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Wang, Ran; He, Chaozheng; Chen, Weixing; Zhao, Chenxu; Huo, Jinrong
Chinese chemical letters, 12/2021, Letnik: 32, Številka: 12Journal Article
The photocatalytic nitrogen reduction reaction (NRR) has mild reaction conditions and only requires sunlight energy as a driving force to replace the traditional ammonia synthesis method. We herein investigate the catalytic activity and selectivity on Penta-B2C for NRR by using density functional theory calculations. Penta-B2C is a semiconductor with an indirect bandgap (2.328 eV) and is kinetically stable based on molecular dynamic simulations. The optical absorption spectrum of Penta-B2C is achieved in the ultraviolet and visible range. Effective light absorption is more conducive to generate photo-excited electrons and improving photocatalytic performances. Rich B atoms as activation sites in Penta-B2C facilitate capturing N2. The activated N2 molecule prefers the side-on adsorption configuration on Penta-B2C, which facilitates the subsequent reduction reaction. Among considered NRR mechanisms on Penta-B2C, the best pathway prefers the enzymatic mechanism, only required a low onset potential of 0.23 V. The hydrogen evolution reaction is inhibited when the hydrogen adsorption concentration is increased or N2 molecules first occupy the adsorption sites. Our results indicate Penta-B2C is a highly reactive and selective photocatalyst for NRR. Our work provides theoretical insights into the experiments and has guiding significance to synthesize efficient NRR photocatalysts. Rich B atoms as activation sites in Penta-B2C facilitate capturing N2. In particular, the activated side-on N2 is further reduced to NH3 through an enzymatic mechanism with an onset potential of 0.23 V. Display omitted
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