Room temperature cells with solid electrolytes

1980 ◽  
pp. 464-482
Author(s):  
T. Dickinson
Keyword(s):  
Solid Electrolytes ◽  
Room Temperature

Mechanosynthesis, Radiation-Thermal Modification and Characterization of Nanostructured Scandia Stabilized Zirconia Ceramics

2008 ◽  
Vol 1122 ◽  
Author(s):  
Vladimir V. Zyryanov ◽  
Nikolay F. Uvarov ◽  
Artem S. Ulihin ◽  
Vladislav A. Sadykov
Keyword(s):  
Solid Electrolytes ◽  
Room Temperature ◽  
Complex Impedance ◽  
Impedance Method ◽  
Sintering Aids ◽  
Zirconia Ceramics ◽  
Operation Temperature ◽  
Cubic Structure ◽  
Xrd Patterns

AbstractSSZ-based ceramics were obtained by sintering of nanopowders derived at room temperature by mechanochemical synthesis from refined technical grade ZrO2 nano-precursors. RT-treatment by 2.5 MeV electrons up to 1563 K was used for the modification of ceramics. Powders and ceramics were characterized by XRD, Raman, SEM and EDS, TEM, SIMS techniques. The phase composition of Zr0.89Sc0.1Ce0.01O1.95 ceramics was very close to cubic structure but better fitting of XRD patterns was obtained for rhombohedral lattice. Conductivity of solid electrolytes for IT SOFC was studied by complex impedance method. To stabilize cubic structure and increase conductivity at operation temperature of To ∼ 1000 K, the composition of SSZ solid electrolyte was optimized by addition of yttria and sintering aids. The interaction of admixtures with minor dopants leading to intergrain phase was revealed. During fast sintering, ceramics keep a memory about inhomogeneous disordered solid solutions in a form of nanostructuring. Conductivity data indicate nanostructuring of ceramics too: activation energies of bulk and grain boundary conductivities are close (Eb ∼ 0.9 eV, Egb ∼ 1.05 eV). Annealing of ceramics at high temperatures increases conductivity at To and promotes grain growth.

Room Temperature Solid Electrolytes for Li-S Solid-State Batteries

2021 ◽  
Vol MA2021-02 (1) ◽  
pp. 152-152
Author(s):  
John Chmiola ◽  
Zachary Favors ◽  
Fabio Albano
Keyword(s):  
Solid State ◽  
Solid Electrolytes ◽  
Room Temperature ◽  
Solid State Batteries

Polymer-in-salt solid electrolytes for lithium-ion batteries

2019 ◽  
Vol 12 (06) ◽  
pp. 1930006 ◽  
Author(s):  
Chengjun Yi ◽  
Wenyi Liu ◽  
Linpo Li ◽  
Haoyang Dong ◽  
Jinping Liu
Keyword(s):  
Ionic Conductivity ◽  
Lithium Ion Batteries ◽  
Smart Grids ◽  
Solid Electrolytes ◽  
Room Temperature ◽  
Lithium Salt ◽  
Lithium Ion ◽  
Solid Polymer Electrolytes ◽  
Solid Polymer ◽  
Polymer Lithium Ion Batteries

Solid-state polymer lithium-ion batteries with better safety and higher energy density are one of the most promising batteries, which are expected to power future electric vehicles and smart grids. However, the low ionic conductivity at room temperature of solid polymer electrolytes (SPEs) decelerates the entry of such batteries into the market. Creating polymer-in-salt solid electrolytes (PISSEs) where the lithium salt contents exceed 50[Formula: see text]wt.% is a viable technology to enhance ionic conductivity at room temperature of SPEs, which is also suitable for scalable production. In this review, we first clarify the structure and ionic conductivity mechanism of PISSEs by analyzing the interactions between lithium salt and polymer matrix. Then, the recent advances on polyacrylonitrile (PAN)-based PISSEs and polycarbonate derivative-based PISSEs will be reviewed. Finally, we propose possible directions and opportunities to accelerate the commercializing of PISSEs for solid polymer Li-ion batteries.

scholarly journals Room-Temperature Mg-Ion Conduction Through Molecular Crystal Mg{N(SO2CF3)2}2(CH3OC5H9)2

2021 ◽  
Vol 9 ◽  
Author(s):  
Takaaki Ota ◽  
Shota Uchiyama ◽  
Keiichi Tsukada ◽  
Makoto Moriya
Keyword(s):  
Crystal Structure ◽  
Solid State ◽  
Ionic Conductivity ◽  
Molecular Crystal ◽  
Solid Electrolytes ◽  
Room Temperature ◽  
Molecular Crystals ◽  
Transference Number ◽  
Ion Conducting ◽  
State Ionic

Molecular crystals have attracted increasing attention as a candidate for innovative solid electrolytes with solid-state Mg-ion conductivity. In this work, we synthesized a novel Mg-ion-conducting molecular crystal, Mg{N(SO2CF3)2}2(CH3OC5H9)2 (Mg(TFSA)2(CPME)2), composed of Mg bis(trifluoromethanesulfonyl)amide (Mg(TFSA)2) and cyclopentyl methyl ether (CPME) and elucidated its crystal structure. We found that the obtained Mg(TFSA)2(CPME)2 exhibits solid-state ionic conductivity at room temperature and a high Mg-ion transference number of 0.74. Contrastingly, most Mg-conductive inorganic solid electrolytes require heating above 150–300°C to exhibit ionic conductivity. These results further prove the suitability of molecular crystals as candidates for Mg-ion-conducting solid electrolytes.

scholarly journals Blend Hybrid Solid Electrolytes Based on LiTFSI Doped Silica-Polyethylene Oxide for Lithium-Ion Batteries

Membranes ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 109 ◽  
Author(s):  
Jadra Mosa ◽  
Jonh Fredy Vélez ◽  
Mario Aparicio
Keyword(s):  
Ionic Conductivity ◽  
Solid Electrolytes ◽  
Room Temperature ◽  
Sol Gel ◽  
Lithium Ion ◽  
Hybrid Structure ◽  
Hybrid Network ◽  
Li Ion Batteries ◽  
Li Ion ◽  
Sol Gel Synthesis

Organic/inorganic hybrid membranes that are based on GTT (GPTMS-TMES-TPTE) system while using 3-Glycidoxypropyl-trimethoxysilane (GPTMS), Trimethyletoxisilane (TMES), and Trimethylolpropane triglycidyl ether (TPTE) as precursors have been obtained while using a combination of organic polymerization and sol-gel synthesis to be used as electrolytes in Li-ion batteries. Self-supported materials and thin-films solid hybrid electrolytes that were doped with Lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) were prepared. The hybrid network is based on highly cross-linked structures with high ionic conductivity. The dependency of the crosslinked hybrid structure and polymerization grade on ionic conductivity is studied. Ionic conductivity depends on triepoxy precursor (TPTE) and the accessibility of Li ions in the organic network, reaching a maximum ionic conductivity of 1.3 × 10−4 and 1.4 × 10−3 S cm−1 at room temperature and 60 °C, respectively. A wide electrochemical stability window in the range of 1.5–5 V facilitates its use as solid electrolytes in next-generation of Li-ion batteries.

scholarly journals CO2-sourced polycarbonates as solid electrolytes for room temperature operating lithium batteries

2019 ◽  
Vol 7 (16) ◽  
pp. 9844-9853 ◽  
Author(s):  
Farid Ouhib ◽  
Leire Meabe ◽  
Abdelfattah Mahmoud ◽  
Nicolas Eshraghi ◽  
Bruno Grignard ◽  
...  
Keyword(s):  
Solid Electrolyte ◽  
Lithium Batteries ◽  
Solid Electrolytes ◽  
Room Temperature ◽  
Electrolyte Membrane ◽  
Temperature Operating

A CO2-sourced self-standing solid electrolyte membrane is prepared and evaluated for room temperature operating lithium batteries.

scholarly journals Effect of Sintering Process on Ionic Conductivity of Li7-xLa3Zr2-xNbxO12 (x = 0, 0.2, 0.4, 0.6) Solid Electrolytes

Materials ◽  
2021 ◽  
Vol 14 (7) ◽  
pp. 1671
Author(s):  
Lei Ni ◽  
Zhigang Wu ◽  
Chuyi Zhang
Keyword(s):  
Ionic Conductivity ◽  
Solid Electrolytes ◽  
High Performance ◽  
Room Temperature ◽  
Process Conditions ◽  
Sintering Process ◽  
Preparation Time ◽  
Conventional Solid State Reaction ◽  
Good Crystallinity ◽  
The Relationship

Garnet-type Li7La3Zr2O12 (LLZO) is considered as a promising solid electrolyte. Nb-doped LLZO ceramics exhibit significantly improved ion conductivity. However, how to prepare the Nb-doped LLZO ceramics in a simple and economical way, meanwhile to investigate the relationship between process conditions and properties in Li7-xLa3Zr2-xNbxO12 ceramics, is particularly important. In this study, Li7-xLa3Zr2-xNbxO12 (LLZNxO, x = 0, 0.2, 0.4, 0.6) ceramics were prepared by conventional solid-state reaction. The effect of sintering process on the structure, microstructure, and ionic conductivity of LLZNxO (x = 0, 0.2, 0.4, 0.6) ceramics was investigated. Due to the more contractive Nb-O bonds in LLZNxO ceramics, the cubic structures are much easier to form and stabilize, which could induce the decreased preparation time. High-performance garnet LLZNxO ceramics can be obtained by optimizing the sintering process with lower calcining temperature and shorter holding time. The garnet samples with x = 0.4 calcined at 850 °C for 10 h and sintered at 1250 °C for 4 h exhibit the highest ionic conductivity of 3.86 × 10−4 S·cm−1 at room temperature and an activation energy of 0.32 eV, which can be correlated to the highest relative density of 96.1%, and good crystallinity of the grains.

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