Proton transport in choline dihydrogen phosphate/H3PO4 mixtures

Literature Information

Publication Date 2010-08-02
DOI 10.1039/C0CP00156B
Impact Factor 3.676
Authors

Usman Ali Rana, Paul M. Bayley, R. Vijayaraghavan, Douglas R. MacFarlane, Maria Forsyth


View Original

Abstract

Mixtures of the plastic crystal material choline dihydrogen phosphate [Choline][DHP] and phosphoric acid, from 4.5 mol% to 18 mol% H3PO4, were investigated and shown to have significantly higher proton conductivity compared to the pure [Choline][DHP]. This was particularly evident from the electrochemical hydrogen reduction reaction and the proton NMR diffusion measurements, in addition to ionic conductivity measured from the impedance spectroscopy. The ionic conductivity was observed to increase by more than an order of magnitude in phase I (i.e. the highest temperature solid phase in [Choline][DHP]) reaching up to 10−2 S cm−1. The multinuclear NMR spectroscopy data suggest that, at least on the timescale of the NMR measurement, the H+ cations and [DHP] anions are equivalent in both phases. The pulsed field gradient NMR diffusion measurements of the 18 mol% acid sample indicate that all three ions are mobile, however the H+ diffusion coefficient is an order of magnitude higher than for the [Choline] cation or the [DHP] anion, and therefore conduction in these materials is dominated by proton conductivity. The thermal stability, as measured by TGA, is unaffected with increasing acid additions and remains high; i.e. no significant mass loss below 200 °C.

Related Literature

Mapping spatially inhomogeneous electrochemical reactions in battery electrodes using high energy X-rays

Olaf J. Borkiewicz, Karena W. Chapman, Peter J. Chupas

2013-04-16 Communication

DOI: 10.1039/C3CP50590A

Influence of the Ce–Zr promoter on Pd behaviour under dynamic CO/NO cycling conditions: a structural and chemical approach

Anna Kubacka, Ana Iglesias-Juez, M. Di Michiel, Mark A. Newton, Marcos Fernández-García

2013-03-18 Paper

DOI: 10.1039/C3CP44293D

Elucidation of structure and nature of the PdO–Pd transformation using in situ PDF and XAS techniques

Jonathan Keating, Gopinathan Sankar, Timothy I. Hyde, Shinji Kohara, Koji Ohara

2013-04-26 Paper

DOI: 10.1039/C3CP50600B

Model of the photoexcitation processes of a two-level molecule coherently coupled to an optical antenna

Masatoshi Nakatani, Atsushi Nobuhiro, Nobuhiko Yokoshi, Hajime Ishihara

2013-03-18 Paper

DOI: 10.1039/C3CP43834A

An ab initio investigation of Li2M0.5N0.5SiO4 (M, N = Mn, Fe, Co Ni) as Li-ion battery cathode materials

Sirous Asgari, Doretta Capsoni, Piercarlo Mustarelli

2013-04-23 Communication

DOI: 10.1039/C3CP51481A

Back cover

Cover

DOI: 10.1039/C3CP90065G

A physicochemical mechanism of chemical gas sensors using an AC analysis

Jaehyun Moon, Jin-Ah Park, Su-Jae Lee, Jeong-Ik Lee, Taehyong Zyung, Eui-Chol Shin, Jong-Sook Lee

2013-04-16 Paper

DOI: 10.1039/C3CP44684K

Ultrafast spectroscopy of linear carbon chains: the case of dinaphthylpolyynes

D. Fazzi, A. Milani, D. Brida, C. Manzoni, E. Cinquanta, M. Devetta, L. Ravagnan, P. Milani, F. Cataldo, L. Lüer, R. Wannemacher, J. Cabanillas-Gonzalez, M. Negro, S. Stagira, C. Vozzi

2013-04-19 Paper

DOI: 10.1039/C3CP50508A

Photoinduced electron transfer of platinum(ii) bipyridine diacetylides linked by triphenylamine- and naphthaleneimide-derivatives and their application to photoelectric conversion systems

Yuma Matsumoto, Mai Tsubamoto, Ryoji Sugimura, Masatoshi Kozaki, Kenshi Kimoto, Munetaka Iwamura, Koichi Nozaki, Naoki Senju, Chiasa Uragami, Yohei Muramatsu, Akinori Konno

2013-02-28 Paper

DOI: 10.1039/C3CP50182E

New Li2FeSiO4–carbon monoliths with controlled macropores: effects of pore properties on electrode performance

George Hasegawa, Mai Sannohe, Yuya Ishihara, Kazuyoshi Kanamori, Kazuki Nakanishi, Takeshi Abe

2013-04-09 Paper

DOI: 10.1039/C3CP50352F

You might also like

Compound Q&A

What precautions should be taken when handling 2-Chloro-1,2-bis(4-methylphenyl)ethanone (CAS: 71193-32-3)?

When handling 2-Chloro-1,2-bis(4-methylphenyl)ethanone (CAS: 71193-32-3), it is ...

71193-32-32-Chloro-1,2-bis(4-m...
Compound Q&A

What industries use 4-Ethoxy-3-(5-methyl-4-oxo-7-propyl-1,4-dihydroimidazo[5,1-f][1,2,4]triazin-2-yl)benzenesulfonyl chloride (CAS: 224789-26-8)?

4-Ethoxy-3-(5-methyl-4-oxo-7-propyl-1,4-dihydroimidazo[5,1-f][1,2,4]triazin-2-yl...

224789-26-84-Ethoxy-3-(5-methyl...
Compound Q&A

How should Methyl 3-Oxo-4-Androsten-17-Carboxylate (CAS: 2681-55-2) be stored?

Methyl 3-Oxo-4-Androsten-17-Carboxylate (CAS: 2681-55-2) should be stored in a c...

2681-55-2Methyl 3-Oxo-4-Andro...
Compound Q&A

What are the main uses of (R)-3-Amino-4-(3-hexylphenylamino)-4-oxobutylphosphonic acid (CAS: 909725-61-7)?

(R)-3-Amino-4-(3-hexylphenylamino)-4-oxobutylphosphonic acid is primarily used i...

909725-61-7(R)-3-Amino-4-(3-hex...
Compound Q&A

What regulatory guidelines apply to 2-Methyl-2-propanyl 3-amino-3-carbamoyl-1-azetidinecarboxylate (CAS: 1254120-14-3)?

2-Methyl-2-propanyl 3-amino-3-carbamoyl-1-azetidinecarboxylate (CAS: 1254120-14-...

1254120-14-32-Methyl-2-propanyl ...
Compound Q&A

Are there alternatives to (E)-4-(tert-Butoxy)-4-oxobut-2-enoic acid (CAS: 135355-96-3) in synthesis?

There are alternative reagents that can be used in synthesis instead of (E)-4-(t...

135355-96-3(E)-4-(tert-Butoxy)-...
Compound Q&A

What are the physical and chemical properties of [2-(3-Chlorophenyl)-1,3-thiazol-4-yl]methanol (CAS: 121202-20-8)?

[2-(3-Chlorophenyl)-1,3-thiazol-4-yl]methanol (CAS: 121202-20-8) is a crystallin...

121202-20-8[2-(3-Chlorophenyl)-...
166249-17-8Methyl (2S)-[(4S)-2,...
Compound Q&A

What is the market or research trend for 1-Bromo-2-isocyanatoethane (CAS: 42865-19-0)?

The market for 1-Bromo-2-isocyanatoethane (CAS: 42865-19-0) is driven by its use...

42865-19-01-Bromo-2-isocyanato...
Compound Q&A

What are the main uses of 4-Nitro-D-phenylalanine hydrochloride (CAS: 147065-06-3)?

4-Nitro-D-phenylalanine hydrochloride (CAS: 147065-06-3) is primarily used in re...

147065-06-34-Nitro-D-phenylalan...

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.