Identification of electrochemical reaction products in lithium–oxygen cells with 7Li nutation spectroscopy

2015 ◽  
Vol 93 (9) ◽  
pp. 976-982 ◽  
Author(s):  
Zoë E.M. Reeve ◽  
Gillian R. Goward ◽  
Alex D. Bain

In the Li–O2 battery system, it is has been shown to be challenging to differentiate the discharge products or determine the electrolyte stability with direct 7Li NMR. Defined 7Li quadrupole lineshapes are not observed for cycled cathodes. Here, 7Li nutation NMR is demonstrated to be an effective method for the identification of Li2O2 in cycled cathodes. The 7Li quadrupole interaction of Li2O2 (35 kHz) and Li2CO3 (120 kHz) are of similar magnitude to typically radiofrequency fields (ranging from 40 to 60 kHz). The 7Li nutation frequency will therefore be influenced by both interactions. The discharge products of the cycled cathodes were determined by comparing the 7Li nutation frequencies of the cycled cathodes to the 7Li nutation frequency of the pristine materials when the applied radiofrequency field was 30 kHz. Li2CO3 was determined to be the main discharge product in the propylene carbonate/dimethyl carbonate and trimethyl phosphate electrolyte systems, since the 7Li nutation frequencies of the cathodes corresponded to the 7Li nutation frequency of pristine Li2CO3. The 7Li nutation frequency of the tetraethylene glycol dimethyl ether cathode was between the 7Li nutation frequencies of both pristine Li2O2 and pristine Li2CO3, indicating that both Li2O2 and Li2CO3 were discharge products influencing the observed nutation frequency. From 7Li nutation NMR the novel trimethyl phosphate electrolyte was determined to be an unsuitable Li–O2 electrolyte, as the fast 7Li nutation frequency indicated that Li2O2 was not a primary discharge species. With 17O NMR, Li2CO3 was confirmed to be a main discharge product formed with the trimethyl phosphate electrolyte.

Detritus ◽  
2021 ◽  
pp. 107-112
Author(s):  
Oscar Sosa ◽  
Sylvie Valin ◽  
Sébastien Thiery ◽  
Sylvain Salvador

The present study investigates the thermochemical conversion of Solid Recovered Fuel (SRF), represented by selected “model materials”. A laboratory-scale induction heated device was specifically developed to achieve fast pyrolysis conditions close to those encountered in a fluidized bed reactor. The novel device can handle up to 5 grams of solid, allowing fast heating rates (near 70°C/s) and a homogeneous distribution of temperature all along the reactor. Pyrolysis tests of a SRF sample and four model materials (Polyethylene, Polyethylene Terephthalate, beech wood, cardboard) were performed at 800°C. The yield and composition of the produced gas for each sample were determined. Experimental results will help to elucidate the relation between the initial components of waste derived fuels and the obtained reaction products.


2014 ◽  
Vol 716-717 ◽  
pp. 94-97
Author(s):  
Yan Xue Li ◽  
Ming Chui Dong ◽  
Peng Cheng Zhao ◽  
Ying Duo Han

In operating of a flow battery, a certain flow rate should be maintained in order to guarantee its performance. But the pump consumed power may cause significant losses for the overall battery system. In this paper, a fresh electrical model is proposed for the novel single flow zinc-nickel battery. The model consists of both battery stack part and pump power part, which consequently not only predicts accurately the battery electrical output, but also estimates the pump consumed power at different electrolyte flow rate. Based on the validated model, the influence of pump power on flow battery’s system efficiency can be evaluated at different operating modes. At last, possible means to further improve the system efficiency of battery is discussed.


2015 ◽  
Vol 44 (3) ◽  
pp. 165-171 ◽  
Author(s):  
G.H. Elgemeie ◽  
K.A. Ahmed ◽  
E.A. Ahmed ◽  
M.H. Helal ◽  
D.M. Masoud

Purpose – The purpose of this paper is to synthesize some novel 2-amino-6,6-dimethyl-9-phenyl-3-(phenyldiazenyl)-6,7-dihydropyrazolo-[5,1-b]quinazolin-8(5H)-one derivatives by multi-component one-pot reaction using a microwave as a new tool for green chemistry. Design/methodology/approach – An equimolor from arylazopyrazole, 5,5-dimethyl-1,3-cyclohexanedione (dimedone) and benzaldehyde derivatives was dissolved in Dimethylformamide (DMF) to be irradiated in a microwave for 15 minutes; after completion of the reaction, as indicated by Thin layer chromatograph (TLC), the reaction mixture was poured into ice water, filtered and then crystallized with an appropriate solvent. Findings – The structure of the synthesized dyes was established and confirmed for the reaction products on the basis of their elemental analysis and spectral data (MS, IR and 1H-NMR). These prepared dyes were used to print polyester and polyamide fabrics using synthetic thickener in the printing paste for the silk screen technique. The synthesized dyes are superior in terms of yield, purity, color strength and fastness properties and will lead to valuable achievements for commercial production. Originality/value – An efficient method for synthesis of pyrazoloquinazolinone dyes was designed. The novel procedure features short reaction time, moderate yields and simple workup. The authors studied its application in printing polyester and polyamide fabrics.


2020 ◽  
Author(s):  
Arbresha Muriqi ◽  
Michael Nolan

Organic-inorganic hybrid materials are a unique class of materials with properties driven by the organic and inorganic components, making them useful for flexible devices. Molecular layer deposition (MLD) offers novel pathways for the fabrication of such hybrids by using inorganic metal precursors and the vast range of organic molecules with tunable properties. To investigate and understand the mechanism of growth a combination of theoretical and experimental data is needed. In this contribution, we present a first principles investigation of the molecular mechanism of the growth of hybrid organic−inorganic thin films of aluminium alkoxides, known as “alucones” grown by MLD. We explore the interactions between precursors by analyzing the MLD reaction products of the alumina surface terminated with Al(CH<sub>3</sub>) groups after the trimethyl aluminium pulse; this yields monomethyl-Al<sub>2</sub>O<sub>3</sub> (Al-CH<sub>3</sub>-Al<sub>2</sub>O<sub>3</sub>) and dimethyl- Al<sub>2</sub>O<sub>3</sub> (Al(CH<sub>3</sub>)<sub>2</sub>- Al<sub>2</sub>O<sub>3</sub>) terminated surfaces. The organic precursors are ethylene glycol (EG), diethylene glycol (DEG), triethylene glycol (TEG) and tetraethylene glycol (FEG). A detailed comparison with alucones grown with ethylene glycol (EG) and glycerol (GL) precursors is presented to assist the interpretation of experimental findings regarding the differences in the hybrid films grown by EG and GL. The results show that Al-O formation with release of methane is favorable for all precursors. EG and GL can lie flat and create so-called double reactions through the reaction of the two terminal hydroxyl groups with the surface fragments. This phenomenon removes active hydroxyl sites for EG. However, for GL the third hydroxyl group is available and growth can proceed. This analysis shows the origin of differences in thickness of alucones found for EG and GL.


2021 ◽  
Vol 9 (36) ◽  
pp. 20725-20736
Author(s):  
Hoai Van T. Nguyen ◽  
Junam Kim ◽  
Kyung-Koo Lee

The trimethyl phosphate-based electrolyte system can be considered as a promising candidate for high-voltage and intrinsically safe supercapacitors.


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