Fe掺杂对Bi2Sr2Co2Oy热电性能和自旋关联的影响

采用固相合成法制备出系列Fe掺杂的Bi2Sr2Co2Oy，样品，并对样品进行XRD分析，电阻率（p）、热电势（固和顺磁共振研究。结果表明：Fe掺杂浓度x≤0．3时样品基本为单相。Fe掺杂使体系的电阻率略微增大，热电势显著升高，这可能与Fe掺杂降低了空穴载流子浓度有关。Fe掺杂浓度x=0．05样品获得最大的功率因子（power factor，S^2／P）。顺磁共振结果显示，不掺Fe的样品有着较强的顺磁共振（ESR）信号，随着Fe含量的增加，ESR信号向低频方向移动，并逐渐宽化减弱直至消失。这表明Fe掺杂改变了体系的自旋关联状态，占据了Co位参与了Co—O—Co之间的自旋关联。研究结果表明合适的元素掺杂可以有效地调整体系的自旋关联状态，改善材料的热电性能。     

Sr对高铁Al-Si合金组织和性能的影响

研究了Sr元素（加入量分别为0．03％、0．06％、0．09％、0．12％和0．18％）对含Fe量为1．2％的ZL102合金的组织和性能的影响。研究发现，随着Sr元素的加入，合金中粗大的针状Fe相开始出现断裂分叉现象，同时针状Fe相的长度也随Sr元素加入量的增加而减小，但Sr对Fe相的针状形貌没有明显改变。随着Sr元素加入量逐渐增加，合金的抗拉强度和伸长率均呈现出先增后减的变化趋势。当Sr元素加入量达到0．12％时，合金材料的综合力学性能最佳。     

Microstructure and properties of (Sr, Ca)CuO2/(Sr, Ca)RuO3 multilayers

Epitaxial multilayer thin films of infinite-layer (Sr, Ca)CuO₂ and perovskite (Sr, Ca)RuO₃ have been prepared on (100) SrTiO₃ substrates by multitarget rf magnetron sputtering. X-ray diffraction analyses revealed that the multilayer structure of (Sr, Ca)CuO₃/(Sr, Ca)RuO₃ was successfully fabricated with a minimum layer thickness of 20 Å. Transmission electron microscopy measurements of the multilayers indicated that there was no dislocation which normally exists in single-layer films with an infinite-layer structure. Resistivities of multilayer films at room temperature ranged from 1 to 10 m cm and showed semiconductor-like dependence against the temperature.     

Structural instabilities and superconductivity in La-214 compounds

In La_2–x Ba _x CuO₄ (LBCO) the transition to a low-temperature tetragonal phase and the suppression of superconductivity occur at the carrier concentration p 1/8 per copper. We will discuss the roles of various material parameters that control this instability. An unusual lattice softening has been found by ultrasonic measurement on La_2–x Sr _x CuO₄ (LSCO). This softening is present only in an in-plane shearing mode and is ascribed to the growth of structural fluctuations in the normal state.These phenomena are closely related because both the structural change in LBCO and the applied strain in LSCO lift the degeneracy of in-plane oxygen sites. They clarify the importance of strong coupling between the normal-state electronic system and the lattice by a Peierls-type mechanism.     

Electrochemically Induced Crystalline-to-Amorphous Transition of Dinuclear Polyoxovanadate for High-Rate Lithium-Ion Batteries

Polyoxometalates are intriguing high-capacity anode materials for alkali-metal-ion storage due to their multi-electron redox capabilities and flexible structure. However, their poor electrical conductivity and high working voltage severely restrict their practical application. Herein, the dinuclear polyoxovanadate Sr₂V₂O₇·H₂O with unusually high electrical conductivity is reported as a promising anode material for lithium-ion batteries. During the initial lithiation process, the Sr₂V₂O₇·H₂O anode experiences an electrochemically induced crystalline-to-amorphous transition. The resulting amorphous structure provides high redox activity and fast reaction kinetics via reversible V^4.9+/V^2.8+ redox couple through the intercalation mechanism. Furthermore, when coupled with the LiFePO₄ cathode, the strong V O bonds of the amorphous anode provide excellent structural stability, with the full-cell capable of performing >12 000 cycles with a capacity retention of 72%. Another advantage of Sr_2xV₂O_7-δ·yH₂O (0.5 ≤ x ≤ 1.0) is its composition adjustability, which enables delicately regulating the Sr vacancy content without destroying the structure. The defect Sr_2xV₂O_7-δ·yH₂O (x = 0.5) electrodes show significantly improved specific capacity and rate capability without sacrificing other key properties, delivering a high specific capacity of 479 mAh g^-1 at 0.1 mA cm^-2 and 41.9% of its capacity in 2 min. Overall, the preliminary study points the way forward for the facile preparation of high-quality polyoxometalates for advanced energy storage applications and beyond.     

Phase equilibria and microstructure development in Mg-rich Mg-Gd-Sr alloys: Experiments and CALPHAD assessment

Mg-Sr alloys are promising to fabricate orthopedic implants. The alloying of rare earth elements such as Gd may improve the comprehensive mechanical properties of Mg-Sr alloys. The information on the phase diagram and the microstructure development are required to design chemical composition and microstructure of Gd alloyed Mg-Sr alloys. The phase equilibria and the microstructure development in Mg-rich Mg-Gd-Sr alloys (Gd, Sr < 30 at. %) are experimentally investigated via phase identification, chemical analysis, and microstructure observation with respect to the annealed ternary alloys. The onset temperatures of liquid formation are measured by differential scanning calorimetry. A thermodynamic database of the Mg-rich Mg–Gd–Sr ternary system is developed for the first time via CALPHAD (CALculation of PHAse Diagram) approach assisted by First-Principles calculations. The thermodynamic calculations with the developed database enable a well reproduction of the experimental findings and the physical-metallurgical understanding of the microstructure formation in solidification and annealing.     

Fe掺杂LSCCF对中低温固体氧化物燃料电池ITSOFC短期输出性能的影响

柠檬酸盐法制备La0.7Sr0.15Ca0.15Co1-xFexO3-δ(x=0.2、0.4、0.6、0.8)阴极材料。该前驱体在900℃处理2h后,XRD证实已经形成完整的钙钛矿结构衍射峰。随Fe掺杂量增加,XRD谱图衍射峰的位置向小角度发生偏移,粉体的晶粒尺寸逐渐变大。SEM观察La0.7Sr0.15Ca0.15Co1-xFexO3-δ粉体其表面活性较高并出现了一定的团聚现象,颗粒尺寸约为5μm。以La0.7Sr0.15Ca0.15Co1-xFexO3-δ为阴极,在氢气/空气中研究了模压法制备的单电池性能,Fe掺杂量对开路电压的高低不起决定性作用,而最高功率密度随Fe掺杂量增加而降低,在650℃最高功率密度由x=0.2时的351.7mW/cm2降为x=0.8时的231.1mW/cm2。     

低温烧结Dy-B-Si-O系玻璃介质掺杂Ba_(0.6)Sr_(0.4)TiO_3陶瓷

采用溶胶-凝胶法制备了Dy-B-Si-O系玻璃介质掺杂Ba0.6Sr0.4TiO3(BST)陶瓷粉体,并烧结成瓷。探讨了玻璃介质对BST陶瓷密度、烧结温度和介电性能的影响,利用扫描电子显微镜(SEM)、自动元件分析仪测试了BST陶瓷的显微结构和介电性能。研究结果表明,添加Dy-B-Si-O系玻璃介质降低了陶瓷烧结温度,提高了陶瓷致密度;随着Dy-B-Si-O系玻璃介质中Dy2O3组分含量的增加,介电常数增大;介电损耗先增大后减小,介电损耗最小值约为0.01,可满足在电压可调电容器上的使用要求。     

钴钇掺杂（Ba,Sr）TiO_3基介电陶瓷的制备与性能研究

采用二次固相反应法制备Ba0.7Sr0.3TiO3介电陶瓷,研究了掺杂钴、钇离子对钛酸锶钡介电性能的影响。结果表明,陶瓷样品Y3＋、Co3＋的最佳掺杂浓度分别为0.04mol%和0.05mol%,最佳烧结温度为1340℃,样品的相对介电常数为4200,介电损耗（tanδ）为0.005。样品的结构为四方晶系,P4mm空间群。获得了高介电常数、低损耗的Ba0.7Sr0.3TiO3介电陶瓷。