Adsorption and Photo-Degradation of Organophosphates on Sulfate-Terminated Anatase TiO2 Nanoparticles

Abstract

The adsorption and photocatalytic degradation of trimethyl phosphate (TMP) and triethyl phosphate (TEP), two environmentally relevant model pollutants, have been studied on commercial anatase TiO2 and sulfate-terminated anatase TiO2 nanoparticles by means of operando diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy and 2D correlation spectroscopy (2D COS). It is concluded that both TMP and TEP adsorb dissociatively on anatase TiO2, while on the sulfate-terminated anatase TiO2, TMP and TEP adsorb associatively. Upon UV illumination, TMP and TEP are completely oxidized on sulfate-terminated anatase TiO2, as evidenced by the evolution of the IR bands characteristic for water and carbon dioxide. In contrast, on anatase TiO2, UV illumination leads to the formation of stable surface-coordinated carboxylate products, which impedes complete oxidation. 2D COS analysis suggests that parallel reaction pathways occur during oxidation under UV illumination, viz. methoxide/ethoxide (ads) → carboxylates (ads) and methoxide/ethoxide (ads) → aldehydes (ads) → carboxylates (ads). A parallel reaction occurs on sulfated TiO2 that yields CO2 and H2O by direct radical reactions with the methoxide groups with little, or no, formation of surface-coordinated intermediates. Sulfated TiO2 favor the formation of aldehyde intermediates, with reaction rates 10 times and 30 times faster for TMP and TEM, respectively, compared with commercial anatase TiO2. About 37% (33%) and 32% (24%) of TMP (TEP) were degraded on sulfated-terminated TiO2 and pure TiO2, respectively, after the first 9 min of UV illumination. We show that the sulfate-functionalization of TiO2 has two main functions. First, it prevents the formation of strongly bonded bridging carboxylates, thereby alleviating deactivation. Second, it promotes full oxidation of the organic side-chains into carbon dioxide and water. Improved electron-hole separation by the electrophilic S(VI) in combination with the blocking of bridging reaction intermediates is proposed to contribute to the improved activity. The presented results give insights into how acidic surface modifications change adsorbate surface chemistries, which can be used to increase the sustained activity of low-temperature photocatalysts.