摘要
The lack of active sites and the low availability of photoelectrons severely limit the photocatalytic reduction of nitrogen to ammonia in semiconductor materials. Here, we successfully designed a BiOBr/O v -TiO 2 -Cu heterojunction catalyst toward N 2 fixation into NH 3 . The optimized BiOBr/O v -TiO 2 -Cu heterojunction has a promising photocatalytic performance and stability with the highest NH 3 yield of 259.82 μmol·g −1 ·h −1 . The combination of detailed theoretical simulation calculations and comprehensive characterizations indicates the BiOBr/O v -TiO 2 -Cu heterojunction with oxygen vacancy (O v ) stabilized Cu nanoparticles (NPs) as active sites can effectively adsorb and activate N 2 molecules. The close contact between BiOBr and Ov-TiO 2 elevates the quick transmission of photogenerated electrons at the interface and the enrichment on Cu NPs. This work not only provides an efficient photocatalyst for the N 2 reduction, but also supplies theoretical support for identifying the active sites and charge transfer kinetics of the nitrogen reduction reaction.
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