共查询到19条相似文献,搜索用时 93 毫秒
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采用脉冲激光淀积法在硅基氧化铝纳米有序孔膜版介质上(膜版孔径平均尺寸20nm,内生长Pt纳米线作为底电极一部分)制备了BaTiO3铁电纳米膜,并对其物性(铁电和介电性能)和微结构进行了表征。结果表明厚度170nm BaTiO3铁电膜的介电常数,随着测量频率的增加(103Hz至106Hz),从400缓慢下降到350;介电损耗在低频区域(103~105Hz)从0.029缓慢增加到0.036,而在高频率区域(〉105Hz)后,则迅速增加到0.07。这是由于BaTiO3铁电薄膜的介电驰豫极化引起的。电滞回线测量结果表明,该薄膜的剩余极化强度为17μC/cm2,矫顽场强为175kV/cm。剖面扫描透射电子显微镜(STEM)图像表明,BaTiO3纳米铁电薄膜与底电极Pt纳米线直接相连接,它们之间的界面呈现一定程度的弯曲。选区电子衍射图和高分辨电子显微像均表明BaTiO3铁电薄膜具有钙钛矿型结构。在BaTiO3纳米铁电薄膜退火晶化处理后,部分Pt纳米线的再生长导致顶端出现分枝展宽现象。为了兼顾氧化铝纳米有序孔膜版内的金属纳米线有序分布和BaTiO3纳米薄膜结晶度,合适的退火温度是制备工艺过程的关键因素。 相似文献
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模板合成法制备ZnO纳米线的研究 总被引:1,自引:0,他引:1
在草酸和硫酸电解液中分别制备了孔径为40 nm和20 nm左右的多孔氧化铝模板,用直流电化学沉积的方法,在模板孔洞内电解沉积Zn,对其进行高温下的氧化,可得到高度有序的ZnO纳米线.扫描电子显微镜观察显示,多晶的Zn纳米线均匀地填充到多孔氧化铝六角排布的孔洞里,直径与模板孔径相当.X射线衍射谱测量证实,制备的Zn纳米线和ZnO纳米线均为多晶结构,并且对比了模板孔径对纳米线结构的影响.测量了多孔氧化铝厚膜和Zn/Al2O3组装体的吸收光谱,发现其在红外波段的吸收系数有逐渐降低的趋势. 相似文献
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通过改变二次氧化过程中的氧化电压,制备了不同孔径的多孔Al(PAA)模板;采用交流电沉积的方法,制备了含Cu阳极PAA膜.X射线衍射(XRD)分析表明,阳极PAA膜上确有Cu生成;扫描电镜(SEM)显示,Cu纳米线粗细均匀,具有很好的线栅结构.Cu/PAA复合膜的透射光谱及偏振光谱表明:这种含Cu纳米线PAA膜在近红外光区有较好的透射率和消光比,且随着膜板孔径(Cu纳米线直径)的增加,样品的透射率下降而其消光比却明显提高.因此,可以通过优化模板参数,制备出实用的Cu/PAA偏振器. 相似文献
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在利用电迁移现象制备铝纳米线的过程中,铝纳米线的生长位置取决于铝原子的积聚位置。为实现铝原子积聚位置控制,基于纳米压痕技术改变试样中铝膜的横截面结构,制备了铝膜试样。通过输入并调节直流电大小使铝膜内产生电迁移现象。试验结果表明,纳米压痕技术可有效提高局部区域的电流密度,显著增强铝原子的电迁移强度,并在压痕区域出现铝原子积聚现象。 相似文献
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将Al片在较高的电压下进行阳极氧化,制备了氧化铝纳米线。其形成机制主要是多孔氧化铝膜生长的同时,其微结构单元阵列在薄膜应力作用下沿薄壁处破裂,从而生成了氧化铝纳米线。扫描电镜和透射电镜观测表明,所得产物结构外形基本一致,呈凹柱面正三棱柱形,表观直径约30~300nm,长度为几微米至数十微米。采用BET法对产物的比表面积进行测量,实验值为5.8×104m2/kg,接近于理论计算值6.2×104m2/kg。实验表明,这种氧化铝一维纳米结构材料对超小Ag和CdS纳米颗粒具有较强的吸附能力,对很难用传统的过滤和离心沉淀法去除的超小纳米颗粒(直径小于10nm)也能做到有效吸附,有望成为超级吸附与过滤材料。 相似文献
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ZHUANG Hui-zhao LI Bao-li XUE Cheng-shan ZHANG Shi-ying WANG De-xiao SHEN Jia-bing 《半导体光子学与技术》2008,14(1):42-47
Large-scale GaN nanowires are successfully synthesized by ammoniating Ga2O3 films on Nb layer deposited on Si(111) substrates at 850 ℃. X-ray diffraction (XRD), scanning electron microscopy (SEM), field-emssion transmission electron microscope(FETEM), Fourier transformed infrared spectrum(FTIR) are used to characterize the structural and morphological properties of the as-synthesized GaN nanowires. The results reveal that the nanowires are pure hexagonal GaN wurtzite structure with a length of about several microns and a diameter between 50 nm and 100 nm. Finally, discussed briefly is the formation mechanism of gallium nitride nanowires. 相似文献
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R. Gunawidjaja C. Jiang S. Peleshanko M. Ornatska S. Singamaneni V.V. Tsukruk 《Advanced functional materials》2006,16(15):2024-2034
Freestanding layer‐by‐layer (LbL) films encapsulating controlled volume fractions (? = 2.5–22.5 %) of silver nanowires are fabricated. The silver nanowires are sandwiched between poly(allylamine hydrochloride)/poly(styrene sulfonate) (PAH/PSS) films resulting in nanocomposite structures with a general formula of (PAH/PSS)10PAH Ag(PAH/PSS)10PAH. The Young's modulus, toughness, ultimate stress, and ultimate strain are evaluated for supported and freestanding structures. Since the diameter of the nanowires (73 nm) is larger than the thickness of the LbL films (total of about 50 nm), a peculiar morphology is observed with the silver nanowires protruding from the planar LbL films. Nanowire‐containing LbL films possess the ability to sustain significant elastic deformations with the ultimate strain reaching 1.8 %. The Young's modulus increases with increasing nanowire content, reaching about 6 GPa for the highest volume fraction, due to the filler reinforcement effect commonly observed in composite materials. The ultimate strengths of these composites range from 60–80 MPa and their toughness reaches 1000 kJ m–3 at intermediate nanowire content, which is comparable to LbL films reinforced with carbon nanotubes. These robust freestanding 2D arrays of silver nanowires with peculiar optical, mechanical, and conducting properties combined with excellent micromechanical stability could serve as active elements in microscopic acoustic, pressure, and photothermal sensors. 相似文献
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The steady-state photoconductivity (PC) response of deep level defects to sub-bandgap illumination was studied in GaN nanowires
(NWs) grown by metalorganic chemical vapor deposition. Photoemission from defects residing in the NW surface depletion region
alters the depletion width, and the PC response arises mainly from the resulting enhancement of the cross-sectional area of
the electrically conductive NW core. The advantages of emphasizing depletion region processes for deep level spectroscopy
of NWs are discussed. A simple electrostatic model was adopted to explain the strong relative increase of sub-bandgap PC response
with decreasing NW width. NW deep level spectra were similar to those widely reported for planar GaN films, suggesting that
the corresponding defects are located throughout the NW volume and are not specific to the surface. 相似文献
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H.F. Al-Taay M.A. Mahdi D. Parlevliet P. Jennings 《Materials Science in Semiconductor Processing》2013,16(1):15-22
Silicon nanowires were grown on ITO-coated glass substrates via a pulsed plasma enhanced chemical vapor deposition method, using tin as a catalyst. The thin films of catalyst, with different thicknesses in the range 10–100 nm, were deposited on the substrates by a thermal evaporation method. The effect of the thickness of the thin film catalyst on the morphology of the silicon nanowires was investigated. The scanning/transmission electron microscopy images showed that the wire diameter increased as the thickness of the thin film catalyst increased. The nanowires grown using a thin film thickness of 10 nm were inhomogeneous in diameter, whereas the other thicknesses led to an increase in the homogeneity of the diameters of the nanowires. The dominant wire diameter of the grown silicon nanowires ranged from 70 to 80 nm with 10 nm catalyst thin film thickness, and increased to a range of 190–200 nm with 100 nm catalyst thin film thickness. 相似文献
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A. Amma B. Razavi S.K. St. Angelo T.S. Mayer T.E. Mallouk 《Advanced functional materials》2003,13(5):365-370
Carbon nanotubules and nanowires were synthesized by pyrolysis of polymer precursors in the pores of alumina membranes. The nanowires were released by dissolving the membranes, and were then made hydrophobic or hydrophilic by chemical surface derivatization. These nanowires could be placed into lithographically defined wells on surfaces by means of electrostatic interactions with monolayers at the bottoms of the wells. 相似文献
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Sujay Phadke Jung‐Yong Lee Jack West Peter Peumans Alberto Salleo 《Advanced functional materials》2011,21(24):4691-4697
Factors affecting charge transport through ZnO nanowire mat films were studied by aligning ZnO nanowires on substrates and coupling experimental measurements with 2D nanowire network simulations. Gallium doped ZnO nanowires were aligned on thermally oxidized silicon wafer by shearing a nanowire dispersion in ethanol. Sheet resistances of nanowire thin films that had current flowing parallel to nanowire alignment direction were compared to thin films that had current flowing perpendicular to nanowire alignment direction. Perpendicular devices showed ~5 fold greater sheet resistance than parallel devices supporting the hypothesis that aligning nanowires would increase conductivity of ZnO nanowire electrodes. 2‐D nanowire network simulations of thin films showed that the device sheet resistance was dominated by inter‐wire contact resistance. For a given resistivity of ZnO nanowires, the thin film electrodes would have the lowest possible sheet resistance if the inter‐wire contact resistance was one order of magnitude lower than the single nanowire resistance. Simulations suggest that the conductivity of such thin film devices could be further enhanced by using longer nanowires. 相似文献
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Si nanowires (Si-NWs) were fabricated by a simple process that consists of deposition of Au thin films, annealing of the Au films to form porous structure and Si wet-etching using the kinetically appearing porous Au films as a template. The deformation behavior of the Au thin films was investigated by scanning electron microscopy and atomic force microscopy. The nanohole diameter and density of the Au films can be controlled by selecting Au film thickness, annealing temperature and annealing time. The formation mechanism of these porous Au films can be explained by a model that consists of nanohole formation at the grain boundaries of the Au films and ridge formation by Au atom diffusion to the hole periphery. The ridge structure suppresses further deformation of the Au films and keeps the nanohole structure kinetically stable. When a thermal energy larger than the activation energy to destroy the ridge structure is supplied, it transforms to the island structure. 相似文献