F.H.Li
金属学报(英文版)
The melting temperature and critical transition temperature T, of YBa2Cu3O7-δ with deferent content additives of PbO and BaPbO3 were studied. When PbO was doped in YBa2Cu3O7-δ the melting temperature of YBa2Cu3O7-δ was reduced, however its superconductivity was weakened. From the XRD pattern of the sintered mixture of YBa2Cu3O7-δ and PbO, it was known that there was a reaction between YBa2Cu3O7-δ and PbO, and the product was BaPbO Hence different contents of BaPbO3 (10mass, 20massand 30mass) were added in YBa2Cu3O7-δ It was proved that there were no reactions between YBa2Cu3O7-δ and BaPbO3.And the superconductivity of the mixtures was much better than that of the samples with PbO additive.
关键词:
YBa2Cu3O7-δ PbO additive
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null
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null
肖剑荣
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徐慧
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李幼真
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刘雄飞
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马松山
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简献忠
中国有色金属学报
使用CF4和CH4为源气体,利用射频等离子体增强化学气相沉积法,制备了a-C:F:H薄膜样品.采用拉曼光谱仪、傅里叶变换红外光谱仪、X射线光电子能谱仪(XPS)对薄膜的结构进行了测试和分析.研究发现:该膜呈空间网状结构,膜内碳与氟、氢的结合主要以sp3形式存在,而sp2形式的含量相对较少;在薄膜内主要含有C-Fx(x=1,2,3)、C-C、C-H2、C-H3等以及不饱和C=C化学键;同时,薄膜中C-C-F键的含量比C-C-F2键的含量要高.在不同功率下沉积的薄膜,其化学键结构明显不同.
关键词:
a-C:F:H薄膜
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等离子体增强化学气相沉积
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低介电常数
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化学键
Journal of Materials Research
The effect of Li(3)N additive on the Li-Mg-N-H system was examined with respect to the reversible dehydrogenation performance. Screening Study with varying Li(3)N additions (5, 10, 20, and 30 mol%) demonstrates that all are effective for improving the hydrogen desorption capacity. Optimally, incorporation of 10 mol% Li(3)N improves the practical capacity from 3.9 wt% to approximately 4.7 wt% hydrogen at 200 degrees C, which drives the dehydrogenation reaction toward completion. Moreover, the capacity enhancement persists well over 10 de-/rehydrogenation cycles. Systematic x-ray diffraction examinations indicate that Li(3)N additive transforms into LiNH(2) and LiH phases and remains during hydrogen cycling. Combined structure/property investigations suggest that the LiNH(2) "seeding" should be responsible for the capacity enhancement, which reduces the kinetic barrier associated with the nucleation of intermediate LiNH(2). In addition, the concurrent incorporation of LiH is effective for mitigating the ammonia release.
关键词:
complex hydrides;improvement;mixtures;imides;amide;h-2
马毅斌
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李宁
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黎德育
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张密林
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黄晓梅
腐蚀学报（英文）
用电化学方法研究了Mg-14Li-1Al-0.1Ce合金在卤素溶液(NaX, X=F, Cl,Br和I)中的腐蚀行为并用失重法测定其腐蚀速率, 用扫描电镜(SEM)观察腐蚀后的表面形貌, 利用XRD检定腐蚀产物的相组成.结果表明, 合金在卤素溶液中的腐蚀速率由低到高的顺序是:NaF<NaI<NaBr<NaCl. 经过48 h腐蚀后, 合金在NaCl、NaBr和NaI溶液中的腐蚀产物层的组分为Mg(OH)2,Li3Mg7和Li0.92Mg4.08,而在NaF溶液中的腐蚀产物层的组分为Li3Mg7和Li0.92Mg4.08. 此外, 合金在NaF溶液中的电化学活性非常低, 出现了钝化现象.电化学阻抗谱表明合金腐蚀产物层不能起到防止基体腐蚀的作用.
关键词:
镁锂合金
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corrosion
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sodium halide
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EIS
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XRD
马毅斌
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李宁
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黎德育
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张密林
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黄晓梅
腐蚀学报（英文）
用电化学方法研究了Mg-14Li-1Al-0．1Ce合金在卤素溶液（NaX，X=F，C1，Br和I）中的腐蚀行为并用失重法测定其腐蚀速率，用扫描电镜（SEM）观察腐蚀后的表面形貌，利用XRD检定腐蚀产物的相组成．结果表明，合金在卤素溶液中的腐蚀速率由低到高的顺序是：NaF〈NaI〈NaBr〈NaCl．经过48h腐蚀后，合金在NaCl、NaBr和NaI溶液中的腐蚀产物层的组分为Mg（OH）2，Li3Mg7和Li0.92Mg4.08，而在NaF溶液中的腐蚀产物层的组分为Li3Mg7和Li0．92Mg4．08．此外，合金在NaF溶液中的电化学活性非常低，出现了钝化现象．电化学阻抗谱表明合金腐蚀产物层不能起到防止基体腐蚀的作用．
关键词:
镁锂合金
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腐蚀
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卤化钠
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EIS
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XRD
林碧洲
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许承晃
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吴季怀
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邱继晨
人工晶体学报
doi:10.3969/j.issn.1000-985X.1998.01.022
描述了掺氧族离子(O2-,S2-,Se2-)NaCl晶体中(F+2)H心的制备过程,报道了氧族离子稳定的(F+2)H心的吸收光谱和发射光谱,测量了这些(F+2)H心的室温避光稳定性.研究表明,氧族离子对F+2心的稳定作用顺序为O2-＜Se2-＜S2-,而受这三种离子扰动的(F+2)H心的光谱峰位相对于纯F+2心的移动大小亦为这一顺序.这一顺序与它们相应元素的电子亲合能顺序相同(分别为1.47,2.02,2.07eV).从而,纠正了根据离子大小为预测的结果O2-＜S2-＜Se2-.本文结果对(F+2)H色心激光晶体材料的研究具有指导意义.研究还表明,随着离子半经的增大,生长出优质的掺杂晶体越来越困难.
关键词:
色心激光
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激活心
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掺杂效应
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稳定性
Journal of Physical Chemistry C
The Li-Mg-N-H system was prepared by reacting magnesium amide [Mg(NH(2))(2)] with lithium nitride (Li(3)N) and investigated with regard to the hydrogen storage properties. Our study shows that the present method is superior to the conventional route in enhancing the reversible dehydrogenation properties. Through optimizing the Li(3)N:Mg(NH(2))(2) ratio in the starting materials, the reversible capacity of U-Mg-N-H system increases to 4.9 wt %, 18% higher than that typically obtained from the Mg(NH(2))(2) + 2LiH mixture at 200 degrees C. Furthermore, increasing the Li(3)N:Mg(NH(2))(2) ratio is effective for mitigating the ammonia release from thus-prepared samples. Combined property/structure investigations indicate that the obtained enhancements should be ascribed to the effects of LiNH(2) and LiH that were in situ generated from the excess Li(3)N. LiNH(2) may promote the dehydrogenation reaction via seeding the reaction intermediate. The concurrently generated LiH acts as an effective ammonia trapping agent. These findings highlight the potential of "intermediate seeding" as a strategy to enhance the reversible hydrogen storage properties of metal-N-H systems.
关键词:
complex hydrides;ultrafast reaction;amide;improvement;desorption;linh2;destabilization;mechanism;mixtures;imides
Physica B-Condensed Matter
The spin-Hamiltonian parameters (g factors g(parallel to), g(perpendicular to) and hyperfine structure constants (161)A(parallel to), (161)A(perpendicular to), (163)A(parallel to), (163)A(perpendicular to)) for Dy(3+) at the tetragonal H(f)(4+) site of H(f)SiO(4) crystal are calculated from the diagonalization (of energy matrix) method. In the method, we add the Zeeman (or magnetic) and hyperfine interaction terms to the conventional Hamiltonian used in the calculations of crystal-field energy levels. The 66 X 66 energy matrix concerning the new Hamiltonian is established by considering the ground multiplet (6)H(15/2) and the first to fifth excited multiplets (6)H(J) (where J=13/2, 11/2,9/2, 7/2 and 5/2), and the crystal-field parameters in the energy matrix are calculated from the superposition model. From the calculations, the spin-Hamiltonian parameters of H(f)SiO(4):Dy(3+) are explained reasonably and the signs of hyperfine structure constants for (161)Dy(3+) and (161)Dy(3+) isotopes in H(f)SiO(4) are suggested. The results are discussed. (C) 2010 Elsevier B.V. All rights reserved.
关键词:
Electron paramagnetic resonance;Crystal-field theory;Point defect;Dy(3+);H(f)SiO(4);superposition-model analysis;single-crystals;paramagnetic-resonance;structure silicates;zircon;growth;hafnon;field;epr;er3
裴增文
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刘晓鹏
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黄倬
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李志念
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王树茂
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蒋利军
稀有金属
doi:10.3969/j.issn.0258-7076.2010.04.013
采用等容法研究了机械球磨工艺制备的Li-Mg-N-H材料储氧性能,结果发现,在室温下采用氦气对样品室体积进行标定时,由于Li-Mg-N-H材料对氦气有一定量的物理吸附,造成准确Li-Mg-N-H材料样品体积标定误差,进而造成Li-Mg-N-H储氢材料在503 K下放氢容量随压力的降低而增加异常变化.为准确标定样品体积,通过对Li-Mg-N-H材料室温氮气吸附容量测定,并采用迭代计算方法获得准确的储氢材料样品体积,进而测定Li-Mg-N-H储氢材料503 K下放氢PCT曲线,其表现为放氢容量随压力降低而减小的正常变化规律.Li-Mg-N-H储氢材料503 K,9.6 MPa氢压下的最大储氢容量为4.81%(质量分数),放氢过程表现为单一放氢平台特性.
关键词:
轻质储氢材料
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Li-Mg-N-H
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储氢性能
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等容测试方法
