311 resultados para NiMn2.0-xFexO4


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Gd1.99-xYxCe0.01SiO5 (Ce:GYSO) crystals (x = 0, 0.0995, 0.199) have been grown by the Czochralski (Cz) method. Crystal structure and the distribution coefficients of Ce have been determined for all three crystals. Spectroscopic measurements indicate that optical transmittance and luminescence intensity of Gd1.99-xYxCe0.01SiO5 (x = 0.0995, 0.199) crystals are Substantially higher than those of Ce:Gd2SiO5 (Ce:GSO), especially at x = 0.0995, which makes them good candidate materials for scintillation applications. The particularly important result is that the alloyed Ce:GYSO crystals can be grown easily by the Cz method and, unlike Ce:GSO, they do not undergo cleavage during the growth process or subsequent mechanical treatment. (c) 2005 Elsevier B.V. All rights reserved.

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采用提拉法生长了Yb掺杂原子数分数为0.5%的Yb:Y3Al5O12。(Yb2YAG)晶体,对晶体的吸收光谱和荧光光谱进行了分析。与Yb掺杂原子数分数为5%的Yb:YAG晶体进行了对比,得出采用940nm激光二极管(LD)抽运晶体最为合适。原子数分数为0.5%的Yb:YAG晶体相对于原子数分数为5%的Yb:YAG晶体白吸收效应的影响要小。测量了原子数分数为0.5%的Yb:YAG晶体的荧光寿命为0.95ms,与理论值很接近。因此采用原子数分数为0.5%的Yb:YAG晶体作为激光工作物质将有利于高效、小型集成

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This paper reports room-temperature ferromagnetism in Co- and Cu-doped In2O3 samples synthesized by a solid-state reaction method. Structure and composition analyses revealed that Co and Cu were incorporated into the In2O3 lattices. Photoluminescence measurement revealed an additional emission at 520 urn from these doped samples. The magnetic measurement showed that additional Cu doping greatly enhanced the ferromagnetism of In1.99Co0.01O3 bulk samples. The implication of the effects of additional Cu doping is also discussed. (c) 2007 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

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ZnO films were fabricated on LiGaO2 (0 0 1), (10 0) and (0 10) planes by RF magnetron sputtering. The structural, morphological and optical properties of as-grown ZnO films were investigated by X-ray diffraction (XRD), atomic force microscopy (AFM), Raman spectra and photoluminescence (PL) spectra. It is found that the orientation of ZnO films is strongly dependent on the substrate plane. [0 0 0 11, [1 (1) over bar 00] and [11 (2) over bar0] oriented ZnO films are deposited on LiGaO2 (001), (100) and (010), respectively. AFM shows the (0001) ZnO film consists of well-aligned regular hexagonal grains. Raman spectra reveal a tensile stress in the (0 0 0 1) ZnO film and a compressive stress in (110 0) and (112 0) ZnO films. PL spectra of all ZnO films exhibit only a near-band-edge UV emission peak. (C) 2008 Elsevier B.V. All rights reserved.

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Nanocrystalline Zn0.95 - xNi0.05AlxO (x = 0.01, 0.02, 0.05 and 0.10) diluted magnetic semiconductors have been synthesized by an auto-combustion method. X-ray diffraction measurements indicate that all Al-doped Zn0.95Ni0.05O samples have the pure wurtzite structure. Transmission electron microscope analyses show that the as-synthesized powders are of the size 40 - 45 nm. High-resolution transmission electron microscope, energy dispersive spectrometer and X-ray photoemission spectroscope analyses indicate that Ni2+ and Al3+ uniformly substitute Zn2+ in the wurtzite structure without forming any secondary phases. The Al doping concentration dependences of cell parameters (a and c), resistance and the ratio of green emission to UV emission have the similar trends. (c) 2007 Elsevier B.V. All rights reserved.

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为了重建东亚季风区域2.5MaB.P.前后植被和气候变化的历史,更好地了解低纬度地区植被变化及其对全球变化的响应,本研究选择了南海南部ODP1143站深海沉积物中的孢粉样品进行研究。通过高分辨率(7ka)的孢粉样品的分析研究,建立起3.0~2.0MaB.P.时段南海深海沉积孢粉组合序列,系统建立了这一时段植被演替序列。在此基础上,重点研究了2.5MaB.P.前后气候变化在南海周边地区植被演替中的响应,为探索和揭示东亚古季风及古环境演变提供了孢粉学依据。 ODP 1143站位于南沙海区,北纬9º22´,东经113º17´,深海柱状样采于水深2772m的大陆坡。本研究以生物地层学和氧同位素年代学为依据建立了年龄框架,对1143站135~95m(3.0~2.6 Ma B. P.)深海沉积中的孢粉样品进行了分析,建立了3.0~2.0MaB.P.时段南海深海沉积孢粉组合序列。孢粉样品处理方法主要是用盐酸去掉钙质和氢氟酸浸泡溶解硅质后,再用筛子将样品在超声波发生器中震荡过滤。孢粉的鉴定和统计在光学透视显微镜下完成。研究结果表明: 1、孢粉谱的主要特征是沉积率变化显著。与3.0~2.6 Ma B. P. 相比,2.6~2.0 Ma B. P.各类型花粉及孢子沉积率均有显著提高。该结果表明2.6 Ma B. P.南海海平面有显著下降,可与北半球冰盖形成、东亚季风增强相对应。 2、2.6 Ma B. P.以来,各类型孢粉沉积率变化与深海氧同位素分期相对应,代表了多次冰期-间冰期旋回。该结果表明南海海平面曾有多次上升和下降。 3、频谱分析结果表明,3.0~2.0 Ma B. P.存在0.1 Ma(偏心率)和46.9ka(斜率)的周期。

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本发明涉及日化领域及医药行业,具体是一种采用海藻糖季铵盐的吸湿 保湿剂及其制备方法。采用海藻糖季铵盐的吸湿保湿剂,以海藻糖季铵盐 作为吸湿保湿剂。制备方法:所述海藻糖季铵盐由按摩尔质量比为1∶4-6 的经碱性异丙醇溶液处理的海藻糖与醚化剂在40℃-60℃条件下反应3-9h, 而后抽滤、烘干即得;所述醚化剂为3-氯-2-羟丙基三甲基氯化铵。本发明 通过有效的合成手段得到的海藻糖季铵盐,生产成本提高甚微,吸湿保湿 性能提高明显。作为一种高效的吸湿保湿因子,本发明得到的海藻糖季铵 盐有望成为透明质酸的替代品用于化妆品中。