Probing Ag nanoparticle surface oxidation in contact with (in)organics: an X‐ray scattering and fluorescence yield approach

Characterizing interfacial reactions is a crucial part of understanding the behavior of nanoparticles in nature and for unlocking their functional potential. Here, an advanced nanostructure characterization approach to study the corrosion processes of silver nanoparticles (Ag‐Nps), currently the most highly produced nanoparticle for nanotechnology, is presented. Corrosion of Ag‐Nps under aqueous conditions, in particular in the presence of organic matter and halide species common to many natural environments, is of particular importance because the release of toxic Ag⁺ from oxidation/dissolution of Ag‐Nps may strongly impact ecosystems. In this context, Ag‐Nps capped with polyvinolpyrrolidone (PVP) in contact with a simple proxy of organic matter in natural waters [polyacrylic acid (PAA) and Cl^? in solution] has been investigated. A combination of synchrotron‐based X‐ray standing‐wave fluorescence yield‐ and X‐ray diffraction‐based experiments on a sample consisting of an approximately single‐particle layer of Ag‐Nps deposited on a silicon substrate and coated by a thin film of PAA containing Cl revealed the formation of a stable AgCl corrosion product despite the presence of potential surface stabilizers (PVP and PAA). Diffusion and precipitation processes at the Ag‐Nps–PAA interface were characterized with a high spatial resolution using this new approach.     

单端面长周期光栅透射模式测量技术

为了实现长周期光栅透射谱测量模式的远距离监测,设计了单端面镀反射膜的测量装置系统,对单端面镀银膜长周期光栅的传感原理做了分析,并从实验的角度分别对单端面镀银膜模式系统和直接透射模式系统的长周期光栅在不同折射率的环境介质中的响应进行了研究,比较了它们的异同。首先,采用2×2单模光纤耦合器分别连接光谱分析仪、光源、长周期光栅。然后,在包含长周期光栅的光纤的另一个端面制备反射银膜。最后,通过测量一系列不同折射率的环境介质,比较了直接透射模式与单端面镀银膜模式下的长周期光栅的响应光谱。实验结果表明:采用波长解调表达时,对于同一种环境介质,两种模式下长周期光栅的响应光谱的谐振波长基本相同;采用功率/峰值解调表达时,随着甘油浓度从水变为80%的甘油溶液,直接透射模式下的光损耗从-6.05 d B变为-9.22 d B,单端面镀银膜模式下的光损耗从-8.03 d B变为-11.33d B。与直接透射模式相比,单端面镀银膜的长周期光栅光谱中的相对光损耗明显增加,谐振峰更尖锐,更有利于谐振波长和谐振峰光损耗值的识别。本研究设计的单端面镀银膜的长周期光栅测量系统不仅保留了长周期光栅透射谱的感应模式,而且使长周期光栅在对环境介质的测量中操作更加灵活方便,尤其是在远距离、恶劣环境或深层液体的折射率测量中具有独特的优势。     

Chitosan loaded with silver nanoparticles,CS‐AgNPs,using thymus syriacus,wild mint,and rosemary essential oil extracts as reducing and capping agents

The present study describes the green method for the preparation of chitosan loaded with silver nanoparticles (CS‐AgNPs) in the presence of 3 different extracted essential oils. The essential oils play dual roles as reductant and capping agents. The reducing power and DPPH (2,2‐diphenyl‐1‐picrylhydrazyl) assay for the 3 essential oils—Thymus syriacus (T), wild mint (M), and rosemary (R)—have been reported. The preparation of CS‐AgNPs was performed by 2 steps. The 3 previously extracted essential oils have been used as reducing and capping agent in the first step, while in the second step, silver nanoparticles were integrated in chitosan. The integration of AgNPs in the structure of chitosan was confirmed by ultraviolet‐visible, Fourier transform infrared spectroscopy, scanning electron microscopy techniques, and energy dispersive X‐ray. Surface plasmon resonance confirmed the formation of CS‐AgNPs with maximum absorbance at λ_max between 405 ‐ 410 and 410 ‐ 430 nm for colloidal and films of CS‐AgNPs, respectively. The intensity of bands at 3408 cm^?1 in the fourier transform infrared spectroscopy measurements was decreased substantially and shifted slightly to lower frequency (?υ = 43 cm^?1). Scanning electron microscopy shows a spherical morphology of AgNPs with size of 62 nm for both colloidal and film samples, and energy dispersive X‐ray analysis shows peaks confirming AgNPs formation.     

掺杂Ag纳米粒子对偶氮聚合物光致异构效应的影响

报道了通过宏观测量偶氮聚合物光致异构效应,及其引起的光学各向异性变化,讨论了一种影响偶氮聚合物顺反异构效应的有效途径。在偶氮高分子聚合物中,添加了不同浓度的Ag纳米粒子,采用了波长为442nm的He-Cd偏振激光为激发光源,当Ag纳米粒子掺杂质量浓度为0.12μg/ml的时候,激发了薄膜样品中Ag纳米粒子的等离子体共振效应,增强了粒子周围纳米尺度的电磁场强度,相当程度上提高了偶氮聚合物光致异构的转换效率;另外,研究了不同的取代基同纳米Ag粒子的相互作用对光致异构效应的影响,探讨了一种能够有效地控制光致异构效应的方法。     

天鹅绒阴极产生的双脉冲强流相对论电子束特性实验研究

在时间分辨的模式下, 实验研究了天鹅绒阴极产生的双脉冲相对论强流电子束的束心运动、束包络和束的发射度. 在实验中, 电子束流强度和电子束心运动用电阻环进行测试, 而电子束和石英玻璃的相互作用产生的契仑科夫辐射用来给出电子束包络和发射度信息. 电子束和石英玻璃作用产生的契仑科夫辐射用1台8幅分幅相机记录. 实验结果表明, 天鹅绒阴极产生的相对论强流双脉冲电子束在束流大小、束心运动轨迹、束包络及束发射度等方面具有较好的一致性.     

微脉冲电子枪的初步实验研究

给出了微脉冲电子枪的模拟计算及其初步实验结果. 该电子枪采用铜铝镁合金作为冷阴极材料, 在以磁控管作为微波功率源的出束实验中得到了100mA/cm²的电流密度.实验结果与次级电子倍增解析计算和SEEG程序的模拟计算结果基本符合, 初步验证了微脉冲电子枪的基本原理, 为今后实验中得到更大的电流密度打下了基础.     

Effect of an aliphatic spacer group on the adsorption mechanism on the colloidal silver surface of L‐proline phosphonodipeptides

A comparative study of molecular structures of five L ‐proline (L ‐Pro) phosphonodipeptides: L ‐Pro‐NH‐C(Me,Me)‐PO₃H₂ (P1), L ‐Pro‐NH‐C(Me,iPr)‐PO₃H₂ (P2), L ‐Pro‐L ‐NH‐CH(iBu)‐PO₃H₂ (P3), L ‐Pro‐L ‐NH‐CH(PA)‐PO₃H₂ (P4) and L ‐Pro‐L ‐NH‐CH(BA)‐PO₃H₂ (P5) has been carried out using Raman and absorption infrared techniques of molecular spectroscopy. The interpretation of the obtained spectra has been supported by density functional theory calculations (DFT) at the B3LYP; 6–31 + + G** level using Gaussian 2003 software. The surface‐enhanced Raman scattering (SERS) on Ag‐sol in aqueous solutions of these phosphonopeptides has also been investigated. The surface geometry of these molecules on a silver colloidal surface has been determined by observing the position and relative intensity changes of the Pro ring, amide, phosphonate and so‐called spacer (−R) groups vibrations of the enhanced bands in their SERS spectra. Results show that P4 and P5 adsorb onto the silver as anionic molecules mainly via the amide bond (∼1630, ∼1533, ∼1248, ∼800 and ∼565 cm⁻¹), Pro ring (∼956, ∼907 and ∼876 cm⁻¹) and carboxylate group (∼1395 and ∼909 cm⁻¹). Coadsorption of the imine nitrogen atom and PO group with the silver surface, possibly by formation of a weaker interaction with the metal, is also suggested by the enhancement of the bands at 1158 and 1248 cm⁻¹. P1, P2 and P3 show two orientations of their main chain on the silver surface resulting from different interactions of the  C CH₃,  NH and  CONH fragments with this surface. Bonding to the Ag surface occurs mainly through the imino atom (1166 cm⁻¹) for P2, while for P1 and P3 it occurs via the methyl group(s) (1194–1208 cm⁻¹). The amide group functionality (CONH) is practically not involved in the adsorption process for P1 and P2, whereas the C_s P bonds do assist in the adsorption. Copyright © 2008 John Wiley & Sons, Ltd.     

赫兹对阴极射线的实验研究及其重要影响

根据赫兹的日记、书信、文集及相关文献,对赫兹所进行的阴极射线的实验研究工作进行了仔细考察,指出他对阴极射线的一系列实验研究为揭示阴极射线的全部特性奠定了重要基础,对勒纳德和汤姆孙在这一领域的研究产生了直接影响．     

基于丝网印刷技术的碳纳米管场发射冷阴极制作

制备了一种新型碳纳米管浆料,并总结了一套阴极制作工艺.实验表明,质量比约为10%的纯化碳纳米管、5%的纳米金属粉末和有机材料混合形成的印刷浆料,其阴极具有较好的发射均匀特性.在浆料制备过程中通过加入表面活性剂使碳纳米管分散更加均匀.用丝网印刷技术制作阴极,并用机械刀刻的办法制作阴、栅两极之间的沟槽,经烧结后分析阴极膜的电阻率和粘附性随阴极材料组分和制作工艺的变化关系,确定较为合适的升温曲线及丝网目数,阴极碳纳米管的均匀性、导电性的提高改善了发射均匀性.该阴极开启场为2.5 V/μm,在电场强度为3.3 V/μm下,阳极电流为5.6 μA,场发射电流稳定,波动小于5%.     

Charge/discharge characteristics of sulfur composite electrode at different temperature and current density in rechargeable lithium batteries

The charge/discharge characteristics of the sulfur composite cathodes were investigated at different temperatures and different current densities. The composite presented the discharge capacities of 854 and 632 mAh g⁻¹ at 60 and −20 °C, respectively, while it had the discharge capacities of 792 mAh g⁻¹ at 25 °C. The composite presented the discharge capacities of 792 and 604 mAh g⁻¹ at 55.6 and 667 mA g⁻¹, respectively, at room temperature. The results showed that the sulfur composite cathodes presented good charge/discharge characteristics between 60 and −20 °C and at a high c-rate up to 667 mA g⁻¹.