4.7 Article

Fabrication and photoelectrochemical properties of silicon nanowires/g-C3N4 core/shell arrays

Journal

APPLIED SURFACE SCIENCE
Volume 396, Issue -, Pages 609-615

Publisher

ELSEVIER
DOI: 10.1016/j.apsusc.2016.10.203

Keywords

PEC; Silicon nanowire/g-C3N4 core/shell arrays; Water splitting

Funding

  1. National Natural Science Foundation of China [21406052, 51602111]
  2. National Natural Science Foundation of Guangdong Province [2014A030308013, 2014B090915005, 2015A030310196, 2015B050501010, 14KJ13]
  3. Pearl River S&T Nova Program of Guangzhou [201506040045]
  4. Guangdong Innovative Research Team Program [2011D039]
  5. PCSIRT Project [IRT13064]

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A photoelectrochemical (PEC) cell made of metal-free carbon nitride (g-C3N4) @siliconnanowire(Si NW) arrays (denoted as Si NWs/g-C3N4) is presented in this work. The as-prepared photoelectrodes with different mass contents of g-C3N4 have been synthesized via a metal-catalyzed electroless etching (MCEE), liquid atomic layer deposition (LALD) and annealing methods. The amount of g-C3N4 on the Si NW arrays can be controlled by tuning the concentration of the cyanamide solution used in the LALD procedure. The dense and vertically aligned Si NWs/g-C3N4 core/shell nanostructures were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD). In comparison with FTO/g-C3N4 and Si NW samples, the Si NWs/g-C3N4 samples showed significantly enhanced photocurrents over the entire potential sweep range. Electrochemical impedance spectroscopy (EIS) was conducted to investigate the properties of the charge transfer process, and the results indicated that the enhanced PEC performance may be due to the increased photo-generated interfacial charge transfer between the Si NWs and g-C3N4. The photocurrent density reached 45 mu A/cm(2) under 100 mW/cm(2) (AM 1.5 G) illumination at 0 V (vs. Pt) in neutral Na2SO4 solution (pH similar to 7.62). Finally, a systematical PEC mechanism of the Si NWs/g-C3N4 was proposed. (C) 2016 Published by Elsevier B.V.

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