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

被引:506
作者
Hoang, Son [1 ]
Guo, Siwei [1 ]
Hahn, Nathan T. [1 ]
Bard, Allen J. [2 ]
Mullins, C. Buddie [1 ,2 ]
机构
[1] Univ Texas Austin, Ctr Nano & Mol Sci, Texas Mat Inst, Ctr Electrochem,Dept Chem Engn, Austin, TX 78712 USA
[2] Univ Texas Austin, Ctr Nano & Mol Sci, Texas Mat Inst, Ctr Electrochem,Dept Chem & Biochem, Austin, TX 78712 USA
关键词
Water photo-oxidation; N-modified TiO2; water oxidation catalyst; hydrothermal synthesis; single crystalline nanowire; photocatalysis; DOPED TITANIUM-DIOXIDE; PHOTOCATALYTIC ACTIVITY; SINGLE-CRYSTALS; THIN-FILMS; NANOMATERIALS; ELECTRODES; DEPENDENCE; ORIGIN; ARRAYS;
D O I
10.1021/nl2028188
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:26 / 32
页数:7
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