通过降低有效的聚合物区域规律性来提高聚烯:富勒烯太阳能电池的热稳定性
Kevin Sivula1, Christine K Luscombe, Barry C Thompson
1Departments of Chemistry and Chemical Engineering, University of California-Berkeley, 718 Latimer Hall, Berkeley, CA 94720-1460, USA.
Journal of the American Chemical Society
|October 26, 2006
概括
将一个共纳体引入到多3-基thiophene (P3HT) 中,可以调整其区域规律性. 较低的区域规律性P3HT (>91%) 产生更热稳定的聚合物太阳能电池与PCBM,保持电子性能.
科学领域:
- 有机电子学有机电子学
- 聚合物化学 聚合物化学
- 材料科学是一种材料科学.
背景情况:
- 聚3-甲 (P3HT) 的区域规律性显著影响其在有机电子中的电子特性和性能.
- 高区域规律性P3HT (>96%) 通常是大量异质连接 (BHJ) 太阳能电池中最佳电荷传输的理想条件.
- BHJ形态的热稳定性对于设备的寿命至关重要.
研究的目的:
- 开发一种简单的方法来调整P3HT的有效区域规律性.
- 调查修改的P3HT区域规律性对BHJ形态和光伏性能的影响.
- 为了比较BHJ的热稳定性,它与不同的P3HT区域规律性混合.
主要方法:
- 通过将3,4-dihexylthiophene作为共称物来合成具有不同区域规律性的P3HT.
- 使用P3HT和烯衍生物PCBM制造大量的异质连接太阳能电池.
- 使用对纳米结构和相分离敏感的技术分析BHJ形态.
- 通过设备测试和回火研究来评估光伏性能和热稳定性.
主要成果:
- 通过引入3,4-dihexylthiophene,建立了一种方法来有效调整P3HT的区域规律性.
- 具有91%区域规律性的P3HT表现出与具有>96%区域规律性的P3HT相似的电子特性.
- 含有91%区域规律性P3HT的BHJ混合物在回火时证明了PCBM与互穿网络的增强热稳定性.
- 尽管区域规律性有所减少,但光伏的性能仍保持不变.
结论:
- 通过共纳体的结合来调整P3HT区域规律性是一种可行的策略,可以提高BHJ形态稳定性.
- 较低的区域规律性P3HT (约91%) 可以导致更强大的有机太阳能电池设备,而不会牺牲电子性能.
- 这种方法为改善聚合物光伏的长期运行稳定提供了一条途径.
相关概念视频
Polymer Classification: Stereospecificity
Polymerization generates chiral centers along the entire backbone of a polymer chain. Accordingly, the stereochemistry of the substituent group has a significant effect on polymer properties. Polymers formed from monosubstituted alkene monomers feature chiral carbons at every alternate position in the polymer backbone. Relative to the predominant orientation of substituents at the adjacent chiral carbons, the polymer can exist in three different configurations: isotactic, syndiotactic, and...
Thermal Electrocyclic Reactions: Stereochemistry
The stereochemistry of electrocyclic reactions is strongly influenced by the orbital symmetry of the polyene HOMO. Under thermal conditions, the reaction proceeds via the ground-state HOMO.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Polymer Classification: Crystallinity
Unlike ionic or small covalent molecules, polymers do not form crystalline solids due to the diffusion limitations of their long-chain structures. However, polymers contain microscopic crystalline domains separated by amorphous domains.
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
Polymer Classification: Architecture
Polymers are classified as linear or branched on the basis of their chain architecture. The polymer chains in linear polymers have a long chain-like structure with minimal to no branching at all. Even if a polymer features large substituent groups on the monomer, which appear as branches to the skeleton, it is not considered a branched polymer. A branched polymer contains secondary polymer chains that arise from the main polymer chain. The branching occurs when the polymer growth shifts from...


