Abstract
The CdS@CdxPb1−xS core–shell photocatalyst was synthesized through cation exchange and demonstrated significant photocatalytic hydrogen production. Initially, the catalyst was inactive due to the formation of an unfavourable Type I heterojunction. However, under continued illumination, electron accumulation in the CdxPb1−xS shell led to electron repulsion, triggering a structural transition from a film-like morphology to quantum dots (QDs). This transition resulted in the formation of a Type II heterojunction between the CdS and PbS components, boosting hydrogen production by 400% compared to CdS nanoparticles. The reversible structural transformation and stable performance over multiple cycles highlight the potential of CdS@CdxPb1−xS nanoparticles as a highly efficient photocatalyst for hydrogen evolution.
| Original language | English |
|---|---|
| Pages (from-to) | 534-542 |
| Number of pages | 9 |
| Journal | Journal of Industrial and Engineering Chemistry |
| Volume | 145 |
| DOIs | |
| State | Published - 2025.05.25 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Cadmium lead sulfide
- Cadmium sulfide
- Hydrogen production
- Photocatalysis
Quacquarelli Symonds(QS) Subject Topics
- Engineering - Chemical
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