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博碩士論文 etd-0726105-135920 詳細資訊
Title page for etd-0726105-135920
論文名稱
Title
以液相沉積法成長氧化鎳電致變色膜
Study of NiO Electrochromic Films Prepared by Liquid Phase Deposition
系所名稱
Department
畢業學年期
Year, semester
語文別
Language
學位類別
Degree
頁數
Number of pages
52
研究生
Author
指導教授
Advisor
召集委員
Convenor
口試委員
Advisory Committee
口試日期
Date of Exam
2005-07-15
繳交日期
Date of Submission
2005-07-26
關鍵字
Keywords
液相沉積法、氧化鎳、電致變色
LPD, NiO, electrochromic
統計
Statistics
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中文摘要
電致變色以外加電場,使離子注入物質之中讓物質產生顏色變化,進而影響物質對於光的穿透能力,此種變色方式稱之為『電致變色』。由於具有光電方面之應用,目前許多工業界與學術界投入研究之中。
本篇論文的目的主要是探討利用液相沉積法成長氧化鎳膜,探討電致變色的能力。利用液相沉積法在透明導電玻璃基板上成長氧化鎳膜,其過程簡單、成本低廉、而且成長溫度低 (40 ℃),因此值得廣泛研究與討論。利用掃描式電子顯微鏡 (SEM)、紫外光可見光譜,探討薄膜的特性,並由實驗結果顯示最大穿透率變化量為48%。
Abstract
The electrochromic materials are capable of changing their optical properties (transmittance and/or reflectance) under applied electric potentials; when that potential is stopped or it goes on reverse, these materials keep or return to its original optical state in a reversible way. The variation of the optical properties is caused by of insertion/extraction of cations in the electrochromic film.
The as-deposited LPD-NiO film is also uniform and transparent. The LPD-NiO film is light gray after coloring; the transparency ratio (ΔT%) can reach about 48% at the wavelength of 550 nm. After annealing in 300oC, the bleached state almost approaches that of original state before colored. We expect that the electrochromic device combined LPD-TiO2 and LPD-NiO films can enhance the coloration efficiency.
目次 Table of Contents
CONTENTS
CHAPTER 1 1
INTRODUCTION 1
1-1 BACKGROUND OF ELECTROCHROMIC 1
1-2 APPLICATIONS OF ELECTROCHROMIC DEVICE 1
1-3 NICKEL OXIDE 4
1-4 MOTIVATION OF LPD-NIO 4
1-5 BACKGROUND OF LPD 5
1-6 MECHANISMS OF LDP-NIO 5
1-7 ADVANTAGE OF LPD 6
REFERENCES 9
CHAPTER 2 11
EXPERIMENTS 11
CURRENT COMPONENTS USED IN ELECTROCHROMIC CELLS 11
Transparent conductors 11
2-1-2 Electrolytes 11
2-2 LIQUID PHASE DEPOSITION SYSTEM 13
2-3 DEPOSITION PROCEDURES 14
2-3-1 ITO-coated glass Cleaning Procedures 14
2-3-2PHOTORESIST COATED 14
2-3-3 Preparation of Deposition Solution 15
2-3-4 Film Growth 16
2-4ANNEALING TREATMENT 16
2-5CHARACTERISTICS 16
2-5-1 Physical Property 16
2-5-2 Optical Property 17
REFERENCES 20
CHAPTER 3 21
RESULTS AND DISCUSSION 21
3-1 ELECTROCHROMIC REACTION 21
3-2 PHYSICAL PROPERTIES OF LPD-NIO FILM 22
3-2-1 SEM view of LPD-NiO Film 22
3-3 OPTICAL PROPERTIES 23
3-4 SPECIFICATION OF ELECTROCHROMIC 23
3-4-1 Operation Voltage(1~5V) 24
3-4-2 Coloration and Bleaching Time(10~15 seconds) 24
3-4-3 Memory Time (about 600 seconds) 25
3-5 SUMMARY 25
REFERENCES 42
CHAPTER 4 43
CONCLUSIONS 43


LIST PICTURE
.
FIGURE 1-1 BASIC DESIGN OF AN ELECTROCHROMIC DEVICE, INDICATING TRANSPORT OF POSITIVE IONS UNDER THE ACTION OF AN ELECTRIC FIELD 8
FIGURE 1-2 THE PRINCIPLES OF FOUR DIFFERENT APPLICATION OF ELECTROCHROMIC DEVICES. ARROWS INDICATE INCOMING AND OUTGOING ELECTROMAGNETIC RADIATION; THE THICKNESS OF THE ARROW SIGNIFIES RADIATION INTENSITY 9
FIGURE 2-1 SCHEMATIC DIAGRAM OF LIQUID PHASE DEPOSITION (LPD) SYSTEM 20
FIGURE 2-2 LPD-NIO DEPOSITION FLOWCHART 21
FIGURE 3-1 SCHEMATIC OF ION INJECTION INTO NICKEL OXIDE FILM. 29
FIGURE 3-2 THICKNESS OF LPD-NIO FILMS DEPOSITIED AT 40℃ AS A FUCTION OF DEPOSITION TIME. 30
FIGURE 3-3 CROSS-SECTIONAL (A) ITO FILM (B) LPD-NIO/ITO FILMS 31
FIGURE 3-4 SURFACE MORPHOLOGY OF 100 NM LDP-NIO FILMS 32
FIGURE 3-5 LPD-NIO/ITO FILMS TRANSMITTANCE SPECTRA OF DIFFERENT LPD- NIO THICKNESS (A) 27 NM (B) 50 NM. 33
FIGURE 3-6 LPD- NIO /ITO FILMS TRANSMITTANCE SPECTRA OF DIFFERENT LPD- NIO THICKNESS (A) 72 NM (B) 100 NM. 34
FIGURE 3-7 LPD-NIO /ITO FILMS TRANSMITTANCE SPECTRA LPD- NIO THICKNESS 128 NM 35
FIGURE 3-8 (A)27 NM(B)50 NM THICKNESS LPD-NIO TRANSMITTANCE SPECTRA ANNEALED 300 ℃ FOR 30 MINS 36
FIGURE 3-9 (A)72 NM(B)100 NM THICKNESS LPD-NIO TRANSMITTANCE SPECTRA ANNEALED 300 ℃ FOR 30 MINS 37
FIGURE 3-10 128 NM THICKNESS LPD-NIO TRANSMITTANCE SPECTRA ANNEALED AT 300 ℃ FOR 30 MINS 38
FIGURE 3-11 PICTURES OF COLORED AND BLEACHED LPD-NIO FILMS 39
FIGURE 3-12 PICTURES OF COLORED AND BLEACHED LPD-NIO FILMS 40
FIGURE 3-13 PICTURE OF COLORED AND BLEACHED LPD-NIO FILMS 41
FIGURE 3-14 OPERATION VOLTAGE 42
FIGURE 3-15 REACTION TIME 43
FIGURE 3-16 MEMORY TIME 44
參考文獻 References
第一章
[1-1] H. Nagayama, H. Honda, and H. Kawahara, “A New Process for Silica Coating, “Journal of The Electrochemical Society, vol.135, pp.2013-2016, 1988
[1-2] K. Tsukuma, T. Akiyama, H. Imai, ”Liquid phase deposition film of tin oxide, “Journal of Non-Crystalline Solide, vol. 210, pp.48-54, 1997
[1-3] S. Deki, Y. Aoi, J. Okibe, H. Yanagimoto, A. Kajinami and M. Mizuhata,” Preparation and characterization of iron oxyhydroxide and iron oxide thin films by liquid-phase deposition, “Journal of Material Chemistry, vol. 7, pp. 1769-1768, 1997
[1-4] S DEKI , Y AOI , A KAJINAMI, “ A novel wet process for the preparation of vanadium dioxide thin film, “Journal of Materials Science, vol. 32, pp.4269-4273, 1997
[1-5] J. Ino, A. Hishinuma, H. Nagayama, H. Kawahara, “US Patent 4 882 183, 1989
[1-6] R. H. Schmitt, H. L. Glove, R. D. Brown, ”The Equivalent Conductance of the Hexafluorocomplexes of Group IV (Si, Ge, Sn, Ti, Zr, Hf) ,” Journal of the American Chemical Society, vol. 82, pp.5292-5295,1960
[1-7] Christian A. Wamser, “Equilibria in the System Boron Trifluoride--Water at 25°, “Journal of the American Chemical Society, vol.73, pp. 409-416,1951
[1-8] K. Shimizu, H. Imai, H. Hirashima, K. Tsukumab, “Low-temperature synthesis of anatase thin films on glass and organic substrates by direct deposition from aqueous solutions, “Thin Solid Films, vol.351, pp. 220-224, 1999
第二章
[2-1] M. J. Edgell, N. A. Pirie, S. C. Mugford, J. E. Castle, vol.137, pp.201-206
[2-2] Hashimoto, S.; Terada, J. U.S. Patent 5,777,779, 1998
[2-3] Nagai, J.; Seike, T. U.S. Patent 5,721,633, 1998
[2-4] Zhang, J.; Benson, D.; Tracy, C.E. U.S. Patent 5,716,736, 1998
[2-5] Van Dine, J.; Parkhe, V.D.; Klein, L.C.; Trumbore, F.A. U.S. Patent 5,659,417, 1997
[2-6] Varaprasad, D.; Agrawal, A.; Zhao, M.; Allemand, P.;Dornan, C.; Lynam, N. EP 0 612 826, A1, 1994
[2-7] Tonar, W.L.; Anderson, J.S.; Theiste, D.A. U.S. Patent 5,679,283, 1997
第三章
[3-1] A. Azensa,*, L. Kullmana, G. Vaivarsa, H. Nordborgb, C.G. Granqvista 3-115 (1998) 449-456
[3-2] Y.G Wu*, G.M. Wu, X.Y. Ni, X. Wu 63 (2000) 217-226
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