The influence of nitrogen doping on reduced graphene oxide as highly cyclable Li-ion battery anode with enhanced performance

A straightforward, one-step route has been established to fabricate reduced- (rGO) and nitrogen-doped reduced graphene oxide (NrGO) with remarkable lithium-ion storage properties. The graphene oxide (GO) was synthesized as starting material by improved Hummers’ method. Thereafter, thermally annealing GO with NH₃ at elevated temperature to synthesize NrGO was yielded a more open structure with nitrogen sites suitable for enhanced Li intercalation. NrGO exhibited a reversible capacity of 240 mAhg^?1 at 10 Ag^-1 after 500 cycles with 90% capacity retention, which is the best result achieved among graphene oxide-based anodes at this current density. In contrast to rGO, NrGO cells exhibited a gradually increasing capacity profile, reaching up to 114% of the initial capacity at 0.1, 2, and 10 Ag^-1 current densities. Results showed that high occupancy of pyridinic N within NrGO enhanced battery performance and cell kinetics upon cycling which offers long-time operability at high current density.     

可靠性工程在电机中的应用

可靠性工程无论在航天技术还是在军事装备以及一般工业产品上都具有极其重要意义和不可估量的经济效益及社会效果。本文简要的介绍了可靠性指标的定义及我国起重冶金用电动机和防爆电动机开展可靠性设计与试验研究情况。     

Unveiling the presence of mixed oxidation states of Europium in Li7+δEuxLa3−δZr2−δO12−δ garnet and its impact on the Li-ion conductivity

Recently, lanthanides have been employed by researchers to examine their impact on the structure and properties of Li₇La₃Zr₂O₁₂ (LLZO) garnets. In this regard, we developed Europium oxide (Eu₂O₃) doped LLZO (Li_7+δEu_xLa_3−δZr_2−δO_12−δ) solid electrolyte which demonstrates a cubic phase with the symmetry of Iad (No.230) at room temperature. In this investigation, different concentrations of Eu ranging from 0.1 to 0.6 atoms per formula unit (pfu) were doped into Li₇La₃Zr₂O₁₂ to evaluate the impact of Eu on the stability of the cubic phase and thereby the ionic conductivity. The results unveiled that upon doping Eu³⁺ ions, the Eu²⁺ state is also formed and is then self-doped into the structure in which Rietveld refinement coupled with XPS, EPR, and solid-state NMR suggests that Eu³⁺ ions most probably partially occupy Zr⁴⁺ (16a) site, the Eu²⁺ ions occupy La³⁺ (24d) site, and the Li⁺ ions occupy two different sites (24d and 96h). It was further found that such a site preference induces distortion at LaO₈ polyhedrons opening up the neck for Li-ions diffusion, thereby enhancing the ionic conductivity. Moreover, it was revealed that Li-ions probably hop from 96h to 24d and then to 96h site to generate the Li-ion movement. Overall, by introducing Eu ions into the LLZO structure, an enhanced bulk ionic conductivity of 0.30 × 10⁻³ S/cm at 298 K with a minimum electronic conductivity of 2.547 × 10⁻⁹ S/cm at 298 K was achieved.     

交流电风扇能效检测方法探讨

针对GB/T 13380-2007《交流电风扇和调速器》中有关交流电风扇能效检测的方法以及所要求的检测系统,对检测所用设备的影响进行分析,通过对检测结果的计算,最终得到测量结果的不确定度,以分析、评估检测结果的可靠性.最后根据现有实验室水平提出了对检测设备改进措施的建议.     

电机冲片、铁心质量对产品的影响

三相异步电动机在检验中,时常发现产品试制鉴定时样品的性能指标符合图纸和产品要求,但在生产时不同厂家或同一厂家,不同批次的产品性能却波动很大,经分析是冲片及铁心的设计制造质量不稳定所致.本文所阐述的是一些对性能有影响,在设计制造中均难以发现的潜在隐患性问题.     

SUPERCRITICAL EXTRACTION AND DESULPHURIZATION OF BEYPAZARI LIGNITE BY ETHYL ALCOHOL/NaOH TREATMENT 1. EFFECT OF ETHYL ALCOHOL/COAL RATIO AND NaOH

ABSTRACT

The solubilization and desulphurization of Beypazari lignite with supercritical ethyl alcohol/NaOH was investigated. Supercritical experiments of 60?minutes were done in microreactors of 15?ml at 245°C by changing the ethyl alcohol/coal ratio from 3 to 20 under a nitrogen atmosphere. As the ethyl alcohol/coal ratio was increased the yield of solubilization and desulphurization also increased. Higher yields of extraction in the case of ethyl alcohol/NaOH experiments may be due to the fact that alcohols can transfer hydrogen more easily in the presence of bases. The average molecular weights of liquid products obtained in experiments with ethylalcohol/coal ratios of 3,6 and 20 were 430,450 and 465, respectively. In experiments with ethylalcohol/NaOH system as the ethylalcohol/coal ratio was increased from 3 to 20 the sulphur content of the coal decreased to 0·75%. In experiments with greater ethylalcohol/coal ratios mercaptane type sulphur chemicals have been extracted,disulphides were missing in these extracts.     

Conversion of methane to styrene over the mixed catalyst La2O3 + MoO3/HZSM-5

The gas‐phase hydrogenation of crotonaldehyde has been performed over unsupported Mo₂N and over Mo₂N supported on two carbonaceous materials, an activated carbon (AC) and a high surface area graphite (G). These catalysts were in situ prepared by the temperature‐programmed reaction of MoO₃ and carbon‐supported Mo precursors with NH₃. It is found that selectivity to the unsaturated alcohol is maximum for the Mo₂N/G sample, where crotylalcohol selectivities exceed the 60% during all time in reaction. Higher selectivity surface sites are associated with the (200) planes of the γ‐Mo₂N crystallites. This revised version was published online in July 2006 with corrections to the Cover Date.     

SUPERCRITICAL EXTRACTION OF ISRAELI MISHOR ROTEM OIL SHALE 1. BATCH EXTRACTION WITH TOLUENE

ABSTRACT

Recovery of organic material from Israeli Mishor Rotem oil shale with toluene under supercritical conditions was investigated. The rate of solubilization, change of structural aspects and molecular weights of solubilized products with time were investigated. Experiments to recover organic material from shale were performed in a stainless steel high pressure autoclave. Shale Sample was charged in a sintered glass crucible suspended from the cap of the autoclave; toluene was the solvent in all experiments. Solvent/shale ratio was 20; experimental temperature was 34O^°C. The gaseous products were analyzed by gas chromatography. Molecular weights of the organic material recovered was measured by gel permeation chromatography technique. FTIR spectra of the organic material recovered and fractions isolated by extractive and chromatographical methods were measured. The amount of kerogen remaining in the spent shale was determined by oxidative derivative thermal gravimetry. A steady state in the production of solubles was reached within 60 minutes at 340^°C with a yield of 60 percent. After this time no further amounts of organic material was recovered. The molecular weights of the recovered organic material decreased at extended times after the steady state was reached. It appeared that the structure of the organic material recovered remained unchanged until the steady state condition is reached whereupon some structural changes occurred. At extended times the organic material was converted into more aromatic and less hydroxyl containing structures of lower molecular weight. The organic material recovered upon reaching steady state was fractionated into 63 percent oils (pentane solubles) and 32 percent asphaltenes (toluene solubles). The oile contained aliphatics and monoaromatic structures and the asphaltenes contained polyaromatic polar structures. Gases which constituted 4 percent of the initial kerogen were produced during the heating period to 340^°C. The amount of carbon monoxide produced remained constant and amounts of hydrogen, carbon dioxide and methane decreased after supercritical conditions were attained.