Graphitic-N highly doped graphene-like carbon: A superior metal-free catalyst for efficient reduction of CO2
[Display omitted] •The N-species in NG-T can be fine-tuned by the pyrolysis conditions, facilitating differentiating functions among different N-species.•The C atoms next to the graphitic-N species serves as active sites for efficient CO2 conversion.•The optimized catalyst is capable of achieving a...
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Veröffentlicht in: | Applied catalysis. B, Environmental Environmental, 2021-12, Vol.298, p.120510, Article 120510 |
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Sprache: | eng |
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•The N-species in NG-T can be fine-tuned by the pyrolysis conditions, facilitating differentiating functions among different N-species.•The C atoms next to the graphitic-N species serves as active sites for efficient CO2 conversion.•The optimized catalyst is capable of achieving a selectivity of 95.0 % in converting CO2 into CO, comparable to the metal-based catalysts.
For metal-free nitrogen(N)-doped carbon catalysts, diverse N-bearing species embedded in the carbon framework are generally regarded as chemical promoters that can upgrade their catalytic performance for CO2 electroreduction reaction (CO2RR). However, it is still a controversy as to which N species plays a dominant role. Herein, a type of large surface area (371 m2/g), N-rich (11.0 wt%) graphene-like carbon electrocatalyst (NG-1000) is fabricated via facile pyrolysis from a precursor composite of dicyandiamide and phthalocyanine. The N-species in the NG-T (T = 700–1000 °C) can be fine-tuned, thus facilitating differentiating functions of the various N-species. Based on the comprehensive analysis of original Pc/CNTs and NG-T catalysts, we identified that the C atoms next to the graphitic-N species in NG-1000 serves as the main active species for CO2RR. In addition, such a non-metal based electrocatalyst is capable of achieving an excellent selectivity of 95.0 % at −0.72 V versus RHE to convert CO2 into CO, with a CO current density of 9.07 mA cm−2, comparable to the state-of-the-art metal-based electrocatalysts. |
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ISSN: | 0926-3373 1873-3883 |
DOI: | 10.1016/j.apcatb.2021.120510 |