4.7 Article

Theoretical Screening of Single Atoms Supported on Two-Dimensional Nb2CN2 for Nitrogen Fixation

期刊

ACS APPLIED NANO MATERIALS
卷 3, 期 11, 页码 11274-11281

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsanm.0c02380

关键词

N-functionalized MXenes; single-atom catalyst; NRR; selectivity; transition metals

资金

  1. Science and Technology Development Fund from Macau SAR [0102/2019/A2, 0035/2019/AGJ, 0154/2019/A3, 0081/2019/AMJ, 199/2017/A3, 0125/2018/A3]
  2. Multi-Year Research Grant from Research & Development Office at University of Macau [MYRG2017-00027-FST, MYRG2018-00003-IAPME, MYRG2017-00149-FST]

向作者/读者索取更多资源

Massively converting nitrogen gas to ammonia is a key process in modern agricultural and industrial fields. The conventional Haber-Bosch process for NH3 production has to be carried out under extreme conditions, leading to high energy consumption and huge emission of greenhouse gases. Electrochemical N-2 reduction is a promising way for NH3 production due to its sustainable process and feasibility in an ambient environment. In this work, we screen the transition metals (TM), including 26 elements, supported on two-dimensional (2D) Nb2CN2 (TM-Nb2CN2) for their applications in the electrochemical reduction of N-2 (NRR) based on first-principles calculations. We show that most SACs can bind with Nb2CN2 strongly through a TM-3N configuration. We find that Mn-Nb2CN2 is a promising candidate for the N-2 reduction reaction (NRR), with a low overpotential of 0.51 V through the distal mechanism. Importantly, TM-Nb2CN2 presents high selectivity to NRR by blocking the hydrogen adsorption and preventing the hydrogen evolution reaction. Moreover, the scaling relationship and Bader charge analysis provide an insightful understanding of the mechanism for NRR on single-atom catalysts (SACs) anchored on 2D MXenes. Our findings may guide the design of novel substrates for SACs with effectively improved performance.

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