Tungsten-based Lindqvist and Keggin type polyoxometalates as efficient photocatalysts for degradation of toxic chemical dyes.

Photocatalytic dye degradation employing polyoxometalates (POMs) has been a research focus for several years. We report the facile synthesis of tungsten-based Lindqvist and Keggin-type POMs that degrade toxic chemical dyes, methyl orange (MO) and methylene blue (MB), respectively. The Lindqvist POM, sodium hexatungstate, NaWO, degrades MO under 100 W UV light irradiation within 15 min, whereas the Keggin POM, AgPWVO, degrades MB under 20 W visible light source within 180 min. The effect of various operating parameters, such as photocatalyst concentration, pH, time, and initial dye concentration, were assessed in the degradation of both dyes. The photoelectrochemical performance of the as-synthesized polyoxometalates shows that the AgPWVO shows 2.4 times higher photocurrent density than NaWO at a potential of 0.9 V vs. Ag/AgCl. Electrochemical impedance analysis reveals that AgPWVO exhibits much lower charge transfer resistance as compared to NaWO, which indicates facile charge transfer at the electrode-electrolyte interface. Further Mott-Schottky measurements reveal that both the catalysts possess n-type semiconductivity and the charge carrier concentration of AgPWVO (5.89 × 10 cm) is 1.4 times higher as compared to NaWO (4.25 × 10 cm). This work offers a new paradigm for designing polyoxometalates suitable for efficient photocatalytic degradation of organic dyes.