Related Experiment Video
Updated: Mar 20, 2026

Morphology Control for Fully Printable Organic–Inorganic Bulk-heterojunction Solar Cells Based on a Ti-alkoxide and Semiconducting Polymer
Published on: January 10, 2017
Hydrogen-bonded oligothiophene rosettes with a benzodithiophene terminal unit: self-assembly and application to bulk
Hayato Ouchi1, Xu Lin1, Takahiro Kizaki2
1Department of Applied Chemistry and Biotechnology, Graduate School of Engineering, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522, Japan. yagai@faculty.chiba-u.jp.
Abstract:
Benzodithiophene-functionalized oligothiophene with barbituric acid hydrogen-bonding unit self-assembles into nanoscopic structures via the formation of rosettes. The nanostructures show a power conversion efficiency of 3% upon mixing with PC61BM in bulk-heterojunction solar cells without thermal annealing.
More Related Videos
06:49In situ Grazing Incidence Small Angle X-ray Scattering on Roll-To-Roll Coating of Organic Solar Cells with Laboratory X-ray Instrumentation
Published on: March 2, 2021
11:38Influence of Hybrid Perovskite Fabrication Methods on Film Formation, Electronic Structure, and Solar Cell Performance
Published on: February 27, 2017
Related Concept Videos
Thermal and Photochemical Electrocyclic Reactions: Overview
Thermal Electrocyclic Reactions: Stereochemistry
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.