13 October 2016 Visible-light-driven hydrogen evolution with polyoxometalate as electron relay
Xing Liu, Yuexiang Li, Shaoqin Peng, Hua Lai, Zhengji Yi
Author Affiliations +
Abstract
A visible-light-driven hydrogen evolution system was constructed in one step with xanthene dye as photosensitizer, triethanolamine (TEOA) as electron donor, Pt as cocatalyst, and Keggin-type silicon-tungsten polyoxometalate (POM) as electron relay. The average rate of hydrogen evolution from the eosin Y−POM−TEOA−PtCl2-6 systems is 51.8  μ mol h−1, and the apparent quantum yield is 8.9% during 20 h irradiation (λ>420  nm;, a high-pressure Hg lamp was used as the light source). Ultraviolet–visible absorption spectra and fluorescence spectra were used to study the mechanism of charge transfer. A radical anion Dye−, which generates from quenching of the triplet-excited state 3Dye* by sacrificial electron donor, was considered the main species for transmitting electrons to POM and then to Pt. SiW9O10−34, derived from SiW12O4−40, is the main form of POM in our reaction system, which can mediate the electron transfer from Dye− to Pt, so an enhanced hydrogen evolution was realized. The present study highlights POM as electron relay in the photocatalytic hydrogen evolution process, which is expected to contribute to the development of functional and efficient artificial photosynthetic systems.
© 2016 Society of Photo-Optical Instrumentation Engineers (SPIE) 1947-7988/2016/$25.00 © 2016 SPIE
Xing Liu, Yuexiang Li, Shaoqin Peng, Hua Lai, and Zhengji Yi "Visible-light-driven hydrogen evolution with polyoxometalate as electron relay," Journal of Photonics for Energy 6(4), 046501 (13 October 2016). https://doi.org/10.1117/1.JPE.6.046501
Published: 13 October 2016
Lens.org Logo
CITATIONS
Cited by 4 scholarly publications.
Advertisement
Advertisement
RIGHTS & PERMISSIONS
Get copyright permission  Get copyright permission on Copyright Marketplace
KEYWORDS
Hydrogen

Relays

Platinum

Dysprosium

Absorption

Visible radiation

Quantum efficiency

Back to Top