Electrochemical Properties of Lithium Titanate Synthesized by Reassembly of Nanosheets

2007 ◽  
Vol 350 ◽  
pp. 139-142 ◽  
Author(s):  
Keigo Sato ◽  
Shinya Suzuki ◽  
Masaru Miyayama

The electrochemical properties of titanate nanosheets and layer-structured lithium titanate obtained by restacking of titanate nanosheets were investigated in comparison with those of layer-structured lithium titanate obtained by ion-exchange. Restacked lithium titanate was synthesized by reassembling titanate nanosheets with LiOH aqueous solution. The nanosheets were 50-200 nm wide and 1.7 nm thick. The crystal structure inside the nanosheets was the same as that the of parent material. The oxidation current peaks observed in cyclic voltammograms of titanate nanosheets and restacked material were 1.6 V (Li/Li+), which was lower than that of ion-exchanged material by 0.3 V. The discharge capacity of restacked material was 96 mAh g-1, indicating that 32% of the titanium ions were reduced.

2012 ◽  
Vol 608-609 ◽  
pp. 894-897
Author(s):  
Hai Tao Wang ◽  
Zhen Jin ◽  
Yu Chun Qin

Three kinds of ions (I-、Fe2+and MnO4-) were appended into the methanol aqueous solution respectively as an additive and the Cyclic voltammograms of the aqueous solutions were studied. The results showed that Fe2+had obvious promotion effect for electro-oxidation of methanol and could improve the methanol anodic oxidation current by 85 percent. The promotion effect of the thulium Ions were related with the electronic distribution of these elements and their adsorption on the Pt electrode surface. I-and MnO4-could facilitate the electro-oxidation of methanol at different extent.


2015 ◽  
Vol 60 (2) ◽  
pp. 941-944 ◽  
Author(s):  
M. Matsunami ◽  
T. Hashizume ◽  
A. Saiki

Abstract Na+ or K+ ion rechargeable battery is started to garner attention recently in Place of Li+ ion cell. It is important that A+ site ion can move in and out the positive-electrode materials. When K2Ta2O6 powder had a pyrochlore structure was only dipped into NaOH aqueous solution at room temperature, Na2Ta2O6 was obtained. K2Ta2O6 was fabricated from a tantalum sheet by a hydrothermal synthesize with KOH aqueous solution. When Na2Ta2O6 was dipped into KOH aqueous solution, K2Ta2O6 was obtained again. If KTaO3 had a perovskite structure was dipped, Ion-exchange was not observed by XRD. Because a lattice constant of pyrochlore structure of K-Ta-O system is bigger than perovskite, K+ or Na+ ion could shinny through and exchange between Ta5+ and O2− ion site in a pyrochlore structure. K+ or Na+ ion exchange of A2Ta2O6 pyrochlore had reversibility. Therefore, A2Ta2O6 had a pyrochlore structure can be expected such as Na+ ion rechargeable battery element.


2011 ◽  
Vol 23 (9) ◽  
pp. 2344-2352 ◽  
Author(s):  
Kunimitsu Kataoka ◽  
Junji Awaka ◽  
Norihito Kijima ◽  
Hiroshi Hayakawa ◽  
Ken-ichi Ohshima ◽  
...  

ChemInform ◽  
2011 ◽  
Vol 42 (27) ◽  
pp. no-no
Author(s):  
Kunimitsu Kataoka ◽  
Junji Awaka ◽  
Norihito Kijima ◽  
Hiroshi Hayakawa ◽  
Ken-ichi Ohshima ◽  
...  

2012 ◽  
Vol 519 ◽  
pp. 124-127 ◽  
Author(s):  
Ji Zhao Zou ◽  
Qian Gang Fu ◽  
Xie Rong Zeng ◽  
Fei Deng ◽  
Ye Yan

LiMn1-xFexPO4 cathode materials were synthesized by microwave hydrothermal using ascorbic acid as reducing agent. The crystal structure, microstructure, electrochemical properties were characterized by XRD and SEM, the discharge capacity and cycling performance were compared. The results show that the lattice parameters of LiMnPO4 decreased by doping Fe, and the doping amount is x = 0.4, the discharge capacity of the prepared material reaches to 145 mAh/g, which has improved of 76.8% compared with the undoped LiMnPO4 at 0.1C.


1993 ◽  
Vol 48 (4) ◽  
pp. 418-424 ◽  
Author(s):  
Emerich Eichhorn ◽  
Anton Rieker ◽  
Bernd Speiser ◽  
Jürgen Sieglen ◽  
Joachim Strähle

N,N′-Bis(salicylidene)ethylenediaminatocobalt(III) hydroxide is treated with chloroform in methanol to yield the corresponding chloride in pure, crystalline form. Results of the crystal structure determination compare well with those in earlier reports of dimeric [Co(salen)Cl]2 units and incorporated CHCl3 molecules. Electrochemical experiments in DMF and pyridine show that the chloride fully dissociates in these donor solvents. Thus, the quasireversible oneelectron reduction to Co(salen) is observed in cyclic voltammograms.


2020 ◽  
Vol 16 ◽  
Author(s):  
Reda M. El-Shishtawy ◽  
Abdullah M. Asiri ◽  
Nahed S. E. Ahmed

Background: Color effluents generated from the production industry of dyes and pigments and their use in different applications such as textile, paper, leather tanning, and food industries, are high in color and contaminants that damage the aquatic life. It is estimated that about 105 of various commercial dyes and pigments amounted to 7×105 tons are produced annually worldwide. Ultimately, about 10–15% is wasted into the effluents of the textile industry. Chitin is abundant in nature, and it is a linear biopolymer containing acetamido and hydroxyl groups amenable to render it atmospheric by introducing amino and carboxyl groups, hence able to remove different classes of toxic organic dyes from colored effluents. Methods: Chitin was chemically modified to render it amphoteric via the introduction of carboxyl and amino groups. The amphoteric chitin has been fully characterized by FTIR, TGA-DTG, elemental analysis, SEM, and point of zero charge. Adsorption optimization for both anionic and cationic dyes was made by batch adsorption method, and the conditions obtained were used for studying the kinetics and thermodynamics of adsorption. Results: The results of dye removal proved that the adsorbent was proven effective in removing both anionic and cationic dyes (Acid Red 1 and methylene blue (MB)), at their respective optimum pHs (2 for acid and 8 for cationic dye). The equilibrium isotherm at room temperature fitted the Freundlich model for MB, and the maximum adsorption capacity was 98.2 mg/g using 50 mg/l of MB, whereas the equilibrium isotherm fitted the Freundlich and Langmuir model for AR1 and the maximum adsorption capacity was 128.2 mg/g. Kinetic results indicate that the adsorption is a two-step diffusion process for both dyes as indicated by the values of the initial adsorption factor (Ri) and follows the pseudo-second-order kinetics. Also, thermodynamic calculations suggest that the adsorption of AR1 on the amphoteric chitin is an endothermic process from 294 to 303 K. The result indicated that the mechanism of adsorption is chemisorption via an ion-exchange process. Also, recycling of the adsorbent was easy, and its reuse for dye removal was effective. Conclusion: New amphoteric chitin has been successfully synthesized and characterized. This resin material, which contains amino and carboxyl groups, is novel as such chemical modification of chitin hasn’t been reported. The amphoteric chitin has proven effective in decolorizing aqueous solution from anionic and cationic dyes. The adsorption behavior of amphoteric chitin is believed to follow chemical adsorption with an ion-exchange process. The recycling process for few cycles indicated that the loaded adsorbent could be regenerated by simple treatment and retested for removing anionic and cationic dyes without any loss in the adsorbability. Therefore, the study introduces a new and easy approach for the development of amphoteric adsorbent for application in the removal of different dyes from aqueous solutions.


CrystEngComm ◽  
2021 ◽  
Author(s):  
Anna A Mukhacheva ◽  
Vladislav Komarov ◽  
Vasily Kokovkin ◽  
Alexander S. Novikov ◽  
Pavel A Abramov ◽  
...  

The [{(C6H6)Ru}2W8O30(OH)2]6– hybrid (organometallic-POM) anion was used as a pH-tunable building block to create special conditions for realizing π-π interactions in the crystal structure. Changing pH of aqueous solution of...


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