Abstract

Graphitic carbon nitrides (g-C3N4) have come into researchists’ horizons for their diversified merits, such as the especial graphite-phase 2D laminar framework, competitive price, innoxious, eligible bandgap (∼2.7 eV) and acceptable consistency. Whereas limited by the disadvantages of inferior specific surface area and fast recombination of photo-generated charge pairs, the pragmatic applicability of g-C3N4 turns out to be still lacking. In our work, g-C3N4 (GCN) and Eu-doped g-C3N4 (Eu/CN) with different Eu/g-C3N4 molar ratios (1%, 2%, 3%, 4%) were synthesized by an impregnating method and characterized through a series of measurements. Photocatalytic activities of Eu/CN catalysts manifest preeminent H2 generation capacity and stability excited by solar light. The highest H2 generation rate without any co-catalyst is 128.8 μmol g−1 h−1 over the 3% Eu/CN, achieving 117.1-fold as high as that of GCN (1.1 μmol g−1 h−1). Eu doping is proven to slightly widen the bandgap of the samples, resulting in the conduction band of samples more negative and the reduction reaction more effortlessly. Simultaneously, Eu doping changes the molecular structure of g-C3N4 and forms more nitrogen defects. Photo-excited electrons can be captured by the defective sites derived from the defect levels, and the recombination rate of photoinduced carriers will be significantly inhibited, accordingly facilitating the high-efficiency separation of photo-induced carriers and improving photocatalytic efficiency. This study provides an advantageous instruction for the implementation of rare earth metals application in improving the separation and transfer rate of photo-induced electrons (e−) and holes (h+) over g-C3N4.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call