# Nonadiabatic Surface Hopping Dynamics of Photocatalytic Water Splitting Process with Heptazine–(H2O)4 Chromophore

## TL;DR

This study explores how water cluster size affects the efficiency of photocatalytic water splitting using heptazine-based materials.

## Contribution

The paper introduces new insights into the differential decay behavior during the EDPT process in heptazine–water clusters.

## Key findings

- The EDPT mechanism in heptazine–(H2O)4 produces a heptazinyl radical and an OH biradical.
- The quantum yield for EDPT in heptazine–(H2O)4 is 6.5%, lower than in heptazine–H2O.
- The de-excitation process involves both fast and slow decay modes, influencing photochemical efficiency.

## Abstract

Recent research on the use of heptazine-based polymeric carbon nitride materials as potential photocatalysts for hydrogen evolution has made significant progress. However, the impact of the water cluster’s size on the time-dependent photochemical mechanisms during the water splitting process of heptazine–water clusters remains largely unexplored. Here, we present a Landau–Zener trajectory surface hopping dynamics calculation for heptazine–(H2O)4 clusters at the ADC(2) level. The electron-driven proton transfer (EDPT) mechanism reaction from water to hydrogen-bonded heptazine–water clusters was confirmed using this method, yielding a heptazinyl radical and an OH biradical as products. The calculated quantum yield of the EDPT for the heptazine–(H2O)4 complex was 6.5%, which was slightly lower than that of the heptazine–H2O complex (9%), suggesting that increasing the water cluster size does not significantly enhance the efficiency of hydrogen transfer. Interestingly, our results show that the de-excitation of the heptazine–water complex from the excited state to the ground state via the EDPT process follows both fast and slow decay modes, which govern population relaxation and facilitate the photochemical water splitting reaction. This newly identified differential decay behavior offers valuable insights that could help deepen our understanding of the EDPT process, potentially improving the efficiency of water splitting under sunlight.