Related Experiment Video
Updated: Jan 31, 2026

Determination of the Gas-phase Acidities of Oligopeptides
Published on: June 24, 2013
Computational Insight into the Photocatalytic Splitting of H2S during Gas-Solid Phase and Aqueous Phase Reactions
Yue-Wen Yang1, Zhi-Hao Luo1, Jia-Sheng Zhou1
1Department of Physics, City University of Hong Kong, Hong Kong SAR 999077, P. R. China.
Abstract:
Hydrogen sulfide (H2S) is a hazardous byproduct of industrial processes and poses significant environmental and health risks. Conventional methods for H2S removal are not cost-effective, motivating the exploration of photocatalytic splitting of H2S to both remove H2S and generate hydrogen. Recent advancements in the use of graphitic carbon nitride materials (g-CN), consisting of heptazine units, have shown impressive progress in the photocatalytic splitting of H2S. This study employs excited-state nonadiabatic dynamics simulations to investigate the molecular-level mechanisms of photoinduced H2S splitting in both gas-solid and aqueous phases. Using a H2S···heptazine model, the gas-solid phase reaction reveals an electron-driven proton transfer (EDPT) process as the key reaction pathway. In the aqueous phase, the photocatalyst significantly improves light absorption efficiency, as the H2S···(H2O)4 cluster absorbs only a limited range of ultraviolet light. Moreover, the study demonstrates that the photoinduced holes transfer from the photocatalyst to H2S and water molecules, which is a crucial step in enhancing the detachment of hydrogen atoms and their subsequent possible combination to form hydrogen gas. These findings provide valuable insights into the charge carrier dynamics and reaction mechanisms, elucidating the potential for efficient hydrogen production from the photocatalytic splitting of hazardous H2S.
Related Concept Videos
Phase Diagrams
Phase Transitions
Phase I Reactions: Hydrolytic Reactions
An important hydrolytic reaction is ester hydrolysis. Ester bonds, often found in prodrugs, are broken down, increasing the solubility of drugs like aspirin and lidocaine for more straightforward elimination. Amide hydrolysis is another critical reaction, targeting amide bonds prevalent...
Phase II Reactions: Acetylation Reactions
The substrates for acetylation are typically drugs or their metabolites with an amino, sulfonamide, or hydrazine functional group. Acetylation can occur at several points in the drug molecule, including primary, secondary, and...
Phase I Reactions: Reductive Reactions
Phase II Reactions: Methylation Reactions
The mechanism of methylation unfolds in two stages. The first stage sees a methyltransferase enzyme facilitating the transfer of a methyl group from S-adenosylmethionine (SAM) to the substrate, forming S-adenosylhomocysteine (SAH). The second stage involves further metabolism of SAH into homocysteine, which can be recycled...

![Solid-phase Synthesis of [4.4] Spirocyclic Oximes](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F58508.jpg&w=3840&q=50)