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Updated: Feb 20, 2026

Morphology Control for Fully Printable Organic–Inorganic Bulk-heterojunction Solar Cells Based on a Ti-alkoxide and Semiconducting Polymer
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Morphology Control for Fully Printable Organic–Inorganic Bulk-heterojunction Solar Cells Based on a Ti-alkoxide and Semiconducting Polymer

Published on: January 10, 2017

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高性能テナー有機太陽電池の非融合環ポリマー受容体による結晶化行動を調節する

Tingting Wang1, Wenliang Li1, Xiaohong Zhao1

  • 1College of Chemistry and Chemical Engineering/Film Energy Chemistry For Jiangxi Provincial Key Laboratory (FEC)/Institute of Polymers and Energy Chemistry (IPEC), Nanchang University, Nanchang, China.

Small (Weinheim an der Bergstrasse, Germany)
|February 18, 2026
PubMed
まとめ

有機太陽電池に非融合リングポリマー受容体 (PW1) を加えることで,活性層の結晶化が改善され,電力変換効率 (PCE) と安定性が向上します. この戦略は,パフォーマンスとデバイスの長寿を向上させます.

キーワード:
結晶性規制について非融合リングポリマー受容器オーガニック・ソーラー・セル安定性の安定性についてです.第三コンポーネントの第3コンポーネント

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Polymer Classification: Crystallinity01:21

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...
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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...
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Ring-opening metathesis polymerization or ROMP involves strained cycloalkenes as starting materials. The mechanism of ROMP proceeds by reacting cycloalkene with Grubbs catalyst to give metallacyclobutane intermediate which undergoes a ring-opening reaction to form new carbene. The new carbene reacts with another molecule of cycloalkene. Repetition of these steps leads to the formation of an unsaturated open-chain polymer product. All these steps are reversible, however, relieving the ring...
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