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Photocatalytic Activities Enhanced by Au-Plasmonic Nanoparticles on TiO(2) Nanotube Photoelectrode Coated with MoO(3)

Although TiO(2) was formerly a common material for photocatalysis reactions, its wide band gap (3.2 eV) results in absorbing only ultraviolet light, which accounts for merely 4% of total sunlight. Modifying TiO(2) has become a focus of photocatalysis reaction research, and combining two metal oxide...

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Detalles Bibliográficos
Autores principales: Li, Chia-Jui, Tseng, Chuan-Ming, Lai, Sz-Nian, Yang, Chin-Ru, Hung, Wei-Hsuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5630543/
https://www.ncbi.nlm.nih.gov/pubmed/28986769
http://dx.doi.org/10.1186/s11671-017-2327-y
Descripción
Sumario:Although TiO(2) was formerly a common material for photocatalysis reactions, its wide band gap (3.2 eV) results in absorbing only ultraviolet light, which accounts for merely 4% of total sunlight. Modifying TiO(2) has become a focus of photocatalysis reaction research, and combining two metal oxide semiconductors is the most common method in the photocatalytic enhancement process. When MoO(3) and TiO(2) come into contact to form a heterogeneous interface, the photogenerated holes excited from the valence band of MoO(3) should be transferred to the valence band of TiO(2) to effectively reduce the charge recombination of photogenerated electron–hole pairs. This can efficiently separate the pairs and promote photocatalysis efficiency. In addition, photocurrent enhancement is attributed to the strong near-field and light-scattering effects from plasmonic Ag nanoparticles. In this work, we fabricated MoO(3)-coated TiO(2) nanotube heterostructures with a 3D hierarchical configuration through two-step anodic oxidation and a facile hydrothermal method. This 3D hierarchical structure consists of a TiO(2) nanotube core and a MoO(3) shell (referred to as TNTs@MoO(3)), as characterized by field emission scanning electron microscopy and X-ray photoelectron spectroscopy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s11671-017-2327-y) contains supplementary material, which is available to authorized users.