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Silole 나노입자, 그래핀 및 다공성 실리콘 유도체의 기능화를 통한 센서의 개발

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Author(s)
조현
Issued Date
2011
Abstract
In Chapter 1, we have synthesized the siloles derivatives to develop a new optical probe for florescence turn off detection biomolecules. 1-methyl-1-hydro-2,3,4,5-tetra- phenyl silole were derived with allylamines to give amine functionalized silole via hydrosilylation. Amine-functionalized silole were further derived with biotin to give biotin-functionalized silole. These biotin-functionalized molecules were used for the detection of biomolecules such as avidin and streptavidin through the quenching of photoluminescence. Our results indicated that biotinylated-silole nano aggregate are highly sensitive and selective to detect the avidin/streptavidin without any other interference.
In chapter 2, we have described the Silole derivatives have an optical and electrical properties which is useful in electronic devices, such as electron transporting materials, light-emitting diodes (LEDs), and chemical sensors. New synthetic routs for silole-derivatized graphene oxide have been developed from the hydrosilylation reaction of 1-methyl-1-aminopropyl-tetraphenylsilole with graphene oxide. Photoluminescence behaviors for the 1-methyl-1-aminopropyl-tetraphenylsilole, graphene oxide, and silole-derivatized graphene oxide were investigated by the measurement of photoluminescence. Prepared graphene oxide and 1-methyl-1-aminopropyl-tetraphenylsilole displayed an emission band at 295 and 480 nm, respectively. Optical behavior of silole-derivatized graphene oxide were investigated by the absorption and fluorescence spectroscopy. The silole-derivatized graphene oxide showed an interesting optical properties. Energy migration by an electron transfer between graphene oxide and silole moiety was observed. The silole-derivatized graphene oxide was further characterized by UV-vis and IR spectroscopy as well as the surface electron micrograph and transmission electron micrograph. Further details for the electronic behaviors of silole-derivatized graphene oxide and reduction to the silole-derivatized graphene will be discussed.
In chapter 3, we have discussed the Nanocrystalline porous silicon (PSi) surfaces used to detect nitroaromatic compounds in vapor phase. The mode of photoluminescence (PL) is emphasized as a sensing attitude or detection technique. Quenching of PL from nanocrystalline porous surfaces as a transduction mode is measured upon the exposure of nitroaromatic compounds. To verify the detection of explosives, the surface of PSi is functionalized with different groups. The quenching mechanism of PL is attributed to the electron transfer behaviors of quantum-sized nano-crystallites in the PSi matrix to the analytes (nitroaromatics). An attempt has been done to prove that the surface-derivatized photoluminescent PSi surfaces can act as versatile substrates for sensing behaviors due to having a large surface area and highly sensitive transduction mode. The detection of analyte was achieved by means of photoluminescence quenching of PSi. The quenching efficiency is in the order of TNT > PA > DNT. The electron transfer efficiency is in the order of PA > TNT > DNT.
Alternative Title
Development of Sensor Based on Functionalzation of Silole Nanoparticles, Graphene and Porous Silicon Derivatives
Alternative Author(s)
Cho, Hyun
Affiliation
조선대학교 화학과
Department
일반대학원 화학과
Advisor
손홍래
Awarded Date
2012-02
Table Of Contents
TABLE OF CONTENTS
TABLE OF CONTENTS...................................................I
LIST OF SYMBOLS AND ABBREVIATIONS......................VII
LIST OF TABLES..........................................................IX
LIST OF SCHEMES.......................................................X
LIST OF FIGURES.........................................................XI
Abstract.....................................................................XIII

Development of Sensor Based on Functionalzation of Silole Nanoparticles, Graphene and Porous Silicon Derivatives

Chapter One. Detection of Avidin and Streptavidin by Using Fluorescent Organosilicon Compounds

1.Introduction................................................................2

2.Experimental Section..................................................4

2.1.Generals................................................................4

2.2.Syntheses..............................................................5

2.2.1. Preparation of 1-Methyl-1-hydro-2,3,4,5-Tetraphenylsilole 1........................................................5

2.2.2. Preparation of 1-Methyl-1-(3-amino)propyl-2,3,4,5-Tetraphenylsilole 2........................................................5

2.2.3. Synthesis of Biotinlyled-silole 3...........................6

2.2.4. Preparation of Biotinylated-silole Nanoaggregates 4................................................................................6

3. Results and Discussion.............................................7

4. Conclusions...........................................................19

5. References.............................................................20


Chapter Two. Synthesis of Silole-derivatized base on Graphene and Optical Characterization

1. Introduction.............................................................23

2. Experimental Section...............................................26

2.1. Generals............................................................26

2.2. Syntheses..........................................................27

2.2.1.Preparation of Graphene Oxide 1.........................27

2.2.2. Preparation of 1-Methyl-2,3,4,5-tetraphenyl-1hydro-silole 2......................................................................27

2.2.3. Preparation of 1-Methyl-1-(3-amino)propyl-2,3,4,5-tetraphenylsilole 3......................................................28

2.2.4. Syntheses of Methyl silole graphene oxide 4.......28

2.2.5. Syntheses of Amino propyl silole graphene oxide 5................................................................................28

2.2.6. Syntheses of Amino propyl silole graphene 6........28

3. Results and Discussion............................................30

3.1. FE-SEM Images of graphite, GO, and MSGO...........30

3.2. Comparison for PL Efficiency GO, Silole, and MSGO.32

3.3. FT-IR Data of GO and MSGO..................................33

3.4. Absorption and Photoluminescence Spectrum of MSGO........................................................................34

3.5. Comparison for PL Efficiency MSGO and MSG.........35

4. Conclusions............................................................39

5. References..............................................................40


Chapter Three. Fabrication and Optical Characterization of Full Color Stop Band Based on Rugate-Structured Porous Silicon

1. Introduction.............................................................43

2. Experiments............................................................45

2.1.Materials & Instrument............................................45

2.1.1. Materials..........................................................45

2.1.2. Instruments.......................................................45

2.2. Experiments.........................................................46

2.2.1. Preparation of Porous Silicon..............................46

2.2.2. Process for surface Derivatization of Porous Silicon Samples.....................................................................47

2.2.3. Synthesis of TNT (2,4,6-trinitrotoluene)................48

2.2.4. Preparation of Gas Samples...............................48

2.2.5. Characterization................................................48

3. Results and Discussion.............................................50

4.. Conclusions...........................................................56

5. References..............................................................57
Degree
Master
Publisher
조선대학교 화학과
Citation
조현. (2011). Silole 나노입자, 그래핀 및 다공성 실리콘 유도체의 기능화를 통한 센서의 개발.
Type
Dissertation
URI
https://oak.chosun.ac.kr/handle/2020.oak/9275
http://chosun.dcollection.net/common/orgView/200000256597
Appears in Collections:
General Graduate School > 3. Theses(Master)
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