Mechanism of Silver Nanoparticles Deposition by Electrolysis and Electroless Methods on a Graphite Substrate

This study shows a silver electrodeposition model (EDM) on a graphite ‎substrate. The electrolyte was a 0.01 M solution of pure silver and chromium nitrate using an ‎electrolyzing cell. EDC with current density up to 20 mA/cm2 and 15 mV and pulse current were studied. Results revealed that silver deposited at a ‎rate of 0.515 mg/cm2/min with 12 mA /cm2 that decreases to 0.21 and 0.16 mg/cm2.min ‎with the decrease of current density to 6 and 5 mA/cm2 respectively. The model postulates that ‎silver ions (a) were first hydrated before diffusing (b) from the solution bulk to ‎the cathode vicinity, the next step (c) involved the chemical adsorption of these ions on certain ‎accessible sites of the graphite substrate (anode), the discharged entities (d) adhere to the graphite ‎surface by Van der Vales force. Silver ions are deposited because the ‎discharge potential of silver is low (0.38 mV) as compared to other metal ions like chromium (0.82 mV). Pulse ‎current controls silver deposition due to flexibility in controlling steps (a) - (c) of the ‎deposition mechanisms.

Correction: Complexing agent study via computational chemistry for environmentally friendly silver electrodeposition and the application of a silver deposit

Correction for ‘Complexing agent study via computational chemistry for environmentally friendly silver electrodeposition and the application of a silver deposit’ by Anmin Liu et al., RSC Adv., 2014, 4, 40930–40940, DOI: 10.1039/C4RA05869K.

Indirect (hydrogen-driven) electrodeposition of porous silver onto a palladium membrane

Hydrogen permeation through a pure palladium film (25 μm thickness, optically dense) is employed to trigger electron transfer (hydrogen-driven) reactions at the external palladium | aqueous electrolyte interface of a two-compartment electrochemical cell. Two systems are investigated to demonstrate feasibility for (i) indirect hydrogen-mediated silver electrodeposition with externally applied potential and (ii) indirect hydrogen-mediated silver electrodeposition driven by external formic acid decomposition. In both cases, porous metal deposits form as observed by optical and electron microscopies. Processes are self-limited as metal deposition blocks the palladium surface and thereby slows down further hydrogen permeation. The proposed methods could be employed for a wider range of metals, and they could provide an alternative (non-electrochemical or indirect) procedure for metal removal or metal recovery processes or for indirect metal sensing.