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It is of great theoretical and practical significance to study the regulation of the structure, morphology and properties of nanomaterials by using high voltage electric field in the field of functional materials. Here, ZnO nanocrystalline powders are synthesized under the condition of high voltage electric field. The effect of electric field on the structure, point defect and Raman spectrum of ZnO is studied.The structure, Raman shift and defect distribution of the product are characterized by (XRD), scanning electron microscope (SEM) and Raman spectroscopy (Raman spectroscopy).The results show that the complete crystallization time and temperature of zinc oxide under high voltage electric field are longer and higher than those without electric field. The direct current electric field can significantly promote the nucleation of zinc oxide in the precursor and reduce the rate of crystallization.The morphologies of ZnO obtained under different electric field intensities are obviously different. At a lower electric field intensity, ZnO presents lamellar or stripy morphology that is formed by many 50 nm-diameter nanoparticles. At a higher electric field intensity, ZnO exhibits short conical particles. It can be inferred that the high voltage electric field inhibits the growth of zinc oxide along the c axis (the strongest polar direction).The Raman spectra of the cathode surface and the anode surface showing obvious difference after the nano-ZnO powder has been polarized in the DC electric field.The intensity of the second-order optical phonon mode A1(LO) on the anode surface at 1050 cm–1 increases significantly under the condition of obvious leakage current, and the ratio (I1/I2) of Raman intensity (I1 = 438 cm–1 and I2 = 1050 cm–1) is linearly related to the field strength of the polarized electric field.When the positive and negative sides of the sample disc turn over, the 1050 cm–1 peak increases on the anode surface and tends to disappear on cathode surface.The zinc vacancies with negative charge move toward the anode and the concentration of zinc vacancies on one side of the anode increases significantly, which makes the surface of zinc oxide nanoparticles in the local area of the anode surface exhibit obvious negative electric properties, and increases the local electric field significantly to form a double Shaw base barrier.The Raman shift of 1050 cm–1 belongs to the second order optical phonon A1 (LO) vibrational mode, which is usually in inactive or silent state. When the current passes through, the grain boundary double Schottky barrier is established, which enhances the vibration of the A1 (LO) phonon and increases its Raman frequency shift.It can be concluded that the enhancement of the 1050 cm–1 Raman peak on the anode surface is related to the redistribution of defects in ZnO grains and the double Schottky barrier.
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Keywords:
- external electric field /
- nano zinc oxide /
- Raman spectra /
- crystallization /
- defect
[1] Zhao L H, Gao Z Y, Zhang J, Lu L W, Zou D S 2018 Appl. Phys. Express 11 115001
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图 1 高压直流电场条件下纳米氧化锌晶化实验装置示意图
Figure 1. Schematic diagram of experimental device for nano ZnO crystallization under high voltage DC electric field.
图 2 不同晶化时间纳米氧化锌的XRD图谱. (a)无外电场; (b)有外电场
Figure 2. XRD patterns of nano-ZnO synthesized for different time: (a) Without external electric field; (b) under external electric field
图 3 不同晶化温度所得纳米氧化锌的XRD图谱 (a)无外电场; (b)有外电场
Figure 3. XRD patterns of nano-ZnO synthesized at different temperatures: (a) Without external electric field; (b) under external electric field.
图 4 不同电场强度下合成纳米氧化锌的显微形貌 (a)1 kV/cm; (b)4 kV/cm; (c)6 kV/cm; (d)7 kV/cm
Figure 4. Microphotographs of nano-ZnO synthesized under different electric field intensities: (a) 1 kV/cm; (b) 4 kV/cm; (c) 6 kV/cm; (d) 7 kV/cm
图 5 纳米氧化锌极化产物的拉曼光谱图 (a)阴极面; (b)阳极面
Figure 5. Raman spectra of polarized nano-ZnO: (a) Cathode surface; (b) anode surface.
图 6 漏电电流及拉曼峰1050 cm–1强度与电场强度之间的关系
Figure 6. Relationship of leakage current, and 1050 cm–1 Raman intensity with electric intensity
图 7 拉曼峰438 cm–1和1050 cm–1的强度比(I1/I2)与电场强度的关系
Figure 7. Relationship of strength ratio of Raman peak I1(438 cm–1)/I2(1050 cm–1) with electric field intensity.
图 8 二次反向极化后纳米氧化锌拉曼图谱的变化
Figure 8. Changes of Raman spectra of nano-ZnO after secondary reverse polarization
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[1] Zhao L H, Gao Z Y, Zhang J, Lu L W, Zou D S 2018 Appl. Phys. Express 11 115001
Google Scholar
[2] Singh B K, Tripathi S 2018 J. Lumin. 198 427
Google Scholar
[3] Savarimuthu K, Sankararajan R, Govindaraj R, Narendhiran S 2018 Nanoscale 10 16022
Google Scholar
[4] Sivakumar A, Murugesan B, Loganathan A, Sivakumar P 2017 J. Taiwan Inst. Chem. E 78 462
Google Scholar
[5] Tang X Y, Gao H, Wu L L, Wen J, Pan S M, Liu X, Zhang X T 2015 Chinese Phys. B 24 394
Google Scholar
[6] Wang S B, Wu Y C, Miao R, Zhang M W, Lu X X, Zhang B, Kinstler A, Ren Z Y, Guo Y B, Lu T F, Suib S L, Gao P X 2017 Cryst. Eng. Comm. 19 5128
Google Scholar
[7] Sapkota G, Gryczynski K, Mcdougald R, Neogi A, Philipose U 2012 J. Electron Mater. 41 2155
Google Scholar
[8] Omidvar A 2018 Vacuum 147 126
Google Scholar
[9] Patterson S, Arora P, Price P, Dittmar J W, Das V K, Pink M, Stein B, Morgan D G, Losovyj Y, Koczkur K M, Skrabalak S E, Bronstein L M 2017 Langmuir 33 14709
Google Scholar
[10] Meng P F, Yang X, Hu J, He J L 2017 Mater. Lett. 209 413
Google Scholar
[11] Li Y, Zhao F X, Lian X X 2016 Mater. Sci-Poland 34 708
Google Scholar
[12] Wu W H, Tang S B, Gu J J, Cao X R 2015 Rsc. Adv. 5 99153
Google Scholar
[13] Kou L Z, Zhang Y, Li C, Guo W L, Chen C F 2011 J. Phys. Chem. C 115 2381
Google Scholar
[14] Jammula R K, Srikanth V V S S, Hazra B K, Srinath S 2016 Mater. Design 110 311
Google Scholar
[15] Gorai P, Seebauer E G 2017 Solid State Ionics 301 95
Google Scholar
[16] Xue F, Zhang L M, Feng X L, Hu G F, Fan F R, Wen X N, Zheng L, Wang Z L 2015 Nano Res. 8 2390
Google Scholar
[17] Nakamura T, Nagata T, Hayakawa R, Yoshimura T, Oh S, Hiroshiba N, Chikyow T, Fujimura N, Wakayama Y 2017 Jpn. J. Appl. Phys. 56 032501
Google Scholar
[18] Li C P, Dai W, Xu S, Li X W, Gao C Y, Chen X M, Yang B H 2015 J. Electron Mater. 44 1095
Google Scholar
[19] Mikkelsen A, Wojciechowski J, Rajnak M, Kurimsky J, Khobaib K, Kertmen A, Rozynek Z 2017 Materials 10 329
Google Scholar
[20] Li C, Vaynzof Y, Lakhwani G, Beirne G J, Wang J P, Greenham N C 2017 J. Appl. Phys. 121 144503
Google Scholar
[21] 安跃华, 熊必涛, 邢云, 申婧翔, 李培刚, 朱志艳, 唐为华 2013 62 073103
Google Scholar
An Y H, Xiong B T, Xing Y, Shen J X, Li P G, Zhu Z Y, Tang W H 2013 Acta Phys. Sin. 62 073103
Google Scholar
[22] 李酽, 李娇, 陈丽丽, 连晓雪, 朱俊武 2018 67 140701
Google Scholar
Li Y, Li J, Chen L L, Lian X X, Zhu J W 2018 Acta Phys. Sin. 67 140701
Google Scholar
[23] Hansen M, Truong J, Xie T, Hahm J I 2017 Nanoscal 9 8470
Google Scholar
[24] Cusco R, Alarcon-Llado E, Ibanez J, Artus L, Jimenez J, Wang B G, Callahan M J 2007 Phys. Rev. B 75 5202
Google Scholar
[25] Lorite I, Diaz-Carrasco P, Gabas M, Fernandez J F, Costa-Kramer J L 2013 Mater. Lett. 109 167
Google Scholar
[26] Du G T, Ma Y, Zhang Y T, Yang T P 2005 Appl. Phys. Lett. 87 946
Google Scholar
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