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Facile synthesis and characterization of V2O5 nanobelt bundles containing plasmonic Ag for photoelectrochemical water splitting under visible light irradiation
摘要: V2O5 nanobelt bundle (NBB) photoanodes were synthesized from commercial V2O5 powder via a facile, room-temperature aqueous solution technique. The V2O5 NBBs were several micrometers long and 15–25 nm wide, with an orthorhombic V2O5 structure, a crystallite size of 63 nm, and an optical bandgap of 2.19 eV. The V2O5 NBBs containing plasmonic Ag showed signi?cantly lower charge transfer resistance than the pure V2O5 NBBs. The charge transfer resistance was further reduced to 21.02 Ω by adding 10% methanol to the 0.1 M KOH electrolyte as a hole scavenger. The water-splitting activity of the V2O5 and V2O5/Ag photoanodes was tested in 0.1 M KOH; a very low photocurrent density of 0.5 μA/cm2 was observed under visible light illumination. The low photocurrent was ascribed to a build-up of photogenerated holes at the photoelectrode/aqueous electrolyte. The addition of methanol drastically increased the photocurrent of the V2O5 NBB photoelectrode. A maximum photocurrent density of 0.2 mA/cm2 was achieved for up to 230 s under light illumination for the V2O5 NBBs containing plasmonic Ag in KOH and methanol, which was 400 times higher than that of the photoanode without a hole scavenger.
关键词: Aqueous electrolyte,Nanowires,Hole scavenger,Ag plasmonic,Water splitting activity
更新于2025-09-16 10:30:52
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Photocatalytic hydrogen evolution from water using fluorene and dibenzothiophene sulfone conjugated microporous and linear polymers
摘要: Three series of conjugated microporous polymers (CMPs) were studied as photocatalysts for hydrogen production from water using a sacrificial hole scavenger. In all cases, dibenzo[b,d]thiophene sulfone polymers outperformed their fluorene analogs. A porous network, S-CMP3, showed the highest hydrogen evolution rate of 6076 μmol h-1 g-1 (λ > 295 nm) and 3106 μmol h-1 g-1 (λ > 420 nm), with an external quantum efficiency of 13.2% at 420 nm. S-CMP3 outperforms its linear structural analog, P35, while in other cases, non-porous linear polymers are superior to equivalent porous networks. This suggests that microporosity might be beneficial for sacrificial photocatalytic hydrogen evolution, if suitable linkers are used that do not limit charge-transport and the material can be wetted by water as studied here by water sorption and quasi-elastic neutron scattering.
关键词: fluorene,sacrificial hole scavenger,conjugated microporous polymers,photocatalytic hydrogen evolution,dibenzo[b,d]thiophene sulfone
更新于2025-09-04 15:30:14