摘要
An interlocking “ T -shape” structure was built by uniform filling β-PbO 2 crystalline inside the trace Ti 3+ self-doping TiO 2 nanotube arrays (TNAs) channels and depositing the cauliflower-like β-PbO 2 clusters on its upper surface through a facile current pulse deposition method. We elaborated the interfacial engineering strategy for generating compact oxide layers at TNAs bottoms and growing β-PbO 2 crystalline from the selectively conductive TNAs bottoms. Different characterization techniques and electrochemical analyses were conducted to characterize the morphology, structure, and electrochemical property of the β-PbO 2 partial filling/covering TNAs (β-PbO 2 /TNAs/Ti) materials. We also systematically investigated and elucidated the performance and mechanism of β-PbO 2 /TNAs/Ti anode activated peroxymonosulfate (PMS) system via berberine removal/mineralization, reactive oxygen species (ROS) identification/contribution, intermediates analysis, energy consumption and practical applicability estimation. Results illustrated that filling β-PbO 2 inside TNAs can efficiently improve the directional electron-transfer efficiency, oxygen evolution over-potential, tolerance to the varied water matrices and service lifetime of β-PbO 2 /TNAs/Ti anode activated PMS system. The ROS including • OH, S O 4 ∙ - and 1 O 2 that generated from PMS electro-activation are responsible for efficient berberine degradation through two pathways. This study will provide a general approach to construct the versatile tube-filled TNAs-based materials for wide applications in water/wastewater treatment.
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