Related Experiment Video
Updated: Jun 13, 2025

Integrating a Triplet-triplet Annihilation Up-conversion System to Enhance Dye-sensitized Solar Cell Response to Sub-bandgap Light
Published on: September 12, 2014
Exploring the triplet state properties of thio-benzothioxanthene imides with applications in TTA-upconversion and
Xiaoping Chen1, Hui Liang1, Xitong He1
1School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, P. R. China. smji@gdut.edu.cn.
Abstract:
Thio-benzothioxanthene imide (BTXI) exhibits long excited state lifetime (τT = 17.7 μs) and high ISC efficiency (ΦΔ = 97%). For the first time, BTXI derivatives were used as photosensitizers for triplet-triplet annihilation upconversion, achieving the highest efficiency of 13.8%. In addition, thio-BTXI derivatives were used as photoinitiators for photopolymerization, resulting in a series of green light-activated radical polymerization systems.
More Related Videos
08:51Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
06:08Time-resolved Photophysical Characterization of Triplet-harvesting Organic Compounds at an Oxygen-free Environment Using an iCCD Camera
Published on: December 27, 2018
Related Concept Videos
Thermal and Photochemical Electrocyclic Reactions: Overview
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
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.
Aromatic Hydrocarbon Cations: Structural Overview
Removing one hydrogen from the intervening CH2 group...
Cycloaddition Reactions: MO Requirements for Photochemical Activation
Woodward–Hoffmann Selection Rules and Microscopic Reversibility