Abstract
Enriched macro/mesoporous graphitic-C3N4 (g-C3N4) micro-rods (CNRs) are prepared by direct calcination of reflux treated ethylene diphosphonic acid-melamine complex fiber network. The optimized phosphorous doped CNRs (P-CNRs) exhibit a high hydrogen-evolution rate of 4960 μmol h−1 g−1 (5.5 times that of pristine g-C3N4) with a remarkable recycling stability. The significantly enhanced performance is found to be attributed to the intentionally designed morphology and electronic properties of P-CNRs. This distinctive hierarchical architecture of CNRs enhances the light scattering, and provides a high specific surface area and thus more catalytically active sites. The P doping of g-C3N4 greatly increases the visible light absorption, narrows the band gap. It also results in a boost in the density state of the conduction band as revealed by the electron paramagnetic resonance (EPR) spectra. The strong visible light emission quenching, observed from the photoluminescence of P-CNRs and photocurrent measurements, implies an enhanced charge transfer/separation process. This work presents a very simple and direct method of designing and developing high-performance visible light driven catalysts for hydrogen production.
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