Electrochemical lithiation of Ge: New insights by operando spectroscopy and diffraction
Artikel i vetenskaplig tidskrift, 2018
The relatively high cost of metallic germanium (Ge) as a lithium-ion battery negative electrode material is more than counterbalanced by its high capacity, high lithium diffusivity, and electronic conductivity. Using a unique and highly complementary set of operando characterization techniques, we propose a complete mechanism for the reversible lithiation of Ge. The electrochemical mechanism is found to be determined by the process of discharge/charge: (i) independent of the charge/discharge rate amorphous a-LiGe is proposed as the first intermediate during the lithiation of c-Ge, followed by Li 7 Ge 3 , and (ii) at low potential Li 15 Ge 4 is observed, but only for moderate rates and never at low rates, where indeed an "overlithiated" phase is preferred. The complementarity of the data obtained from XAS, Raman spectroscopies, and XRD, all in operando mode, was crucial in order to understand the complex mechanism based on reversible formation of the various crystalline and amorphous phases.
Författare
L. C. Loaiza
Université de Picardie Jules Verne
N. Louvain
Université de Montpellier
Centre national de la recherche scientifique (CNRS)
B. Fraisse
Université de Montpellier
Athmane Boulaoued
Université de Montpellier
Chalmers, Fysik, Kondenserade materiens fysik
A. Iadecola
Centre national de la recherche scientifique (CNRS)
Patrik Johansson
Chalmers, Fysik, Kondenserade materiens fysik
L. Stievano
Université de Montpellier
Centre national de la recherche scientifique (CNRS)
V. Seznec
Université de Picardie Jules Verne
Centre national de la recherche scientifique (CNRS)
L. Monconduit
Université de Montpellier
Centre national de la recherche scientifique (CNRS)
Journal of Physical Chemistry C
1932-7447 (ISSN) 1932-7455 (eISSN)
Vol. 122 7 3709-3718Ämneskategorier
Oorganisk kemi
Materialkemi
Annan fysik
Annan kemi
Drivkrafter
Hållbar utveckling
Styrkeområden
Transport
Energi
Materialvetenskap
DOI
10.1021/acs.jpcc.7b11249