Bonding in silver-oxygen compounds from Ag L3 XANES spectroscopy

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Authors

  • P. Behrens

External Research Organisations

  • University of Konstanz
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Details

Original languageEnglish
Pages (from-to)235-239
Number of pages5
JournalSolid state communications
Volume81
Issue number3
Publication statusPublished - Jan 1992
Externally publishedYes

Abstract

Compounds containing cations with a valence electron configuration that can formally be described as (n-1)d10ns0 (Cu+, Ag+, Au+, Hg2+) exhibit a variety of unusual structural properties, e.g. low coordination numbers and short cation-cation distances. The incorporation of d electrons from the closed d10 sub-shell has been debated for a long time as a reason for this extraordinary behaviour. Ag L3 XANES spectra of oxidic silver(I) compounds exhibit a prominent peak at the rising edge. By comparison with the XANES spectrum of a Ag(III) periodate complex this peak is assigned to a transition from initial 2p states to 4d final states, proving that in oxidic Ag(I) compounds the closed-shell configuration 4d10 is broken. The intensity of the peak signalling unoccupied 4d states is related to the degree of covalent bonding in a compound.

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Bonding in silver-oxygen compounds from Ag L3 XANES spectroscopy. / Behrens, P.
In: Solid state communications, Vol. 81, No. 3, 01.1992, p. 235-239.

Research output: Contribution to journalArticleResearchpeer review

Behrens P. Bonding in silver-oxygen compounds from Ag L3 XANES spectroscopy. Solid state communications. 1992 Jan;81(3):235-239. doi: 10.1016/0038-1098(92)90506-5
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