Hydrated lithium nido-boranes for solid-liquid hybrid batteries

Hydridoborate salts are considered as promising solid-state electrolyte candidates for the development of solid-state batteries (SSBs). The presence of coordinated water in the crystal structure may facilitate the migration of the cation, yielding compounds with high ionic conductivity. In the prese...

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Main Authors: Souza, Diego H.P., Humphries, Terry D., Liu, Yu, Gradišek, A., D'Angelo, A.M., Buckley, Craig E., Paskevicius, Mark
Format: Journal Article
Language:English
Published: ROYAL SOC CHEMISTRY 2022
Subjects:
Online Access:http://purl.org/au-research/grants/arc/LE170100199
http://hdl.handle.net/20.500.11937/97011
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author Souza, Diego H.P.
Humphries, Terry D.
Liu, Yu
Gradišek, A.
D'Angelo, A.M.
Buckley, Craig E.
Paskevicius, Mark
author_facet Souza, Diego H.P.
Humphries, Terry D.
Liu, Yu
Gradišek, A.
D'Angelo, A.M.
Buckley, Craig E.
Paskevicius, Mark
author_sort Souza, Diego H.P.
building Curtin Institutional Repository
collection Online Access
description Hydridoborate salts are considered as promising solid-state electrolyte candidates for the development of solid-state batteries (SSBs). The presence of coordinated water in the crystal structure may facilitate the migration of the cation, yielding compounds with high ionic conductivity. In the present study, two samples of hydrated LiB11H14, here called LiB11H14·2H2O and a-LiB11H14·(H2O)n (n < 2), demonstrate remarkably different properties as solid-state electrolytes. LiB11H14·2H2O is identified as a new class of ionic liquid, as it melts at ≈70 °C, whereas the sample a-LiB11H14·(H2O)n undergoes a polymorphic phase transition close to this temperature, reaching the liquid-like ionic conductivity of 3.2 × 10−2 S cm−1 at 70 °C and an oxidative stability limit of 2.8 V against Li+/Li. Galvanostatic cycling and battery tests were conducted with a-LiB11H14·(H2O)n as the solid-state electrolyte (SSE) at 60 °C with the addition of traces of either the ionic liquid (IL) LiB11H14·2H2O or the liquid electrolyte (LE) 1.0 M LiPF6 EC/DMC (v/v = 50/50) at their interfaces. Galvanostatic experiments for the cell Li/IL/SSE/IL/Li showed an overpotential of only 21 mV after 9 days cycling (48 h at 25 μA cm−2 and 168 h at 50 μA cm−2), and the battery Li/LE/SSE/SSE + TiS2 retained 83% of its capacity shown in the first cycle at 0.4C after 50 cycles. LiB11H14·2H2O and 1.0 M LiPF6 EC/DMC work effectively as wetting agents to improve SSE/Li contact.
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institution Curtin University Malaysia
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publishDate 2022
publisher ROYAL SOC CHEMISTRY
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spelling curtin-20.500.11937-970112025-02-28T05:58:49Z Hydrated lithium nido-boranes for solid-liquid hybrid batteries Souza, Diego H.P. Humphries, Terry D. Liu, Yu Gradišek, A. D'Angelo, A.M. Buckley, Craig E. Paskevicius, Mark Science & Technology Physical Sciences Technology Chemistry, Physical Energy & Fuels Materials Science, Multidisciplinary Chemistry Materials Science LI-ION CONDUCTIVITY STATE LI VIBRATIONAL SPECTROSCOPY HIGH-PRESSURE ELECTROLYTE STABILITY LI7LA3ZR2O12 COMBINATION PERFORMANCE GENERATION Hydridoborate salts are considered as promising solid-state electrolyte candidates for the development of solid-state batteries (SSBs). The presence of coordinated water in the crystal structure may facilitate the migration of the cation, yielding compounds with high ionic conductivity. In the present study, two samples of hydrated LiB11H14, here called LiB11H14·2H2O and a-LiB11H14·(H2O)n (n < 2), demonstrate remarkably different properties as solid-state electrolytes. LiB11H14·2H2O is identified as a new class of ionic liquid, as it melts at ≈70 °C, whereas the sample a-LiB11H14·(H2O)n undergoes a polymorphic phase transition close to this temperature, reaching the liquid-like ionic conductivity of 3.2 × 10−2 S cm−1 at 70 °C and an oxidative stability limit of 2.8 V against Li+/Li. Galvanostatic cycling and battery tests were conducted with a-LiB11H14·(H2O)n as the solid-state electrolyte (SSE) at 60 °C with the addition of traces of either the ionic liquid (IL) LiB11H14·2H2O or the liquid electrolyte (LE) 1.0 M LiPF6 EC/DMC (v/v = 50/50) at their interfaces. Galvanostatic experiments for the cell Li/IL/SSE/IL/Li showed an overpotential of only 21 mV after 9 days cycling (48 h at 25 μA cm−2 and 168 h at 50 μA cm−2), and the battery Li/LE/SSE/SSE + TiS2 retained 83% of its capacity shown in the first cycle at 0.4C after 50 cycles. LiB11H14·2H2O and 1.0 M LiPF6 EC/DMC work effectively as wetting agents to improve SSE/Li contact. 2022 Journal Article http://hdl.handle.net/20.500.11937/97011 10.1039/d2se00843b English http://purl.org/au-research/grants/arc/LE170100199 ROYAL SOC CHEMISTRY fulltext
spellingShingle Science & Technology
Physical Sciences
Technology
Chemistry, Physical
Energy & Fuels
Materials Science, Multidisciplinary
Chemistry
Materials Science
LI-ION CONDUCTIVITY
STATE LI
VIBRATIONAL SPECTROSCOPY
HIGH-PRESSURE
ELECTROLYTE
STABILITY
LI7LA3ZR2O12
COMBINATION
PERFORMANCE
GENERATION
Souza, Diego H.P.
Humphries, Terry D.
Liu, Yu
Gradišek, A.
D'Angelo, A.M.
Buckley, Craig E.
Paskevicius, Mark
Hydrated lithium nido-boranes for solid-liquid hybrid batteries
title Hydrated lithium nido-boranes for solid-liquid hybrid batteries
title_full Hydrated lithium nido-boranes for solid-liquid hybrid batteries
title_fullStr Hydrated lithium nido-boranes for solid-liquid hybrid batteries
title_full_unstemmed Hydrated lithium nido-boranes for solid-liquid hybrid batteries
title_short Hydrated lithium nido-boranes for solid-liquid hybrid batteries
title_sort hydrated lithium nido-boranes for solid-liquid hybrid batteries
topic Science & Technology
Physical Sciences
Technology
Chemistry, Physical
Energy & Fuels
Materials Science, Multidisciplinary
Chemistry
Materials Science
LI-ION CONDUCTIVITY
STATE LI
VIBRATIONAL SPECTROSCOPY
HIGH-PRESSURE
ELECTROLYTE
STABILITY
LI7LA3ZR2O12
COMBINATION
PERFORMANCE
GENERATION
url http://purl.org/au-research/grants/arc/LE170100199
http://hdl.handle.net/20.500.11937/97011