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Tailoring TiO(2) Nanotube‐Interlaced Graphite Carbon Nitride Nanosheets for Improving Visible‐Light‐Driven Photocatalytic Performance
Rapid recombination of photoinduced electron–hole pairs is one of the major defects in graphitic carbon nitride (g‐C(3)N(4))‐based photocatalysts. To address this issue, perforated ultralong TiO(2) nanotube‐interlaced g‐C(3)N(4) nanosheets (PGCN/TNTs) are prepared via a template‐based process by tre...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6010724/ https://www.ncbi.nlm.nih.gov/pubmed/29938167 http://dx.doi.org/10.1002/advs.201700844 |
Sumario: | Rapid recombination of photoinduced electron–hole pairs is one of the major defects in graphitic carbon nitride (g‐C(3)N(4))‐based photocatalysts. To address this issue, perforated ultralong TiO(2) nanotube‐interlaced g‐C(3)N(4) nanosheets (PGCN/TNTs) are prepared via a template‐based process by treating g‐C(3)N(4) and TiO(2) nanotubes polymerized hybrids in alkali solution. Shortened migration distance of charge transfer is achieved from perforated PGCN/TNTs on account of cutting redundant g‐C(3)N(4) nanosheets, leading to subdued electron–hole recombination. When PGCN/TNTs are employed as photocatalysts for H(2) generation, their in‐plane holes and high hydrophilicity accelerate cross‐plane diffusion to dramatically promote the photocatalytic reaction in kinetics and supply plentiful catalytic active centers. By having these unique features, PGCN/TNTs exhibit superb visible‐light H(2)‐generation activity of 1364 µmol h(−1) g(−1) (λ > 400 nm) and a notable quantum yield of 6.32% at 420 nm, which are much higher than that of bulk g‐C(3)N(4) photocatalysts. This study demonstrates an ingenious design to weaken the electron recombination in g‐C(3)N(4) for significantly enhancing its photocatalytic capability. |
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