RISS 학술연구정보서비스

검색
다국어 입력

http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.

변환된 중국어를 복사하여 사용하시면 됩니다.

예시)
  • 中文 을 입력하시려면 zhongwen을 입력하시고 space를누르시면됩니다.
  • 北京 을 입력하시려면 beijing을 입력하시고 space를 누르시면 됩니다.
닫기
    인기검색어 순위 펼치기

    RISS 인기검색어

      Anthracene과 Dibenzothiophene을 포함하는 OTFT 물질의 합성과 OTFT 특성에 관한 연구

      한글로보기

      https://www.riss.kr/link?id=T10883392

      • 0

        상세조회
      • 0

        다운로드
      서지정보 열기
      • 내보내기
      • 내책장담기
      • 공유하기
      • 오류접수

      부가정보

      다국어 초록 (Multilingual Abstract) kakao i 다국어 번역

      This article describes the synthesis and OTFT characteristics of anthracene and dibenzothiophene derivatives.
      The OTFT materials were synthesized by well knowen reaction, bromination, Suzuki coupling, Yamamoto reaction, etc.
      Monomers, polymers, and oligomers were characterized by the spectroscopic methods such as UV-visible, FT-IR, and 1H-NMR spectroscopies.
      The resulting polymers were soluble in common organic solvents such as toluene, xylene, chlorobenzene, etc. The oligomers were well soluble in hot aromatic solvent, toluene, xylene, chlorobenzene.
      The obtained polymers and oligomers showed high thermal stabilities with high Td's(Td : 298 oC - 441 oC), which were characterized by TGA.
      Optical properties of these polymers and oligomer were characterized by UV-visible and photoluminescence (PL) spectra, which were measured in solution and film, respectively. The polymers and oligomers were red shift solution to film in UV-visible and photoluminescence (PL) spectra. The materials were good orderness and stacking, respectively.
      The thin-film transistor (TFT) performances of dibenzothiophene derivatives are examined. Through studied of the thin film morphology using X-ray diffraction (XRD) and atomic force microscopy. Due to the extended π-conjugation and efficient hole injection, the devices exhibited hole mobility of up to 0.026 cm2/Vs. The devices showed very low subthreshold-slope of 0.4 V/dec.
      번역하기

      This article describes the synthesis and OTFT characteristics of anthracene and dibenzothiophene derivatives. The OTFT materials were synthesized by well knowen reaction, bromination, Suzuki coupling, Yamamoto reaction, etc. Monomers, polymers, and ol...

      This article describes the synthesis and OTFT characteristics of anthracene and dibenzothiophene derivatives.
      The OTFT materials were synthesized by well knowen reaction, bromination, Suzuki coupling, Yamamoto reaction, etc.
      Monomers, polymers, and oligomers were characterized by the spectroscopic methods such as UV-visible, FT-IR, and 1H-NMR spectroscopies.
      The resulting polymers were soluble in common organic solvents such as toluene, xylene, chlorobenzene, etc. The oligomers were well soluble in hot aromatic solvent, toluene, xylene, chlorobenzene.
      The obtained polymers and oligomers showed high thermal stabilities with high Td's(Td : 298 oC - 441 oC), which were characterized by TGA.
      Optical properties of these polymers and oligomer were characterized by UV-visible and photoluminescence (PL) spectra, which were measured in solution and film, respectively. The polymers and oligomers were red shift solution to film in UV-visible and photoluminescence (PL) spectra. The materials were good orderness and stacking, respectively.
      The thin-film transistor (TFT) performances of dibenzothiophene derivatives are examined. Through studied of the thin film morphology using X-ray diffraction (XRD) and atomic force microscopy. Due to the extended π-conjugation and efficient hole injection, the devices exhibited hole mobility of up to 0.026 cm2/Vs. The devices showed very low subthreshold-slope of 0.4 V/dec.

      더보기

      목차 (Table of Contents)

      • I 서론
      • 1. OTFT 서론 1
      • 2. OTFT의 동작원리 2
      • 3. OTFT 특성 4
      • 4. OTFT 재료 6
      • I 서론
      • 1. OTFT 서론 1
      • 2. OTFT의 동작원리 2
      • 3. OTFT 특성 4
      • 4. OTFT 재료 6
      • II OTFT 특성에 관한 연구
      • 1. Dibenzothiophene유도체의 합성과 OTFT특성에 관한 연구 15
      • 1). 실험 15
      • (1) 실험재료 및 기기 15
      • (2) Oligomer의 합성 16
      • 2). 결과 및 고찰 22
      • (1) Oligomer의 확인 22
      • (2) 열적특성 24
      • (3) 광학적 특성 27
      • (4) OTFT 특성 29
      • 3). 결론 34
      • 2. Anthracene을 포함하는 고분자의 합성 35
      • 1). 실험 35
      • (1) 실험재료 및 기기 35
      • (2) 단량체 합성 36
      • (3) 고분자 합성 41
      • 2). 결과 및 고찰 44
      • (1) 단량체 확인 44
      • (2) 고분자 확인 46
      • (3) 중합체의 용해도 및 분자량 47
      • (4) 열적특성 49
      • (5) 전기 광학적 특성 52
      • (6) 표면에너지 특성 54
      • 3) 결론 56
      • 3. TIPS anthracene 유도체의 합성 57
      • 1). 실험 57
      • (1) 실험재료 및 기기 57
      • (2) Oligomer의 합성 58
      • 2). 결과 및 고찰 66
      • (1) Oligomer의 확인 66
      • (2) 열적특성 69
      • (3) 전기 광학적 특성 70
      • 3). 결론 75
      • 참고문헌 76
      더보기

      분석정보

      View

      상세정보조회

      0

      Usage

      원문다운로드

      0

      대출신청

      0

      복사신청

      0

      EDDS신청

      0

      동일 주제 내 활용도 TOP

      더보기

      주제

      연도별 연구동향

      연도별 활용동향

      연관논문

      연구자 네트워크맵

      공동연구자 (7)

      유사연구자 (20) 활용도상위20명

      이 자료와 함께 이용한 RISS 자료

      나만을 위한 추천자료

      해외이동버튼