Water oxidation by a nickel-glycine catalyst

Research output: Contribution to journalArticle

53 Citations (Scopus)

Abstract

The utilization of solar energy requires an efficient means for its storage as chemical energy. In bioinspired artificial photosynthesis, light energy can be used to drive water oxidation, but catalysts that produce molecular oxygen from water are needed to avoid excessive driving potentials. In this paper, we demonstrate the utility of a novel complex utilizing earth-abundant Ni in combination with glycine as an efficient catalyst with a modest overpotential of 0.475 ± 0.005 V at a current density of 1 mA/cm2 at pH 11. Catalysis requires the presence of the amine moiety with the glycine most likely coordinating the Ni in a 4:1 molar ratio. The production of molecular oxygen at a high potential is verified by measurement of the change in oxygen concentration, yielding a Faradaic efficiency of 60 ± 5%. The catalytic species is most likely a heterogeneous Ni-hydroxide formed by electrochemical oxidation. This Ni species can achieve a current density of 4 mA/cm2 that persists for at least 10 h. Based upon the observed pH dependence of the current amplitude and oxidation/reduction peaks, the catalytic mechanism is an electron-proton coupled process.

Original languageEnglish
Pages (from-to)10198-10201
Number of pages4
JournalJournal of the American Chemical Society
Volume136
Issue number29
DOIs
Publication statusPublished - Jul 23 2014

Fingerprint

Molecular oxygen
Nickel
Glycine
Amino acids
Current density
Oxygen
Oxidation
Catalysts
Photosynthesis
Water
Electrochemical oxidation
Solar Energy
Solar energy
Catalysis
Amines
Protons
Earth (planet)
Oxidation-Reduction
Electrons
Light

ASJC Scopus subject areas

  • Chemistry(all)
  • Catalysis
  • Biochemistry
  • Colloid and Surface Chemistry

Cite this

Water oxidation by a nickel-glycine catalyst. / Wang, Dong; Ghirlanda, Giovanna; Allen, James Paul.

In: Journal of the American Chemical Society, Vol. 136, No. 29, 23.07.2014, p. 10198-10201.

Research output: Contribution to journalArticle

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