Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Electrodeposition01:08

Electrodeposition

Electrodeposition is a technique used to separate an analyte from interferents by electrochemical processes. Here, the analyte is a metal ion that can be deposited on an electrode immersed in the sample solution. The electrochemical setup consists of an anode and a cathode. When an electric current is applied to the setup, oxidation occurs at the anode. At the cathode, which consists of a large metal surface, metal ions undergo reduction and deposit onto the surface.
Electrodeposition can...
Extraction: Advanced Methods00:56

Extraction: Advanced Methods

Metal ions can be separated from one another by complexation with organic ligands–the chelating agent– to form uncharged chelates. Here, the chelating agent must contain hydrophobic groups and behave as a weak acid, losing a proton to bind with the metal. Since most organic ligands used in this process are insoluble or undergo oxidation in the aqueous phase, the chelating agent is initially added to the organic phase and extracted into the aqueous phase. The metal-ligand complex is formed in...
Precipitation and Co-precipitation01:17

Precipitation and Co-precipitation

Precipitation and coprecipitation methods can be used to separate a mixture of ions in a solution. In qualitative inorganic analysis, ions that form sparingly soluble precipitates with the same reagent are separated based on the differences in solubility products. For example, consider the separation of Cu(II) and Fe(II) ions by precipitation as insoluble sulfides. First, copper(II) sulfide is precipitated by the addition of acidic H2S, where the dissociation of H2S is suppressed. Adding H2S...
Types of Reversible Electrodes01:24

Types of Reversible Electrodes

For electrode reversibility to be maintained, all the reactants and products involved in the half-reaction must be present at the electrode. There are several types of reversible electrodes (half-cells).In metal-metal-ion electrodes, a metal balances electrochemically with a solution of its own ions. Examples are Cu2+|Cu and Zn2+|Zn. Metals that react with the solvent, like group 1 and most group 2 metals, which react with water, and zinc, which reacts with aqueous acidic solutions, cannot be...
Microbial Leaching01:27

Microbial Leaching

Microbial leaching, also known as bioleaching, is an environmentally favorable method for extracting metals from low-grade ores using specific microorganisms. This biotechnological approach is particularly valuable for mining operations targeting copper, gold, and uranium, where traditional extraction methods may be economically or environmentally impractical.Copper Leaching and Microbial CatalysisIn copper bioleaching, crushed ore is arranged into heaps and irrigated with a dilute sulfuric...
Formation of Complex Ions03:45

Formation of Complex Ions

A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Pivotal influence of ligand field stabilization energy on the extraction order of divalent metal ions by acidic extractants.

Reaction chemistry & engineering·2026
Same author

Solvation of copper(ii), zinc(ii) and lead(ii) in monoethanolamine solutions attained <i>via</i> leaching of microwave-assisted-roasted sulfidic tailings.

RSC advances·2026
Same author

Thermodynamic model for methanesulphonic acid recovery by tri-<i>n</i>-butyl phosphate.

RSC advances·2026
Same author

Recovery of metallic iron from the loaded organic phase after solvent extraction by precipitation-stripping with hydrogen gas.

RSC advances·2026
Same author

Solubility and antisolvent crystallization of lithium hydroxide monohydrate in various organic solvents.

Physical chemistry chemical physics : PCCP·2026
Same author

Solvation structures of potassium bis(trifluoromethylsulfonyl)imide-glyme highly concentrated electrolytes and cycling on organic cathodes.

Dalton transactions (Cambridge, England : 2003)·2026

Related Experiment Video

Updated: Jun 3, 2026

Solar-Driven Electrochemical Green Fuel Production from CO2 and Water Using Ti3C2Tx MXene-Supported CuZn and NiCo Catalysts
10:15

Solar-Driven Electrochemical Green Fuel Production from CO2 and Water Using Ti3C2Tx MXene-Supported CuZn and NiCo Catalysts

Published on: November 7, 2025

Copper(I)-containing ionic liquids for high-rate electrodeposition.

Neil R Brooks1, Stijn Schaltin, Kristof Van Hecke

  • 1Katholieke Universiteit Leuven, Department of Chemistry, Celestijnenlaan 200F, P.O. Box 2404, 3001 Heverlee, Belgium. Neil.Brooks@chem.kuleuven.be

Chemistry (Weinheim an Der Bergstrasse, Germany)
|March 19, 2011
PubMed
Summary

New copper-containing ionic liquids enable efficient copper electrodeposition from non-aqueous electrolytes at high current densities. These novel materials offer improved metal solubility and mass transport for advanced electrochemical applications.

More Related Videos

Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
06:53

Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks

Published on: June 9, 2023

Accumulation and Analysis of Cuprous Ions in a Copper Sulfate Plating Solution
07:00

Accumulation and Analysis of Cuprous Ions in a Copper Sulfate Plating Solution

Published on: March 20, 2019

Related Experiment Videos

Last Updated: Jun 3, 2026

Solar-Driven Electrochemical Green Fuel Production from CO2 and Water Using Ti3C2Tx MXene-Supported CuZn and NiCo Catalysts
10:15

Solar-Driven Electrochemical Green Fuel Production from CO2 and Water Using Ti3C2Tx MXene-Supported CuZn and NiCo Catalysts

Published on: November 7, 2025

Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
06:53

Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks

Published on: June 9, 2023

Accumulation and Analysis of Cuprous Ions in a Copper Sulfate Plating Solution
07:00

Accumulation and Analysis of Cuprous Ions in a Copper Sulfate Plating Solution

Published on: March 20, 2019

Area of Science:

  • Electrochemistry
  • Materials Science
  • Inorganic Chemistry

Background:

  • Ionic liquids (ILs) are salts that are liquid at or below 100°C, offering unique solvent properties.
  • Non-aqueous electrolytes are crucial for specific electrochemical processes, including metal deposition.
  • Copper electrodeposition often faces challenges with solubility and mass transport in conventional electrolytes.

Purpose of the Study:

  • To synthesize novel metal-containing ionic liquids based on copper.
  • To investigate their application as non-aqueous electrolytes for high-current-density copper electrodeposition.
  • To characterize the structure and electrochemical behavior of these new ionic liquids.

Main Methods:

  • Synthesis of copper(I) ionic liquids with bis(trifluoromethylsulfonyl)amide anion ([Tf(2)N]) and acetonitrile (CH(3)CN) ligands.
  • Electrochemical characterization, including cyclic voltammetry and galvanostatic deposition.
  • Structural analysis of the synthesized ionic liquids.

Main Results:

  • Successful synthesis of [Cu(CH(3)CN)(n)][Tf(2)N] (n=2, 4) ionic liquids.
  • Demonstration of copper electrodeposition at current densities exceeding 25 A dm(-2) using these electrolytes.
  • Identification of a tetrahedral copper(I) cation analogous to quaternary ammonium and phosphonium ILs.
  • Formation of a concentrated non-aqueous electrolyte [Cu(CH(3)CN)(2)][Tf(2)N] at elevated temperatures.

Conclusions:

  • The novel copper-containing ionic liquids are effective non-aqueous electrolytes for high-performance copper electrodeposition.
  • The unique structure of the copper(I) cation enhances metal solubility and mass transport.
  • These ionic liquids represent a promising advancement for electrochemical copper plating technologies.