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Title Page
Abstract
Contents
Chapter 1. Introduction 26
1.1. Optical encryption system using nanocomposite 26
1.2. Anticounterfeiting printing technique 30
1.3. References 32
Chapter 2. Highly Stable Upconverting Nanocrystal-Polydiacetylenes Nanoplates for Orthogonal Dual Signaling-Based Detection of Cyanide 34
2.1. Introduction 34
2.2. Result and Discussion 36
2.3. Experimental Section 53
2.4. Conclusion 55
2.5. References 56
Chapter 3. Multi-Color Luminescence Transition of Upconversion Nanocrystals via Crystal Phase Control with SiO₂ for High Temperature Thermal Labels 60
3.1. Introduction 60
3.2. Result and Discussion 62
3.3. Experimental Section 82
3.4. Conclusion 83
3.5. References 83
Chapter 4. Facile Microfluidic Fabrication of 3D Hydrogel SERS Substrate with High Reusability and Reproducibility via Programmable Maskless Flow Microlithography 86
4.1. Introduction 86
4.2. Result and Discussion 89
4.3. Experimental Section 107
4.4. Conclusion 110
4.5. References 111
Chapter 5. Dynamic Multimodal Holograms of Conjugated Organogels via Dithering mask lithography 114
5.1. Introduction 114
5.2. Result and Discussion 116
5.3. Experimental Section 146
5.4. Conclusion 152
5.5. References 152
Chapter 6. Summary 156
Appendix-Research achievements 159
Figure 1.1. Example of counterfeit product damage in newspaper, journal, and advertising 26
Figure 1.2. Anticounterfeit product a RFID, b fluorescence optical system, c hologram 27
Figure 1.3. Photochromism materials a Spiropyran derivative, b Diarylethene, c Oxazolidine 28
Figure 1.4. Photoluminsecence materials a Fluorescence dye, b Quantum dots, c Polymer dots, d... 28
Figure 1.5. Photonic crystal as structural color emission materials a colloidal nanocrystal clusters, b... 29
Figure 1.6. Metallic nanoparticles selectively absorb and scatter light of different wavelengths, which... 30
Figure 1.7. Printing technique a Direct printing, b Templated printing 31
Figure 2.1. The schematic of fabricating highly stacked PCDA-Co nanoplates, a, Synthesis of PCDA-... 36
Figure 2.2. SEM image of isolated PCDA-Co nanoplates. 39
Figure 2.3. a Color change observed in isolated PCDA-Co nanoplates (RPCDA/Co=0.33) in solution upon...[이미지참조] 39
Figure 2.4. Rapid color changes observed for isolated PCDA-Co nanoplates in solution after treatment... 40
Figure 2.5. Color change observed in isolated PCDA-Co nanoplates (RPCDA/Co=0.33) in solution, after...[이미지참조] 40
Figure 2.6. Change in UV-vis absorption intensities of isolated PCDA-Co nanoplates upon treatment... 41
Figure 2.7. Color changes observed for solution-phase isolated PCDA-Co nanoplates prepared using... 42
Figure 2.8. Color changes observed in solution for isolated PCDA-Co nanoplates fabricated using... 42
Figure 2.9. Bright-field microscopy images of a isolated PCDA-Co nanoplates and b agglomerated... 43
Figure 2.10. Color change observed in agglomerated PCDA-Co nanoplates (RPCDA/Co=0.33) in solution...[이미지참조] 44
Figure 2.11. Changes in UV-vis absorption intensities of isolated PCDA-Co nanoplates in solution upon... 45
Figure 2.12. SEM images of isolated PCDA-Co nanoplates in solution based on various initial molar... 45
Figure 2.13. Color changes observed for highly stacked PCDA-Co nanoplates prepared using various... 46
Figure 2.14. Color change observed in highly stacked PCDA-Co nanoplates films upon treatment with... 46
Figure 2.15. Color changes observed for highly stacked PCDA-Co nanoplates prepared using various... 47
Figure 2.16. a XPS and b Raman spectra of highly stacked PCDA-Co nanoplates film before/after... 48
Figure 2.17. XRD spectra of a isolated PCDA-Co nanoplates, and b agglomerated PCDA-Co... 49
Figure 2.18. Changes observed in SEM images of a isolated PCDA-Co nanoplates, b agglomerated... 50
Figure 2.19. SEM image of UCNs incorporated into highly stacked PCDA-Co nanoplates. 51
Figure 2.20. a Color and luminescence changes of UCNs/PCDA-Co nanoplate composites film upon... 52
Figure 2.21. a Schematic of the portable detection system, b Selective detection of CN ions with the... 53
Figure 3.1. Scheme of the crystal phase transition of UCNs through an annealing process involving... 62
Figure 3.2. Luminescence image and XRD data of UCNs/metalloid oxide composite compared to those... 63
Figure 3.3. Schematic representation of the fabrication of UCNs-embedded microparticles with/without... 64
Figure 3.4. a Luminescence color image and b transmittance of UCNs in PUA. 64
Figure 3.5. Change in the luminescence color and efficiency of UCNs with/without SiO₂ NPs after the... 65
Figure 3.6. Luminance of UCNs with and without SiO₂ NPs after the annealing process at 900 ℃. Inset:... 66
Figure 3.7. Normalized luminescence spectra of the four types of UCNs with different reconversion... 68
Figure 3.8. Change in the crystal structure and morphology of UCNs with and without SiO₂E NPs in... 69
Figure 3.9. XRD, luminescence spectrum, and SEM analysis of UCNs with and without SiO₂ NPs.... 70
Figure 3.10. Fourier-transform infrared spectra of an UCNs- and SiO₂ NPs-embedded PUA film, a... 71
Figure 3.11. Variation in the XRD pattern according to the concentration of SiO₂ NPs. The UCNs- and... 72
Figure 3.12. XRD patterns revealing the crystal phase transition of UCNs. XRD pattern of a pristine... 73
Figure 3.13. Comparison of the luminescence spectra of cubic NaREF₄ and hexagonal apatite UCNs.... 74
Figure 3.14. Structural and electronic properties, and the proposed energy transfer mechanism of three... 75
Figure 3.15. Energy level diagrams of Er3+ doped in three crystal phases. Energy level diagrams of Er3+...[이미지참조] 76
Figure 3.16. Phonon density of states of Er3+ in three types of crystal phases. Phonon density of states...[이미지참조] 77
Figure 3.17. XRD patterns of Tm3+-doped UCNs without/with SiO₂ NPs after annealing at 900 ℃: a...[이미지참조] 79
Figure 3.18. Electronic properties and phonon density of states of Tm3+ in cubic NaREF₄ and hexagonal...[이미지참조] 79
Figure 3.19. Demonstration of multiple luminescence color changing high temperature labeling systems,... 81
Figure 4.1. Schematic illustration of computer controlled 3D hydrogel-based SERS platform fabrication... 89
Figure 4.2. Schematic illustration of the UV LED installed DMD lithography system. 90
Figure 4.3. The fabrication and characterization of the microposts array, a Bright-field optical... 91
Figure 4.4. a 365 nm UV-light intensity profile through 20x projection lens, b Z-stack image of... 92
Figure 4.5. a Bright-field optical micrographs of PEGDA hydrogel micro-post fabricated without AA... 93
Figure 4.6. Energy-dispersive X-ray spectroscopy (EDS) spectra of PEGDA/AA/Ag hydrogel micro-... 95
Figure 4.7. UV-Vis absorption spectra of the 1 µM R6G in PEGDA/AA and PEGDA/AAmide micro-... 96
Figure 4.8. a Bright-field optical micrograph and b UV-Vis absorption spectra of the micro-post array... 96
Figure 4.9. SERS detection of R6G using the micropost array, Bright-field optical micrograph of the... 97
Figure 4.10. The normal Raman spectrum of aqueous 10-1 M R6G molecules adsorbed on PEGDA...[이미지참조] 98
Figure 4.11. Calculated results of SERS enhancement factor of Ag NP systems, a Model system of Ag... 101
Figure 4.12. The reliability and reproducibility of measurements for R6G by the PEGDA/AA/Ag... 102
Figure 4.13. The reusability, continuous multitarget sensing capability, and a demonstration of the... 104
Figure 4.14. The effect of washing solvent on recovering the pristine state of the PEGDA/AA/Ag micro-... 105
Figure 4.15. SERS spectra of GHB (5.0 M) and 40% EtOH in PEGDA/AA/Ag micro-posts and Raman... 106
Figure 5.1. a Depending on immersion solvent, PDA organogels acting as volume phase holographic... 115
Figure 5.2. a Schematic showing fabrication of conjugated PDA organogels. Two-dimensionally... 116
Figure 5.3. a Bright-field microscopy images of crosslinked HD-DA microstructures according to 365... 116
Figure 5.4. Bright-field images of crosslinked HD-DA microstructures by changing 365 nm UV... 118
Figure 5.5. Bright-field microscope images of crosslinked a HD-DA and b HDDA microstructures... 118
Figure 5.6. Bright-field (left) and fluorescence (right) microscopy images show reversible volume and... 119
Figure 5.7. UV-Vis spectra a and fluorescence emission spectra b of PDA organogels immersed in ACN... 119
Figure 5.8. Comparison of an area of top region of PDA microstructure and their fluorescence intensity... 120
Figure 5.9. 3D simulation result (left) shows predicted deformed shape, and each cut plane of simulation... 121
Figure 5.10. Organogel crosslinked without dithering pattern into a disk shape and shrunk in MeOH... 122
Figure 5.11. Bright-field microscopy images of PDA organogel microstructure (left) composed of 2D... 122
Figure 5.12. Refractive indices of rod and matrix when exposed to a ACN and b water. 123
Figure 5.13. Confocal microscopy image of rod and matrix in conjugated PDA organogel microstructure,... 123
Figure 5.14. Structural color of the patterned PDA organogel. Structural color of the patterned PDA... 124
Figure 5.15. Schematic of the imaging setup for structural color of dithering mask patterned organogel... 124
Figure 5.16. a Schematic of the diffraction efficiency measuring system. Transmitted and diffracted... 124
Figure 5.17. Confocal microscopy images of dithering mask patterned conjugated PDA organogel... 126
Figure 5.18. When organogel contracted in water, a three-dimensional view (left) and a cross-sectional... 127
Figure 5.19. Bright-field (top row) and fluorescence microscopy images (bottom row) of dithering mask... 127
Figure 5.20. a Bright-field micrographs (top row), widefield fluorescence micrographs (middle row),... 128
Figure 5.21. FEA results showing that solvent exchange shrank the organogel patterned with a square... 129
Figure 5.22. Orthogonal confocal microscopy image (left) of square dithering mask patterned PDA... 129
Figure 5.23. Line profile of initial fluorescence intensity of uniform PDA organogel. Uniform... 129
Figure 5.24. Fluorescence expression predicted for the patterned organogel in FEA results after... 130
Figure 5.25. Bright-field and fluorescence microscopy images of dithering mask patterned PDA... 131
Figure 5.26. Bright-field and fluorescence microscopy images of PDA organogel microstructures upon... 131
Figure 5.27. Changing of signal shape with varying contraction level. Modeled fluorescence signals... 132
Figure 5.28. Light propagation simulations, a The 3D organogel structure was divided into N=90 layers.... 133
Figure 5.29. a Expected fluorescence intensity based on fluorescence expression and illumination... 133
Figure 5.30. a Bright-field and b fluorescence microscopy images of hexagon patterned PDA organogel... 134
Figure 5.31. Bright-field and fluorescence microscopy image of dithering mask patterned fluorescein... 135
Figure 5.32. Fabrication process of shape morphing PDA organogel microstructure.. 135
Figure 5.33. a A dithering mask used for the organogel microstructure (a square dithering pattern for... 136
Figure 5.34. Microarray consisting of organogels patterned with horizontal lines on the right of the red... 137
Figure 5.35. a Horizontal lined dithering mask pattern image. Bright-field microscopy images of... 137
Figure 5.36. Dynamic flip-flop structural color systems displaying letter changes from T to E and T to... 138
Figure 5.37. a Fabrication of letter transition systems using four types of dithering masks. Hexagon... 138
Figure 5.38. Selective patterning of conjugated PDA organogel for structural color and 1,6-hexanediol... 139
Figure 5.39. Free-standing flexible films with embedded holographic lettering fabricated using... 139
Figure 5.40. a A schematic diagram of encryption process that generates a specific dithering pattern in... 140
Figure 5.41. Structural color displayed by encoded organogel matrices with varying matrix size. 0° and... 140
Figure 5.42. Encrypted information, structural color, bright-field image, and maginified bright-field images... 141
Figure 5.43. Structural colors displayed by 4x3 micro-array of 4x4 encoded organogel matrices. 141
Figure 5.44. Encrypted information (left) and structural color (right) of PDA organogel microstructures... 142
Figure 5.45. An array of structural color displayed by an imprinted flexible PDMS film. Scale bar is 200 ㎛. 142
Figure 5.46. Encoded organogel matrices in the form of free-floating microparticles. Scale bar is 200 ㎛. 142
Figure 5.47. A computer-assisted method to convert digital color images to structural color encrypted holograms. 143
Figure 5.48. Structural color encrypted PDA organogel micro-particles displaying The Starry Night,... 143
Figure 5.49. Selective structural color change of masterpiece encrypted microstructures by changing... 143
Figure 5.50. Structural color (top), bright-field (middle), and maginified bright-field (bottom) images of... 144
Figure 5.51. Transmittance of photo-crosslinked HD-DA film. 144
Figure 5.52. Structural color on-off PDA organogel microstructures patterned with two types of line... 145
Figure 5.53. Selective structural color changing of PDA organogels by rotating the portable imaging... 146
Figure 5.54. a A flexible free-standing PDMS film encoded with Van Gogh self-portrait hologram and... 146
As new authentic products are introduced into the market, counterfeiting has always been on the rise. In 2015, the global economic loss caused by counterfeiting is more than 1.7 trillion US dollars and has been increasing annually. Therefore, an inexpensive but efficient anticounterfeiting platform must be developed to end counterfeiting. In this work, we present new optical encryption system which is used Upconversion nanoparticle (UCNs), SERS and new micro structural coloration system to prevent counterfeiting.
In Chapter 2, we developed practical dual signaling capability of the PDA sensor system, upconverting nanocrystals (UCNs) are incorporated into highly stacked PDA-metal nanoplates, and practical dual signaling (orthogonal changes in luminescence and visible color) is demonstrated using a portable detection system. Lanthanide ion-doped UCNs have superior optical stability against environmental changes. In addition, UCNs release a large anti Stokes shift luminescence at a visible range under near-infrared light (NIR) irradiation and therefore 980 nm NIR laser of excitation. One of the conjugated polymers, Polydiacetylene (PDA), have unique optical properties that cause blue-to-red color change and red fluorescence emission in response to external stimuli. Based on their stimuliresponsive unique optical properties, we fabricate the highly stable polydiacetylene introduction of metal cation, and develop the practical dual signaling sensor having colorimetric and luminescent transition by combining PDA organogel with luminescent upconverting nanocrystals (UCNs).
In Chapter 3, we present thermally responsive UCNs system. Spectrally tunable microarchitectures are effective information media because they act as carriers of luminescent materials that change their properties in response to external stimuli. However, it is challenging to meet the stringent requirements of practical applications, such as in optical labeling systems underhigh-temperature conditions. Lanthanide ion-doped UCNs-based labeling systems that can deliver the desired information in micro-sized solid architectures have been developed in a scalable manner. we report a strategy to modulate the predetermined luminescence color of lanthanide-ion doped UCNs with large enhancement in luminescence intensity upon heating with silica nanoparticles.
In Chapter 4, we realized silver nanoparticles (AgNPs) based 3D microstructure for chemical sensing and encoding. While superior signal enhancing effect and distinctive optical property of AgNPs have been explored to construct the chemical detectible 3D silver structure in the microfluidic device, conventional methods require sophisticated structure or additional treatment to upgrade sensitivity of the substrate, which cause long production time, low reusability, and poor reproducibility. we suggest a facile and simple technique for preparing highly sensitive 3D hydrogel surface enhanced Raman spectroscopy (SERS) substrate. We can fabricate any number of precisely specified hydrogel microstructures by automated and programmed maskless flow microlithography. Then, AgNPs are uniformly synthesized inside of the microstructures by UV induced photo-reduction. Using our substrate, a signal for target molecule can be noticeably amplified with high sensitivity (enhancement factor: 2.4x108). Also, since the microstructures have porous network, there is no need for additional treatment to decrease the distance between the target molecule and AgNPs, and the fabricated SERS substrate is reusable over 20 times by washing the SERS substrate using methanol. In addition, our system can detect multi-target without interference of former molecules (rhodamine 6G (R6G), three isomers of aminobenzoic acid (ABA), and γ-hydroxybutyric acid (GHB)).
In Chapter 5, we report a polydiacetylene (PDA) organogel that reversibly displays 3 modes of holograms in a single architecture. Using dithering mask lithography, we realized two-dimensional patterns with varying crosslinking density on a conjugated polydiacetylene. In protic solvents, the organogel contracts anisotropically to develop optical and structural heterogeneities along the third dimension, displaying holograms in the form of three-dimensional full parallax signals, both in fluorescence and bright-field microscopy imaging. In aprotic solvents, these heterogeneities diminish as organogels expand, recovering the two-dimensional periodicity to display a third hologram mode based on iridescent structural colors. Our study presents a next-generation hologram manufacturing method for multi-level encryption technologies.*표시는 필수 입력사항입니다.
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