In a typical degradation experiment, 50 mg of the photocatalyst was fully mixed with 100 mL of Rh B (10 mg L−1) by ultrasonic treatment for 5 min. Before exposure to light, the reaction system achieved adsorption–desorption equilibrium by magnetic stirring for 30 min in darkness. At designated intervals, 3.0 mL suspension was collected and centrifuged at 12 000 rpm for 10 min. Finally, the concentration of Rh B in the supernatant was estimated using a Unico UV-2800A spectrophotometer at the characteristic wavelength of 552 nm.
In the photocatalytic H2 generation test, 30 mg of sample deposited with 1.0 wt% Pt was fully suspended into 50 mL ultrapure water containing 10% (vol/vol) triethanolamine (TEOA), where TEOA was used as the hole scavenger and Pt was used as the co-catalyst. H2 evolution during the photocatalytic reaction was calculated using an online gas chromatograph (Agilent, GC-8890) equipped with a thermal conductivity detector and high-purity nitrogen was used as the carrier gas.