Electrochemical kinetics of CuCl(aq)/HCl(aq) electrolyzer for hydrogen production via a Cu-Cl thermochemical cycle

Derek Hall, Eric G. LaRow, Rich S. Schatz, Justin R. Beck, Serguei Lvov

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

An electrochemical kinetics investigation of the CuCl(aq)/HCl(aq) electrolyzer identified methods to significantly reduce the platinum loadings required to achieve a high cell current density of 0.5 A/cm2 at 0.7 V. As the CuCl(aq)/HCl(aq) electrolyzer is a key component of the Cu-Cl thermochemical cycle, the economic viability of the Cu-Cl thermochemical cyclewas significantly improved by reducing the loading required to achieve 0.5 A/cm2. Electrochemical impedance spectroscopy (EIS) and linear sweep voltammetry (LSV) with a rotating disc electrode were employed to investigate the kinetics of the aqueous CuII/CuI chloride complexes reaction on platinum and glassy carbon using a three-electrode cell. It was found that the standard exchange current density of the anodic CuII/CuI electrochemical reaction on platinum, 4-12 A/cm2, was significantly larger than the values reported for the HER cathodic reaction thus far. In addition, SEM was used to observe the effectiveness of different catalyst application techniques. Through SEM observations, and electrochemical data analysis, the amount of platinum used in a laboratory scale CuCl(aq)/HCl(aq) electrolyzer was reduced from 0.8 mg/cm2 applied to both electrodes to 0.4 mg/cm2 on the cathode and zero at the anode while still maintaining a current density of 0.5 A/cm2 at 0.7 V of applied potential difference.

Original languageEnglish (US)
Pages (from-to)F108-F114
JournalJournal of the Electrochemical Society
Volume162
Issue number1
DOIs
StatePublished - Jan 1 2014

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hydrogen production
Hydrogen production
Platinum
platinum
cycles
Kinetics
Current density
kinetics
current density
Electrodes
electrodes
Scanning electron microscopy
scanning electron microscopy
glassy carbon
Glassy carbon
rotating disks
Rotating disks
Voltammetry
cells
Electrochemical impedance spectroscopy

All Science Journal Classification (ASJC) codes

  • Electronic, Optical and Magnetic Materials
  • Renewable Energy, Sustainability and the Environment
  • Condensed Matter Physics
  • Surfaces, Coatings and Films
  • Electrochemistry
  • Materials Chemistry

Cite this

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title = "Electrochemical kinetics of CuCl(aq)/HCl(aq) electrolyzer for hydrogen production via a Cu-Cl thermochemical cycle",
abstract = "An electrochemical kinetics investigation of the CuCl(aq)/HCl(aq) electrolyzer identified methods to significantly reduce the platinum loadings required to achieve a high cell current density of 0.5 A/cm2 at 0.7 V. As the CuCl(aq)/HCl(aq) electrolyzer is a key component of the Cu-Cl thermochemical cycle, the economic viability of the Cu-Cl thermochemical cyclewas significantly improved by reducing the loading required to achieve 0.5 A/cm2. Electrochemical impedance spectroscopy (EIS) and linear sweep voltammetry (LSV) with a rotating disc electrode were employed to investigate the kinetics of the aqueous CuII/CuI chloride complexes reaction on platinum and glassy carbon using a three-electrode cell. It was found that the standard exchange current density of the anodic CuII/CuI electrochemical reaction on platinum, 4-12 A/cm2, was significantly larger than the values reported for the HER cathodic reaction thus far. In addition, SEM was used to observe the effectiveness of different catalyst application techniques. Through SEM observations, and electrochemical data analysis, the amount of platinum used in a laboratory scale CuCl(aq)/HCl(aq) electrolyzer was reduced from 0.8 mg/cm2 applied to both electrodes to 0.4 mg/cm2 on the cathode and zero at the anode while still maintaining a current density of 0.5 A/cm2 at 0.7 V of applied potential difference.",
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Electrochemical kinetics of CuCl(aq)/HCl(aq) electrolyzer for hydrogen production via a Cu-Cl thermochemical cycle. / Hall, Derek; LaRow, Eric G.; Schatz, Rich S.; Beck, Justin R.; Lvov, Serguei.

In: Journal of the Electrochemical Society, Vol. 162, No. 1, 01.01.2014, p. F108-F114.

Research output: Contribution to journalArticle

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