TY - JOUR
T1 - In situ and operando investigation of the dynamic morphological and phase changes of a selenium-doped germanium electrode during (de)lithiation processes
AU - Li, Tianyi
AU - Lim, Cheolwoong
AU - Cui, Yi
AU - Zhou, Xinwei
AU - Kang, Huixiao
AU - Yan, Bo
AU - Meyerson, Melissa L.
AU - Weeks, Jason A.
AU - Liu, Qi
AU - Guo, Fangmin
AU - Kou, Ronghui
AU - Liu, Yuzi
AU - De Andrade, Vincent
AU - De Carlo, Francesco
AU - Ren, Yang
AU - Sun, Cheng-Jun
AU - Mullins, C. Buddie
AU - Chen, Lei
AU - Fu, Yongzhu
AU - Zhu, Likun
PY - 2020/1/14
Y1 - 2020/1/14
N2 - To understand the effect of selenium doping on the good cycling performance and rate capability of a Ge0.9Se0.1 electrode, the dynamic morphological and phase changes of the Ge0.9Se0.1 electrode were investigated by synchrotron-based operando transmission X-ray microscopy (TXM) imaging, X-ray diffraction (XRD), and X-ray absorption spectroscopy (XAS). The TXM results show that the Ge0.9Se0.1 particle retains its original shape after a large volume change induced by (de)lithiation and undergoes a more sudden morphological and optical density change than pure Ge. The difference between Ge0.9Se0.1 and Ge is attributed to a super-ionically conductive Li-Se-Ge network formed inside Ge0.9Se0.1 particles, which contributes to fast Li-ion pathways into the particle and nano-structuring of Ge as well as buffering the volume change of Ge. The XRD and XAS results confirm the formation of a Li-Se-Ge network and reveal that the Li-Se-Ge phase forms during the early stages of lithiation and is an inactive phase. The Li-Se-Ge network also can suppress the formation of the crystalline Li15Ge4 phase. These in situ and operando results reveal the effect of the in situ formed, super-ionically conductive, and inactive network on the cycling performance of Li-ion batteries and shed light on the design of high capacity electrode materials. © 2019 The Royal Society of Chemistry.
AB - To understand the effect of selenium doping on the good cycling performance and rate capability of a Ge0.9Se0.1 electrode, the dynamic morphological and phase changes of the Ge0.9Se0.1 electrode were investigated by synchrotron-based operando transmission X-ray microscopy (TXM) imaging, X-ray diffraction (XRD), and X-ray absorption spectroscopy (XAS). The TXM results show that the Ge0.9Se0.1 particle retains its original shape after a large volume change induced by (de)lithiation and undergoes a more sudden morphological and optical density change than pure Ge. The difference between Ge0.9Se0.1 and Ge is attributed to a super-ionically conductive Li-Se-Ge network formed inside Ge0.9Se0.1 particles, which contributes to fast Li-ion pathways into the particle and nano-structuring of Ge as well as buffering the volume change of Ge. The XRD and XAS results confirm the formation of a Li-Se-Ge network and reveal that the Li-Se-Ge phase forms during the early stages of lithiation and is an inactive phase. The Li-Se-Ge network also can suppress the formation of the crystalline Li15Ge4 phase. These in situ and operando results reveal the effect of the in situ formed, super-ionically conductive, and inactive network on the cycling performance of Li-ion batteries and shed light on the design of high capacity electrode materials. © 2019 The Royal Society of Chemistry.
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U2 - 10.1039/c9ta09750c
DO - 10.1039/c9ta09750c
M3 - RGC 21 - Publication in refereed journal
SN - 2050-7488
VL - 8
SP - 750
EP - 759
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 2
ER -