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Cu/TiO2 Derived from Cu-Doped MIL-125 for Enhanced Photocatalytic CO2-to-CH4 Conversion
Haopeng Cui1, Zhiying Li1, Siyu Huang1
1School of Environment and Architecture, University of Shanghai for Science and Technology, Shanghai 200093, China.
Molecules (Basel, Switzerland)
|July 15, 2026
Summary
Copper-modified titanium dioxide (Cu/TiO2) photocatalysts were synthesized from a metal-organic framework precursor. Optimized calcination temperature significantly enhanced CO2 reduction to methane, achieving high efficiency and selectivity for solar fuel production.
Area of Science:
- Materials Science
- Catalysis
- Renewable Energy
Background:
- Photocatalytic CO2 reduction to methane is a key strategy for solar fuel production.
- Challenges include poor charge separation, CO2 activation, and multi-electron transfer kinetics.
Purpose of the Study:
- To develop efficient Cu/TiO2 photocatalysts for CO2 reduction.
- To investigate the effect of calcination temperature on catalyst performance.
Main Methods:
- Synthesis of Cu-modified defective MIL-125(Ti) precursor (Cu-MIL-125).
- Temperature-controlled calcination to produce Cu/TiO2.
- Characterization of structural, chemical, and electronic properties.
- Evaluation of photocatalytic CO2 reduction to CH4.
Main Results:
- Cu/TiO2 catalysts were successfully synthesized, with properties dependent on calcination temperature.
- The optimal catalyst (450 Cu/TiO2) achieved a CH4 formation rate of 15.90 μmol g-1 h-1 (9.8-fold enhancement).
- High CH4 selectivity (93.05%) was observed, confirmed by isotope labeling and in situ spectroscopy.
Conclusions:
- Calcination temperature critically influences Cu/TiO2 structure and photocatalytic activity.
- Metal-organic framework-derived Cu/TiO2 shows promise for efficient solar fuel production.
- This study provides a practical route for designing advanced photocatalysts.

