4.5 Article

Electrochemical fabrication of ultrafine g-C3N4 quantum dots as a catalyst for the hydrogen evolution reaction

Journal

NEW CARBON MATERIALS
Volume 37, Issue 2, Pages 392-399

Publisher

ELSEVIER
DOI: 10.1016/S1872-5805(21)60045-8

Keywords

g-C3N4; Electrochemical exfoliation; Al3+ ions; QDs; HER

Funding

  1. Natural Science Foundation of China [91845109, 21872169, 22109171, 22172190]
  2. CAS Project for Young Scientists in Basic Research [YSBR-022]
  3. Young Cross Team Project of CAS [JCTD-2021-14]
  4. Jiangsu Planned Projects for Postdoctoral Researc Funds [2021K226B]

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Graphite-like carbon nitride (g-C3N4) is a promising metal-free material with high in-plane elemental nitrogen concentration and superior stability. This study presents a rapid method for synthesizing ultrafine g-C3N4 quantum dots (QDs) using electrochemical exfoliation with Al3+ ions as an intercalation agent. The obtained QDs exhibit small size and thickness, and show excellent hydrogen evolution reaction performance in an acidic electrolyte.
Because of its high concentration of in-plane elemental nitrogen, superior chemical/thermal stability, tunable electronic band structure and environmentally friendly nature, graphite-like carbon nitride (g-C3N4) is a new promising metal-free material that has drawn much attention in photo-/electric catalysis. Compared with the regulation of the band structure in photocatalysis, the deliberate synthesis of g-C3N4 electrocatalysts is mainly focused on the construction of catalytic sites and the modulation of the charge transfer kinetics. This work reports a rapid method for synthesizing ultrafine g-C3N4 quantum dots (QDs) by electrochemical exfoliation using Al3+ ions as an intercalation agent. Uniform g-C3N4 QDs with small lateral size and thickness were collected more easily due to the higher charge density and stronger electrostatic force of Al3+ ions in the lattice of the host material, compared to conventional univalent alkali cations. The QDs had an average lateral dimension and thickness of 3.5 nm and 1.0 nm, respectively, as determined by TEM and AFM measurements. The presence of a large number of C/N defects was verified by the UV-vis spectra. The ultrafine g-C(3)N(4)QDs had a superior hydrogen evolution reaction performance with an ultra-low onset-potential approaching 0 V, and a low overpotential of 208 mV at 10 mA cm(-2), as well as a remarkably low Tafel slope (52 mV.dec(-1)) in an acidic electrolyte.

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