z-logo
open-access-imgOpen Access
Mechanism of Silver Nanoparticles Deposition by Electrolysis and Electroless Methods on a Graphite Substrate
Author(s) -
Mahmoud A. Rabah,
AUTHOR_ID,
Nabil Nassif Girgis,
AUTHOR_ID
Publication year - 2022
Publication title -
al-mağallaẗ al-akādīmiyyaẗ li-l-abḥāṯ wa-al-našr al-ʿilmī
Language(s) - English
Resource type - Journals
ISSN - 2706-6495
DOI - 10.52132/ajrsp.e.2022.33.1
Subject(s) - graphite , electrolysis , materials science , anode , electrolyte , substrate (aquarium) , deposition (geology) , cathode , chromium , silver nanoparticle , current density , inorganic chemistry , adsorption , chemical engineering , analytical chemistry (journal) , nanotechnology , chemistry , metallurgy , nanoparticle , electrode , paleontology , oceanography , physics , quantum mechanics , chromatography , sediment , engineering , biology , geology
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.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here