N-doped graphitic carbon encapsulating cobalt nanoparticles derived from novel metal–organic frameworks for electrocatalytic oxygen evolution reaction
Nitrogen-doped carbon catalysts with hierarchical porous structure are promising oxygen evolution reaction (OER) catalysts due to the faster mass transfer and better charge carrying ability. Herein, an exquisite high nitrogen-containing ligand was designed and readily synthesized from the low-cost b...
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Veröffentlicht in: | Chinese chemical letters 2023-08, Vol.34 (8), p.108056-477, Article 108056 |
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Sprache: | eng |
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Zusammenfassung: | Nitrogen-doped carbon catalysts with hierarchical porous structure are promising oxygen evolution reaction (OER) catalysts due to the faster mass transfer and better charge carrying ability. Herein, an exquisite high nitrogen-containing ligand was designed and readily synthesized from the low-cost biomolecule adenine. Accordingly, three new MOFs (TJU-103, TJU-104 and TJU-105) were prepared using the Co(II) or Mn(II) ions as metal nodes. Through rationally controlling pyrolysis condition, in virtue of the high nitrogen content in well-defined periodic structure of the pristine MOFs, TJU-104–900 among the derived MOFs with hierarchical porous structure, i.e., N-doped graphitic carbon encapsulating homogeneously distributed cobalt nanoparticles, could be conveniently obtained. Thanks to the synergistic effect of the hierarchical structure and well dispersed active components (i.e., C=O, Co‒Nx, graphitic C and N, pyridinic N), it could exhibit an overpotential of 280 mV@10 mA/cm2 on carbon cloth for OER activity. This work provides the inspiration for fabrication of nitrogen-doped carbon/metal electrocatalysts from cost-effective and abundant biomolecules, which is promising for practical OER application.
One-step pyrolysis of novel MOFs with high N content rigid ligand allows for making porous N-doped graphitic carbons encapsulating metal nanoparticles as high-performance OER catalysts. [Display omitted] |
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ISSN: | 1001-8417 1878-5964 |
DOI: | 10.1016/j.cclet.2022.108056 |