Physicochemical properties of pentaglyme–sodium bis(trifluoromethanesulfonyl)amide solvate ionic liquid

Literature Information

Publication Date 2014-04-25
DOI 10.1039/C4CP00746H
Impact Factor 3.676
Authors

Shoshi Terada, Toshihiko Mandai, Risa Nozawa, Kazuki Yoshida, Kazuhide Ueno, Seiji Tsuzuki, Masayoshi Watanabe


View Original

Abstract

The physicochemical properties of pentaglyme (G5) and sodium bis(trifluoromethanesulfonyl)amide (Na[TFSA]) binary mixtures were investigated with respect to salt concentration and temperature. The density, viscosity, ionic conductivity, self-diffusion coefficient, and oxidative stability of a series of binary mixtures were measured, and the mixtures were examined as electrolytes for Na secondary batteries. An equimolar mixture of G5 and Na[TFSA] formed a low melting solvate, [Na(G5)1][TFSA], which exhibited an ionic conductivity of 0.61 mS cm−1 at 30 °C. The ionicity (Λimp/Λideal) of the glyme–Na[TFSA] mixture was estimated from the molar conductivity of electrochemical impedance measurements (Λimp) and the Walden plot (Λideal). [Na(G5)1][TFSA] possessed a high ionicity of 0.63 at 30 °C, suggesting that [Na(G5)1][TFSA] is highly dissociated into a [Na(G5)1]+ cation and a [TFSA]− anion, regardless of the extreme salt concentration in the liquid. The oxidative stabilities of G5–Na[TFSA] mixtures were investigated by linear sweep voltammetry, and the higher concentration resulted in higher oxidative stability due to the lowering of the HOMO energy level of G5 by complexation with the Na+ ion. In addition, battery tests were performed using the mixtures as electrolytes. The [Na|[Na(G5)1][TFSA]|Na0.44MnO2] cell showed good charge–discharge cycle stability, with a discharge capacity of ca. 100 mA h g−1, while the [Na(G5)1.25][TFSA] system, containing excess G5, showed poor stability.

Related Literature

Donor–acceptor nanoensembles of soluble carbon nanotubes

G. N. A. Rahman, Jeff Ramey, Massimo Marcaccio, Demis Paolucci, Francesco Paolucci, Shuhui Qin, Warren T. Ford, Domenico Balbinot, Norbert Jux, Nikos Tagmatarchis, Maurizio Prato

2004-08-10 Communication

DOI: 10.1039/B406933A

Metal-chelating nanoparticles as selective fluorescent sensor for Cu2+

Rachel Méallet-Renault, Robert Pansu, Sonia Amigoni-Gerbier, Chantal Larpent

2004-09-07 Communication

DOI: 10.1039/B407766K

Photochemical polymerization of thiophene derivatives in aqueous solution

Sergey A. Piletsky, Elena V. Piletska, Kal Karim, Frank Davis, Seamus P. J. Higson, Anthony P. F. Turner

2004-08-20 Communication

DOI: 10.1039/B408387C

The surprisingly beneficial effect of soft donors on the performance of early transition metal olefin polymerisation catalysts

Daniel C. H. Oakes, Brian S. Kimberley, Vernon C. Gibson, David J. Jones, Andrew J. P. White, David J. Williams

2004-08-23 Communication

DOI: 10.1039/B409870F

Oligomer preparation from hexane by radical polyaddition with bis(α-trifluoromethyl-β,β-difluorovinyl) terephthalate

Tadashi Narita, Hiroshi Hamana, Satoshi Hattori

2004-09-07 Communication

DOI: 10.1039/B406116K

Structurally diverse Rh(i) and Mn(i) complexes derived from the new ambidentate indeneligand, (1-{iPr2P(S)}-2-{NMe2})C9H6

Dominik Wechsler, Robert McDonald, Michael J. Ferguson, Mark Stradiotto

2004-09-21 Communication

DOI: 10.1039/B410328A

Fabrication and photoluminescence of chemically stable La2O3:Eu3+–La2Sn2O7 core–shell-structured nanoparticles

Eiji Hosono, Shinobu Fujihara

2004-08-13 Communication

DOI: 10.1039/B408495K

Molecular tectonics: design of luminescent H-bonded molecular networks

Sylvie Ferlay, Mir Wais Hosseini, Véronique Bulach, Jean-Marc Planeix

2004-09-07 Communication

DOI: 10.1039/B410459P

The anion sequence in the phase transformation of mesostructures templated by non-ionic block copolymers

Jiawei Tang, Chengzhong Yu, Xufeng Zhou, Xiaoxia Yan, Dongyuan Zhao

2004-08-25 Communication

DOI: 10.1039/B408100E

You might also like

Compound Q&A

What is the market or research trend for N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0)?

N-(4-Methoxybenzyl)-2-pyridinamine (CAS: 52818-63-0) is increasingly being used ...

52818-63-0N-(4-Methoxybenzyl)-...
Compound Q&A

What precautions should be taken when handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate (CAS: 1050507-06-6)?

When handling Ethyl 4-(2-chlorophenyl)-1,3-thiazole-2-carboxylate, appropriate p...

1050507-06-6Ethyl 4-(2-chlorophe...
Compound Q&A

What regulatory guidelines apply to diethyldiselane (CAS: 628-39-7)?

Diethyldiselane (CAS: 628-39-7) is classified under the Globally Harmonized Syst...

628-39-7Diethyldiselane
Compound Q&A

What is the market or research trend for oxocopper (CAS: 12053-18-8)?

The market for oxocopper (CAS: 12053-18-8) is primarily driven by its use in cat...

12053-18-8oxocopper; oxo-(oxoc...
Compound Q&A

What is the market or research trend for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-carboxylic acid?

The market for 5-{[(2-Methyl-2-propanyl)oxy]carbonyl}-5-azaspiro[2.4]heptane-7-c...

1268519-54-55-{[(2-Methyl-2-prop...
Compound Q&A

What is 2-(1-Pyrrolidinyl)-4-pyridinamine (CAS: 35981-63-6)?

2-(1-Pyrrolidinyl)-4-pyridinamine is a chemical compound with the CAS number 359...

35981-63-62-(1-Pyrrolidinyl)-4...
Compound Q&A

What are the physical and chemical properties of 2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1)?

2-(3-Pyridinyl)-1-azabicyclo[2.2.2]octane (CAS: 91556-75-1) is a crystalline sol...

91556-75-12-(3-Pyridinyl)-1-az...
Compound Q&A

How is (S)-Alpha-allyl-proline hydrochloride (CAS: 129704-91-2) typically synthesized?

(S)-Alpha-allyl-proline hydrochloride is usually synthesized via a Wittig reacti...

129704-91-2(S)-Alpha-allyl-prol...
Compound Q&A

What is 3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5)?

3-Methyl-1,2-oxazole-5-carboxylic acid (CAS: 4857-42-5) is an organic compound w...

4857-42-53-Methyl-1,2-oxazole...
Compound Q&A

How is Lys-SMCC-DM1 (CAS: 1281816-04-3) typically synthesized?

Lys-SMCC-DM1 is synthesized via a multi-step process involving the coupling of S...

1281816-04-3Lys-SMCC-DM1

Source Journal

Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
Self-citation Rate: 10.3%
Articles per Year: 3036

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.