4.8 Article

Visible Light Driven Photoelectrochemical Water Oxidation on Nitrogen-Modified TiO2 Nanowires

Journal

NANO LETTERS
Volume 12, Issue 1, Pages 26-32

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/nl2028188

Keywords

Water photo-oxidation; N-modified TiO2; water oxidation catalyst; hydrothermal synthesis; single crystalline nanowire; photocatalysis

Funding

  1. Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences of the U.S. Department of Energy [DE-FG02-09ER16119]
  2. Welch Foundation [F-1436, F-0021]

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We report hydrothermal synthesis of single crystalline TiO2 nanowire arrays with unprecedented small feature sizes of similar to 5 nm and lengths up to 4.4 mu m on fluorine-doped tin oxide substrates. A substantial amount of nitrogen (up to 1.08 atomic %) can be incorporated into the TiO2 lattice via nitridation in NH3 flow at a relatively low temperature (500 degrees C) because of the small cross-section of the nanowires. The low-energy threshold of the incident photon to current efficiency (IPCE) spectra of N-modified TiO2 samples is at similar to 520 nm, corresponding to 2.4 eV. We also report a simple cobalt treatment for improving the photoelectrochemical (PEC) performance of our N-modified TiO2 nanowire arrays. With the cobalt treatment, the IPCE of N-modified TiO2 samples in the ultraviolet region is restored to equal or higher values than those of the unmodified TiO2 samples, and it remains as high as similar to 18% at 450 nm. We propose that the cobalt treatment enhances PEC performance via two mechanisms: passivating surface states on the N-modified TiO2 surface and acting as a water oxidation cocatalyst.

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