Abstract
Elemental red phosphorus (red P) is a new class of photocatalysts with a desirable bandgap of ~1.7 eV and has a strong visible-light response. Here, we show that the efficiency of red P is limited by severe electron trapping at deep traps that are intrinsic to the different crystal facets of the red P. To overcome this, we synthesized the red P/RGO (reduced graphene oxide) composite in a one-step ampoule chemical vapor deposition synthesis that formed a conducive interface between the red P photocatalyst and the RGO acceptor for efficient interfacial charge transport. As substantiated through photoelectrochemical characterization and ultrafast (femtoseconds) transient absorption spectroscopy, the interfacing with RGO provided a rapid pathway for the photocharges in red P to be interfacially separated, thereby circumventing the slower the charge trapping process. As a result, up to a sevenfold increase in the photocatalytic hydrogen production rate (apparent quantum yield = 3.1% at 650 nm) was obtained for the red P/RGO relative to the pristine red P.
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CITATION STYLE
Jing, L., Zhu, R., Ng, Y. H., Hu, Z., Teoh, W. Y., Phillips, D. L., & Yu, J. C. (2020). Visible-light photocatalysis and charge carrier dynamics of elemental crystalline red phosphorus. Journal of Chemical Physics, 153(2). https://doi.org/10.1063/5.0013142
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