The electrocatalytic nitrogen reduction reaction (NRR) is proposed as an alternative to the Haber-Bosch process, but the development of efficient NRR electrocatalysts remains a challenging task. MoSe2 has superior conductivity compared to MoS2, making it promising in the NRR field. Unfortunately, the scarcity of active sites and competitive hydrogen evolution reaction (HER) hinder its broader applications. Here, Se-vacancy-rich MoSe2 is designed through Cr doping, allowing for targeted regulations of architectural and electronic structure by leveraging the dual effects of doping and VSe. Further mechanistic studies innovatively find that the Cr-induced multi-vacancy (18.75% concentration) exerts inverse contributions to NRR on 2H- and 1T-MoSe2, reflecting boosted and depressed effects, respectively. Consequently, suitable doping effectively facilitates NRR and eases the competition from HER, realizing excellent NH3 yield (51.53 ± 2.45 µg h-1 mg-1 cat) and Faradaic efficiency (63.37%) in MSC-1. This work paves the opportunity for MoSe2-based electrocatalysts toward boosted NRR.
Keywords: heteroatom doping; hydrogen evolution reaction; molybdenum diselenide; nitrogen reduction reaction; vacancy engineering.
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