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Synthesis and Stability Study of Conjugated Organic Materials for Organic Photovoltaics.
Synthesis and Stability Study of Conjugated Organic Materials for Organic Photovoltaics.
- 자료유형
- 학위논문
- Control Number
- 0017163031
- International Standard Book Number
- 9798383692110
- Dewey Decimal Classification Number
- 620.11
- Main Entry-Personal Name
- Zhong, Xiaowei.
- Publication, Distribution, etc. (Imprint
- [S.l.] : The University of North Carolina at Chapel Hill., 2024
- Publication, Distribution, etc. (Imprint
- Ann Arbor : ProQuest Dissertations & Theses, 2024
- Physical Description
- 240 p.
- General Note
- Source: Dissertations Abstracts International, Volume: 86-02, Section: B.
- General Note
- Advisor: You, Wei.
- Dissertation Note
- Thesis (Ph.D.)--The University of North Carolina at Chapel Hill, 2024.
- Summary, Etc.
- 요약Organic Solar Cells (OSCs) have achieved efficiencies up to 20%, yet their stability remains a pressing concern, especially for high-efficiency systems like Bulk Heterojunction (BHJ) solar cells. This thesis examines the chemical and morphological stability of OSCs, from the perspectives of the roles of donor and acceptor materials' chemical structures. We first developed a modified synthetic method to D18 series polymers which have shown record-high efficiencies in OSCs. With a well-defined polymerization method, we were able to access high-molar-mass conjugated polymers and control the molar mass distribution readily. Next, we modified the synthesis of commonly employed small molecule acceptors (SMAs), the other key component for donor-acceptor based BHJ OSCs. Our improved and much simpler synthesis of Fused Ring Electron Acceptors (FREAs) enabled further exploration of the structural effects on both morphological and chemical stability. This led to the observation of the intrinsic instability of prevailing SMAs. The polarized double bonds are responsible for most chemical instability observed with SMAs. Larger differences between the donor moiety and the acceptor moiety on each side of the double bonds can lead to higher instability, yet steric hindrance can effectively protect the double bond from decomposition. With these synthetic tools, we then synthesized SMAs with extended backbone lengths, which could exhibit smaller diffusion coefficients towards more stable morphology. Finally, to understand why polymerized SMAs (PSMAs) usually present low molar-mass, we synthesized high-molar-mass PSMAs and modified the purification process to prevent unintended degradation of PSMAs, aiming to achieve both better morphological and chemical stability. These advancements should contribute to the development of more stable and efficient OSCs.
- Subject Added Entry-Topical Term
- Materials science.
- Subject Added Entry-Topical Term
- Organic chemistry.
- Subject Added Entry-Topical Term
- Molecular chemistry.
- Index Term-Uncontrolled
- Organic Solar Cells
- Index Term-Uncontrolled
- Bulk Heterojunction
- Index Term-Uncontrolled
- Small molecule acceptors
- Index Term-Uncontrolled
- Fused Ring Electron Acceptors
- Added Entry-Corporate Name
- The University of North Carolina at Chapel Hill Materials Science
- Host Item Entry
- Dissertations Abstracts International. 86-02B.
- Electronic Location and Access
- 로그인을 한후 보실 수 있는 자료입니다.
- Control Number
- joongbu:655131
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