4.7 Article

FeS2/MoS2@RGO hybrid materials derived from polyoxomolybdate-based metal-organic frameworks as high-performance electrocatalyst for ammonia synthesis under ambient conditions

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 445, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.136797

Keywords

Polyoxometalates; Metal -organic frameworks; Bimetallic sulfide; Electrocatalysts; Nitrogen reduction reaction

Funding

  1. Major Research Plan National Natural Science Foundation of China [92061102]
  2. National Natural Science Foundation of China [22171059]
  3. Outstanding Youth Project of Natural Science Foundation in Heilongjiang Province [YQ2020B005]
  4. University Nursing Program for Young Scholars with Creative Talents in Heilongjiang Province [UNPYSCT-2018213]
  5. ERDF A way of making Europe
  6. Opening Foundation of Key Laboratory of Functional Inorganic Material Chemistry (Heilongjiang University, Ministry of Education)
  7. Generalidad Valenciana [Prometeo/2019/076]
  8. MCIN [CTQ2017-87201-P, MCIN/AEI/10.13039/501100011033]

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In this work, a one-pot hydrothermal synthesis process was used to successfully synthesize nanostructured bimetallic sulfides with the assistance of an iron-based metal-organic framework and a molybdenum-based polyoxometalate. The synthesized FeS2/MoS2@RGO catalyst showed excellent electrocatalytic activity and stability towards nitrogen reduction reaction in both acidic and alkaline solutions, with high Faradaic efficiency and NH3 yield rate.
The electrocatalytic nitrogen reduction reaction (NRR) provides a promising way for storage and sustainable utilization of ammonia. In order to reduce the cost of ammonia synthesis and promote large-scale production, it is very important to develop stable and highly active electrocatalysts. In this work, we demonstrate an iron-based metal-organic framework (MIL-100) and molybdenum-based polyoxometalate (PMo12) host-guest-assisted strategy for synthesizing nanostructured bimetallic sulfides through a one-pot hydrothermal synthesis process. FeS2/MoS2 particles are evenly distributed on reduced graphene oxide (RGO) with high conductivity, forming a well-defined nanoflower structure. Benefiting from the synergistic effect of FeS2, MoS2 (with inherent rich catalytically active sites and uniform nanoflower structure) and RGO, the as-synthesized FeS2/MoS2@RGO achieves electrocatalytic activity and stability towards NRR in both basic and acidic solutions. The electrochemical results show a high Faradaic efficiency (FE) of 38.6 % and NH3 yield rate of 41.1 mu g h-1 mgcat -1 at -0.2 V with respect to a reversible hydrogen electrode (RHE) in acidic potassium sulfate, and FE of 9.62 % and NH3 yield rate of 10.35 mu g h-1 mgcat-1 at -0.4 V vs. RHE in alkaline potassium hydroxide solution at room temperature. Density functional theory (DFT) calculation indicates that NRR on FeS2/MoS2 has optimized nitrogen binding and ammonia release which promotes the fast kinetics process through the distal mechanism, and the protonation of N2 to form *N2H species is the rate-determining step (RDS) with the maximum Delta G values (+0.43 eV). This work develop a general and promising method for the design of efficient and low cost pH-universal NRR electrocatalysts.

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