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Autor(en) / Beteiligte
Titel
Two-dimensional graphdiyne analogue containing Mo-coordinated porphyrin covalent organic framework as a high-performance electrocatalyst for nitrogen fixation
Ist Teil von
  • Applied surface science, 2022-04, Vol.580, p.152359, Article 152359
Ort / Verlag
Elsevier B.V
Erscheinungsjahr
2022
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Synopsis: Two-dimensional Mo-PDY exhibits excellent electrocatalytic activity for N2 reduction to NH3 with an extremely low overpotential (0.14 V), effectively suppressing competing hydrogen evolution reaction. [Display omitted] •The proposed TM-PDYs are constructed by butadiyne linkages between TM-coordinated phenylporphyrin rings.•The Mo-PDY possesses outstanding electrocatalytic activity to reduce N2 into NH3.•The NRR proceeds with an ultralow overpotential (0.14 V) by distal mechanism in principle.•The origin of the excellent NRR reactivity of Mo-PDY can be well interpreted by the distribution of spin density, Bader charge analyses and bond length variation. Graphdiyne (GDY), as a burgeoning two-dimensional (2D) material, is regarded as an excellent carbon support owing to its unique polyyne structure, but lack of active sites. Meanwhile, metalloporphyrins can anchor various metals as eminent catalytic center and have been extensively applied in various electrochemical reactions, including N2 reduction reaction (NRR). Integrating metalloporphyrins connected by polyynes as GDY analogues may create facile and charming heterogeneous electrochemical catalysts by merging their complementary advantages and broad prospects. Herein, the electrocatalytic behaviors of a sequence of 2D metalloporphyrin-based GDY analogues connected by butadiyne (TM-PDYs, TM = Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Ru, Rh, Pd, Ag, and W, respectively) toward NRR have been investigated by employing first-principles calculations. The computations demonstrate that 2D Mo-PDY owns superior electrocatalytic property for N2 fixation with an ultralow overpotential of 0.14 V via the preferred distal pathway among the 19 candidates, together with the capability of inhibiting the competing hydrogen evolution reaction (HER). This work not only puts forward an innovative idea based on multi-active components to realize attainable functional 2D lattices for the design of high-performance catalysts, but also promotes more experimental researches in this field to achieve sustainable NH3 production.
Sprache
Englisch
Identifikatoren
ISSN: 0169-4332
eISSN: 1873-5584
DOI: 10.1016/j.apsusc.2021.152359
Titel-ID: cdi_crossref_primary_10_1016_j_apsusc_2021_152359

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