The Electro-Deposition/Dissolution of CuSO4 Aqueous Electrolyte Investigated by In Situ Soft X-ray Absorption Spectroscopy.
Juan-Jesus Velasco-VelezKatarzyna SkorupskaElias FreiYu-Cheng HuangChung Li DongBing-Jian SuCheng-Jhih HsuHung-Yu ChouJin-Ming ChenPeter StrasserRobert SchlöglAxel Knop-GerickeCheng-Hao ChuangPublished in: The journal of physical chemistry. B (2017)
The electrodeposition nature of copper on a gold electrode in a 4.8 pH CuSO4 solution was inquired using X-ray absorption spectroscopy, electrochemical quartz crystal microbalance, and thermal desorption spectroscopy techniques. Our results point out that the electrodeposition of copper prompts the formation of stable oxi-hydroxide species with a formal oxidation state Cu+ without the evidence of metallic copper formation (Cu0). Moreover, the subsequent anodic polarization of Cu2Oaq yields the formation of CuO, in the formal oxidation state Cu2+, which is dissolved at higher anodic potential. It was found that the dissolution process needs less charge than that required for the electrodeposition indicating a nonreversible process most likely due to concomitant water splitting and formation of protons during the electrodeposition.
Keyphrases
- solid state
- high resolution
- aqueous solution
- single molecule
- ionic liquid
- metal organic framework
- hydrogen peroxide
- oxide nanoparticles
- gold nanoparticles
- magnetic resonance imaging
- magnetic resonance
- risk assessment
- electron transfer
- human health
- climate change
- silver nanoparticles
- tandem mass spectrometry
- molecularly imprinted