Core–shell defective TiO2 nanoparticles by femtosecond laser irradiation with enhanced photocatalytic performance†
*a
Michael A.
Pope
ah
and
Abstract
Engineering defects in titanium dioxide (TiO2) is becoming increasingly important to enhance its photocatalytic performance by increasing active sites and lowering its band gap from the UV region to the visible light region. Herein, we demonstrate a simple method to create stable surface defects by exposing TiO2 dispersions to femtosecond laser irradiation. When using an 800 nm wavelength source, little change to the TiO2 dispersion is observed. However, including the second harmonic of this source (400 nm wavelength) creates stable, dark colored, defective TiO2, also known as black TiO2. This occurs without the formation of a rutile phase, previously thought to be necessary for black TiO2 formation. We demonstrate that the surface oxygen vacancy concentration can be tuned to a maximum of 8% with irradiation time. Beyond this, defect annihilation is observed. Unlike irradiation using longer pulse width lasers (e.g. nanosecond and picosecond lasers), which are known to create more bulk defects, modification using femtosecond pulse widths only modifies a thin shell at the surface, leaving the bulk of the particles unaffected. The most defective TiO2 exhibits enhanced photocatalytic performance under UV light owing to the formation of defects which act as trapping states for photogenerated electron/hole pairs.
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