Journal
ACS OMEGA
Volume 5, Issue 30, Pages 18919-18934Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsomega.0c02142
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Funding
- University of Auckland FRDF fund
- New Zealand Synchrotron Group Ltd
- MacDiarmid Institute for Advanced Materials and Nanotechnology
- Dodd Walls Centre for Photonic and Quantum Technologies
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This study systematically evaluates the performance of a series of TiO2 nanoflower (TNF) photocatalysts for aqueous methylene blue photo-oxidation under UV irradiation. TNF nanoflowers were synthesized from Ti(IV) butoxide by a hydrothermal method and then calcined at different temperatures (T = 400-800 degrees C) for specific periods of time (t = 1-5 h). By varying the calcination conditions, TNF-T-t photocatalysts with diverse physicochemical properties and anatase/rutile ratios were obtained. Many of the TNF-T-1 photocatalysts demonstrated remarkable activity for aqueous methylene blue photo-oxidation at pH 6 under UV excitation (365 nm), with activities following the order TNF-700-1 > TNF-600-1 > TNF-500-1 > TNF-400-1 similar to P25 TiO2 >> TNF-800-1. The activity of the TNF-700-1 photocatalyst (99% anatase, 1% rutile) was 2.3 times that of P25 TiO2 at pH 6 and 14.4 times that of P25 TiO2 at pH 4. Prolonged calcination of the TNFs at 700 degrees C proved detrimental to dye degradation performance due to excessive rutile formation, which reduced the photocatalyst surface area and suppressed OH center dot generation. The outstanding activities of TNF-700-1 and TNF-600-1 are attributed to their hierarchical nanoflower morphology which benefitted UV absorption, a near-ideal anatase crystallite size for efficient charge separation, and their unusually low isoelectric point (IEP = 4.3-4.5).
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