Journal
APPLIED SURFACE SCIENCE
Volume 427, Issue -, Pages 1202-1216Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.apsusc.2017.08.053
Keywords
Silver chalcogen compounds; Electronic structure; Photocatalytic performance; Band gap; Free radical
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Funding
- National Natural Science Foundation of China [21476146, 21676168]
- Outstanding Young Scholar Fund of Sichuan University [2015SCU04B06]
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Four silver chalcogen compounds, Ag2O, Ag2S, Ag2Se and Ag2Te, can be utilized as visible-light-driven photocatalysts. In this research, the electronic structures of these compounds were analyzed by simulation and experiments to systematically reveal the relationship between photocatalytic performance and energetic structure. All four chalcogenides exhibited interesting photocatalytic activities under ultraviolet, visible and near-infrared light. However, their photocatalytic performances and stability significantly depended on the band gap width, and the valence band and conduct band position, which was determined by their composition. Increasing the X atomic number from O to Te resulted in the upward movement of the valence band top and the conduct band bottom, which resulted in narrower band gaps, a wider absorption spectrum, a weaker photo-oxidization capacity, a higher recombination probability of hole and electron pairs, lower quantum efficiency, and worse stability. Among them, Ag2O has the highest photocatalytic performance and stability due to its widest band gap and lowest position of VB and CB. The combined action of photogenerated holes and different radicals, depending on the different electronic structures, including anion ozone radical, hydroxide radical, and superoxide radical, was observed and understood. The results of experimental observations and simulations of the four silver chalcogen compounds suggested that a proper electronic structure is necessary to obtain a balance between photocatalytic performance and absorbable light region in the development of new photocatalysts. (C) 2017 Elsevier B.V. All rights reserved.
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