在Si(111)上脉冲ArF准分子激光淀积晶态定向α-SiC薄膜

报道用脉冲ArF激光烧蚀SiC陶瓷靶,在800℃Si(111)衬底上淀积SiC薄膜,再经920℃真空(10-3Pa)退火处理,制备出晶态α-SiC薄膜.用FTIR、XPS、SEM、XRD、TEM、PL谱等分析方法,研究了薄膜的表面形态、晶体结构、微结构、组成、化学态和光致发光等.结果表明,在920℃较低温度下,SiC薄膜经非晶核化--长大过程,生成了晶态α-SiC(0001)∥Si(111)高度定向外延膜,薄膜内C/Si比约为1.01.表面有污染C及少量氧化态Si和C.室温下用280nm光激发薄膜,在341nm处有较强发光峰,半峰宽45nm,显示出较好的短波发光性质.     

HFCVD法制备SiC材料及室温光致发光

利用热丝化学气相沉积法(HFCVD)以CH4和SiH4作为反应气体在Si衬底上制备了SiC薄膜。用X射线衍射(XRD)、傅立叶红外吸收谱(FTIR)等手段对样品进行了结构和组分分析，分析结果表明已经在Si衬底上制备了SiC薄膜。对所制备的SiC薄膜进行了光致发光测试，在室温下观察到了薄膜峰值位于417nm和436nm的较强的可见光发射，认为这两个相近的蓝光发射起源可能是光激发载流子从SiC晶粒核心激发．然后转移到SiC晶粒表面发光中心上的辐射复合。     

纳米6H-SiC薄膜的等离子体化学气相沉积及其紫外发光

采用螺旋波等离子体化学气相沉积技术在Si(100)衬底上制备了具有纳米结构的碳化硅(SiC)薄膜.通过X射线衍射、傅里叶红外吸收和扫描电子显微镜等技术对所制备薄膜的结构、形貌以及键合特性进行了分析,利用光致发光技术研究了样品的发光特性.分析表明,在500℃的衬底温度和高氢气稀释条件下,所制备的纳米SiC薄膜红外吸收谱主要表现为SiC TO声子吸收,X射线衍射显示所制备的纳米SiC薄膜为6H结构.采用氙灯作为激发光源,不同氢气流量下所制备的样品在室温下呈现出峰值波长可变的紫外发光.     

纳米6H-SiC薄膜的等离子体化学气相沉积及其紫外发光

采用螺旋波等离子体化学气相沉积技术在Si(100)衬底上制备了具有纳米结构的碳化硅(SiC)薄膜.通过X射线衍射、傅里叶红外吸收和扫描电子显微镜等技术对所制备薄膜的结构、形貌以及键合特性进行了分析,利用光致发光技术研究了样品的发光特性.分析表明,在500℃的衬底温度和高氢气稀释条件下,所制备的纳米SiC薄膜红外吸收谱主要表现为SiC TO声子吸收,X射线衍射显示所制备的纳米SiC薄膜为6H结构.采用氙灯作为激发光源,不同氢气流量下所制备的样品在室温下呈现出峰值波长可变的紫外发光.     

热丝化学气相沉积制备多晶硅薄膜的研究

采用热丝化学气相沉积技术制备了多晶硅薄膜。利用Raman、XRD、SEM等检测手段,系统研究了沉积气压、衬底温度、衬底与热丝间距离、衬底种类等实验参数对多晶硅薄膜晶态比、晶面择优取向、晶粒尺寸的影响。得出优化条件:沉积气压42 Pa,衬底温度250℃,衬底与热丝间距离48 mm,在玻璃衬底上制备出晶态比Xc>90%,择优取向为(111),横向晶粒尺寸为200~500 nm,纵向晶粒尺寸为30 nm左右的优质多晶硅薄膜。     

nc-SiC/SiO_2镶嵌薄膜材料的制备、结构和发光特性

采用二氧化硅/碳化硅复合靶,用射频磁控共溅射技术和后高温退火的方法在Si(111)衬底上制备了碳化硅纳米颗粒/二氧化硅基质(nc-SiC/SiO2)镶嵌结构薄膜材料。用X射线衍射(XRD),傅里叶红外吸收(FTIR),扫描电子显微镜(SEM)和光致发光(PL)实验分析了薄膜的微结构以及光致发光特性。实验结果表明,样品薄膜经高温退火后,部分无定形SiC发生晶化,形成β-SiC纳米颗粒而较均匀地镶嵌在SiO2基质中。以280nm波长光激发薄膜表面,有较强的365nm的紫外光发射以及458nm和490nm处的蓝光发射,其发光强度随退火温度的升高显著增强,发光归结为薄膜中与Si—O相关的缺陷形成的发光中心。     

SiC纳米晶薄膜的制备及发光性质研究

用射频磁控溅射及后退火(800℃、1000℃和1200℃)方法,在Si(111)衬底上制备出了SiC纳米晶(nc-SiC)薄膜。傅立叶变换红外光谱(FTIR)、X射线衍射谱(XRD)及扫描电子显微镜(SEM)形貌像等研究表明,制备出的nc-SiC薄膜具有立方结构;样品经800℃、1000℃退火后,表面的纳米晶粒分别为10nm和20nm左右;而1200℃退火后,样品晶化完全。光致发光(PL)研究表明,nc-SiC薄膜室温条件下发射蓝光,发光峰峰位随退火温度的降低发生蓝移且发光峰强度变大;1000℃退火后样品的发光峰在478nm,800℃退火后发光峰在477nm,800℃退火比1000℃退火的样品发光强度高4倍。     

垂直靶向脉冲激光沉积制备ZnO纳米薄膜

用一种新颖的制备纳米粒子与薄膜的垂直靶向脉冲激光沉积(VTPLD)方法,在室温及空气气氛下,于玻璃基底上成功地制备出ZnO纳米薄膜.用扫描电子显微镜(SEM)和X射线衍射(XRD)仪对ZnO纳米薄膜的表面形貌和结构进行了表征,用荧光光谱仪对薄膜的光致发光(PL)性能进行了测量.结果表明,当激光功率为13 W时,沉积出的粒子大小较均匀,尺寸在40 nm左右,且粒子排列呈现出一定方向性;当激光功率为21 W时,沉积的ZnO纳米薄膜图呈现出微纳米孔的连续薄膜.在玻璃基底上沉积的ZnO纳米薄膜有一主峰对应的(002)衍射晶面,表明ZnO纳米薄膜具有良好的c轴取向性.不同激光功率下沉积ZnO纳米薄膜经500 ℃热处理后的PL峰,其强度随激光能量而变化,最大发光波长位于412 nm.     

氨化温度对Si基GaN纳米结构质量的影响(英文)

通过磁控溅射技术在Si(111)衬底上沉积Ga2O3/Co薄膜,然后在不同温度下氨化制得GaN纳米结构。采用X射线衍射(XRD)、傅里叶红外吸收谱(FTIR)、扫描电子显微镜(SEM)、高分辨透射电镜(HRTEM)和光致发光谱(PL)对样品的结构、形貌和光学特性进行了表征。结果显示合成的GaN纳米结构具有六方纤锌矿结构,且纳米结构的生长受温度影响很大。PL谱显示在388nm处有一强的紫外发光峰,表明其在低维激光器件方面的应用优势。同时对纳米结构的生长机制进行了简单讨论。     

多孔Si/纳米ZnS复合材料发光的研究

利用脉冲激光沉积(PLD)分别在Si片和多孔Si衬底上沉积了ZnS薄膜,考察衬底对ZnS薄膜结构和发光性能的影响。X射线衍射(XRD)和扫描电镜(SEM)测量表明,两种衬底上制备的ZnS薄膜均沿立方相结构β-ZnS(111)晶向择优取向生长。多孔Si衬底上生长的ZnS薄膜表面有很多凹坑,而Si衬底上生长的ZnS薄膜表面相对比较平整。光致发光(PL)谱显示,ZnS薄膜沉积后,多孔Si的发光峰强度减小且峰位发生蓝移。根据ZnS薄膜具有较高透射率的特点,把透射出ZnS的多孔Si的橙红光和ZnS的发光叠加,多孔Si/ZnS纳米薄膜复合体系在可见光区有很强的PL现象。     

SiC/SiO_2镶嵌结构薄膜光致发光特性研究

采用 SiC/SiO_2复合靶,用射频磁控共溅射技术和高温退火的方法制备了 SiC/SiO_2纳米镶嵌结构复合薄膜,并应用傅里叶红外吸收(FTIR),X 射线衍射(XRD),扫描电镜(SEM)和光致发光(PL)实验分析了薄膜的结构、表面形貌以及光致发光性能。结果表明,样品经高温退火后在 SiO_2基质中有 SiC 纳米颗粒形成。以 280 nm 波长光激发样品薄膜表面,显示出较强的 365 nm 的紫外光发射以及 458 nm 和 490 nm 处的蓝光发射,其发光强度随退火温度从 800℃升高至 1 050℃而增强。其发光归结为薄膜中与 Si-O 相关的缺陷形成的发光中心。     

Investigation of luminescence from SiC nano-granule films on porous glass substrate

SiC granule films were fabricated onto porous glass substrate by RF-magnetron sputtering. Photoluminescence （PL） measurements show that there are light emissions at three different wavelengths. Ultraviolet emission peaked at 360 nm originated from the band-band transmission of SiC nanoparticles with relatively small size. The 370 nm light emission was due to the luminescence of the nano-skeletons of porous glass that was formed during the etching of the glass substrate. The blue emission at about 460 nm was associated with the recombination of the excited electron and O-deficient defects appeared at the interface between SiC nanoparticles and the porous glass. Furthermore, the optimal PL performance was obtained when SiC deposited time was I h and the glass substrate was etched for 20 min in the annealing sample （450 ℃）.     

用ECRCVD法制备的纳米碳化硅薄膜及其室温下的强光发射

用电子回旋共振化学气相沉积(ECRCVD)方法制备了纳米碳化硅薄膜.实验中发现:在高氢稀释反应气体和高微波功率条件下,可以得到结构上具有纳米碳化硅晶粒镶嵌在碳化硅无序网络中的薄膜.用高分辩透射电子显微镜、傅里叶红外吸收谱、Raman散射和X射线光电子谱等分析手段对薄膜的结构进行了分析.在室温条件下,薄膜能够发出强烈的短波长可见光,发光峰位于能量为2.64eV处.瞬态光谱研究表明样品的光致发光寿命为纳秒数量级,表现出直接跃迁复合的特征.这种材料有希望在大面积平面显示器件中得到应用.     

The Effect of Substrate Material and Postannealing on the Photoluminescence and Piezo Properties of DC-Sputtered ZnO

Abstact Zinc oxide (ZnO) thin films were deposited on various substrates by DC sputtering deposition. Thermal annealing was performed at up to 1,200°C in N₂ for 30 min. The effect was investigated using x-ray diffraction (XRD), photoluminescence (PL) spectra, scanning electron microscopy (SEM), and piezoresponse force microscopy (PFM). The influence on PL response depends both on substrate material and annealing temperature. The PFM images reveal that the ZnO films have inversion domains. While annealing improves the piezoresponse, the inversion domains still persist. The cross-sectional analysis of the inversion domains shows domain boundary widths of approximately 1.5 nm. (Received ...; accepted ...)     

Photoluminescence origin of nanocrystalline SiC films

The nanocrystalline SiC films were prepared on Si then annealed at 800℃ and 1 000℃ for 30 minutes （111） substrates by rf magnetron sputtering and in a vacuum annealing system. The crystal structure and crystallization of as-annealed SiC films were determined by the Fourier transform infrared （FIR） absorption spectra and the X-ray diffraction （XRD） analysis. Measurement of photoluminescence （PL） of the nanocrystalline SiC （nc-SiC） films shows that the blue light with 473 nm and 477 nm wavelengths emitted at room temperature and that the PL peak shifts to shorter wavelength side and the PL intensity becomes stronger as the annealing temperature decreases. The time-resolved spectrum of the PL at 477 nm exhibits a bi-exponential decay process with lifetimes of 600 ps and 5 ns and a characteristic of the direct band gap. The strong blue light emission with short PL lifetimes suggests that the quantum confinement effect of the SiC nanocrystals resulted in the radiative recombination of the direct optical transitions.     

Si基GaN薄膜的制备方法及结构表征

分别采用射频磁控溅射、热壁化学气相沉积(CVD)、电泳沉积法制备GaN薄膜。利用扫描电镜(SEM)、荧光光谱仪对样品进行结构、形貌和发光特性的分析比较。射频磁控溅射方法中,把SiC中间层沉淀到Si衬底上,目的是为了缓冲由GaN外延层和Si衬底的晶格失配造成的应力。结果证实了SiC中间层提高了GaN薄膜的质量。热壁化学气相沉积法制备GaN晶体膜时,选择H2作反应气体兼载体,有利于GaN膜的形成。电泳沉积法显示所得样品为六方纤锌矿结构的GaN多晶薄膜。结果表明:溅射法制备的GaN薄膜结晶效果好;CVD法制备时GaN薄膜应用范围广;电泳沉积法操作方便、简单易行。     

石英衬底上磁控溅射SiC膜退火形成SiC纳米线

用射频磁控溅射法在石英片上溅射SiC膜,然后在氮气气氛下1150℃退火3h后,在石英衬底上生长出SiC纳米线。用x射线衍射(XRD)、扫描电镜(SEM)和x光电子能谱(XPS)对样品进行了结构、形貌及组分分析。SEM结果表明,SiC纳米线的直径为20～80纳米,其长度可达7～8微米,甚至于长达十几个微米。     

Structure and photoluminescence properties of InN films grown on porous silicon by MOCVD

In this work, indium nitride (InN) films were successfully grown on porous silicon (PS) using metal oxide chemical vapor deposition (MOCVD) method. Room temperature photoluminescence (PL) and field emission scanning electron microscopy (FESEM) analyses are performed to investigate the optical, structural and morphological properties of the InN/PS nanocomposites. FESEM images show that the pore size of InN/PS nanocomposites is usually less than 4 μm in diameter, and the overall thickness is approximately 40 μm. The InN nanoparticles penetrate uniformly into PS layer and adhere to them very well. Nitrogen (N) and indium (In) can be detected by energy dispersive spectrometer (EDS). An important gradual decrease of the PL intensity for PS occurs with the increase of oxidation time, and the PL intensity of PS is quenched after 24 h oxidization. However, there is a strong PL intensity of InN/PS nanocomposites at 430 nm (2.88 eV), which means that PS substrate can influence the structural and optical properties of the InN, and the grown InN on PS substrate has good optical quality.