Abstract
Integrating semiconductors into metal-organic frameworks (MOFs) typically compromises porosity due to pore blockage or coverage. Conversely, we report a CdS/UiO-66-NH2 composite, achieving a 1.5-fold increase in specific surface area. Through in-situ synthesis, CdS clusters are embedded into the tetrahedral pores of UiO-66-NH2. Structural analysis utilizing Rietveld-refined synchrotron X-ray diffraction (SXRD) and density functional theory (DFT) reveals the confined CdS clusters modulate the rotation of organic linkers, synchronously expanding the framework by a guest-induced gate-opening effect. In addition, CdS/UiO-66-NH2 heterostructure significantly facilitates efficient charge carrier separation. Consequently, the optimized CdS/UiO-66-NH2 exhibits a more than doubled photocatalytic water splitting rate compared to pristine UiO-66-NH2. This work offers molecular-level insights into leveraging structural flexibility for constructing high-efficiency photocatalysts.
| Original language | English |
|---|---|
| Article number | 176362 |
| Journal | Chemical Engineering Journal |
| Volume | 537 |
| DOIs | |
| Publication status | Published - 1 Jun 2026 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- CdS
- Composite
- Gate-opening effect
- Liner rotation
- UiO-66-NH MOF
ASJC Scopus subject areas
- Environmental Chemistry
- General Chemistry
- General Chemical Engineering
- Industrial and Manufacturing Engineering
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