YBa_2Cu_3O(7-δ)在超导转变点处的比热反常

用连续量热法,在80—120K 对超导体 YBa_2Cu_3O_(7-δ)的比热进行了测量.结果表明在超导转变点 T_(mid)=92.4K 时,比热跳跃△Cp=7.1J/mol·K,由此计算出的△Cp/γT_c=2.05,比由 BCS 弱耦合理论推导出的1.43要大的多.说明高 T_c 氧化物 YBa_2Cu_3O_(7-δ)是具有强耦合相互作用行为,并由德拜公式拟合晶格比热计算出(?)_D=424.7K.     

(Bi,Pb)-Sr-Ca-Cu-O体系110K超导体的相转变及超导电性

品质优良的110K超导体(Bi,Pb)₂Sr₂Ca₂Cu₃O_y的单相多晶样品已制备,其零电阻温度为107K。讨论了2201相,2212相和2223相的形成和转变以及淬火温度对其的影响。测量了样品的复磁化率,结果表明超导体晶粒间的Josephson结的耦合强度与样品的制备过程有关,对不同热处理的样品测其比热;△c(107K)=5.3J/molK,索末菲常数v=34.6mJ/molK,比热跳跃与热处理     

新型Pr基大块非晶及其特性研究

用铜模吸铸法获得了直径为5mm的一种新的Pr基大块非晶.与以往其他稀土-过渡金属(RE-TM)大块非晶不同的是，这种新的Pr基大块非晶具有明显的玻璃转变和稳定的过冷液相区，且其玻璃转变温度在目前已知的大块非晶中是最低的，T_g=409K.研究了该大块非晶的玻璃转变动力学，并给出了Kauzmann温度T_k、Vogel-Fulcher温度T⁰_g及脆性参数m等重要参数. 关键词： 大块非晶 玻璃转变 脆性参数m     

新型BCN化合物的结构表征和相转变

将石墨和六方氮化硼(h-BN)混合粉球磨120h形成的非晶B-C-N粉在4.5GPa，1600K等温退火45min. XRD，TEM和Raman散射测量结果表明，高压合成的产物由晶格常数为a₁=0.2551nm，c₁=0.6716nm的六方Ⅰ相和a₂=1.2360nm，c₂=0.8570nm的六方Ⅱ相组成，其中六方Ⅱ相为B-C-N 新相. 在室温该新相在1279，1368，1398cm^-1出现三个特征Raman峰. 变温Raman测量结果表明，在测量温度T=93K时，样品中的主要相为六方Ⅰ相，随着温度的升高，六方Ⅰ相逐渐向六方Ⅱ相转变，当T>473K时，六方Ⅰ相完全转变成六方Ⅱ相. 当温度从673K降到93K过程中，样品又从六方Ⅱ相逐渐变回到六方Ⅰ相. 对这一相变的机理进行了讨论. 关键词： B-C-N 机械球磨 高温高压 相转变     

Pd-Ni-P大块金属玻璃的形成及其转变动力学

本文报道了Pd-Ni-P合金的过冷实验结果,研究了冷却速度对合金过冷行为的影响。通过将样品包裹在B₂O₃中从而减少样品的表面非均匀生核,使得样品在极低的冷却速度下形成大块金属玻璃。在玻璃转变温度(T_g=590K)处,冷却速度低达1K/s。利用经典的均匀生核与非均匀生核理论,计算了Pd₄₀Ni₄₀P₂₀合金的温度、时间转变曲线(即TTT图)。确定了合金的临界冷却速度。对结果进行了详细的讨论。 关键词：     

重电子金属CeCu(6-x)Nix低温电阻与比热的研究

测量了重电子金属CeCu6-xNix(x=0,005,01,015,02)01K—250K的低温电阻和5K—70K低温比热,发现样品电阻的极大值温度随着掺Ni含量的增大而急剧下降,这一现象反映少数与Ni邻近的Ce离子在极低温下磁矩的加强和整个Ce离子点阵对导电电子相干散射的减弱.与此相反,低温电子比热系数γ在较低温度下近于常数,而在8K附近因有效质量变大而明显上升,但γ明显上升的温度,对Ni的含量却不敏感,表明绝大部分Ce离子的状况并未受到影响 关键词： 重费米子系统 低温比热 低温电阻     

K0.3MoO3和Tl0.3MoO3派尔斯相变临界行为的比热研究

采用连续绝热加热法测量了K_0.3MoO₃和Tl_0.3MoO₃在100—220K温度范围内的比热。发现K_0.3MoO₃和Tl_0.3MoO₃分别在177.5K和172.3K发生派尔斯相变。对派尔斯相变附近比热临界行为的研究表明,K_0.3MoO₃和Tl_0.3MoO₃的临界区域宽度分别为6K和8K,临界行为属于三维XY模型普适类。 关键词：     

准一维有机超导体(TMTSF)2ClO4的高精度温差电动势研究

测量了准一维有机超导体(TMTSF)2ClO4单晶a方向不同降温速率下的高精度温差电动势(6—280K).高温下的温差电动势表现出线性行为，不能被正常的一维电子能带理论所解释.在240K左右观察到温差电动势斜率发生反常突变.在140K左右温差电动势向下逐渐偏离线性行为，这与1D—2D的维度渡越相关.对阴离子有序—无序相变温度Ta（Ta=24K）附近的温差电动势结果与比热和电阻率的数据进行了比较.对于极慢速降温的温差电动势，求导后可以看到相变的痕迹.随着通过Ta降温速率的增大，在Ta之下的温差电动势数值出现了一个逐渐增大的整体抬高.对此进行了讨论. 关键词： 低维体系 输运性质 温差电动势     

准一维有机超导体(TMTSF)_2ClO_4的高精度温差电动势研究

测量了准一维有机超导体 (TMTSF) 2 ClO4 单晶a方向不同降温速率下的高精度温差电动势 (6— 2 80K) .高温下的温差电动势表现出线性行为 ,不能被正常的一维电子能带理论所解释 .在 2 4 0K左右观察到温差电动势斜率发生反常突变 .在 14 0K左右温差电动势向下逐渐偏离线性行为 ,这与 1D— 2D的维度渡越相关 .对阴离子有序—无序相变温度Ta(Ta=2 4K)附近的温差电动势结果与比热和电阻率的数据进行了比较 .对于极慢速降温的温差电动势 ,求导后可以看到相变的痕迹 .随着通过Ta 降温速率的增大 ,在Ta 之下的温差电动势数值出现了一个逐渐增大的整体抬高 .对此进行了讨论 .     

Zr-Ti-Cu-Ni-Be大块非晶低温比热

测量了Zr₄₁Ti₁₄Cu_12.5Ni₁₀Be_22.5大块非晶及不同退火条件的样品在液氦温区的比热.低温下的比热数据可用电子比热和声子比热两部分的贡献来拟合,发现非晶的电子比热系数γ值比其他样品大,德拜温度从非晶到平衡相依次增大,并从电子态密度和德拜理论出发,初步解释了这种差异. 关键词： 低温比热 大块非晶     

Pressure and temperature induced modification of luminescence from tetracene single crystals

Fluorescence spectra of crystalline tetracene have been recorded in the temperature range 120 to 300 K under hydrostatic pressure up to 600 MPa. From discontinuities in both emission spectra and spectral intensities it is concluded that two phase transitions occur. The room temperature phase is transformed to a low temperature phase/high pressure phase I at T^I_t (p = 0) = 182 K, the temperature coefficient being dT^I_t/dp = 0.395 K/MPa. The phase transition is induced by a decrease of the specific volume under pressure and/or upon cooling. Lack of a significant shift of the origin of the fluorescence band near T^I_t at constant pressure is an artifact resulting from the neglect of reabsorption effects. The Stokes shift is 260 cm^-1, independent of temperature and crystal modification. In accord with previous Raman data a second phase transition occurs at T^II_t (p) = 143 K, the pressure shift being dT^II_t/dp = 0.088 K/MPa.In addition, the shift of the triplet energy as a function of pressure as well as the pressure-dependence of the rate constants governing fission of a singlet exciton into a pair of triplets is discussed utilizing their magnetic field dependences.     

Nb3Sn正常-超导转变时的比热反常

在16.0°K—20.3°K之间测量了Nb₃Sn样品的热容量。Nb₃Sn在临界温度附近的比热跳跃值ΔC=2.21(±5％)焦耳/克分子·度。样品的临界温度T_c=17.88°K,转变宽度ΔT_c≈0.2°K。ΔC值利用热力学关系式确定了Nb₃Sn在0°K时的热力学临界场H₀=5300奥斯特。利用本文的结果和文献上关于热膨胀系数的跳跃值Δα及?T/?P值验证了热力学关系式。扼要地描述了比热测量装置.     

Effect of γ irradiation on the structural and thermal properties of [N(C2H5)4]2ZnBr4 in the vicinity of a first-order phase transition

The unit cell parameters a and c of nonirradiated [N(C₂H₅)₄]₂ZnBr₄ crystals in the temperature region 90–300 K and of samples irradiated with γ rays to doses of 10⁶ and 5 × 10⁶ R in the 270-to 300-K interval were measured using x-ray diffraction. The data obtained were used to derive the thermal expansion coefficients α_a and α_c. It is shown that the parameter a increases and the parameter c decreases with increasing temperature. In the vicinity of the phase transition (PT) at T = 285 K, the temperature dependences of a(T) and c(T) reveal anomalies in the form of jumps and the α_a(T) and α_c(T) curves have a maximum and a minimum, respectively. The heat capacity of nonirradiated and irradiated [N(C₂H₅)₄]₂ZnBr₄ samples was measured by adiabatic calorimetry. A maximum was found in the C _p(T) curve at T = 285 K. Both x-ray diffraction and heat capacity measurements showed that the PT temperature decreased after γ irradiation.     

The heat capacity of the layer compounds (CH3CH2CH2NH3)2MnCl4 and (CH3CH2CH2NH3)2CdCl4 from 10 K TO 300 K

The heat capacity of the layer compounds tetrachlorobis (n-propylammonium) manganese II and tetrachlorobis (n-propylammonium) cadmium II, (CH₃CH₂CH₂NH₃)₂MnCl₄ and (CH₃CH₂CH₂NH₃)₂CdCl₄ respectively, has been measured over the temperature range 10 K ?T ? 300 K.Two known structural phase transitions were observed for the Mn compound in this temperature region: at T = 112.8 ± 0.1 K (ΔH_t= 586 ± 2 J mol^?1; ΔS_t = 5.47 ± 0.02 J K^?1mol^?1) and at T =164.3 ± (ΔH_t = 496 ± 7 J mol^?1; ΔS_t =3.29 ± 0.05 J K^?1mol^?1). The lower transition is known to be from a monoclinic structure to a tetragonal structure, while the upper is from the tetragonal phase to an orthorhombic one. From comparison with the results for the corresponding methyl Mn compound it is deduced that the lower transition primarily involves changes in H-bonding while the upper transition involves motion in the propyl chain.A new structural phase transition was observed in the Cd compound at T= 105.5 ± 0.1 K (ΔH_t= 1472.3 ± 0.1 J mol^?1; ΔS_t = 13.956 ± 0.001 J K^?1mol^?1), in addition to two transitions that have been observed previously by other techniques. The higher of these transitions(T = 178.7 ± 0.3 K; ΔH_t = 982 ± 4 J mol^?1 ΔS_t = 6.16 ± 0.02 J K^? mol^?1) is known to be between two orthorhombic structures, while the structural changes at the lower transition (T= 156.8 ± 0.2 K; ΔH_t = 598 ± 5 J mol^?1, ΔS_t = 3.85 ± 0.03 J K^?1 mol^?1) and at the new transition are not known. It is proposed that these two transitions correspond respectively to the tetragonal to orthorhombic and monoclinic to tetragonal transitions in the propyl Mn compounds.In addition to the structural phase transitions (CH₃CH₂CH₂NH₃)₂MnCl₄ magnetically orders at t? 130 K. The magnetic contribution to the heat capacity is deduced from the heat capacity of the corresponding diamagnetic Cd compound and is of the form expected for a quasi 2-dimensional Heisenberg antiferromagnet.     

The heat capacity of the layer compound tetrachlorobis (methylammonium) manganese—II (CH3NH3)2MnCl4, from 10 to 300k

The heat capacity of the layer compound, tetrachlorobis (methylammonium) manganese II, (CH₃NH₃)₂MnCl₄, has been measured over the range 10K <T<300K. In this region, two structural phase transitions have been observed previously by other techniques: one transition is from a monoclinic low temperature (MLT) phase to a tetragonal low temperature (TLT) phase, and the other is from TLT to an orthorhombic room temperature (ORT) phase. The present experiments have shown that the lower transition (MLT→TLT) occurs at T = 94.37±0.05K with ΔH_t = 727±5 J mol^?1 and ΔS_t = 7.76±0.05 J K^?1 mol^?1, and the upper transition (TLT→ORT) takes place at T = 257.02±0.07K with ΔH_t = 116±1J mol^?1 and ΔS_t = 0.451±0.004 J K^?1mol^?1. These results are discussed in the light of recent measurements on (CH₃NH₃)₂CdCl₄, and also with regard to a recent theoretical model of the structural phase transitions in compounds of this type.In addition to the structural phase transitions, (CH₃NH₃)₂MnCl₄ also undergoes magnetic ordering at T < 150K. The magnetic component to the heat capacity, as deduced from a corresponding states comparison of the heat capacity of the present compound with that of the Cd compound, is shown to be consistent with the behaviour expected for a quasi 2-dimensional Heisenberg antiferromagnet.     

C<Subscript>60</Subscript> heat capacity anomaly at the orientational phase transition

An orientational phase transition in C60 crystals was studied by differential scanning calorimetry with the highest resolution provided by this method. The temperature dependence of the specific heat ΔC _p (T) was found to have a double peak in the range 250–270 K. An analysis of the temperature dependences of heat capacity in the region of the peaks revealed that the lower temperature peak follows a power law of the type ΔC _p = A/(T?T₀)^1/2 characteristic of order-disorder second-order phase transitions, while the high-temperature peak can be identified with a diffuse Λ-shaped first-order phase transition.     

Dielectric response of the relaxor ferroelectric Pb(Mg1/3Nb2/3)O3 in the nonergodic state after a DC electric field is turned off

The Pb(Mg_1/3Nb_2/3)O₃ (PMN) relaxor system is used as an example to analyze the temperature dependences of the low-frequency dielectric permitivity (?′(T)) measured during zero-field heating (ZFH) from T = 10 K to T = 300 K after using different field cooling (FC) conditions. No changes in the temperature dependences of the permittivity have been detected during the transition from a nonergodic relaxor state (NERS) into an ergodic relaxor state (ERS) (at T _f ≈ 216 K). However, the difference Δ?′(T) between the curves corresponding to different field cooling conditions in the same electric field has different shapes and different values below and above T → (T _f + 9 K)^? (for E _dc = 1.52 kV/cm). The reduced permittivities ?′_r(T, f) recorded under different cooling conditions are shown to change their behavior when passing through T = T _f + 9 K. In NERS, these curves diverge: the stronger the field (0 ≤ E _dc ≤ 3 kV/cm), the larger the divergence. In ERS, however, the ?′_r(T, f) curves coincide under different cooling conditions irrespective of the field. The character of the changes in Δ?′(T) and ?′_r (T, f) during the NERS-ERS transition is frequency-independent. The difference in the behavior of the dielectric response during ZFH after cooling in different (ZFC, FC) modes (even in a weak field), for both transition through T _f and cooling down to T = 10 K, indicates different NERSs forming under these conditions. The contribution to ?′(T) from slowly relaxing regions (ω ～ 0.1 mHz), whose polarization is reoriented after the field is turned off, is responsible for the fact that, during the NERS-ERS transition, the ?′_r(T, f) curves coincide at a temperature that is higher than T = T _f.     

Phase transition in electronic manganite Ca0.85Sm0.15MnO3

The resistivity, the magnetic susceptibility, the magnetization, and the specific heat of electronic manganite Ca_0.85Sm_0.15MnO₃ were studied. The data obtained suggest that this compound undergoes phase transition into the insulator antiferromagnetic state at T _c ～115 K and displays negative magnetoresistance at T<T _c . A minor ferromagnetic component of 0.025µ_B in the magnetization of Ca_0.85Sm_0.15MnO₃ may be caused by the deviation of this composition from the exact stoichiometry Mn³⁺: Mn⁴⁺=1: 8. The Debye temperature Θ_D=575 K and the entropy of phase transition ΔS=5.1 J/(mol K) were derived from the temperature dependence of specific heat.     

Nd1.85Ce0.15CuO4－δ单晶c-轴方向电阻的低场行为

采用自助熔剂缓冷法成功地生长出了Nd_1.85Ce_{0. 15}CuO_4-δ单晶，其零场下零电阻温度约为21K. 在0—0.5T范围内分别测量了磁场平行和垂直样品表面的电阻转变曲线以及0.5T不同角度下的电阻转变曲线. 结果显示磁场平行和垂直样品表面时的转变温度T_p随磁场的变化均服从H=H₀(1-T_p(h)/T_p(0))²关系. 0.5T 关键词： 1.85Ce_0.15CuO_4-δ单晶')" href="#">Nd_1.85Ce_0.15CuO_4-δ单晶 输运性质     

Ferroelastic phase transition and anomalous elastic and thermal properties of betaine borate (CH3)3NCH2COO·H3BO3

The temperature and pressure derivatives of the elastic constants of orthorhombic betaine borate, (CH₃)₃NCH₂COO·H₃BO₃, have been determined by measuring temperature and stress induced shifts of resonance frequencies of thick plates at ca. 15 MHz in the range between 140 and 300 K and 0 and 3 kbar. The elastic ‘shear’ resistance c₄₄ exhibits a value as low as 0.0492×10¹⁰Nm^-2at 293 K. With decreasing temperature c₄₄ approaches zero at ca. 142.5 K, indicating an acoustic soft mode behaviour connected with a ferroelastic phase transition. The softening of c₄₄ is described in a good approximation by c₄₄(T)_p=0 =alogT/T₀ with a=0.0663×10¹⁰Nm^-2 and T₀ = 139.5 K. Further, c₄₄ decreases with increasing pressure according to the linear relation c₄₄(p)_{T=293 K} = 0.0492?0.184×10^-4p (p in bar, c₄₄ in 10¹⁰ Nm^-2). All other elastic constants show a quite normal temperature and pressure dependence. At 293 K the transition is induced by a pressure of 2.65 kbar. The transition temperature T_c depends linearly on pressure according to T_c = 142.5+0.0568 p (pinbar, T_cinK). Passing through the transition no discontinuous change of the lattice constants is observed. The three principal coefficients of thermal expansion and the pressure derivatives of the dielectric constants exhibit discontinuities at the transition. The transition is of strongly second order.