Ultra-fast microwave irradiation: a superior method of fabricating ZnO quantum wires

IF 1.6 4区 化学 Q3 CHEMISTRY, INORGANIC & NUCLEAR
Salahuddin Sourav, Shamsun Alam, Harinarayan Das
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引用次数: 0

Abstract

ZnO nanorods were successfully synthesized by the microwave irradiation method in this project. The procedure verified the highest yields, least expense, and fastest synthesis of pure, fine-grained, single-phase ZnO nanorods; additionally, the procedure is ecologically friendly. Same-scale size nanorods displayed varying d-spacing values with the Hold time changed at a constant temperature of 150 °C in the microwave reactor, as supported by the TEM results. HRTEM pictures verified the ZnO nanorods’ perfect form. The quality of the nanoparticles’ crystallization was demonstrated by SAED patterns and data. The hexagonal wurtzite structure of ZnO nanorods is further supported by the matching of the diffraction rings in the SAED image with the peaks in the XRD pattern. Based on the data analysis, we concluded that the d-spacing values in ZnO nanorods at various nanometer scales increased. The absence of diffraction peaks from other contaminants indicated a high level of purity in ZnO samples. All the diffraction peaks were in good arrangement with those of the hexagonal structure of ZnO. Only the elements zinc (Zn) and oxygen (O) appeared in the EDX data, and the mass fraction was calculated. In the UV–visible absorbance spectrum, the absorbance peak located at the wavelength of 376 nm was the characteristic peak for hexagonal wurzite ZnO. The bandgap for ZnO nanorods held for one minute at a constant temperature of 150 °C is 3.24 eV; the binding energy gap for samples maintained for five minutes is 3.25 eV; and the binding energy gap for samples held for fifteen minutes is 3.28 eV, as determined by the UV–vis data. The presence of a peak at 432 cm−1 at 1 min Hold Time ZnO nanorods FTIR data, 434 cm−1 in 5 min Hold time ZnO nanorods FTIR data, and 451 cm−1 proved a characteristic vibration of the Zn–O bond in the wurzite structure of ZnO. Therefore, at a constant temperature of 150 °C, the distinctive peaks of ZnO nanorods increased with variations in hold duration.

Abstract Image

超快微波辐照:一种制造氧化锌量子线的优越方法
本项目采用微波辐照法成功合成了氧化锌纳米棒。该方法以最高的产率、最低的成本和最快的速度合成了纯净、细粒度、单相的氧化锌纳米棒;此外,该方法还具有生态友好性。在微波反应器中,温度恒定为 150 °C,随着保温时间的变化,相同尺寸的纳米棒显示出不同的 d 距值,TEM 结果也证明了这一点。HRTEM 照片验证了氧化锌纳米棒的完美形态。SAED 图样和数据证明了纳米颗粒的结晶质量。SAED 图像中的衍射环与 XRD 图样中的峰值相匹配,进一步证实了氧化锌纳米棒的六方菱面体结构。根据数据分析,我们得出结论:氧化锌纳米棒在不同纳米尺度上的 d 距值都有所增加。没有其他污染物的衍射峰表明氧化锌样品的纯度很高。所有衍射峰都与 ZnO 的六边形结构的衍射峰排列一致。EDX 数据中只出现了锌(Zn)和氧(O)元素,并计算出了质量分数。在紫外-可见吸收光谱中,波长为 376 nm 的吸收峰是六方菱锌矿 ZnO 的特征峰。根据紫外可见光数据测定,在 150 °C 恒温下保持一分钟的氧化锌纳米棒的带隙为 3.24 eV;保持五分钟的样品的结合能隙为 3.25 eV;保持十五分钟的样品的结合能隙为 3.28 eV。在保持时间为 1 分钟的 ZnO 纳米棒傅立叶变换红外光谱数据中出现了 432 cm-1 的峰值,在保持时间为 5 分钟的 ZnO 纳米棒傅立叶变换红外光谱数据中出现了 434 cm-1 的峰值,在 451 cm-1 的峰值证明了 ZnO 锆石结构中 Zn-O 键的特征振动。因此,在 150 °C 的恒温条件下,氧化锌纳米棒的特征峰随保持时间的变化而增加。
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来源期刊
Transition Metal Chemistry
Transition Metal Chemistry 化学-无机化学与核化学
CiteScore
3.60
自引率
0.00%
发文量
32
审稿时长
1.3 months
期刊介绍: Transition Metal Chemistry is an international journal designed to deal with all aspects of the subject embodied in the title: the preparation of transition metal-based molecular compounds of all kinds (including complexes of the Group 12 elements), their structural, physical, kinetic, catalytic and biological properties, their use in chemical synthesis as well as their application in the widest context, their role in naturally occurring systems etc. Manuscripts submitted to the journal should be of broad appeal to the readership and for this reason, papers which are confined to more specialised studies such as the measurement of solution phase equilibria or thermal decomposition studies, or papers which include extensive material on f-block elements, or papers dealing with non-molecular materials, will not normally be considered for publication. Work describing new ligands or coordination geometries must provide sufficient evidence for the confident assignment of structural formulae; this will usually take the form of one or more X-ray crystal structures.
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