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Enhanced Solar Photothermal Catalysis over Solution Plasma Activated TiO(2)

Colored wide‐bandgap semiconductor oxides with abundant mid‐gap states have long been regarded as promising visible light responsive photocatalysts. However, their catalytic activities are hampered by charge recombination at deep level defects, which constitutes the critical challenge to practical a...

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Detalles Bibliográficos
Autores principales: Yu, Fei, Wang, Changhua, Li, Yingying, Ma, He, Wang, Rui, Liu, Yichun, Suzuki, Norihiro, Terashima, Chiaki, Ohtani, Bunsho, Ochiai, Tsuyoshi, Fujishima, Akira, Zhang, Xintong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7435248/
https://www.ncbi.nlm.nih.gov/pubmed/32832348
http://dx.doi.org/10.1002/advs.202000204
Descripción
Sumario:Colored wide‐bandgap semiconductor oxides with abundant mid‐gap states have long been regarded as promising visible light responsive photocatalysts. However, their catalytic activities are hampered by charge recombination at deep level defects, which constitutes the critical challenge to practical applications of these oxide photocatalysts. To address the challenge, a strategy is proposed here that includes creating shallow‐level defects above the deep‐level defects and thermal activating the migration of trapped electrons out of the deep‐level defects via these shallow defects. A simple and scalable solution plasma processing (SPP) technique is developed to process the presynthesized yellow TiO(2) with numerous oxygen vacancies (Ov), which incorporates hydrogen dopants into the TiO(2) lattice and creates shallow‐level defects above deep level of Ov, meanwhile retaining the original visible absorption of the colored TiO(2). At elevated temperature, the SPP‐treated TiO(2) exhibits a 300 times higher conversion rate for CO(2) reduction under solar light irradiation and a 7.5 times higher removal rate of acetaldehyde under UV light irradiation, suggesting the effectiveness of the proposed strategy to enhance the photoactivity of colored wide‐bandgap oxides for energy and environmental applications.