《电动力学》课程中引入普通物理知识的探索

《电动力学》是研究电磁现象的经典的动力学理论,它主要研究电磁场的基本属性、运动规律以及电磁场和带电物质的相互作用,对本科生来说这是一门相对较为难学的课程,其难点为数学知识:散度和旋度,重点为麦克斯韦方程组。在课堂教学中,通过引入一些相关的普通物理知识,采用通俗形象、层层铺垫等方法进行教学,将其化难为易,让学生们循序渐进地掌握《电动力学》的基本知识。实践教学效果良好。

《电动力学》教学改革的探索与思考

本文从教学实践出发,就<电动力学>课程建设中有关教学思想的转变、教学内容的更新及教学方法的改革等问题进行了分析与讨论.

Sn nucleation and growth from Sn(II)dissolved in ethylene glycol:Electrochemical behavior and temperature effect

Thermodynamic and kinetic aspects of Sn nucleation and growth processes onto a glassy carbon electrode from SnCl2·2H2O dissolved in ethylene glycol solutions were studied.Typical reduction and oxidation peaks observed in voltammograms have demonstrated the capability of ethylene glycol solutions to electrodeposit Sn.The temperature-dependence of diffusion coefficient values derived from potentiodynamic and potentiostatic studies helped to determine and validate estimations of the activation energy for Sn(II)bulk diffusion.Chronoamperometric results have identified that,the suitable model to describe the early stage of Sn electrodeposition could be composed of Sn three-dimensional nucleation and diffusion-controlled growth and water reduction contributions,which was duly validated by theoretical and experimental approaches.From the model,typical kinetic parameters such as the nucleation frequency of Sn(A),number density of Sn nuclei(N_(0)),and diffusion coefficient of Sn(II)ions(D),were determined.The presence of Sn nuclei with excellent quality and their structures were verified using SEM,EDX,and XRD techniques.

Modulation of Electronic States in Bimetallic-doped Nitrogen-Carbon Based Nanoparticles for Enhanced Oxygen Reduction Kinetics

Controlling the local electronic structure of active ingredients to improve the adsorption desorption characteristics of oxygen-containing intermediates over the electrochemical liquid-solid interfaces is a critical challenge in the field of oxygen reduction reaction(ORR)catalysis.Here,we offer a simple approach for modulating the electronic states of metal nanocrystals by bimetal co-doping into carbon-nitrogen substrate,allowing us to modulate the electronic structure of catalytic active centers.To test our strategy,we designed a typical bimetallic nanoparticle catalyst(Fe-Co NP/NC)to flexibly alter the reaction kinetics of ORR.Our results from synchrotron Xray absorption spectroscopy and X-ray photoelectron spectroscopy showed that the co-doping of iron and cobalt could optimize the intrinsic charge distribution of Fe-Co NP/NC catalyst,promoting the oxygen reduction kinetics and ultimately achieving remarkable ORR activity.Consequently,the carefully designed Fe-Co NP/NC exhibits an ultra-high kinetic current density at the operating voltage(71.94 mA/cm^(2)at 0.80 V),and the half-wave potential achieves 0.915 V,which is obviously better than that of the corresponding controls including Fe NP/NC,Co NP/NC.Our findings provide a unique perspective for optimizing the electronic structure of active centers to achieve higher ORR catalytic activity and faster kinetics.

从教学实践看课堂教学中多媒体的使用

近年来，多媒体越来越普遍地应用到高等学校的课堂教学中，并以其强大的优势对传统的板书教学造成巨大的影响。笔者在吉林师范大学物理学院从事多轮的《电动力学》教学工作，在实践中使用过传统的板书教学、完全使用多媒体（采用PowerPoint结合MATLAB软件）教学、多媒体辅助板书教学三种教学方式。为探讨三种教学方式的课堂教学效果，笔者设计了符合本课程特点的调查问卷，对吉林师范大学物理学院2003级本科3、4班共63名同学进行了问卷调查。

Development and simulation of electric vehicle based on ADVISOR

Based on the electric vehicle simulator ADVISOR（ advanced vehicle simulator）, the electric vehicle which has a wheel driving system was developed and named ELVEC. The ELVEC consists of wheel, axle, body, motor/controller, energy storage, power bus, etc. The acceleration, grading, driving speed and fuel economy of the ELVEC are analyzed. The results show that the ELVEC has good dynamic performance and fuel economy. It is suitable for the driving conditions of the start-accelerate-stop and the low speed driving conditions in urban areas. At the same time, the motor performance, energy storage （batteries） and energy management of the ELVEC are simulated. It is concluded that the efficiencies of the motor, batteries and driveline are high, and the energy management and the fuzzy logic control strategy are efficient.

Anodic behavior and microstructure of Al/Pb-Ag anode during zinc electrowinning

Anodic behaviors and oxygen evolution kinetics of Pb-0.8%Ag and Al/Pb-0.8%Ag anodes during the initial 24 h zinc electrowinning were investigated with cyclic voltammetry （CV） curves and electrochemical impedance spectroscopy （EIS）. The results reveal that the anodic behaviors and reaction kinetics of the two anodes vary a lot during the anodic polarization which indicate the formation and stabilization of anodic layer. Compared with conventional Pb-0.8%Ag anode, A1/Pb-0.8%Ag anode has longer time of anodic polarization. At the very beginning of anodic polarization, the two anodes all exhibit higher potential of oxygen evolution reaction （OER） since the reaction is controlled by the transformation step of intermediates. Then, its OER potential is largely diminished and OER rate is deduced from the formation and adsorption of the first intermediate （S-OHms）. In the prolonged anodie polarization, the anodie potential of A1/Pb-0.8%Ag gradually decreases and the final value is more stable than that of conventional Pb-0.8%Ag anode. On the anodic layer after 24 h of anodic polarization, the OER potential is controlled by the formation and adsorption of intermediate. The microstructures of A1/Pb-0.8%Ag and Pb-0.8%Ag anodes after 24 h of anodie polarization were analyzed by scanning electron microscope （SEM）.

Effects of stoichiometric ratio La/Mg on structures and electrochemical performances of as-cast and annealed La-Mg-Ni-based A_2B_7-type electrode alloys

In order to investigate the influences of the stoichiometric ratio of La/Mg （increasing La and decreasing Mg on the same mole ratio） on the structure and electrochemical performances of the La-Mg-Ni-based A2B7-type electrode alloy, the as-cast and the annealed ternary Lao.8＋xMgo.2_xNi3.5 （x=0-0.05） electrode alloys were prepared. The characterization of electrode alloys by X-ray diffraction （XRD） and scanning electron microscopy （SEM） shows that all the as-cast and the annealed alloys hold two major phases of （La,Mg）2Ni7 and LaNi5 as well as a residual phase of LaNi3. Moreover, the increase of La/Mg ratio brings on a decline of （La,Mg）2Ni7 phase and a rise of LaNi5 and LaNi3 phases. The variation of La/Mg ratio gives rise to an evident change of the electrochemical performances of the alloys. The discharge capacities of the as-cast and the annealed alloys evidently decrease with growing the La/Mg ratio, while the cycle stabilities of the alloys visibly augment under the same condition. Furthermore, the high rate discharge ability （HRD）, the electrochemical impedance spectrum （EIS）, the Tafel polarization curves, and the potential step measurements all indicate that the electrochemical kinetic properties of the alloy electrodes increase with the La/Mg ratio rising.

Phase structure and electrochemical properties of La_(0.7)Ce_(0.3)Ni_(3.75)Mn_(0.35)Al_(0.15)Cu_(0.75-x)Fe_x hydrogen storage alloys

La0.7Ce0.3Ni3.75Mn0.35Al0.15Cu0.75-xFex （x=0-0.20） hydrogen storage alloys were synthesized by induction melting and subsequent annealing treatment, and phase structure and electrochemical characteristics were investigated. All alloys consist of a single LaNi5 phase with CaCu5 structure, and the lattice constant a and the cell volume （V） of the LaNi5 phase increase with increasing x value. The maximum discharge capacity gradually decreases from 319.0 mA？h/g （x=0） to 291.9 mA？h/g （x=0.20） with the increase in x value. The high-rate dischargeability at the discharge current density of 1200 mA/g decreases monotonically from 53.1% （x=0） to 44.2% （x=0.20）. The cycling stability increases with increasing x from 0 to 0.20, which is mainly ascribed to the improvement of the pulverization resistance.

CHAOTIC TRANSDUCER

Utilizing the character of chaos, the sensitivity to the initial conditions, the concept and the structure of so-called chaotic transducer based on Tent map is provided in this paper creatively. The possibility of applying the basic theory of symbolic dynamics to the measurement is presented and proved. Then, the theoretical model of chaotic transducer is realized by using the switched capacitor and the basic experimental results are given. The transducer has such characters as high sensitivity, resolution, the simple structure and combining signal amplification with A/D. The new area of the application of chaos is exploited. Meanwhile, it provides a new method of exploring the structure of new type transducer.

Photoionization Mass Spectrometric and Kinetic Modeling of Low-pressure Pyrolysis of Benzene

Pyrolysis of benzene at 30 Torr was studied from 1360 K to 1820 K in this work. Synchrotron vacuum ultraviolet photoionization mass spectrometry was employed to detect the pyroly- sis products such as radicals, isomers and polycyclic aromatic hydrocarbons, and measure their mole fraction profiles versus temperature. A low-pressure pyrolysis model of benzene was developed and validated by the experimental results. Rate of production analysis was performed to reveal the major reaction networks in both fuel decomposition and aromatic growth processes. It is concluded that benzene is mainly decomposed via H-abstraction reaction to produce phenyl and partly decomposed via unimolecular decomposition reac- tions to produce propargyl or phenyl. The decomposition process stops at the formation of acetylene and polyyne species like diacetylene and 1,3,5-hexatriyne due to their high thermal stabilities. Besides, the aromatic growth process in the low-pressure pyrolysis of benzene is concluded to initiate from benzene and phenyl, and is controlled by the even carbon growth mechanism due to the inhibited formation of C5 and C7 species which play important roles in the odd carbon growth mechanism.

Dynamics simulation of tertiary amines adsorbing on kaolinite(001) plane

The collecting power of tertiary amines（DRN,DEN and DPN） on kaolinite follows the order of DENDPNDRN.After reacting with DRN,DEN and DPN,the surface potentials of kaolinite increase remarkably,and the recruitments caused by collectors also follow the order of DENDPNDRN.The results of dynamics simulation show that the geometries of substituent groups bonding to N are deflected and twisted,and some of bond angles are changed when tertiary amines cations adsorb on kaolinite（001） surface.Based on the results of dynamics simulations and quantum chemistry calculations,the electrostatic forces between three tertiary amines cations and 4×4×3（001） plane of kaolinite are 1.38×10？7 N（DRN12H＋）,1.44×10-6 N（DEN12H＋）,1.383×10-6 N（DPN12H＋）,respectively.

Gauge dependence of chiral condensate and fermion mass by an unquenched model

Based on three-dimensional quantum electrodynamics theory,a set of truncated Dyson-Schwinger（D-S） equations are solved to study photon and fermion propagators with the effect of vacuum polarization.Numerical studies show that condensation and the value of fermion mass depends heavily on how the D-S equations are truncated.By solving a set of coupled D-S equations,it is also found that the fermion propagator shows a clear dependence on the order parameter.The truncated D-S equations under unquenched approximation are used to study the mass-function and chiral condensation of the fermions.The results under the unquenched approximation are clearly different from the ones under quenched approximation.With the increase in the order parameter,the fermion condensation in the unquenched approximation decreases when 0≤ξ5,while it increases when ξ5.However,nothing like this is observed in the quenched approximation,which indicates that there may be flaws in the quenched approximations.

A Kinetic Model of Dielectric Ageing

A kinetic model of dielectric ageing is presented. The central finding of this investigation is that there is a power-law relationship between the local electric field concentration and the rate of defect-tip initiated conducting crack growth. By applying such a power-law conducting crack growth rate expression to the evaluation of the life of solid dielectrics, the empirical classical ageing law of insulation materials can be derived theoretically as a lobical result. All the results are universal and agree with the experimental data of oxide films.

Transport Properties of Two Coupled Quantum Dots Under Optical Pumping

Using the Keldysh-Green function,we present a theoretical study on the electron transport properties of two coupled quantum dots under optical pumping. Plateaus in the I-V curve and resonant peaks in the transmission coefficient occur and can be explained by the local electron density of states in the quantum dots. The effects of the optical pumping frequency and intensity on the transport properties of the system are also discussed. The electron dynamical localization phenomenon occurs when the optical pumping frequency is equal to the discrete hole energy level. This result can be used to realize optical control switches.

Multiple solutions and fermion mass effect in QED_3

Due to the negligible non-perturbation effect in the low-energy region, quantum chromodynamics （QCD） is limited to be applied to hadron problems in particle physics. However, QED has mature non-perturbation models which can be applied to Fermi acting-energy between quark and gluon. This paper applies quantum electrodynamics in 2 ＋ 1 dimensions （QED3） to the Fermi condensation problems. First, the Dyson-Schwinger equation which the fermions satisfy is constructed, and then the Fermi energy gap is solved. Theoretical calculations show that within the chirality limit, there exist three solutions for the energy gap; beyond the chirality limit, there are two solutions; all these solutions correspond to different fermion condensates. It can be concluded that the fermion condensates within the chirality limit can be used to analyze the existence of antiferromagnetic, pseudogap, and superconducting phases, and two fermion condensates are discovered beyond the chirality limit.

Kinetics Study on O2 Adsorption and OHad Desorption at Pt（111）, Its Implication to Oxygen Reduction Reaction Kinetics

Kinetics of dissociative O2 adsorption, OHad desorption, and oxygen reduction reaction （ORR） at Pt（111） electrode in 0.1 mol/L HClO4 has been investigated. Reversible OHad adsorption/desorption occurs at potentials from 0.6 V to 1.0 V （vs. RHE） with the exchange current density of ca. 50 mA/cm^2 at 0.8 V, the fast kinetics of OHad desorption indicates that it should not be the rate determining step for ORR. In the kineticor kinetic-mass transport mix controlled potential region, ORR current at constant potential displays slight decrease with reaction time. ORR current in the positive-going potential scan is slightly larger than that in the subsequent negative-going scan with electrode rotation speed （〉800 r/min） and slow potential scan rate （〈100 mV/s）. The open circuit potential of Pt/0.1 mol/L HClO4 interface increases promptly from 0.9 V to 1.0 V after switch from O2 free- to O2-saturated solution. The increase of open circuit potential as well as ORR current decays under potential control due to the accumulation of OHad from dissociative adsorption of O2. It indicates that at Pt（111） the net rate for O2 decomposition to OHad is slightly faster than that for OHad removal, one cannot simply use the assumption of rate determining step to discuss ORR kinetics. Instead, the ORR kinetics is determined by both the kinetics for O2 decomposition to OHad as well as the thermo-equilibrium of OHad＋H^＋＋e→←H2O.