Zn$lt;sub$gt;1-$lt;i$gt;x$lt;/i$gt;$lt;/sub$gt;Mg$lt;sub$gt;$lt;i$gt;x$lt;/i$gt;$lt;/sub$gt;O薄膜的光致发光特性研究

采用脉冲激光沉积方法在单晶Si（100）衬底上制备出c轴取向的Zn_1-xMg_xO单晶薄膜,通过荧光光谱仪研究了薄膜的光致发光特性.实验结果表明,Mg含量增加,Zn_1-xMg_xO单晶薄膜的紫外发光峰蓝移,发光峰强度减弱,缺陷发光强度增强.同时发现,由于Mg的掺杂,引入了一些束缚能较大的局域束缚态.对于氧气氛下制备的样品,实验发现紫外峰和绿光带发光峰同时增强,但是R值减小,紫外峰红移.对绿光发光机理研究发现,绿光发光带主要与锌空位、氧间隙（O_i）或锌位氧（O_Zn）等缺陷有关,它是由多个缺陷发光峰组成,各缺陷发光峰强度相对变化导致了绿光发光带的整体移动. 关键词： 1-xMg_xO薄膜')" href="#">Zn_1-xMg_xO薄膜 光致发光 脉冲激光沉积     

Ca$lt;sub$gt;2$lt;/sub$gt;Si（O$lt;sub$gt;4-$lt;i$gt;x$lt;/i$gt;$lt;/sub$gt;N$lt;sub$gt;$lt;i$gt;x$lt;/i$gt;$lt;/sub$gt;）：Eu$lt;sup$gt;2+$lt;/sup$gt;绿色荧光粉的制备及其发光性能

利用在Ca-Si-O干凝胶前驱体中添加Si₃N₄的方法于非还原气氛下合成了含N固溶体Ca₂Si（O_4-xN_x）：Eu²⁺绿色荧光粉. 通过X射线衍射仪、扫描电子显微镜以及荧光分光光度计分别分析了产物的物相结构、颗粒形貌和发光性能. 结果显示,Si₃N₄与前驱体的混合物在非还原气氛（纯氮气）下于1100℃焙烧后获得含N固溶体Ca₂Si（O_4-xN_x）：Eu²⁺荧光粉,特别是其中Eu³⁺被还原为Eu²⁺,产物的晶体结构与βup -Ca₂SiO₄相一致. Ca₂Si（O_4-xN_x）：Eu²⁺能够被270–400 nm 范围内的紫外线有效激发,其发射光谱呈宽带发射. 随着N含量的增加,发射峰出现一定程度红移（501–504 nm）,而且发光强度显著提高. 当Eu²⁺浓度为0.25 mol%时发光强度达最大值,浓度超过0.25 mol%时,发光强度显著降低,出现浓度猝灭 效应. 关键词： 白光LED 荧光粉 溶胶凝胶法 3N₄')" href="#">Si₃N₄     

营造·感悟·探究·应用

笔者有幸观摩了一堂第七届全国中学物理青年教师教学大赛录像课——由天津市南开中学贾双老师执教的“自由落体运动”,感受颇多．这是一堂在新课程理念下有意义、有效率、有生成性且非常精彩的课．现重现最精彩的教学片段．     

直接带隙Ge$lt;sub$gt;1-$lt;em$gt;x$lt;/em$gt;$lt;/sub$gt;Sn$lt;sub$gt;$lt;em$gt;x$lt;/em$gt;$lt;/sub$gt;本征载流子浓度研究

通过合金化改性技术, Ge可由间接带隙半导体转变为直接带隙半导体. 改性后的Ge半导体可同时应用于光子器件和电子器件, 极具发展潜力. 基于直接带隙Ge_1-xSn_x半导体合金8带Kronig-Penny模型, 重点研究了其导带有效状态密度、价带有效状态密度及本征载流子浓度, 旨在为直接带隙改性Ge半导体物理的理解及相关器件的研究设计提供有价值的参考. 研究结果表明: 直接带隙Ge_1-xSn_x合金导带有效状态密度随着Sn组分x的增加而明显减小, 价带有效状态密度几乎不随Sn组分变化. 与体Ge半导体相比, 直接带隙Ge_1-xSn_x合金导带有效状态密度、价带有效状态密度分别低两个和一个数量级; 直接带隙Ge_1-xSn_x合金本征载流子浓度随着Sn组分的增加而增加, 比体Ge半导体高一个数量级以上. 关键词： 1-xSn_x')" href="#">Ge_1-xSn_x 直接带隙 本征载流子浓度     

Co掺杂对Mn$lt;sub$gt;3$lt;/sub$gt;Sn$lt;sub$gt;1-$lt;em$gt;x$lt;/em$gt;$lt;/sub$gt;Co$lt;sub$gt;$lt;em$gt;x$lt;/em$gt;$lt;/sub$gt;C$lt;sub$gt;1.1$lt;/sub$gt;化合物的磁性质、熵变以及磁卡效应的影响

利用固态反应法制备了Mn₃Sn_1-xCo_xC_1.1 （x=0.05,0.1,0.2） 系列化合物,研究了Co掺杂对其磁性质、相变、熵变的影响. 随着Co掺杂量的增加,样品的居里温度由283 K先降到212 K （Mn₃Sn_0.9Co_0.1C_1.1） 后又升到332 K （Mn₃Sn_0.2Co_0.8C_1.1）,相变类型由一级相变逐渐转变为二级相变. 增大Co的掺杂量,Mn₃Sn_1-xCo_xC_1.1化合物的熵变峰值逐渐减小,磁熵变温区由9 K展宽到300 K. 当Co掺杂量为0.2时,相对制冷量达到最高,为103 J/kg （磁场强度为1.6 MA/m）. 由于室温附近良好的磁致冷效应,该类材料在磁制冷领域可能具有重要的应用前景. 关键词： 磁性质 相变 磁卡效应 相对制冷量     

MC与$lt;i$gt;M$lt;/i$gt;$lt;sub$gt;$lt;i$gt;n$lt;/i$gt;+1$lt;/sub$gt;$lt;i$gt;AC$lt;/i$gt;$lt;sub$gt;$lt;i$gt;n$lt;/i$gt;$lt;/sub$gt;稳定性与电子特征的第一性原理研究

研究MC与M_n+1AC_n(M=Sc, Ti, V, Cr, Mn; A=Al, Si, P, S; n=1, 2, 3)结构的稳定性与电子特征有利于探究三元层状结构M_n+1AC_n稳定性的内在原因和设计新型M_n+1AC_n结构. 第一性原理计算研究表明, M-3d与C-2p轨道间的电子转移对MC与M_n+1AC_n 的形成焓有较大影响. 供电子能力较强的前过渡金属可以形成稳定的MC结构. 计算结果显示, MC结构是缺电子体系, 其趋向于与具有一定供电子能力的MA结构结合形成M_n+1AC_n. 与M₂PC和M₂SC 相比, M₂AlC和M₂SiC可以更为容易地被分离成二维 M₂C结构. 关键词： MAX相结构 第一性原理 电子结构 过渡金属碳化物     

O<Subscript>2</Subscript> photodesorption from AuO<Stack><Subscript>2</Subscript><Superscript>−</Superscript></Stack> and Au<Subscript>2</Subscript>O<Stack><Subscript>2</Subscript><Superscript>−</Superscript></Stack>

Using time-resolved photoelectron spectroscopy, the decay channels of AuO₂⁻ and Au₂O₂⁻ following photoexcitation with 3.1-eV photons have been studied. For AuO₂⁻, a state with a rather long lifetime of 30 ps has been identified. Its decay path could not be determined but photodesorption can be excluded. For Au₂O₂⁻, the spectra indicate O₂ desorption after 3.1-eV photoexcitation on a time scale of 1 ps. While comparing these results on Au _n O₂⁻ with analogous data on Ag _n O₂⁻ clusters, a discernible pattern emerges: for dissociatively bound O₂(AuO₂⁻, Ag₃O₂⁻), there are long-living excited states which do not decay by oxygen desorption, while for molecular chemisorption (Au₂O₂⁻, Ag₂O₂⁻, Ag₄O₂⁻, Ag₈O₂⁻), the 3.1-eV photoexcitation triggers fast O₂ desorption with a high quantum yield.     

相位物体$lt;i$gt;Z$lt;/i$gt;-扫描研究金属簇合物［$lt;i$gt;Tp$lt;/i$gt;*W($lt;i$gt;μ$lt;/i$gt;$lt;sub$gt;3$lt;/sub$gt;-S)$lt;sub$gt;3$lt;/sub$gt;Cu$lt;sub$gt;3$lt;/sub$gt;$lt;i$gt;Py$lt;/i$gt;$lt;sub$gt;3$lt;/sub$gt;($lt;i$gt;μ$lt;/i$gt;$lt;sub$gt;3$lt;/sub$gt;-Br)］($lt;i$gt;PF$lt;/i$gt;$lt;sub$gt;6$lt;/sub$gt;)/DMF溶液的瞬态热致非线性折射

在纳秒时域,采用相位物体（PO）Z-扫描技术研究了一种新型金属簇合物溶液的瞬态热致非线性效应.该方法的最大优点是很容易区分瞬态热致非线性折射和三阶非线性折射.本文利用PO Z-扫描和传统Z-扫描研究了在8 ns脉宽、不同能量激光脉冲作用下［Tp*W（μ₃-S）₃Cu₃Py₃（μ₃-Br）］（PF₆）/DMF溶液的光学非线性.从声波方程和热传导方程出发,对实验结果进行了理论分析和数值模拟,理论值和实验结果很好的吻合.研究结果表明,样品溶液的非线性折射主要来源于瞬态热致非线性效应. 关键词： Z-扫描')" href="#">相位物体 Z-扫描 瞬态热致非线性折射 光克尔效应 DMF     

Tb$lt;sub$gt;0.3$lt;/sub$gt;Dy$lt;sub$gt;0.6$lt;/sub$gt;Pr$lt;sub$gt;0.1$lt;/sub$gt;(Fe$lt;sub$gt;1-$lt;i$gt;x$lt;/i$gt;$lt;/sub$gt;Al$lt;sub$gt;$lt;i$gt;x$lt;/i$gt;$lt;/sub$gt;)$lt;sub$gt;1.95$lt;/sub$gt;合金的磁性、磁致伸缩和穆斯堡尔谱研究

系统研究了室温下Tb_0.3Dy_0.6Pr_0.1（Fe_1-xAl_x）_1.95 （x=0.05,0.1,0.15,0.2,0.25,0.3）合金中元素Al替代Fe对结构、磁性、磁致伸缩性能和自旋重取向的影响.测量结果发现,x<0.2时Tb_0.3Dy_0.6Pr_0.1（Fe_1-xAl_x）_1.95合金基本上是纯的单相,x=0.2时出现其他杂相,杂相随Al替代量的增加不断增多.随Al替代量x的增加,点阵常数a接近于线性增大,Curie温度T_C逐渐下降,而矫顽力H_c急剧下降.振动样品磁强计（VSM）测量发现,磁化强度M随Al替代量x的变化较为复杂.VSM计和磁致伸缩效应测量共同表明,少量Al的替代有利于降低磁晶各向异性,而且随着Al替代量x的增多磁致伸缩系数快速减小,x>0.15时巨磁致伸缩效应消失.穆斯堡尔效应研究发现,随Al含量的增加Tb_0.3Dy_0.6Pr_0.1（Fe_1-xAl_x）_1.95合金中易磁化轴可能在{110}面逐渐偏离了立方晶体的主对称轴,发生自旋重取向,从而引起合金宏观磁性、磁致伸缩性能的变化. 关键词： 磁致伸缩 立方Laves相 自旋重取向 穆斯堡尔谱     

钙钛矿型锰氧化物(La$lt;sub$gt;0.8$lt;/sub$gt;Eu$lt;sub$gt;0.2$lt;/sub$gt;)$lt;sub$gt;4/3$lt;/sub$gt;Sr$lt;sub$gt;5/3$lt;/sub$gt;Mn$lt;sub$gt;2$lt;/sub$gt;O$lt;sub$gt;7$lt;/sub$gt;的磁性和电性研究

采用传统固相反应法制备钙钛矿型锰氧化物 (La_0.8Eu_0.2)_4/3Sr_5/3Mn₂O₇多晶样品, X-射线衍射分析表明, 样品(La_0.8Eu_0.2)_4/3Sr_5/3Mn₂O₇结构呈现良好的单相. 通过磁化强度随温度的变化曲线(M-T)、不同温度下磁化强度随磁场的变化曲线(M-H)和电子自旋共振谱发现: 在300 K以下, 随着温度的降低, 样品先后经历了二维短程铁磁有序转变 (T_C^2D ≈ 282 K)、三维长程铁磁有序转变(T_C^3D ≈ 259 K)、奈尔转变(T_N ≈ 208K)和电荷有序转变(T_CO ≈ 35 K); 样品 (La_0.8Eu_0.2)_4/3Sr_5/3Mn₂O₇在T_N以下, 主要处于反铁磁态; 在T_C^3D达到370 K时, 样品处于铁磁-顺磁共存态, 在370 K以上时样品进入顺磁态. 此外, 分析电阻率随温度的变化曲线(ρ-T)得到: 样品在金属-绝缘转变温度(T_P ≈ 80 K)附近出现最大磁电阻值, 其位置远离T_C^3D, 表现出非本征磁电阻现象, 其磁电阻值约为61%. 在T_CO以下, 电阻率出现明显增长, 这是由于温度下降使原本在高温部分巡游的e_g电子开始自发局域化增强所致. 通过对 (La_0.8Eu_0.2)_4/3Sr_5/3Mn₂O₇的ρ-T 曲线拟合, 发现样品在高温部分的导电方式基本遵循小极化子的导电方式. 关键词： 磁性 电性 金属-绝缘转变温度 电子自旋共振     

Mixed spin- and spin- Ising models with random nearest-neighbour interactions

Using the effective field theory with correlations, we study mixed spin?3/2 and spin?1/2 Ising models with random bonds and crystal-field interactions on the honeycomb lattice. The nearest-neighbour couplings J_ij are taken as random variables with distribution P(J_ij) = pδ(J_ij ? J)+(1 ? p)δ(J_ij ? αJ), where J > 0 and |α| ≤ 1. In a certain range of negative values of α, the phase diagrams exhibit re-entrant behaviour. In detail, we investigate separately two kinds of disorder: Bond dilution (α = 0) and random ±J interactions (α = ?1). In both cases, the influence of the an-isotropy on the phase diagrams shows some new outstanding features.     

Inelastic neutron scattering and lattice dynamics of NaNbO<Subscript>3</Subscript> and Sr<Subscript>0.70</Subscript>Ca<Subscript>0.30</Subscript>TiO<Subscript>3</Subscript>

NaNbO₃ and (Sr,Ca)TiO₃ exhibit an unusual complex sequence of temperature- and pressure-driven structural phase transitions. We have carried out lattice dynamical studies to understand the phonon modes responsible for these phase transitions. Inelastic neutron scattering measurements using powder samples were carried out at the Dhruva reactor, which provide the phonon density of states. Lattice dynamical models have been developed for SrTiO₃ and CaTiO₃ which have been fruitfully employed to study the phonon spectra and vibrational properties of the solid solution (Sr,Ca)TiO₃.      

Influence of <Emphasis Type="Italic">CP</Emphasis> and <Emphasis Type="Italic">CPT</Emphasis> on production and decay of Dirac and Majorana fermions

The consequences of CP and CPT invariance for production and subsequent decay of Dirac and Majorana fermions in polarized fermion-antifermion annihilation are analytically studied. We derive general symmetry relations for the production spin density matrix and for the three-particle decay matrices and obtain constraints for the polarization and the spin-spin correlations of Dirac and Majorana fermions. We prove that only for Majorana fermions the energy and opening angle distribution factorizes exactly into contributions from production and decay if CP is conserved. Received: 6 November 2001 / Revised version: 23 April 2002 / Published online: 12 July 2002     

Thermodynamic and elastic properties of AgInSe<Subscript>2</Subscript> and AgInTe<Subscript>2</Subscript>

The specific heat at constant volume as a function of temperature, the elastic constants, compressibility coefficients, and bulk moduli of AgInSe₂ and AgInTe₂ crystals with a chalcopyrite structure have been calculated in terms of the density functional theory using the pseudopotential method. A comparison of the calculated specific heat for the tellurium compound with the results of measurements has demonstrated good agreement between theory and experiment. The bulk moduli of the AgInSe₂ and AgInTe₂ crystals calculated from first principles (60.4 and 50.1 GPa, respectively) somewhat exceed the results available in the literature, which were obtained earlier from approximate semiempirical formulas.     

Structures and stability of Al<Subscript><Emphasis Type="Bold">7</Emphasis></Subscript>C and Al<Subscript><Emphasis Type="Bold">7</Emphasis></Subscript>N clusters

We report results of the atomic and electronic structures of Al₇C cluster using ab initio molecular dynamics with ultrasoft pseudopotentials and generalized gradient approximation. The lowest energy structure is found to be the one in which carbon atom occupies an interstitial position in Al₇ cluster. The electronic structure shows that the recent observation [Chem. Phys. Lett. 316, 31 (2000)] of magic behavior of Al₇C^- cluster is due to a large highest occupied and lowest unoccupied molecular orbital (HOMO-LUMO) gap which makes Al₇C^- chemically inert. These results have further led us to the finding of a new neutral magic cluster Al₇N which has the same number of valence electrons as in Al₇C^- and a large HOMO-LUMO gap of 1.99 eV. Further, calculations have been carried out on (Al₇N)₂ to study interaction between magic clusters. Received 28 July 2001     

The ρ-π Puzzle of J/φ and φ′ Decays

The recent BES Collaboration data on φ →PV, particularly the isospin violating mode φ′ → π^oω^o and finding of a finite number for B(φ′ → K^*OK^O), enable us now to deal more precisely about the challenges to theory concerning this extraordinary and remarkableso-called ρ-π puzzle of J/φ and φ′ decays. In terms of the existing data and deploying the simplest phenomenology, measurement of φ′ → π⁺π^- and whether a finite number for the K^*+K^- mode might require a significantly large accumulation of data remain interesting questions.     

Raman and FTIR spectroscopy study of LiFeTiO<Subscript>4</Subscript> and Li<Subscript>2</Subscript>FeTiO<Subscript>4</Subscript>

We report the Fourier transform infrared (FTIR)–Raman spectroscopy study of spinel Li–Fe–Ti–O oxides viz., LiFeTiO₄ and Li₂FeTiO₄ in order to probe structural details such as type of bonding networks viz., octahedral and tetrahedral, and type of different atomic bonds present in those materials. Both the samples were prepared through solid-state reaction route prior to high-energy ball-milling. All the phases prepared through solid-state reaction and ball-milled were probed using X-ray diffraction, field emission scanning electron microscopy, and FTIR–Raman spectroscopy. X-ray diffraction study indicates spinel phase formation with Fd3m space group symmetry for both LiFeTiO₄ and Li₂FeTiO₄. However, pure phase of Li₂FeTiO₄ was not achieved in these preparation routes, rather mixed phases of Li₂FeTiO₄ and Fe₂TiO₄ were achieved. Field emission scanning electron microscopy (FESEM) analysis indicated porous microstructure for LiFeTiO₄ while more agglomerated microstructure for Li₂FeTiO₄. Ball-milling reduces the grain size partly for both the samples. FTIR–Raman spectroscopy indicates the presence of LiO₄ tetrahedral, LiO₆ and TiO₆ octahedral in the spinel network. Presence of Li–Li–O type bonding was also indicated from spectroscopy analysis. Existence of Fe₂TiO₄ phase with Li₂FeTiO₄ was also identified from both FTIR and Raman spectrum. Effect of ball-milling on the spectrum has been exhibited by broadening and peak shifting the FTIR–Raman spectrum, arising from the enhanced lattice strain and structural disorder.     

“q-hat” and jet quenching

We discuss bremsstrahlung rates for a weakly coupled fast jet propagating in dense nuclear matter. A time-dependent radiation rate which smoothly merges with previous limits is introduced, exhibiting a clear transition between two regimes after a traversed length of order one to several fermis. The different physical processes probed in the two regimes are discussed.     

Band structure and the magnetic and elastic properties of SrFeO<Subscript>3</Subscript> and LaFeO<Subscript>3</Subscript> perovskites

The band structure and the magnetic and elastic characteristics of SrFeO₃ and LaFeO₃ perovskites with ferromagnetic and antiferromagnetic collinear spin configurations (of the A, C, and G types) are investigated using the ab initio pseudopotential method (the VASP program package) with the inclusion of the single-site Coulomb correlations (the LSDA + U formalism). It is shown that, in the pressure range 0–50 GPa, the most stable states are the ferromagnetic metal state for the SrFeO₃ compound and the antiferromagnetic insulator state of the G type for the LaFeO₃ compound.