基于遥感-过程耦合模型的1988～2004年青海三江源区净初级生产力模拟

三江源区不仅是地处青藏高原的全球气候变化的敏感区,也是我国甚至亚洲最重要河流的上游关键源区。作为提供物质基础的植被净初级生产力(Netprimaryproduction,NPP),是评价生态系统状况的重要指标。该文应用已在碳通量观测塔验证,扩展到区域水平的遥感-过程耦合模型GLOPEM-CEVSA,以空间插值的气象数据和1km分辨率的AVHRR遥感反演的FPAR数据为模型主要输入,模拟并分析了1988～2004年该区NPP时空格局及其控制机制。结果表明,该区植被平均NPP为143.17gC·m–2·a–1,呈自东南向西北逐渐降低的空间格局,其中,以森林NPP最高(267.90gC·m–2·a–1),其次为农田(222.94gC·m–2·a–1)、草地(160.90gC·m–2·a–1)和湿地(161.36gC·m–2·a–1),荒漠最低(36.13gC·m–2·a–1)。其年际变化趋势在空间上呈现出明显的差异,西部地区NPP表现为增加趋势,每10a增加7.8～28.8gC·m–2;而中、东部表现为降低趋势,每10a降低13.1～42.8gC·m–2。根据显著性检验,NPP呈增加趋势(趋势斜率b>0),显著性水平高于99%和95%的区域占研究区总面积的13.43%和20.34%,主要分布在西部地区;NPP呈降低趋势(趋势斜率b<0),显著性水平高于99%和95%的区域占研究区面积的0.75%和3.77%,主要分布在中、东部地区,尤以该区长江和黄河等沿线区分布更为集中,变化显著性也更高。三江源NPP的年际变化趋势的气候驱动力分析表明,整个区域水平上该地区植被生产力受气候变化的主导,西部地区暖湿化趋势,造成了该地区生产力较为明显的、大范围的增加趋势;但东、中部地区则主要受人类活动的影响,特别是长江、黄河等河流沿线,是人类居住活动密集的地区,造成这些地区放牧压力较大、草地退化严重,而该地区暖干化趋势加剧了这一过程。

BaYF_5:Ce~(3+)纳米粒子的制备与光谱性质

在水/十六烷基三甲基溴化铵(CTAB)/正丁醇/正辛烷微乳液体系中成功的合成了BaYF5:Ce3+纳米粒子。运用X射线衍射(XRD)、环境扫描电子显微镜(ESEM)和荧光光谱等测试技术对所制备产物进行了表征。

LaGaO3 : A (A=Sm3+ and/or Tb3+) as promising phosphors for field emission displays

LaGaO3:Sm3+, LaGaO3:Tb3+ and LaGaO3: Sm3+, Tb3+ phosphors were prepared through a Pechini-type sol-gel process. X-Ray diffraction, field emission scanning electron microscopy, photoluminescence (PL), and cathodoluminescence (CL) spectroscopy were utilized to characterize the synthesized phosphors. Under excitation with ultraviolet light (250-254 nm), the LaGaO3: Sm3+, LaGaO3: Tb3+ and LaGaO3: Sm3+, Tb3+ phosphors mainly show the characteristic broadband emission (from 300 to 600 nm with a maximum around 430 nm) of the LaGaO3 host lattice, accompanied by the weak emission of Sm3+ ((4)G(5/2) -> H-6(5/2), H-6(7/2), H-6(9/2) transitions) and/or Tb3+ (D-5(3,4) -> F-7(6,5,4,3) transitions). However, under excitation by low-voltage electron beams (1-3 kV), the LaGaO3: Sm3+, LaGaO3: Tb3+ and LaGaO3: Sm3+, Tb3+ phosphors exhibit exclusively the characteristic emissions of Sm3+ and/or Tb3+ with yellow (Sm3+), blue (Tb3+, with low concentrations) and white (Sm3+ + Tb3+) colors, respectively.

Synthesis, characterization and mechanism of cetyltrimethylammonium bromide bilayer-encapsulated gold nanosheets and nanocrystals

Single-crystal Au nanosheets and fcc gold nanocrystals of uniform size were synthesized by a novel and simple route. The results of field-emission scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD) indicated the formation of the single-crystal structure of gold nanosheets and fcc nanocrystals. Energy-dispersive analysis of X-ray (EDAX) showed absorbance of cetyltrimethylammonium bromide (CTAB) molecules onto the surface of gold nanostructures.

The direct electrochemistry behavior of Cyt c on the modified glassy carbon electrode by SBA-15 with a high-redox potential

It is discovered that SBA-15 (santa barbara amorphous) can provide the favorable microenvironments and optimal direct electron-transfer tunnels (DETT) of immobilizing cytochrome c (Cyt c) by the preferred orientation on it. A high-redox potential (254 mV vs. Ag/AgCl) was obtained on glassy carbon (GC) electrode modified by immobilizing Cyt c on rod-like SBA-15. With ultraviolet-visible (UV-vis), circular dichroism (CD), FTIR and cyclic voltammetry, it was demonstrated that immobilization made Cyt c exhibits stable and ideal electrochemical characteristics while the biological activity of immobilized Cyt c is retained as usual.

Aggregation-based growth of silver nanowires at room temperature

We describe an aggregation-based growth mechanism for formation of silver nanowires at room temperature. It is found that the pH of solution and the concentration of L-cysteine capping molecules have an important effect on the formation and growth of nanowires. Characterization by atomic force microscopy (AFM) and UV-vis spectroscopy recorded as time clearly shows that the silver nanowires are grown at the expense of nanoparticles.

Synthesis and properties of novel soluble polyimides having a spirobisindane-linked dianhydride unit

A new synthetic procedure was elaborated allowing the preparation of semiaromatic dianhydride. N-Methyl protected 4-chlorophthalic anhydride was nitrated with HNO3 to produce N-methyl-4-chloro-5-nitrophthalimide (1). The aromatic nucleophilic substitution reaction between 5,5',6,6'-tetrahydroxy-3,3,3',3'-tetramethyl-1,1-spirobisindane and 1 afforded spirobisindane-linked bis(N-methylphthalimide) (2), which was hydrolyzed and subsequently dehydrated to give the corresponding dianhydride (3). The latter was polymerized with five different aromatic diamines to afford a series of aromatic polyimides. The properties of polyimides such as inherent viscosity, solubility, UV transparency and thermal stability were investigated to illustrate the contribution of the introduction of spirobisindane groups into the polyimide backbone. The resulting polyimides were readily soluble in polar solvents such as chloroform, THF and N-methyl-2-pyrrolidone. The glass-transition temperatures of these polyimides were in the range of 254-292 degrees C. The tensile strength, elongation at break, and Young's modulus of the polyimide film were 68.8-106.6 MPa, 5.9-9.8%, 1.7-2.0 GPa, respectively. The polymer films were colorless and transparent with the absorption cutoff wavelength at 286-308 nm.