Related Experiment Video

Updated: Mar 16, 2026

Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions
10:21

Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions

Published on: October 5, 2019

9.1K

Salicylic Acid-Based Organic Dyes Acting as the Photosensitizer for Solar Cells

Sungjun Hong, Jae-Hyeong Park, Ah-Reum Han

    Journal of Nanoscience and Nanotechnology
    |August 4, 2016
    PubMed

    More Related Videos

    Integrating a Triplet-triplet Annihilation Up-conversion System to Enhance Dye-sensitized Solar Cell Response to Sub-bandgap Light11:26

    Integrating a Triplet-triplet Annihilation Up-conversion System to Enhance Dye-sensitized Solar Cell Response to Sub-bandgap Light

    Published on: September 12, 2014

    13.1K
    Electrospinning of Photocatalytic Electrodes for Dye-sensitized Solar Cells09:30

    Electrospinning of Photocatalytic Electrodes for Dye-sensitized Solar Cells

    Published on: June 28, 2017

    10.2K

    Related Concept Videos

    Aryldiazonium Salts to Azo Dyes: Diazo Coupling01:11

    Aryldiazonium Salts to Azo Dyes: Diazo Coupling

    The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the para...
    3.8K
    Photochemical Electrocyclic Reactions: Stereochemistry01:26

    Photochemical Electrocyclic Reactions: Stereochemistry

    The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
    Selection Rules: Photochemical Activation
    2.4K
    Cycloaddition Reactions: MO Requirements for Photochemical Activation01:12

    Cycloaddition Reactions: MO Requirements for Photochemical Activation

    Some cycloaddition reactions are activated by heat, while others are initiated by light. For example, a [2 + 2] cycloaddition between two ethylene molecules occurs only in the presence of light. It is photochemically allowed but thermally forbidden.
    2.8K