TY - JOUR
T1 - Can Substitutions Affect the Oxidative Stability of Lithium Argyrodite Solid Electrolytes?
AU - Banik, Ananya
AU - Liu, Yunsheng
AU - Ohno, Saneyuki
AU - Rudel, Yannik
AU - Jiménez-Solano, Alberto
AU - Gloskovskii, Andrei
AU - Vargas-Barbosa, Nella M.
AU - Mo, Yifei
AU - Zeier, Wolfgang G.
N1 - Funding Information:
The research was supported by the Federal Ministry of Education and Research (BMBF) within project FESTBATT under grant number 03XP0430F. This research used resources at the P22 beamline at the light source PETRA III of DESY, a member of the Helmholtz Association (HGF). A.B. and S.O. gratefully acknowledge the Alexander von Humboldt Foundation for financial support through a Postdoctoral Fellowship. Y.L. and Y.M. acknowledge the funding support from the National Science Foundation HDR Program under award number 1940166, and the computational facilities from the University of Maryland supercomputing resources and the Maryland Advanced Research Computing Center (MARCC).
Publisher Copyright:
© 2022 American Chemical Society
PY - 2022/2/28
Y1 - 2022/2/28
N2 - Lithium-ion conducting argyrodites are among the most studied solid electrolytes due to their high ionic conductivities. A major concern in a solid-state battery is the stability of the solid electrolyte. Here, we present a systematic study on the influence of cationic and anionic substitution on the electrochemical stability of Li6PS5X using stepwise cyclic voltammetry, optical band gap measurements, and hard X-ray photoelectron spectroscopy along with first-principles calculations. We observe that on going from Li6PS5Cl to Li6+xP1-xMxS5I (M = Si4+, Ge4+), the oxidative stability does not change. Considering the chemical bonding shows that the valence band edges are mostly populated by nonbonding orbitals of the PS43- units or unbound sulfide anions and that simple substitutions in these sulfide-based solid electrolytes cannot improve oxidative stabilities. This work provides insights into the role of chemical bonding on the stability of superionic conductors and shows that alternative strategies are needed for long-term stable solid-state batteries.
AB - Lithium-ion conducting argyrodites are among the most studied solid electrolytes due to their high ionic conductivities. A major concern in a solid-state battery is the stability of the solid electrolyte. Here, we present a systematic study on the influence of cationic and anionic substitution on the electrochemical stability of Li6PS5X using stepwise cyclic voltammetry, optical band gap measurements, and hard X-ray photoelectron spectroscopy along with first-principles calculations. We observe that on going from Li6PS5Cl to Li6+xP1-xMxS5I (M = Si4+, Ge4+), the oxidative stability does not change. Considering the chemical bonding shows that the valence band edges are mostly populated by nonbonding orbitals of the PS43- units or unbound sulfide anions and that simple substitutions in these sulfide-based solid electrolytes cannot improve oxidative stabilities. This work provides insights into the role of chemical bonding on the stability of superionic conductors and shows that alternative strategies are needed for long-term stable solid-state batteries.
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U2 - 10.1021/acsaem.1c03599
DO - 10.1021/acsaem.1c03599
M3 - Article
AN - SCOPUS:85124956942
SN - 2574-0962
VL - 5
SP - 2045
EP - 2053
JO - ACS Applied Energy Materials
JF - ACS Applied Energy Materials
IS - 2
ER -