Skip to content Skip to navigation
University of Warwick
  • Study
  • |
  • Research
  • |
  • Business
  • |
  • Alumni
  • |
  • News
  • |
  • About

University of Warwick
Publications service & WRAP

Highlight your research

  • WRAP
    • Home
    • Search WRAP
    • Browse by Warwick Author
    • Browse WRAP by Year
    • Browse WRAP by Subject
    • Browse WRAP by Department
    • Browse WRAP by Funder
    • Browse Theses by Department
  • Publications Service
    • Home
    • Search Publications Service
    • Browse by Warwick Author
    • Browse Publications service by Year
    • Browse Publications service by Subject
    • Browse Publications service by Department
    • Browse Publications service by Funder
  • Statistics
  • Help & Advice
University of Warwick

The Library

  • Login

Measurement of solute partitioning across liquid/liquid interfaces using scanning electrochemical microscopy-double potential step chronoamperometry (SECM-DPSC): Principles, theory, and application to ferrocenium ion transfer across the 1,2-dichloroethane/aqueous interface

Tools
- Tools
+ Tools

UNSPECIFIED. (2001) Measurement of solute partitioning across liquid/liquid interfaces using scanning electrochemical microscopy-double potential step chronoamperometry (SECM-DPSC): Principles, theory, and application to ferrocenium ion transfer across the 1,2-dichloroethane/aqueous interface. JOURNAL OF PHYSICAL CHEMISTRY B, 105 (48). pp. 12019-12031. ISSN 1089-5647

Full text not available from this repository.
Official URL: http://dx.doi.org/10.1021/jp010591v

Abstract

SECM-DPSC is extended as an approach for probing the transfer of a target electrogenerated species across the interface between two immiscible phases, by developing a theoretical model for reversible phase transfer. The SECM-DPSC technique involves the electrogeneration of a target species at an UME positioned close to an interface in an initial (forward) potential step. After a defined period, this species is then collected back at the UME by reversing the potential step. The numerical treatment for calculating the UME current-time response during the forward and reverse potential steps is outlined, without restriction on the partition coefficient of the solute between the two phases, thereby building on an earlier model (Slevin, C. J.; Macpherson, J. V.; Unwin, P. R. J. Phys. Chem. B 1997, 101, 10851). It is shown that the technique can be used to measure both the partition coefficient and kinetics of phase transfer. The approach is illustrated through experimental studies of the transfer of the oxidized form of ferrocene (Fc) and derivatives across a 1,2-dichloroethane (DCE)/ aqueous interface, with ClO4- present in excess in each phase. The transfer of ferrocenium and dimethyl-ferrocenium, accompanied by ClO4- to maintain charge neutrality, are both found to be diffusion limited (rate constants > 0.5 cm s(-1)), even on the fastest time scales accessible with SECM. In contrast, deca-methylferrocenium ion does not appear to transfer across the interface under the defined conditions. In certain cases, such as slightly elevated temperatures, UME oxidation of ferrocene derivatives in the vicinity of the DCE/aqueous interface, was found to be accompanied by interfacial instabilities akin to a Marangoni phenomenon. SECM may provide a new method for initiating and monitoring such effects.

Item Type: Journal Article
Subjects: Q Science > QD Chemistry
Journal or Publication Title: JOURNAL OF PHYSICAL CHEMISTRY B
Publisher: AMER CHEMICAL SOC
ISSN: 1089-5647
Date: 6 December 2001
Volume: 105
Number: 48
Number of Pages: 13
Page Range: pp. 12019-12031
Identification Number: 10.1021/jp010591v
Publication Status: Published
URI: http://wrap.warwick.ac.uk/id/eprint/11506

Data sourced from Thomson Reuters' Web of Knowledge

Request changes to a record

Actions (login required)

View Item View Item
twitter

Email us: publications@warwick.ac.uk
Contact Details
About Us