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1.
Effect of nickel coating on electrochemical performance of graphite anodes for lithium ion batteries
Among the different materials often studied and proposed as negative electrodes for lithium-ion batteries, graphite anodes
are the most used in commercial batteries. For this study, synthetic graphite was tested. During the first discharge 0.2 Li
ions were consumed for the formation of the SEI film and the capacity reaches about 387 mAh/g. But at the end of the first
charge only 72% of the initial charge was recovered (the reversible capacity is about 279 mAh/g). In order to improve this
performance we have deposited metallic nickel on graphite with the intention to obtain a homogeneous thin layer able to modify
the nature of the SEI film, to allow the diffusion of lithium ions through the protective layer, and also to increase the
performance of graphite electrodes. The results show a decrease of the irreversible capacity loss (16% instead of 28% for
pure graphite electrodes) as well as better cycleability for a nickel-deposited graphite electrode with only 11% weight ratio
of nickel. On the other hand, an increase of the nickel content decreases this performance. 相似文献
2.
James W. Pavlik Theppawut Israsena Na Ayudhaya Chennagiri R. Pandit Supawan Tantayanon 《Journal of heterocyclic chemistry》2004,41(1):61-67
Trifluromethyl substitution on the pyrazole ring was found to enhance photoreactivity via the P4 pathway which involves interchange of the N2‐C3 ring atoms. Thus, 1‐methyl‐3‐(trifluromethyl)pyrazole (1) and 1‐methyl‐5‐(trifluromethyl)pyrazole (3) transposed with a P4/P6 or P4/P6+P7 ratio of 2.1:1. 1‐methyl‐4‐(trifluromethyl)pyrazole (2) transposed regiospecifically by the P4 transposition pathway. Compounds 2 and 3 were also observed to undergo photocleavage to yield enaminonitrile and enaminoisocyanide products. 相似文献
3.
Usually, numerical self-consistent calculations predict a much larger intrinsic bistability region than actually is measured in resonant tunneling diodes (RTDs). In addition, numerical calculations have shown that scattering in the well reduces bistability. We used a unified treatment of current flowing from continuum states and emitter quasi-bound states to show numerically and analytically that not only the scattering in the quantum well but also the scattering in the emitter reduces bistability. Moreover, within the Hartree approximation, bistability occurs by tunneling resonantly between emitter quasi-bound state and well quasi-bound state as a pitchfork bifurcation. 相似文献
4.
We give an overview of studies of models for semiflexible, equilibrium polymers with special emphasis on our work on both lattice and continuum models for such systems. We show, principally by Monte Carlo simulations, that, once monomers self assemble to form polymers, their semiflexibility leads to nematic phases at low temperatures. Attractive wall potentials encourage the adsorption of these equilibrium polymers on surfaces. Rapid cooling leads to the formation of glasses with entangled polymers. Shear promotes nematic ordering, but, at high shear rates, this tendency decreases since the equilibrium polymers are torn apart. A version of our model in which the polymers are directed shows the polymer analog of bosonic Mott-insulating, mass-density-wave, and supersolid phases. We give a brief comparison of our work with other studies and also explore the experimental implications of our study. 相似文献
5.
6.
Conjugated esters and amides react with aryldiazonium salts at room temperature (MeCN) to form the corresponding iminium hydrazone derivatives, which can be thermally cyclized to cinnoline-3-esters and cinnoline-3-amides. In general the intermediate iminium salts derived from the enamine amides cyclize faster than those from the enamine esters. Furthermore, the ease of cyclization depends upon the structure of the base-component of the enamine ester or the amide and the substituent in the aryl moiety of the diazonium salt. The configurational structure of the iminium hydrazones, studied by NMR spectroscopy, has been shown to involve H-bonding of the hydrazonyl N-H with the ester or the amide CO group. 相似文献
7.
A series of monoacylated piperazine derivatives were obtained by the reaction of carboxylic acids with 2-chloro-4,6-dimethoxy-1,3,5-triazine in dichloromethane at room temperature. Good to excellent yields, short reaction times and mild reaction conditions are important features of this methodology. 相似文献
8.
V. Anuradha D. D. Hai R. Shivaji 《Proceedings of the American Mathematical Society》1996,124(3):757-763
We consider the existence of positive solutions to the BVP
where . Our results extend some of the existing literature on superlinear semipositone problems and singular BVPs. Our proofs are quite simple and are based on fixed point theorems in a cone.
9.
Carbenes3a-e add to the α-side of the first double bond of dienamine2 (title compound) to give 1 : 1 adducts4a-e, Chlorofluorocarbene3e gives, in addition, ketone7, corresponding to β-addition at the second double bond of2, and a 2 : 1 adduct8. The reaction of2 with dichlorocarbene3a yields, besides4a, novel ring-expansion products5 and6 corresponding to addition of two moles of3a. Ethoxycarbonylcarbene3f reacts with the dienamine (2) to give isomeric esters9 and10a,b. The structure assignments and the mechanism of formation of the reaction products are discussed. 相似文献
10.
Alkylation of 4-ethoxy-2-hydroxypyrimidines (10a, b), via their anions, provides a convenient procedure for preparing N1-substituted derivatives. Reaction of 10a, b with t-butyl 4-bromo-2-benzyloxycarbamidobutyrate (17) gives good yields of the N1-alkylated products 18a, b. The latter have been converted to uracil- (20a), thymine- (20b) and cytosine- (21) substituted -aminobutyric acids. 相似文献