TY - JOUR
T1 - Fast Ionic Conductivity in the Most Lithium-Rich Phosphidosilicate Li14SiP6
AU - Strangmüller, Stefan
AU - Eickhoff, Henrik
AU - Müller, David
AU - Klein, Wilhelm
AU - Raudaschl-Sieber, Gabriele
AU - Kirchhain, Holger
AU - Sedlmeier, Christian
AU - Baran, Volodymyr
AU - Senyshyn, Anatoliy
AU - Deringer, Volker L.
AU - Van Wüllen, Leo
AU - Gasteiger, Hubert A.
AU - Fässler, Thomas F.
N1 - Publisher Copyright:
Copyright © 2019 American Chemical Society.
PY - 2019/9/11
Y1 - 2019/9/11
N2 - Solid electrolytes with superionic conductivity are required as a main component for all-solid-state batteries. Here we present a novel solid electrolyte with three-dimensional conducting pathways based on "lithium-rich" phosphidosilicates with ionic conductivity of σ > 10-3 S cm-1 at room temperature and activation energy of 30-32 kJ mol-1 expanding the recently introduced family of lithium phosphidotetrelates. Aiming toward higher lithium ion conductivities, systematic investigations of lithium phosphidosilicates gave access to the so far lithium-richest compound within this class of materials. The crystalline material (space group Fm3m), which shows reversible thermal phase transitions, can be readily obtained by ball mill synthesis from the elements followed by moderate thermal treatment of the mixture. Lithium diffusion pathways via both tetrahedral and octahedral voids are analyzed by temperature-dependent powder neutron diffraction measurements in combination with maximum entropy method and DFT calculations. Moreover, the lithium ion mobility structurally indicated by a disordered Li/Si occupancy in the tetrahedral voids plus partially filled octahedral voids is studied by temperature-dependent impedance and 7Li NMR spectroscopy.
AB - Solid electrolytes with superionic conductivity are required as a main component for all-solid-state batteries. Here we present a novel solid electrolyte with three-dimensional conducting pathways based on "lithium-rich" phosphidosilicates with ionic conductivity of σ > 10-3 S cm-1 at room temperature and activation energy of 30-32 kJ mol-1 expanding the recently introduced family of lithium phosphidotetrelates. Aiming toward higher lithium ion conductivities, systematic investigations of lithium phosphidosilicates gave access to the so far lithium-richest compound within this class of materials. The crystalline material (space group Fm3m), which shows reversible thermal phase transitions, can be readily obtained by ball mill synthesis from the elements followed by moderate thermal treatment of the mixture. Lithium diffusion pathways via both tetrahedral and octahedral voids are analyzed by temperature-dependent powder neutron diffraction measurements in combination with maximum entropy method and DFT calculations. Moreover, the lithium ion mobility structurally indicated by a disordered Li/Si occupancy in the tetrahedral voids plus partially filled octahedral voids is studied by temperature-dependent impedance and 7Li NMR spectroscopy.
UR - http://www.scopus.com/inward/record.url?scp=85072058811&partnerID=8YFLogxK
U2 - 10.1021/jacs.9b05301
DO - 10.1021/jacs.9b05301
M3 - Article
C2 - 31403777
AN - SCOPUS:85072058811
SN - 0002-7863
VL - 141
SP - 14200
EP - 14209
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 36
ER -