Department of Textile Engineering, Chemistry and Science, North Carolina State University, Raleigh, North Carolina 27695-8301, United States.
Langmuir. 2013 Mar 26;29(12):4159-66. doi: 10.1021/la400281c. Epub 2013 Mar 15.
We report on the synthesis of tuned energy band gap Mg(x)Zn(1-x)O nanofibers (NFs) with different Mg(2+) content via the sol-gel electrospinning (ES) technique wherein the addition of the doping material affects not only the morphologies of as-spun ZnAc/PVA and MgAc/ZnAc/PVA nanofibers but also the crystal microstructure and optical properties of calcined ZnO and Mg(x)Zn(1-x)O nanofibers. Following an appropriate aqueous solution preparation of magnesium acetate (MgAc) and zinc acetate (ZnAc) with poly(vinyl alcohol) (PVA), electrospinning is performed and then as-spun nanofibers are calcined in an air atmosphere at 600 °C for 3 h. As-spun and calcined nanofiber diameters and morphologies are evaluated with scanning (SEM) and transmission (TEM) electron microscopies, whereas crystalline microstructural interpretations of ZnO and Mg(x)Zn(1-x)O are conducted with wide-angle X-ray diffraction spectra (XRD). Surface chemical composition and elemental evaluation of calcined nanofibers are examined with X-ray photoelectron spectroscopy (XPS), and optical properties and crystal defect analyses of the calcined nanofibers are conducted with photoluminescence spectra (PL). We observe a sharp reduction in fiber diameter upon calcination as a result of the removal of organic species from the fibers and conversion of ceramic precursors into ceramic nanofibers, and the appearance of a range of fiber morphologies from "bead in a string" to "sesame seed" coverage depending on fiber composition. Because Zn(2+) and Mg(2+) have similar ionicity and atomic radii, some Zn(2+) atoms are replaced by Mg(2+) atoms in the crystals, leading to a change in the properties of crystal lattices. The band gap energy of the calcined fibers increases significantly with addition of Mg(2+) along with an increase in the ultraviolet (UV) photoluminescence emission of the fibers.
我们报告了通过溶胶-凝胶静电纺丝(ES)技术合成具有不同 Mg(2+)含量的调谐能带隙 Mg(x)Zn(1-x)O 纳米纤维(NFs),其中掺杂材料的添加不仅影响了 ZnAc/PVA 和 MgAc/ZnAc/PVA 纳米纤维的形态,而且影响了煅烧 ZnO 和 Mg(x)Zn(1-x)O 纳米纤维的晶体微结构和光学性质。在适当的水溶液中制备了乙酸镁(MgAc)和乙酸锌(ZnAc)与聚乙烯醇(PVA)之后,进行静电纺丝,然后将所得的初生纳米纤维在空气气氛中于 600°C 下煅烧 3 h。使用扫描电子显微镜(SEM)和透射电子显微镜(TEM)评估初生和煅烧纳米纤维的直径和形态,而 ZnO 和 Mg(x)Zn(1-x)O 的晶体微观结构解释则使用广角 X 射线衍射谱(XRD)进行。使用 X 射线光电子能谱(XPS)检查煅烧纳米纤维的表面化学成分和元素评价,使用光致发光光谱(PL)进行煅烧纳米纤维的光学性质和晶体缺陷分析。我们观察到,由于纤维中有机物质的去除和陶瓷前体转化为陶瓷纳米纤维,纤维直径在煅烧后急剧减小,并且根据纤维成分,出现了一系列纤维形态,从“串珠”到“芝麻种子”覆盖。由于 Zn(2+)和 Mg(2+)具有相似的离子性和原子半径,因此在晶体中一些 Zn(2+)原子被 Mg(2+)原子取代,导致晶格性质发生变化。随着 Mg(2+)的加入,煅烧纤维的能带隙能量显著增加,同时纤维的紫外(UV)光致发光发射增加。