Electrochemical insertion of lithium into pyrite from nonaqueous electrolytes at room temperature. An in situ Fe K-edge X-ray absorption fine structure study

D. A. Tryk, S. Kim, Y. Hu, W. Xing, Daniel Alberto Scherson, M. R. Antonio, V. Z. Leger, G. E. Blomgren

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Abstract

The effects of lithium ion insertion on the structural and electronic properties of FeS2 (pyrite) have been examined in situ by Fe K-edge X-ray absorption fine structure (XAFS) using electrodes and electrolytes similar to those found in conventional, ambient-temperature, primary Li/FeS2 batteries. A substantial reduction in the amplitudes of the Fe-S and Fe-Fe backscattering was observed as the amount of intercalated lithium in the FeS2 lattice was increased from 0 to 2 Li+ equivalents, (Li+)eq. After the insertion of 2 (Li+)eq, the second-shell Fe-S interaction and the distant Fe-Fe interactions were no longer discernible in the Fourier transform (FT) data. Curve-fitting analysis of the κ3 X(k) extended X-ray absorption fine structure for this latter material yielded an average Fe-S distance, d(Fe-S) = 2.31 +/- 0.02 A, which is about 0.05 A longer than d(Fe-S) in crystalline pyrite. In addition, the X-ray absorption near-edge structure revealed a rounding of the otherwise highly structured edge of FeS2 as the amount of inserted lithium was increased. This behavior is consistent with the formation of Fe1-xS and thus supports the assignment made on the basis of in situ 57Fe Mossbauer effect spectroscopy of the same system.

Original languageEnglish
Pages (from-to)3732-3735
Number of pages4
JournalJournal of physical chemistry
Volume99
Issue number11
DOIs
Publication statusPublished - 1995 Jan 1
Externally publishedYes

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ASJC Scopus subject areas

  • Engineering(all)
  • Physical and Theoretical Chemistry

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