Integrating Mo2Bx (x=1, 4) with CdS for efficient photocatalytic hydrogen production

Molybdenum based compounds, such as MoCx, MoSe2, MoS2 MoPx, MoOx and their derivatives, have been considered as the alternative catalysts for platinum (Pt) whether in electrocatalytic or photocatalytic hydrogen evolution reaction (HER). This means molybdenum based compounds have great application potential in solving the energy crisis and environmental pollution. Herein, for the first time, the unexplored Mo2Bx (x = 1 or 4) were investigated as the active components in a visible-light driven photocatalytic hydrogen production system. Experimental results demonstrate that they both exhibit excellent hydrogen evolution activities when combined with CdS or organic photosensitizers. Additionally, for the same kind of light-harvesting material, the photocatalytic HER activity of Mo B-2(4) is obviously better than that of Mo2B. This clearly indicates the photocatalytic activities of them are affected by the content of electron deficient atom boron (B) in Mo2Bx samples and exhibits a strong B dependence in photocatalytic HER. The reason for this B dependency is studied in detail by photo/electrochemical methods and optical characterizations in this work, where it is essentially caused by the difference in the electron transfer (ET) rates between light-harvesting material and Mo2Bx samples and just manifested as B dependency. Additionally, the relation between photocatalysis and electrocatalysis in HER is discussed.

Automated summary

Molybdenum based compounds, such as MoCx, MoSe2, MoS2 MoPx, MoOx and their derivatives, have been considered as alternative catalysts to platinum in hydrogen evolution reactions. Mo2Bx (x = 1 or 4) has been investigated for the first time as active components in a visible-light driven photocatalytic hydrogen production system, showing excellent hydrogen evolution activities. The electron deficient atom boron (B) content in Mo2Bx samples affects their photocatalytic activities, with Mo B-2(4) exhibiting better activity than Mo2B due to differences in electron transfer rates.