期刊
ACS CATALYSIS
卷 3, 期 11, 页码 2547-2555出版社
AMER CHEMICAL SOC
DOI: 10.1021/cs400466b
关键词
photocatalysis; flux synthesis; layered-niobate; solar energy; band engineering
资金
- Research Corporation for Science Advancement
Layered DionJacobson phases RbLaNb2O7 and RbA(2)Nb(3)O(10) (A = Ca, Sr) and the RuddlesdenPopper phase Rb2La2Ti3O10 were prepared by solid-state methods at a reaction time of 50 h and a temperature of 1100 degrees C. The products were silver-exchanged within a AgNO3 flux at a reaction time of 24 h and a temperature of 250 degrees C. Substitution of silver cations into the interlayer spacing of the layered structures is found to decrease the optical bandgap sizes on average by similar to 0.5 to similar to 1.0 eV. The products were found by scanning electron microscopy (SEM) to exhibit irregularly shaped platelet morphologies with an average size of similar to 15 mu m across their lateral dimensions and stepped edges ranging from similar to 20 to similar to 300 nm in height. Significant increases in photocatalytic hydrogen production rates for all silver-exchanged products were observed. The silver-exchanged RbA(2)Nb(3)O(10) layered structures exhibited the highest photocatalytic hydrogen formation rates under ultraviolet and visible irradiation (similar to 13,616 mu mol H-2.g(1).h(1)). These rates were 10 times higher than prior to silver exchange (similar to 1,418 mu mol H-2.g(1).h(1)). However, photocatalytic activity under only visible light irradiation is not observed. It is also found that the silver cations located at the surfaces are reduced to Ag(s) after prolonged UV and visible light exposure in solution, which functions to increase their activity under UV irradiation. Electronic-structure calculations based on density functional theory show that the highest-energy valence band states are composed of Ag 4d-orbital and O 2p-orbital contributions within the interlayer spacing of the structure. The lowest-energy conduction band states arise from the Nb/Ti d-orbital and O 2p-orbital contributions that are confined to the two-dimensional niobate/titanate sheets within the structures and along which the excited-electrons can preferentially migrate.
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