Electrochemical Analysis of Lithium-Ion Transfer Reaction through the Interface between Ceramic Electrolyte and Ionic Liquids

2012 ◽  
Vol 159 (11) ◽  
pp. A1766-A1769 ◽  
Author(s):  
Fumihiro Sagane ◽  
Takeshi Abe ◽  
Zempachi Ogumi
Author(s):  
Yasuyuki Kondo ◽  
Tomokazu Fukutsuka ◽  
Yuko Yokoyama ◽  
Yuto Miyahara ◽  
Kohei Miyazaki ◽  
...  

AbstractGraphitic materials cannot be applied for the negative electrode of sodium-ion battery because the reversible capacities of graphite are anomalously small. To promote electrochemical sodium-ion intercalation into graphitic materials, the interfacial sodium-ion transfer reaction at the interface between graphitized carbon nanosphere (GCNS) electrode and organic electrolyte solutions was investigated. The interfacial lithium-ion transfer reaction was also evaluated for the comparison to the sodium-ion transfer. From the cyclic voltammograms, both lithium-ion and sodium-ion can reversibly intercalate into/from GCNS in all of the electrolytes used here. In the Nyquist plots, the semi-circles at the high frequency region derived from the Solid Electrolyte Interphase (SEI) resistance and the semi-circles at the middle frequency region owing to the charge-transfer resistance appeared. The activation energies of both lithium-ion and sodium-ion transfer resistances were measured. The values of activation energies of the interfacial lithium-ion transfer suggested that the interfacial lithium-ion transfer was influenced by the interaction between lithium-ion and solvents, anions or SEI. The activation energies of the interfacial sodium-ion transfer were larger than the expected values of interfacial sodium-ion transfer based on the week Lewis acidity of sodium-ion. In addition, the activation energies of interfacial sodium-ion transfer in dilute FEC-based electrolytes were smaller than those in concentrated electrolytes. The activation energies of the interfacial lithium/sodium-ion transfer of CNS-1100 in FEC-based electrolyte solutions were almost the same as those of CNS-2900, indicating that the mechanism of interfacial charge-transfer reaction seemed to be the same for highly graphitized materials and low-graphitized materials each other. Graphic abstract


2011 ◽  
Vol 115 (26) ◽  
pp. 12990-12994 ◽  
Author(s):  
Toyoki Okumura ◽  
Tomokazu Fukutsuka ◽  
Keisuke Matsumoto ◽  
Yuki Orikasa ◽  
Hajime Arai ◽  
...  

2014 ◽  
Vol 161 (14) ◽  
pp. A1939-A1942 ◽  
Author(s):  
Yuya Ishihara ◽  
Kohei Miyazaki ◽  
Tomokazu Fukutsuka ◽  
Takeshi Abe

ACS Omega ◽  
2021 ◽  
Author(s):  
Yasuyuki Kondo ◽  
Tomokazu Fukutsuka ◽  
Yuko Yokoyama ◽  
Yuto Miyahara ◽  
Kohei Miyazaki ◽  
...  

Membranes ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 359
Author(s):  
László Koók ◽  
Piroska Lajtai-Szabó ◽  
Péter Bakonyi ◽  
Katalin Bélafi-Bakó ◽  
Nándor Nemestóthy

Hydrophobic ionic liquids (IL) may offer a special electrolyte in the form of supported ionic liquid membranes (SILM) for microbial fuel cells (MFC) due to their advantageous mass transfer characteristics. In this work, the proton and ion transfer properties of SILMs made with IL containing imidazolium cation and [PF6]− and [NTf2]− anions were studied and compared to Nafion. It resulted that both ILs show better proton mass transfer and diffusion coefficient than Nafion. The data implied the presence of water microclusters permeating through [hmim][PF6]-SILM to assist the proton transfer. This mechanism could not be assumed in the case of [NTf2]− containing IL. Ion transport numbers of K+, Na+, and H+ showed that the IL with [PF6]− anion could be beneficial in terms of reducing ion transfer losses in MFCs. Moreover, the conductivity of [bmim][PF6]-SILM at low electrolyte concentration (such as in MFCs) was comparable to Nafion.


Carbon ◽  
2021 ◽  
Vol 176 ◽  
pp. 655
Author(s):  
Tomokazu Fukutsuka ◽  
Yuto Miyahara ◽  
Kohei Miyazaki ◽  
Takeshi Abe

2004 ◽  
Vol 151 (11) ◽  
pp. A1950 ◽  
Author(s):  
Takeshi Abe ◽  
Masahiro Ohtsuka ◽  
Fumihiro Sagane ◽  
Yasutoshi Iriyama ◽  
Zempachi Ogumi

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