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In this work, we mainly investigate the influence of structure water on crystal structure, electronic structure, band structure, and charge separation of WO3·2H2O. It is found, for the first time, that although water is a weak electron donor, a ligand-to-metal charge transfer (LMCT) from H2O to W occurs. The structure water contributes to the conduction band (CB) of WO3·2H2O, and the band gap of WO3·2H2O is obviously narrowed, thus increasing the light absorption obviously. Moreover, the results of EIS, photocurrent spectra, and PL show that structure water in WO3·2H2O also improves the charge separation and transfer efficiency of the catalyst. This is the first investigation on the LMCT transfer from structure water (a weak electron donor) to tungsten, which obviously improves light absorption and charge separation. Under visible light irradiation (λ ≥ 420 nm), WO3·2H2O nanosheets have a photocatalytic activity 2.3 times higher than that of WO3 for the degradation of methylene blue (MB). The kind number of photochemical materials can be increased greatly, because structure water-contained compounds widely exist in nature.

In this work, we mainly investigate the influence of structure water on crystal structure, electronic structure, band structure, and charge separation of WO

From the viewpoint of engineering application, it is highly desirable to develop a low-cost, fossil energy–saving degradation technology. In this work, hydrated molybdenum oxide (MoO3·0.55H2O) is prepared by a simple chemical method. It is interesting that under indoor natural ambient conditions, 79% of methylene blue is degraded by hydrated molybdenum oxide after 150 min, but under the same conditions, anhydrous molybdenum oxide does not have any degradation activity. It is found that the outstanding ambient activity of hydrated molybdenum oxide is mainly attributed to the photothermal synergistic effect caused by structure water. On one hand, the coordination of structure water with molybdenum brings about the Jahn–Teller distortion of MoO6 octahedron, giving rise to Lewis acid sites that promote the adsorption and activation of oxygen. O2–temperature-programmed desorption and H2–temperature-programmed reduction profiles show that compared with MoO3, MoO3·0.55H2O has a higher oxygen adsorption ability and a higher oxidation ability. Jahn–Teller effect is mainly responsible for the thermocatalytic activity. On the other hand, the ligand-to-metal charge transfer (LMCT) transfer from structure water to molybdenum obviously increases the light absorption, thus LMCT is mainly responsible for the photocatalytic activity The most important is that compared with conventional photocatalysis, no artificial light source equipment is required; compared with thermocatalysis, no extra heating equipment is needed. Thus, this mild degradation process is low-cost, energy-saving and space-saving, which is very promising for indoor or limited space cleaning.