类金刚石碳纳米线的制备及生长机理

采用热蒸发法制备了类金刚石碳纳米线,利用透射电子显微镜(TEM)和高分辨率透射电子显微镜(HRTEM)对样品的形貌和结构进行观察,发现该碳纳米线具有圆形实心结构,表面光滑,直径10～40 nm;拉曼光谱研究显示特征峰出现在1 352 cm-1和1 586 cm-1处,为典型的类金刚石结构.用CO辅助生长机理解释类金刚石碳纳米线的形成过程.     

钽催化磁控溅射法制备GaN纳米线

利用磁控溅射技术通过氮化Ga2O3/Ta薄膜,合成大量的一维单晶纤锌矿型氮化镓纳米线.用X射线衍射、扫描电子显微镜、高分辨透射电子显微镜,选区电子衍射和光致发光谱对制备的氮化镓进行了表征.结果表明;制备的GaN纳米线是六方纤锌矿结构,其直径大约20～60 nm,其最大长度可达10 μm左右.室温下光致发光谱测试发现363 nm处的较强紫外发光峰.另外,简单讨论了氮化镓纳米线的生长机制.     

氨化Si基Ga2O3/V膜制备GaN纳米线

氨化硅基钒应变层氧化镓膜制备了大量氮化镓纳米线,X射线衍射、扫描电子显微镜和透射电子显微镜观察发现,纳米线具有十分光滑且干净的表面,其直径为20～60 nm左右,长度达到十几微米.高分辨透射电子显微镜和选区电子衍射分析结果表明,制备的氮化稼纳米线为六方纤锌矿结构.光致发光谱显示制备的氮化稼纳米线有良好的发光特性.另外,简单讨论了氮化稼纳米线的生长机制.     

表面活性剂辅助水热法制备ZnS纳米线

用十二烷基硫醇做表面活性剂,用水热法在180℃,12 h条件下制备了ZnS纳米线.实验发现硫醇可以诱导ZnS纳米粒子沿着一维方向生长.所得产物ZnS纳米线为六方纤锌矿结构,直径为50 nm～100 nm,长度10 μm～20 μm.用X射线衍射(XRD)、透射电子显微镜(TEM)、扫描电子显微镜(SEM)、荧光发射光谱(PL)和紫外漫反射光谱(UV)等手段对所得纳米线进行了表征,并初步探讨了硫醇在限制ZnS纳米晶一维方向生长的机理.     

Preparation of GaN Nanorods by Rare Earth Metal Tb Catalyst-Assisted Process

利用稀土金属Tb作为催化剂,通过氨化磁控溅射在Si(111)衬底上的Ga203/Tb薄膜制备出GaN纳米棒.X射线衍射和傅里叶红外吸收谱测试结果表明,制备的样品为六方结构的GaN.利用扫描电子显微镜、透射电子显微镜和高分辨透射电子显微镜对样品进行测试,结果显示样品为单晶结构的纳米棒,直径为80～200 nm,长度达几十微米.最后简单地讨论了GaN纳米棒的生长机制.     

氨化磁控溅射Ga2O3/BN薄膜制备GaN纳米棒

利用射频磁控溅射技术在Si(111)衬底上制备Ga2O3/BN薄膜,在氨气中退火合成了大量的一维GaN纳米棒.用X射线衍射(XRD)、选区电子衍射(SAED)、傅立叶红外透射谱(FTIR)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)和光致发光谱(PL)对样品的晶体结构、元素成分、形貌特征和光学特性进行了分析.结果表明GaN纳米棒为六方纤锌矿结构的单晶相,其直径在150 nm～400 nm左右,长度可达几十微米.室温下光致发光谱的测试发现了较强的372nm处的强紫外发光峰和420nm处的蓝色发光峰.     

氨化磁控溅射Ga2O3/BN薄膜制备GaN纳米棒

利用射频磁控溅射技术在Si(111)衬底上制备Ga2O3/BN薄膜,在氨气中退火合成了大量的一维GaN纳米棒.用X射线衍射(XRD)、选区电子衍射(SAED)、傅立叶红外透射谱(FTIR)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)和光致发光谱(PL)对样品的晶体结构、元素成分、形貌特征和光学特性进行了分析.结果表明:GaN纳米棒为六方纤锌矿结构的单晶相,其直径在150 nm～400 nm左右,长度可达几十微米.室温下光致发光谱的测试发现了较强的372nm处的强紫外发光峰和420nm处的蓝色发光峰.     

氨化合成一维GaN纳米线

用氨化溅射Ga2O3薄膜的方法，成功地合成了一维GaN纳米线。用X射线衍射仪(XRD)、扫描电镜(SEM)、透射电镜(TEM)和高分辨电镜(HRTEM)对样品进行了分析。生成的GaN纳米线平直光滑，其直径为20nm～90nm，长可达50μm；纳米线为高质量的单晶六方纤锌矿GaN，沿[110]方向生长。用此工艺制备GaN纳米线，避免了在制备过程中引入杂质，合成的纳米线纯度较高。     

稀土金属Tb催化制备GaN纳米棒(英文)

利用稀土金属Tb作为催化剂,通过氨化磁控溅射在Si(111)衬底上的Ga2O3/Tb薄膜制备出GaN纳米棒。X射线衍射和傅里叶红外吸收谱测试结果表明,制备的样品为六方结构的GaN。利用扫描电子显微镜、透射电子显微镜和高分辨透射电子显微镜对样品进行测试,结果显示样品为单晶结构的纳米棒,直径为80～200nm,长度达几十微米。最后简单地讨论了GaN纳米棒的生长机制。     

Sb2S3纳米线的制备和表征

以硫化钠(Na2S)和氯化锑(SbCl3)为原料,采用水热法在240 ℃下反应12 h 制备了大量高长径比的Sb2S3纳米线.X射线粉末衍射测试结果表明,所制备的产物是正交Sb2S3晶相,其晶胞参数为:a=1.123 nm,b=1.131 nm,c=0.3840 nm.通过扫描电子显微镜(SEM)、透射电子显微镜(TEM)和高分辨透射电镜(HRTEM)分析表明:所制备的Sb2S3纳米线为单晶并且沿[001]晶面生长,其直径为100～250 nm,长为100 μm.初步讨论了Sb2S3纳米线的生长机制.     

Effect of ammoniating temperature on microstructure and optical properties of one-dimensional GaN nanowires doped with magnesium

One-dimensional GaN nanowires doped with Mg element have been successfully prepared on Si (1 1 1) substrates by magnetron sputtering through ammoniating Ga₂O₃/Mg thin films, and the effect of the ammoniating temperatures on the microstructure and optical properties of the GaN nanowires was investigated in detail. X-ray diffraction (XRD), X-ray photoelectron spectroscope (XPS), FT-IR spectrophotometer, Scanning electron microscope (SEM), high-resolution transmission electron microscope (TEM), and photoluminescence (PL) spectrum were carried out to characterize the microstructure, morphology, and optical properties of GaN nanowires. The results demonstrate that ammoniating temperature has a significant effect on microstructure, morphology and optical properties of GaN nanowires. GaN nanowires after ammoniation at 900 °C for 15 min are straight, smooth and of uniform thickness along spindle direction with the highest crystalline quality. The growth direction of these nanowires is parallel to [1 0 0] orientation.     

Catalytic Growth of Large-Scale GaN Nanowires

A novel lanthanon seed was employed as the catalyst for the growth of GaN nanowires. Large-scale GaN nanowires have been synthesized successfully through ammoniating Ga₂O₃/Tb films sputtered on Si(111) substrates. Scanning electron microscopy, x-ray diffraction, high-resolution transmission electron microscopy, and Fourier transform infrared spectroscopy were used to characterize the samples. The results demonstrate that the nanowires are single-crystal hexagonal wurtzite GaN. The growth mechanism of GaN nanowires is also discussed.     

Growth and optical properties of gallium nitride nanowires produced via different routes

Several vapor phase processes for the preparation of GaN nanowires, such as chemical vapor deposition (CVD), direct reaction (DR), and hydride vapor phase epitaxial growth (HVPE), have been previously reported. To determine the most appropriate route for fabrication and engineering of GaN nanowires, we prepared nanowires via the three aforementioned routes and characterized their microstructures and photoluminescence (PL) properties. All prepared nanowires were single-crystalline, whowing well-defined crystal structure in X-ray diffraction and transmission electron microscopic analyses. However, high-quality nanowires could most readily be obtained by DR. Large-scale and selective area growth of nanowires could most readily be achieved by CVD and HVPE. PL spectra for the nanowires prepared by HVPE showed a red-shifted center wavelength and wider full width-half maximum (FWHM) value as compared to those prepared by DR or CVD. This indicates the presence of unknown impurities and/or defects in the nanowires prepared by HVPE. Our results indicate that high-quality nanowires can be prepared by DR and CVD, while large-scale selective growth can be achieved by CVD and HVPE.     

Si（111）衬底上生长GaN晶环的研究

利用热壁化学气相沉积在Si(111)衬底上获得GaN晶环，采用扫描电镜(SEM)、选择区电子衍射(SAED)、X射线衍射(XRD)，光致发光(PL)谱和傅里叶红外吸收谱(FTIR)对晶环的组成、结构、形貌和光学特性进行分析。初步结果证明：在Si(111)衬底上获得择优生长的六方纤锌矿结构的GaN晶环。SEM显示在均匀的薄膜上出现直径约为10μm的5品环，由XRD和SAED的分析证实晶环呈六方纤矿多晶结构，FTIR显示GaN薄膜的主要成分为GaN，同时含有少量的C污染，PL测试表明晶环呈现不同于GaN薄膜的发光特性。     

Synthesis of one-dimensional GaN nanorods by Tb intermediate layer with different thicknesses

GaN nanorods were synthesized by magnetron sputtering and ammonification system, and the thickness of Tb intermediate layer was changed to study the effect on GaN nanorods. The resultant was tested by scanning electron microscopy (SEM), X-ray diffraction (XRD), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), and photoluminescence (PL) spectra. The results show that the thickness of Tb layer has an evident effect on the modality, quality, and luminescence properties of GaN nanorods. PL spectra at room temperature show a very strong emission peak at 368 nm and a weak emission peak at 387 nm, and the intensities of the peak for the produced samples reach the maximum when Tb layer is 20 nm. Finally, the optimal thickness of 20 nm of Tb intermediate layer for synthesizing GaN nanostructures is achieved.     

热壁化学气相沉积Si基GaN晶体膜的研究

采用热壁化学气相沉积工艺在Si(111)衬底上生长GaN晶体膜，并对其生长条件进行研究。用X射线衍射(XRD)、扫描电镜(SEM)、荧光光谱(PL)对样品进行结构、形貌和发光特性的分析。测试结果表明：用此方法得到了六方纤锌矿结构的GaN晶体膜。实验结果显示：采用该工艺制备GaN晶体膜时，选择H2作反应气体兼载体，对GaN膜的形成起着非常有利的作用。     

Preparation and Properties of GaN Micro-Ribbons on Ga-Diffused Si （111） Substrates

用射频磁控溅射工艺在室温扩镓硅衬底上沉积Ga2O3膜,然后在氨气气氛下氮化Ga2O3膜得到GaN微米带,用X射线衍射(XRD)、扫描电镜(SEM)、选区电子衍射(SAED)、X射线光电子能谱(XPS)及光致发光谱(PL)对薄膜样品进行了结构、表面形貌、组分及发光特性分析.SEM图像显示直径约为100 nm～300 nm微米带随机分布在GaN薄膜表面.XRD、XPS及SAED分析表明GaN微米带呈六方闪锌矿多晶结构,择优沿[001]方向生长.P1显示了可能由量子限制效应引起的发光峰,其相对于报道的GaN晶体发光峰有显著蓝移.     

氨化Si基Ga2O3／Al2O3制备GaN薄膜

研究了Ga2O3／Al2O3膜反应自组装制备GaN薄膜。首先利用磁控溅射法在硅衬底上制备Ga2O3／Al2O3膜，再将Ga2O3／Al2O3膜在高纯氨气气氛中氨化反应得到了GaN薄膜。用X射线衍射(XRD)，X光光电子能谱(XPS)、扫描电镜(SEM)、透射电镜(TEM)和荧光光谱(PL)对样品进行结构、组分、形貌和发光特性的分析。测试结果表明：用此方法得到了六方纤锌矿结构的GaN晶体膜。