scholarly journals Synthesis of Aromatic and Aliphatic N-Heterocyclic Salts and Their Application as Organic Electrolyte Supporters in Electrochemical Capacitor

2021 ◽  
Vol 11 (19) ◽  
pp. 8824
Author(s):  
Young-Ji Kim ◽  
Jaeyeong Choi ◽  
Soo-Yeoun Kim ◽  
Seong-Ho Choi

Aromatic and aliphatic N-heterocyclic chemical salts were synthesized by counter-anion-exchange reactions after substitution reactions in order to apply them as organic electrolyte supporters in an electrochemical capacitor (super capacitor). The aromatic N-heterocyclic salts were N-methylpyridinium tetrafluoroborate ([MPy]+[BF4]−), N-methylpyridinium hexafluorophosphate ([MPy]+[PF6]−), 1,3-dibuthylimidazolium tetrafluoroborate ([DI]+[BF4]−), 1,3-dibuthylimidazolium hexafluorophosphate ([DI]+[PF6]−), 1-buthyl-4-methyl-1,2,4-triazolium tetrafluoroborate ([BMTA]+[BF4]−), and 1-buthyl-4-methyl-1,2,4-triazolium hexafluorophosphate ([BMTA]+[PF6]−). The aliphatic N-heterocyclic salts were N,N-dimethylpiperilidium tetrafluoroborate ([DMP]+[BF4]−), N,N-dimethylpiperilidium hexafluorophosphate ([DMPy]+[PF6]−), N,N-dimethylpyrrolidium tetrafluoroborate ([DMPy]+[BF4]−) and N,N-dimethylpyrrolidium hexafluorophosphate ([DMPy]+[PF6]−), 1-ethyltriethamine tetrafluoroborate ([E-TEDA]+[BF4]−), and 1-ethyltriethamine hexafluorophosphate ([E-TEDA]+[PF6]−), respectively. We confirmed the successful synthesis of the aromatic and aliphatic N-heterocyclic chemical salts by 1H-NMR, FT-IR, and GC/MS analysis before conducting the counter-anion-exchange reactions. Then, we determined the electrochemical potential of vanadium acetylacetonate (V(acac)3) under acetonitrile in the presence of the N-heterocyclic chemical salts as energy-storage chemicals. By cyclic voltammetry, the maximum voltages with the N-heterocyclic chemical salts in acetonitrile reached 2.2 V under a fixed current value. Charge-discharge experiments were performed in the electrochemical capacitor with an anion-exchange membrane using a non-aqueous electrolyte prepared with a synthesized N-heterocyclic salt in acetonitrile.

Author(s):  
Lucie Zárybnická ◽  
Eliska Stranska

The present work deals with verification stability of the prepared anion-exchange membrane with surface modification in the time. The surface modification of a commercial ultrafiltration poly(ethersulfone) membrane was carried out graft polymerization. Poly(styrene-co-divinylbenzene-co-4-vinylbenzylchloride) surface layer was covalently attached onto commercial ultrafiltration support layer. The membrane was tested from the point of view of water content, ion-exchange capacity, specific resistance, permselectivity, FT-IR spectroscopy and SEM analysis. The tested characteristics (IEC, permselectivity, resistances, structure) of the prepared membrane were same after one year from preparation. The prepared membranes can find use in electrodialysis processes.


Molecules ◽  
2022 ◽  
Vol 27 (2) ◽  
pp. 364
Author(s):  
Prem P. Sharma ◽  
Yeeun Jeon ◽  
Dukjoon Kim

Alkaline stable anion exchange membranes based on the cross-linked poly(arylene ether sulfone) grafted with dual quaternary piperidine (XPAES-DP) units were synthesized. The chemical structure of the synthesized PAES-DP was validated using 1H-NMR and FT-IR spectroscopy. The physicochemical, thermal, and mechanical properties of XPAES-DP membranes were compared with those of two linear PAES based membranes grafted with single piperidine (PAES-P) unit and conventional trimethyl amine (PAES-TM). XPAES-DP membrane showed the ionic conductivity of 0.021 S cm−1 at 40 °C which was much higher than that of PAES-P and PAES-TM because of the possession of more quaternary ammonium groups in the cross-linked structure. This cross-linked structure of the XPAES-DP membrane resulted in a higher tensile strength of 18.11 MPa than that of PAES-P, 17.09 MPa. In addition, as the XPAES-DP membrane shows consistency in the ionic conductivity even after 96 h in 3 M KOH solution with a minor change, its chemical stability was assured for the application of anion exchange membrane fuel cell. The single-cell assembled with XPAES-DP membrane displayed a power density of 109 mWcm−2 at 80 °C under 100% relative humidity.


2000 ◽  
Vol 49 (4) ◽  
pp. 211-218
Author(s):  
F. Elhannouni ◽  
M. Belhadj ◽  
M. Taky ◽  
A. El Midaoui ◽  
L. Echihabi ◽  
...  

Author(s):  
Dongguo Li ◽  
Andrew R Motz ◽  
Chulsung Bae ◽  
Cy Fujimoto ◽  
Gaoqiang Yang ◽  
...  

Interest in the low-cost production of clean hydrogen is growing. Anion exchange membrane water electrolyzers (AEMWEs) are considered one of the most promising sustainable hydrogen production technologies because of their...


Processes ◽  
2021 ◽  
Vol 9 (4) ◽  
pp. 718
Author(s):  
Van Men Truong ◽  
Ngoc Bich Duong ◽  
Hsiharng Yang

Gas diffusion layers (GDLs) play a critical role in anion exchange membrane fuel cell (AEMFC) water management. In this work, the effect of GDL thickness on the cell performance of the AEMFC was experimentally investigated. Three GDLs with different thicknesses of 120, 260, and 310 µm (denoted as GDL-120, GDL-260, and GDL-310, respectively) were prepared and tested in a single H2/O2 AEMFC. The experimental results showed that the GDL-260 employed in both anode and cathode electrodes exhibited the best cell performance. There was a small difference in cell performance for GDL-260 and GDL-310, while water flooding was observed in the case of using GDL-120 operated at current densities greater than 1100 mA cm−2. In addition, it was found that the GDL thickness had more sensitivity to the AEMFC performance as used in the anode electrode rather than in the cathode electrode, indicating that water removal at the anode was more challenging than water supply at the cathode. The strategy of water management in the anode should be different from that in the cathode. These findings can provide a further understanding of the role of GDLs in the water management of AEMFCs.


2021 ◽  
Vol 624 ◽  
pp. 119088
Author(s):  
Lv Li ◽  
Jiaao Wang ◽  
Manzoor Hussain ◽  
Lingling Ma ◽  
Naeem Akhtar Qaisrani ◽  
...  

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