excess Te, were reported. 

The electrodeposition of tellurium and silver has been investigated in dilute aqueous solutions of tellurous acid and Ag " ions (concentrations in the order of 10 to 10 " M) in 0.1 M HCIO4 [164], In particular, cyclic voltammetry experiments were conducted with rotating glassy carbon disk electrodes in baths with various concentration ratios of Ag(I) and Te(IV) precursors, and their outcome was discussed in terms of the voltammetric features. For a Ag(I)/Te(IV) ratio close to 0.8, formation of quasi pure silver telluride, Ag2Te, was reported. The authors, based on their measurements and on account of thermodynamic predictions, assumed that silver is deposited first on the electrode (Ag" + e Ag), and then Te(IV) is reduced on the previous silver deposit with formation of Ag2Te according to the reaction... 

In searching to formulate a mechanism of CuInSc2 phase formation by one-step electrodeposition from acid (pH 1-3) aqueous solutions containing millimolar concentrations of selenous acid and indium and copper sulfates, Kois et al. [178] considered a number of consecutive reactions involving the formation of Se, CuSe, and Cu2Se phases as a pre-requisite for the formation of CIS (Table 3.2). Thermodynamic and kinetic analyses on this basis were used to calculate a potential-pH diagram (Fig. 3.10) for the aqueous Cu+In-i-Se system and construct a distribution diagram of the final products in terms of deposition potential and composition ratio of Se(lV)/Cu(ll) in solution. 

On the other hand, Xiao et al. [215] reported that smooth, dense, and erystalline PbTe films with nearly stoichiometric composition could be obtained by an optimized electrodeposition process from highly acidic (pH 0) tellurite solutions of uncomplexed Pb(II), on Au-coated silicon wafers. The results from electroanalyti-cal studies on Te, Pb, and PbTe deposition with a Pt rde at various temperatures and solution compositions supported the induced co-deposition scheme. The microstructure and preferred orientation of PbTe films was found to change significantly with the deposition potential and electrolyte concentration. At -0.12 V vs. Ag/AgCl(sat. KCl), the film was granular and oriented preferentially in the [100] direction. At potentials more negative than -0.15 V, the film was dendritic and oriented preferentially in the [211] direction (Pig. 3.13). 

Electrodeposition of antimony sesquitelluride, Sb2Tc3, or of (Bii xSbx)2Te3 alloys from aqueous solutions is challenging because it is difficult to achieve a sufficiently high concentration of antimony. Complexing agents such as tartaric acid, citric acid, or FUTA have been used to solubilize Sb in water. 

The UPD and anodic oxidation of Pb monolayers on tellurium was investigated also in acidic aqueous solutions of Pb(II) cations and various concentrations of halides (iodide, bromide, and chloride) [103]. The Te substrate was a 0.5 xm film electrodeposited in a previous step on polycrystalline Au from an acidic Te02 solution. Particular information on the time-frequency-potential variance of the electrochemical process was obtained by potentiodynamic electrochemical impedance spectroscopy (PDEIS), as it was difficult to apply stationary techniques for accurate characterization, due to a tendency to chemical interaction between the Pb adatoms and the substrate on a time scale of minutes. The impedance... 

To deposit Au structures, a Au probe is approached to the surface until a positive feedback is observed. This is due to the regeneration of Cl species on the substrate while Au is deposited from AUCI4 according to the reverse reaction, leading to an increase in the local concentration of Cl. The microelectrode is then left at this position above the substrate for a certain time, after which it is withdrawn from the surface. The potential of the substrate, the electrolyte, and the pH were found to be the most significant parameters determining in determining the rate of Au electrodeposition and its structure (Amman and Mandler, 2001). 

Another example is dendritic crystal growth under diffusion-limited conditions accompanied by potential or current oscillations. Wang et al. reported that electrodeposition of Cu and Zn in ultra-thin electrolyte showed electrochemical oscillation, giving beautiful nanostmctured filaments of the deposits [27,28]. Saliba et al. found a potential oscillation in the electrodeposition of Au at a liquid/air interface, in which the Au electrodeposition proceeds specifically along the liquid/air interface, producing thin films with concentric-circle patterns at the interface [29, 30]. Although only two-dimensional ordered structures are formed in these examples because of the quasi-two-dimensional field for electrodeposition, very recently, we found that... 

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