# Deuteration Induced Electron‐Phonon Coupling Modulation: Suppressing Energy Dissipation and Enhancing Carrier Separation in Organic Photocatalysis

**Authors:** Hongli Sun, Zirui Zhou, Yunfei Ma, Qingzhu Xu, Yanglong Liao, Cheng Han, Yue Zheng, Xiaosong Cao, Yu Wang, Zutao Fan, Jianfeng Zhao, Chenliang Su, Fengtao Fan, Bin Liu

PMC · DOI: 10.1002/advs.202516740 · Advanced Science · 2025-11-19

## TL;DR

This paper shows how replacing hydrogen with deuterium in organic photocatalysts can improve their efficiency by altering electron-phonon interactions.

## Contribution

A novel deuteration strategy is introduced to modulate electron-phonon coupling in organic photocatalysts.

## Key findings

- Deuteration increases the Huang–Rhys factor by ≈1.7-fold, indicating stronger electron-phonon coupling.
- Deuteration lowers exciton binding energy and promotes exciton dissociation.
- The strategy suppresses non-radiative energy dissipation, enhancing photocatalytic hydrogen evolution.

## Abstract

The electron‐phonon coupling in organic photocatalysts offers a great opportunity for tuning carrier behaviors and energy dissipation toward improving photocatalytic efficiency. Adopting strategies to tailor electron‐phonon coupling and revealing the underlying mechanism are therefore essential for the development of high‐efficiency organic photocatalysts. In this work, an isotope substitution strategy is developed by replacing H in high‐frequency C─H oscillators with D to tune the electron‐phonon coupling strength of both 1,2,3,5‐tetrakis(carbazol‐9‐yl)‐4,6‐dicyanobenzene (4CzIPN) and its polymeric derivative. The fitted Huang–Rhys factors exhibit an ≈1.7‐fold increase upon isotopic deuteration, revealing enhanced electron‐phonon coupling. Comprehensive studies demonstrate that the deuteration strategy can effectively lower exciton binding energy, promote exciton dissociation, and suppress non‐radiative energy dissipation, therefore leading to an improved efficiency toward photocatalytic hydrogen evolution. This study highlights the crucial role of electron‐phonon coupling on photocatalytic systems and presents a novel regulatory strategy for designing high‐efficiency organic photocatalysts.

During charge transport, photogenerated carriers exchange energy with lattice vibrations, influencing photocatalytic performance. The deuteration strategy enhances exciton dissociation and suppresses non‐radiative energy loss, significantly improving photocatalytic hydrogen evolution.

## Linked entities

- **Chemicals:** 1,2,3,5‐tetrakis(carbazol‐9‐yl)‐4,6‐dicyanobenzene (PubChem CID 102198498), 4CzIPN (PubChem CID 102198498), deuterium (PubChem CID 24523), hydrogen (PubChem CID 783)

## Full-text entities

- **Chemicals:** 4CzIPN (-), D (MESH:D003903), H (MESH:D006859), 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene (MESH:C586174)

## Full text

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## Figures

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## References

47 references — full list in the complete paper: https://tomesphere.com/paper/PMC12866818/full.md

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Source: https://tomesphere.com/paper/PMC12866818