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Details

Autor(en) / Beteiligte
Titel
Charge Transfer Engineering via Multiple Heteroatom Doping in Dual Carbon-Coupled Cobalt Phosphides for Highly Efficient Overall Water Splitting
Ist Teil von
  • Applied catalysis. B, Environmental, 2020-07, Vol.268, p.118404, Article 118404
Ort / Verlag
Amsterdam: Elsevier B.V
Erscheinungsjahr
2020
Quelle
Access via ScienceDirect (Elsevier)
Beschreibungen/Notizen
  • The charge transfer ability and catalytic activity of CoP@C@rGO can be tuned by incorporating multiple heteroatoms. The triple heteroatoms-doped CoP@C@rGO exhibites an exceptional bifunctional catalytic activity for overall water splitting. [Display omitted] •Dual carbon coupled-CoP with triple heteroatoms doping catalyst was developed•The charge transfer ability could be engineered by multiple heteroatoms doping•The electrocatalyst exhibits a superior electrocatalytic activity•The catalyst towards overall water splliting can afford 10 mA cm–2 at an ultralow voltage of 1.50 V The exploration of non-noble-metal bifunctional electrocatalysts with high activity and stability for overall water splitting is crucial, but remains challenging for hydrogen fuel production. Herein, tuning of the charge transfer ability and catalytic performance of zeolitic imidazolate framework-derived porous carbon/reduced graphene oxide-coupled CoP composites (CoP@C@rGO) was achieved by incorporating multiple heteroatoms. The combined experimental investigation and density functional theory calculations revealed that the electronic interaction within the composites caused by B, N, and S tri-doped heteroatoms effectively induced interfacial charge transfer, which improved the active site accessibility and reduced the energy barriers of the intermediates. From the synergetic effects of the components, the overall water splitting electrolyzer assembled using the newly prepared B,N,S-CoP@C@rGO catalyst required only 1.50 V to drive a current density of 10 mA cm–2, which is superior to the commercial Pt/C and IrO2/C couple (1.56 V).
Sprache
Englisch
Identifikatoren
ISSN: 0926-3373
eISSN: 1873-3883
DOI: 10.1016/j.apcatb.2019.118404
Titel-ID: cdi_proquest_journals_2435540831

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