4.7 Article

Enhanced Photocatalytic Hydrogen Evolution by Star-Shaped Viologen-Sensitized TiO2 Nanoparticles

期刊

ACS APPLIED NANO MATERIALS
卷 6, 期 21, 页码 20173-20182

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsanm.3c03965

关键词

photocatalysis; viologen; hydrogen evolution; sensitization of TiO2; electron-transfermediator

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Viologens can serve as effective electron-transfer mediators and modifiers for semiconductors in photocatalytic systems. In this study, hybrid photocatalysts composed of TiO2 nanoparticles and star-shaped viologen derivatives were prepared for visible-light-driven hydrogen evolution. TPCBP-E_TiO2 exhibited the highest hydrogen evolution activity among the structures, with superior apparent quantum yield and electron transfer efficiency.
Viologens are well-suited for serving as electron-transfer mediators in redox systems due to their low reduction potential and ability to form stable radical cations. Because of this feature, viologens can play a key role in modifying semiconductors toward enhanced photocatalytic performance. Herein, a series of hybrid photocatalysts composed of TiO2 nanoparticles and star-shaped viologen derivatives with different alkyl chains [TPCBP-X_TiO2; X: ethyl (E), butyl (B), hexyl (H) and octyl (O)] were prepared for the photocatalytic hydrogen evolution from water under visible-light irradiation. The TPCBP-X molecules not only provide photosensitization of TiO2 nanoparticles in the visible-light region but also act as an efficient electron-transfer mediator for the transfer of photoinduced electrons to TiO2 and Pt. Among these photocatalysts, TPCBP-E_TiO2 exhibited a 1.013 mmol g(-1) h(-1) H-2 evolution rate with an apparent quantum yield (AQY) of 20.15% (470 nm), which dramatically improved hydrogen evolution activity among the other structures [TPCBP-X_TiO2 (X; B, H, O)] due to the more porous and uniform surface, resulting in its low barrier effect for electron transfer. In addition, in the presence of a Pt cocatalyst, TPCBP-E_TiO2 yielded a H-2 evolution rate of 17.7 mmol g(-1), which is about 2.2 times higher than that of pure TPCBP-E_TiO2 (8.1 mmol g(-1)) after 8 h of visible-light illumination.

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