Abstract
Organic conjugated polymer dots (Pdots) are considered promising photocatalysts for solar-driven hydrogen production. However, the impact of molecular weight on their photocatalytic activity remains unexplored. In this study, four thiophene-quinoxaline (PTQ)-based Pdots (D-A system) with tunable molecular weights were fabricated to elucidate the effects of molecular weight on Pdot photocatalytic activity. These Pdots serve as highly efficient and stable photocatalysts for visible-light-driven hydrogen generation in a solvent-free organic system, which was achieved for the first time. Low-molecular-weight Pdots exhibited minimal aggregation, small particle sizes, uniform morphology, enhanced charge transfer capability, and superior photocatalytic activity with remarkable photostability. Notably, L-PTQ10 and L-PTQ11 demonstrated exceptional hydrogen evolution rates of 15,807 and 10,411 μmol g−¹ h−¹, respectively, when coupled with a Pt cocatalyst. The findings from our DFT and molecular dynamics (MD) calculations strongly support our hypothesis, highlighting the use of low-molecular-weight PTQ-based Pdots as a promising strategy to develop efficient and stable photocatalysts for solar-driven hydrogen production.
| Original language | English |
|---|---|
| Pages (from-to) | 1079-1088 |
| Number of pages | 10 |
| Journal | Polymer Journal |
| Volume | 56 |
| Issue number | 11 |
| DOIs | |
| State | Published - Nov 2024 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© The Author(s), under exclusive licence to The Society of Polymer Science, Japan 2024.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 2 Zero Hunger
-
SDG 7 Affordable and Clean Energy
ASJC Scopus subject areas
- Polymers and Plastics
- Materials Chemistry
Fingerprint
Dive into the research topics of 'Solar-driven photocatalytic hydrogen production thiophene-quinoxaline-based polymer dots with tunable molecular weight'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver