TY - JOUR
T1 - In situ Fe K-edge X-ray absorption fine structure of a pyrite electrode in a Li/polyethylene oxide(LiClO4)/FeS2 battery environment
AU - Totir, Dana A.
AU - Bae, In Tae
AU - Hu, Yining
AU - Antonio, Mark R.
AU - Stan, Mark A.
AU - Scherson, Daniel Alberto
PY - 1997/11/20
Y1 - 1997/11/20
N2 - Electronic and structural properties of materials generated by the reduction and subsequent oxidation of pyrite (FeS2) in a Li+-based solid polymer electrolyte (SPE) have been examined in situ by fluorescence Fe K-edge X-ray absorption fine structure (XAFS) in a Li/SPE/FeS2 battery environment. The in situ X-ray absorption near edge structure (XANES) of fully, i.e., four-electron, discharged FeS2 displayed features consistent with the presence of metallic iron, in agreement with information derived from in situ X-ray diffraction (XRD) and in situ 57Fe Mossbauer effect spectroscopy (MES) reported by other groups. The two-electron reoxidation (half-recharge) of such fully reduced material yielded an in situ XANES very similar to that of genuine crystalline Li2FeS2 prepared and characterized in this laboratory. These spectroscopic findings support conclusions made purely on the basis of electrochemical information, which identified Li2FeS2 as an intermediate in the charge-discharge mechanism of FeS2 in room-temperature Li+-containing electrolytes.
AB - Electronic and structural properties of materials generated by the reduction and subsequent oxidation of pyrite (FeS2) in a Li+-based solid polymer electrolyte (SPE) have been examined in situ by fluorescence Fe K-edge X-ray absorption fine structure (XAFS) in a Li/SPE/FeS2 battery environment. The in situ X-ray absorption near edge structure (XANES) of fully, i.e., four-electron, discharged FeS2 displayed features consistent with the presence of metallic iron, in agreement with information derived from in situ X-ray diffraction (XRD) and in situ 57Fe Mossbauer effect spectroscopy (MES) reported by other groups. The two-electron reoxidation (half-recharge) of such fully reduced material yielded an in situ XANES very similar to that of genuine crystalline Li2FeS2 prepared and characterized in this laboratory. These spectroscopic findings support conclusions made purely on the basis of electrochemical information, which identified Li2FeS2 as an intermediate in the charge-discharge mechanism of FeS2 in room-temperature Li+-containing electrolytes.
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M3 - Article
AN - SCOPUS:0031272977
SN - 1089-5647
VL - 101
SP - 9751
EP - 9756
JO - Journal of Physical Chemistry B
JF - Journal of Physical Chemistry B
IS - 47
ER -