Steering Charge Directional Separation in MXenes/Titanium Dioxide for Efficient Photocatalytic Nitrogen Fixation

Abstract

Photocatalytic nitrogen fixation has attracted much attention because of its ability to synthesize ammonia under mild conditions. However, the ammonia yield is still greatly limited by the sluggish charge separation and extremely high N2 dissociation energy. Herein, two-dimensional Ti3C2 MXene ultrathin nanosheets were introduced to construct Ti3C2/TiO2 composites via electrostatic adsorption for photocatalytic nitrogen fixation. The photocatalytic activity experiments showed that after adding 0.1 wt% Ti3C2, the ammonia yield of the Ti3C2/TiO2 composite reached 67.9 μmol L−1 after 120 min of light irradiation, nearly 3 times higher than that of the monomer TiO2. XPS, DRS, LSV, and FTIR were used to explore the possible photocatalytic nitrogen fixation mechanism. Studies showed that a close interfacial contact has been formed via the bonding mode of =C-O between the Ti3C2 and TiO2 samples. The formed =C-O bond boosts an oriented photogenerated charge separation and transfer in the Ti3C2/TiO2 composite. This work provides a promising idea for constructing other efficient MXene-based composite photocatalysts for artificial photosynthesis.

Keywords

• titanium dioxide
• ultrathin MXene
• nitrogen fixation
• charge separation
• artificial photosynthesis