ZnO纳米管的制备及光学特性研究

ZnO nanotubes have been fabricated through a carbon thermal reduction deposition process. Structure characterization results show that the ZnO nanotubes have a single crystalline wurtzite hexagonal structure pref- erentially oriented in the c-axis. The diameters of ZnO nanotubes are in the range of 90-280 nm and the wall thickness is about 50-100 nm. Room-temperature photoluminescence measurements of the ZnO nanotubes exhibit an intensive ultraviolet peak at 377 nm and a broad peak centered at about 517 nm. The UV emission is caused by the near band edge emission while the green emission may be attributed to both oxygen vacancy and the surface state. Raman and cathodoluminescence spectra are also discussed. Finally, a possible growth mechanism of the ZnO nanotubes is proposed.     

聚苯胺包覆钛酸锂锌负极材料的制备及表征

以钛酸四丁酯、乙酸锌、醋酸锂、苯胺为原料,通过溶胶?凝胶和化学氧化聚合的方法制备了钛酸锂锌/聚苯胺复合材料。利用X射线衍射（XRD）、红外光谱（IR）、扫描电子显微镜（SEM）、透射电镜（TEM）和电化学测试等手段对材料进行了表征及分析。结果表明,复合材料中的聚苯胺为无定型结构,且未引入杂质。当聚苯胺的质量分数为5.3%、电流密度为0.1 A/g时,首次放电比容量为330.0 (mA·h)/g;恒流充放电100圈后,仍然可保持281.3 (mA·h)/g的高放电比容量。     

储氢材料研究进展

氢能是人类未来的理想能源载体,而储氢是氢能实现规模应用的基础。本文综述了储氢材料的种类及其最新研究进展。     

Encapsulation of quantum dots and carbon nanotubes with polypyrrole in a syringe needle for automated molecularly imprinted solid phase pre-concentration of ochratoxin A in red wine analysis

Nanometer-sized semiconductor quantum dots (QDs with CdSe core and ZnS shell) and carbon nanotubes (CNTs with multi-walls) were encapsulated inside a stainless steel syringe needle by electrodeposition of polypyrrole (PPy). By cross-linking the PPy with ethylene glycol dimethacrylate (EGDMA) in the presence of ochratoxin A (OTA) as a template, molecularly imprinted polypyrrole (MIPPy) was formed on the nano-hybrid structure at an increased specific surface area. The MIPPy/CNTs/QDs-modified needle was readily adapted in an autosampler for micro-solid phase preconcentration (μSPP) of OTA from a red wine sample. After pulsed elution (PE) with 2% triethylamine (TEA), the OTA was determined by high performance liquid chromatography (HPLC) with fluorescence detection (FD). In comparison with MIPPy/CNTs, this new nano-hybrid structure of MIPPy/CNTs/QDs significantly improved the % recovery of OTA. The method, MIPPy/CNTs/QDs-μSPP-HPLC-FD, demonstrated that the MIPPy was truly a molecularly imprinted polymer (MIP) with specific recognition for OTA. All red wine matrix components could be differentially washed out, prior to accurate determination of the strongly bound OTA.     

Effect of modified ITO substrate on electrochromic properties of polyaniline films

In this work, we report the morphological and electrochromic properties of electrochemically synthesized polyaniline (PANI) thin films on bare and modified indium–tin oxide (ITO) glass substrates. In the last case, the surface of ITO glass was covered by a self-assembled monolayer of N-phenyl-γ-aminopropyl-trimethoxysilane (PAPTS). Atomic force microscopy images and perfilometry show that smoother and thinner PANI films were grown on PAPTS-modified ITO substrates. PANI-based electrochromic devices (ECDs) were assembled by using a viscous polymeric electrolyte (PE) of LiClO₄ and polymethyl methacrylate (PMMA) co-dissolved in a mixture of propylene and ethylene carbonate. The architectural design of the devices was glass/ITO/PANI/PE/ITO/glass. A dual ECD was also prepared by collocating a poly(3-methylthiophene) (P3MT) thin film as a complementary electrochromic element. The effect of the PAPTS-modified ITO substrate is reflected in a higher optical transmittance at bleach state and a little less color change at 550 nm of PANI-based ECDs.     

碳纳米管电极上的电化学行为分析

用化学方法对碳纳米管进行表面处理 ,用红外谱对处理后的碳纳米管进行表征 ,处理后的碳纳米管表面出现了活性功能团羧基。用这些碳纳米管制成电极 ,对Cd离子在硫酸钠中的电化学行为进行了分析。结果表明 ,从碳纳米管电极上可以观察到很好的、准可逆循环伏安图 ;在扫描速度为 10 0mV·s- 1时 ,氧化还原峰电位分别出现在 - 0 .6 5V和 - 0 .95V对照饱和甘汞电极(SCE)。峰电流与扫描速度的平方根成良好的线性关系 ,说明反应过程是由镉离子的扩散控制的。由循环伏安图相关的电位与扫描速度关系 ,我们导出了电子转移动力学速度参数。由于碳纳米管电极有很好的电化学活性和可重复性 ,它可以成为一种新型的分析电极材料     

Structure changes of single-wall carbon nanotubes and single-wall carbon nanohorns caused by heat treatment

Raman spectra and transmission electron microscope images showed that diameter enlargement of HiPco, a kind of single-wall carbon nanotube, accompanied by tube-wall corrugation was caused by heat treatment (HT) at 1000 to 1700 °C. Further enlargement accompanied by straightening of the tube walls and incorporation of carbon fragments within the tubes became obvious after HT at 1800 to 1900 °C. The transformation of some single-wall carbon nanotubes into multi-wall nanotubes was observed after HT at 2000 °C, and most single-wall tubes were transformed into multi-wall ones by HT at 2400 °C. What influence the Fe contained in the HiPco tubes had on these structure changes was unclear; similar changes were observed in single-wall carbon nanohorns that did not contain any metal. This indicates that thermally induced changes in the structure of single-wall carbon nanotubes can occur without a metal catalyst. Heat treatment increased the integrity of the nanotube-papers, and this increase may have been due to tube-tube interconnections created by HT.     

Alkyl Substituent Effects on the Conductivity of Polyaniline

The oxidative polymerization of aniline hydrochloride derivatives in water at low temperature is studied without lithium chloride. The resulting polymers have high molecular weight but the conductivity of the acid‐doped films is strongly dependent on the alkyl‐substituted chain at the 2‐positions. The root cause of the alkyl‐substitution effects is thoroughly investigated using density functional theory (DFT) methods (B3LYP using 6–1G(d,p) and 6‐311++G(2d,2p) basis sets). Internal structural changes observed on substitution appear to be more significant than a variety of electronic parameters measured using the natural bond orbital (NBO) method. Interplanar angles steadily increase on substitution, whereas ring orbital properties and the amount of ring delocalization remain fairly constant. An investigation into the extent to which lone pair–σ‐orbital overlap is affected by substitution indicates that increasing the steric bulk of the substituent reduces the ability of the lone pair to delocalize into the ring orbitals. However, the amount of overlap between the two is not adversely affected until the dihedral between them is > 30°, a situation that only occurs in i‐propyl and s‐butyl substitution. This finding is completely reflected in the experimental conductivity measurements.