高温高压下碳纳米管的相转变及金刚石的合成

 利用透射电子显微镜（TEM）和扫描电子显微镜（SEM）研究了碳纳米管在高压高温下的相转变。研究发现在高压高温条件下碳纳米管是不稳定的,在5.5 GPa压力下,770 ℃到950 ℃间退火时碳纳米管趋向形成碳纳米葱。在5 GPa、1 000 ℃条件下合成了金刚石。     

5.5 GPa下碳纳米管的热稳定性研究

 利用X射线衍射和透射电子显微镜研究了碳纳米管在5.5 GPa下的热稳定性问题。根据以往的研究在常压真空条件下碳纳米管的热稳定性非常好，其结构在2 800 ℃以下可能并不发生变化。实验中发现，虽然在5.5 GPa压力下冷压作用后碳纳米管的微结构没有明显的改变，但在950 ℃既开始发生改变，转变成类巴基葱和类条带结构，而在1 150 ℃其结构转变成石墨结构。高压是这种转变的主要原因，高压可以促使碳纳米管管结构的破裂，从而减小了它的热稳定性。     

碳纳米管的氧化铝模板法合成及其退火效应研究

结合氧化铝模板制约生长技术和高温退火处理，得到了相当统一的多壁碳纳米管.扫描电子显微镜（SEM）图像表明模板制约生长的初始碳纳米管形貌和尺寸完全受控于模板结构，透 射电子显微镜（TEM）和x射线粉末衍射（XRD）结果显示其管壁结构为无定形碳和石墨纳米 晶组成的混杂结构.为减少晶格缺陷及无定形碳，对初始碳纳米管进行系列高温（1100—240 0℃）退火处理，并初步研究了管壁在高温下的晶化行为.实验证明高温退火是提高多壁碳纳 米管质量的有效途径. 关键词： 氧化铝模板 碳纳米管 高温退火     

碳纳米管熔接金电极的分子动力学模拟

利用分子动力学模拟方法,研究了单壁碳纳米管与Au电极的高温熔接. 模拟结果表明,用端口吸附了Au团簇的碳纳米管在高温下能很好地与Au电极熔接. 首先将Au团簇放置于碳纳米管开口处进行高温退火,退火温度在1100 K左右,Au团簇部分Au原子进入碳纳米管管内,吸入碳纳米管中的Au原子形成壳层螺旋结构的Au纳米线,管外Au团簇呈无定形结构. 然后将吸附了Au团簇的碳纳米管与Au电极进行熔接,高温退火后,碳纳米管与Au电极表面之间形成了稳固的熔接,熔接最佳温度在800 K左右. 关键词： 碳纳米管 金电极 分子动力学模拟     

Si表面间水平碳纳米管束的分子动力学模拟研究

本文采用分子动力学模拟方法研究了Si表面间单壁水平碳纳米管束SWCNT (10,10)的变形和摩擦特性.系统在弛豫平衡后,首先对碳纳米管束施加压力至碳纳米管或Si表面结构破坏.之后在无压力和高压力两种情况下使上表面沿水平方向做剪切运动以研究碳纳米管束的摩擦特性.结果表明,由于碳纳米管的柔韧性,碳纳米管束在加载过程中出现明显变形,但直至3.8 GPa高压下并无结构破坏.系统无压力时SWCNT (10,10)在原地轻微随机滚动,压力为3.8 GPa时,碳纳米管束出现了整体的轻微滑动,同时伴随无规律的轻微滚动, 关键词： 碳纳米管束 摩擦 分子动力学模拟     

多孔氧化铝模板催化制备定向碳纳米管阵列

在不加过渡金属做催化剂的前提下,利用化学气相沉积法在二次阳极氧化法制得的多孔氧化铝模板中制备沉积了定取向碳纳米管阵列。考察了不同沉积温度以及退火处理对沉积结果的影响。温度达到600℃以上时,能得到开口的、定取向的多壁碳纳米管阵列；当沉积温度降至550℃左右时,沉积结果中存在碳纳米管、纳米纤维以及类似于弯曲的竹节状的结构；温度继续降低至500℃以下时,不能得到碳纳米管或碳纳米纤维；从实验结果中可以得出,在氧化铝模板中沉积碳纳米管过程中氧化铝起到了催化乙炔裂解以及催化沉积的碳石墨化成碳纳米管两种作用。另外,退火处理虽然能够提高沉积的碳纳米管的石墨化程度,但是也可能会引入新的缺陷。     

射频等离子体辅助化学气相沉积方法生长碳纳米洋葱

用射频等离子体辅助化学气相沉积方法生长碳纳米洋葱.电子显微镜观察表明,产物中无碳纳米管等伴随生成,因而制得了较高产率、较高纯度的纳米洋葱.尤其是Co-SiO₂催化剂生长的碳纳米洋葱,实心、光滑,且内无催化剂颗粒,其外层由未闭合的、呈波浪状的石墨片构成,显示出与众不同的微观结构和性能.提出了该方法中碳纳米洋葱的生长机理为碳笼由里向外嵌套形成球形粒子.对波浪状、非闭合结构的形成过程进行了讨论. 关键词： 射频等离子体 化学气相沉积 碳纳米洋葱     

CoPt(FePt)-C纳米复合膜的结构与磁性

用磁过滤脉冲真空电弧沉积方法制备了CoPt(FePt) C纳米复合薄膜，并在不同温度下进行了退火处理，研究了薄膜中碳的含量以及退火温度对薄膜结构与磁性能的影响.制备态薄膜经过足够高的温度退火后，x射线衍射和磁力显微镜分析发现，在碳基质中生成了面心四方相的CoPt(FePt)纳米颗粒.对于特定组分为Co24Pt31C45和Fe43Pt35C22的薄膜，矫顽力以及颗粒尺寸都随退火温度的升高而增大，当退火温度为700℃时，Co24Pt31C45薄膜的矫顽力为21×105A/m，晶粒尺寸为17nm;当退火温度为650℃时，Fe43Pt35C22相应值分别为28×105A/m和105nm. 关键词： 磁记录材料 磁性薄膜 CoPt FePt纳米复合薄膜     

连续碳纳米管线及其应用

如何将碳纳米管组装成宏观尺度的结构对于碳纳米管的宏观应用来说具有重要意义．自从碳纳米管被发现以来，在合成大面积碳纳米管阵列方面已经取得很多的进展，并有望应用于场发射平板显示器．然而，在如何将碳纳米管顺排起来连成连续的长线方面则鲜有进展．这里介绍的是作者最近的新发现：当从一种作者称之为“超顺排”碳纳米管阵列中拔出一束碳纳米管时，碳纳米管以可自组织成一条连续的长线．在这个过程中，“超顺排”碳纳米管阵列起的作用如同一个蚕茧，阵列中的碳纳米管则由范德瓦耳斯力首尾相连形成连续的纯碳纳米管线．这种碳纳米管线平行排列起来构成的偏振片可以工作在紫外波段．这种碳纳米管线还可以用作白炽灯的灯丝，仅需很小的功率就可以发出白炽光．不仅如此，这种碳纳米管线经过高温处理后，强度和导电性都得到明显增强，这将使碳纳米管线在宏观领域内得到更多的应用．     

外加电场作用下碳纳米管结构稳定性及结构修饰研究

利用外加电场的方法，对多壁碳纳米管的结构稳定性进行了研究.结果表明当场强达到30 V/nm时，碳纳米管端部的结构失稳，端部碳原子间的π键被打开，外部原子开始进入到碳纳米管的结构中.利用电子显微镜作为纳米加工仪器，通过外加电场的方法在多壁碳纳米管的端部制备了非晶态碳纳米线，形成碳纳米管-纳米线复合结构.碳纳米管和纳米线结合处的σ键作为绝缘界面，形成了电子输运的势垒.     

Transformation of Carbon Nanotubes to Diamond at High Pressure and High Temperature

The synthesis of diamond at high pressure and high temperature and the discovery of fullerenes and carbon nanotubes are among the most important achievements in carbon science. In the present work, we report the synthesis of diamond from carbon nanotubes at 4.5 GPa and 1300°C. Under these conditions, no diamond crystals were obtained when graphite was used as the starting material. The detailed investigation shows that at high pressure and high temperature carbon nanotubes first transform into quasi-spherical onion-like structures and then into diamond crystals. Our work suggests that carbon nanotubes can be used for the synthesis of high-quality diamond crystals at lower pressure and temperature.     

Effect of Pt and Fe catalysts in the transformation of carbon black into carbon nanotubes

In this research carbon nanotubes and carbon nano onion-like structures were synthesized from carbon black using metal catalysts at 400 °C and 700 °C. Platinum and iron-group metals were used as catalysts for the transformation of CB into graphitized nanocarbon and the effect of both metals was compared. The synthesized products were characterized using X-ray diffraction (XRD), transmission electron microscope (TEM), high resolution transmission electron microscope (HRTEM) and Raman spectroscopy. The characterization shows that this process is very efficient in the synthesis of high quality graphitized products from amorphous carbon black, even though the process temperature was relatively low in comparison with previous studies. Distinguished graphitic walls of the newly formed carbon nanostructures were clearly visible in the HRTEM images. Possible growth difference related to the type of catalyst used is briefly explained with the basis of electron vacancies in d-orbitals of metals.     

不同剂量C离子注入Si单晶中Si1-xCx合金的形成及其特征

室温下在单晶Si中注入(0.6—1.5)%的C原子,利用高温退火固相外延了Si_1-xC_x合金,研究了不同注入剂量下Si_1-xC_x合金的形成及其特征.如果注入C原子的浓度小于0.6%,在850—950℃退火过程中,C原子容易与注入产生的损伤缺陷结合,难于形成Si_1-xC_x合金相.随注入C原子含量的增加,C原子几乎全部进入晶格位置形成Si_1-xC_{x 关键词： 1-x}C_x合金')" href="#">Si_1-xC_x合金 离子注入 固相外延     

裂解温度对CVD法制备多壁碳纳米管的影响

用SEM、TEM、HRTEM及拉曼光谱方法研究了催化裂解乙炔制备多壁碳纳米管过程中裂解温度的影响,结果表明,在650℃～700℃裂解乙炔,可获得产量高、直径分布均匀、石墨程度高的多壁碳纳米管,并对裂解温度影响机制进行了分析和探讨。     

碳纳米管掺杂聚丙烯腈/铜室温环化为石墨的拉曼光谱分析及形成机制研究

石墨质碳质材料因具有良好的电学、力学、热学性能而在电子设备,复合材料,电池,传感器中得到广泛应用,但针对生产能耗高,污染大,成本高,不可控等现状是急需解决的核心问题。因此,通过使用较简单和成本低的制造技术在纳米级器件中获得石墨碳结构的方法是一个有吸引力的探索领域。表面等离激元技术因具有环境友好、能耗低等优点而受到广泛关注,利用等离激元技术诱导大分子链状聚合物石墨化就是一种具有广阔前景的制备技术,而Cu作为贱金属具有产量高,价格便宜等优势。基于表面等离激元技术,利用激光辐射粗糙Cu表面上的聚丙烯腈(PAN)+碳纳米管(CNT),而使聚丙烯腈在金属表面被石墨化。通过改变基底刻蚀时间、退火温度、退火时间、激光强度系统地研究了PAN/Cu和PAN+CNT/Cu得到最佳石墨化条件。实验结果表明：以PAN作为探针分子,在2.5 mol·L^-1硝酸刻蚀15min的铜基底上,观察到了增强因子为1.39×10⁴的表面增强拉曼散射(SERS)效应。通过使用拉曼激光作为光源,在退火温度为140℃时,可以观察到石墨化的PAN分子结构缺陷较少,碳氮三键消失,其I     

Ferritin-mixed solution plasma system yielding low-dimensional carbon nanomaterials and their application to flexible conductive paper

We demonstrate the production of low-dimensional carbon nanomaterials using a solution plasma system and their application to flexible conductive paper. The solution plasma system consists of two graphite electrodes and a beaker filled with ferritin-mixed deionized water. Ferritin molecules are used as the growth catalyst of the carbon nanomaterials. A high voltage of 15 kV at a frequency of 25 kHz is supplied to the electrodes using an alternating-current power source. The effects of the graphite rod diameters and the concentration of ferritin molecules are comparatively investigated. The produced carbon nanomaterials are characterized using Raman spectroscopy, scanning electron microscopy, and transmission electron microscopy. We confirmed the synthesis of graphitic platelets, onion-like structures, and carbon nanotubes. Finally, we fabricated flexible conductive papers using the produced materials with a good electrical conductance.     

Effect of hydrogenation on the spectra of electronic and vibrational transitions in single-walled carbon nanotubes

Single-walled carbon nanotubes containing 5.4 wt% H are prepared under a hydrogen pressure of 50 kbar at the temperature T = 500°C. Analysis of the optical transmission spectra has revealed that the hydrogenation of single-walled carbon nanotubes brings about suppression of high-frequency conduction provided by free charge carriers in the nanotubes, the disappearance of interband electronic transitions, and the appearance of an absorption line at 2845 cm^?1 corresponding to stretching vibrations of the C-H bonds. The removal of hydrogen from hydrogenated single-walled carbon nanotubes owing to vacuum annealing at a temperature of 500°C is accompanied by a linear decrease in the intensity of this line as the hydrogen content in the system decreases. This phenomenon indicates that the greater part of the hydrogen atoms in single-walled carbon nanotubes are covalently bonded to the carbon atoms.     

Carbon nanotubes formed in graphite after mechanical grinding and thermal annealing

Multi-walled carbon nanotubes with cylindrical and bamboo-type structures are produced in a graphite sample after mechanical milling at ambient temperature and subsequent thermal annealing up to 1400 °C. The ball milling produces a precursor structure and the thermal annealing activates the nanotube growth. Different nanotubular structures indicate different formation mechanisms: multi-wall cylindrical carbon nanotubes are probably formed upon micropores and the bamboo tubes are produced because of the metal catalysts. A two-dimensional growth governed by surface diffusion is believed to be one important factor for the nanotube growth. A potential industrial production method is demonstrated with advantages of large production quantity and low cost. Received: 17 May 2002 / Accepted: 12 September 2002 / Published online: 4 December 2002 RID="*" ID="*"Corresponding author. Fax: +61-2/6125-8338, E-mail: ying.chen@anu.edu.au