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Details

Autor(en) / Beteiligte
Titel
Boosting electrochemical conversion of CO2 to ethanol through the confinement of pyridinic N-B layer on copper nanoparticles
Ist Teil von
  • Applied catalysis. B, Environmental, 2024-10, Vol.355, p.124168, Article 124168
Ort / Verlag
Elsevier B.V
Erscheinungsjahr
2024
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Developing efficient electrocatalysts for CO2 reduction has gained significant attention in the field of sustainable energy, especially the Cu-based catalysts for CO2 conversion to valuable alcohols. In this study, we developed Cu nanoparticles supported on pyridinic N-B doped graphene nanoribbons/amorphous carbon (Cu/BNC-1) as an electrocatalyst for CO2 reduction, exhibiting substantially improved ethanol (EtOH) conversion rate in terms of activity, selectivity, and stability. The Cu/BNC-1 achieved a remarkable 58.64 % Faradaic efficiency (FE) for producing EtOH at −1.0 V vs. RHE with a current density of 20.4 mA cm−2 in 0.5 M KHCO3 electrolyte. In-situ Raman, FT-IR, and density functional theory (DFT) calculations demonstrated that the high C2+ product selectivity of Cu/BNC-1 attributed to the pyridinic N-B modulation, lowering the CO dimerization barrier. Moreover, the synergistic confinement effect of Cu and BNC can stabilize the C-O bond of the *HOCCH intermediate, thereby increasing the yield of EtOH. [Display omitted] •Cu nanoparticles with B, N co-doped graphene nanoribbons/amorphous carbon was fabricated.•The catalyst showed stable 58 % FE under 20.4 mAcm−2 during 24 h testing in CO2RR to ethanol.•The overall catalytic performance of Cu/BNC-1 was superior to other Cu-based catalysts.•This research highlighted the synergistic effect of Cu and BNC materials.•Pyridinic N-B modulation in Cu/BNC-1 reduced the CO dimerization barrier.
Sprache
Englisch
Identifikatoren
ISSN: 0926-3373
eISSN: 1873-3883
DOI: 10.1016/j.apcatb.2024.124168
Titel-ID: cdi_elsevier_sciencedirect_doi_10_1016_j_apcatb_2024_124168

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