Solar-driven fast photocatalytic hydrogen evolution using size-minimized organic heterojunctions
Pursuing small catalyst sizes has remained a constant endeavor to maximize reaction yields by exposing more active sites and/or enhancing charge extraction. Organic particle photocatalysts typically remain tens to hundreds of nanometers in size, constrained by the quasi-infinite conjugation of commonly used polymers. Here, we reveal the size-minimized organic heterojunction nanoparticles by using all small molecule photovoltaic materials, and significantly enhance their photocatalytic activities for solar-driven hydrogen evolution. Owing to the intrinsically weak intermolecular forces and the absence of molecular entanglement of small molecules, (sub)nanometer-scale diameters of polymer-free nanoparticles are yielded, representing a size reduction of 1-2 orders of magnitude than traditional polymer-containing nanoparticles. Optimized polymer-free nanoparticles attaching on covalent frameworks achieve photocatalytic mass-united hydrogen evolution rates of up to 527.2 ~ 3180.7 mmol h<sup>-1</sup> g<sup>-1</sup> at varied concentrations under simulated sunlight, and the external quantum efficiency is up to 32.8 % at near-infrared light, marking a competitive performance for organic photocatalysts.
Authors
- Wenqin Si
- Dong Qiu
- Yawen Li
- Zhenzhen Zhang
- Heng Liu
- Yan Qiao
- Xinhui Lu
- Tengfei Li
- Yuze Lin
Institutions
- Chinese University of Hong Kong (HK)
- Chinese Academy of Sciences (CN)
- Beijing National Laboratory for Molecular Sciences (CN)
- Institute of Chemistry (CN)
- University of Chinese Academy of Sciences (CN)
Publication Details
- Journal
- Nature Communications
- Published
- 2025-12-30
- DOI
- https://doi.org/10.1038/s41467-025-67811-4
- Primary Topic
- Covalent Organic Framework Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China