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

塔菲尔方程 过电位 材料科学 电化学 催化作用 量子点 电解质 剥脱关节 石墨氮化碳 分解水 化学工程 纳米技术 石墨烯 光催化 物理化学 电极 化学 有机化学 工程类
作者
Nana Yang,Zhi‐Gang Chen,Zhigang Zhao,Yi Cui
出处
期刊:New Carbon Materials [Elsevier BV]
卷期号:37 (2): 392-399 被引量:16
标识
DOI:10.1016/s1872-5805(21)60045-8
摘要

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.
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