Electrochemical fabrication of ultrafine g-C 3 N 4 quantum dots as a catalyst for the hydrogen evolution reaction
New Carbon Materials, ISSN: 1872-5805, Vol: 37, Issue: 2, Page: 392-399
2022
- 16Citations
- 12Captures
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Most Recent News
New Findings from University of Science and Technology China in the Area of Quantum Dots Reported (Electrochemical Fabrication of Ultrafine G-c3n4 Quantum Dots As a Catalyst for the Hydrogen Evolution Reaction)
2023 FEB 06 (NewsRx) -- By a News Reporter-Staff News Editor at Nanotech Daily -- Investigators publish new report on Nanotechnology - Quantum Dots. According
Article Description
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-C 3 N 4 ) 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-C 3 N 4 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-C 3 N 4 quantum dots (QDs) by electrochemical exfoliation using Al 3+ ions as an intercalation agent. Uniform g-C 3 N 4 QDs with small lateral size and thickness were collected more easily due to the higher charge density and stronger electrostatic force of Al 3+ 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.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S1872580521600458; http://dx.doi.org/10.1016/s1872-5805(21)60045-8; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85128302895&origin=inward; https://linkinghub.elsevier.com/retrieve/pii/S1872580521600458; http://dx.doi.org/10.1016/s1872-5805%2821%2960045-8; https://dx.doi.org/10.1016/s1872-5805%2821%2960045-8; http://sciencechina.cn/gw.jsp?action=cited_outline.jsp&type=1&id=7236848&internal_id=7236848&from=elsevier
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