Codoping titanium dioxide nanowires with tungsten and carbon for enhanced photoelectrochemical performance

被引:267
作者
Cho, In Sun [1 ]
Lee, Chi Hwan [1 ]
Feng, Yunzhe [2 ]
Logar, Manca [2 ]
Rao, Pratap M. [1 ]
Cai, Lili [1 ]
Kim, Dong Rip [3 ]
Sinclair, Robert [2 ]
Zheng, Xiaolin [1 ]
机构
[1] Stanford Univ, Dept Mech Engn, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA
[3] Hanyang Univ, Dept Mech Engn, Seoul 133791, South Korea
来源
NATURE COMMUNICATIONS | 2013年 / 4卷
基金
新加坡国家研究基金会;
关键词
DOPED TIO2; WATER; HYDROGEN; PHOTOCATALYSIS; DEGRADATION; EFFICIENT; NANORODS;
D O I
10.1038/ncomms2729
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Recent density-functional theory calculations suggest that codoping TiO2 with donor-acceptor pairs is more effective than monodoping for improving photoelectrochemical water-splitting performance because codoping can reduce charge recombination, improve material quality, enhance light absorption and increase solubility limits of dopants. Here we report a novel ex-situ method to codope TiO2 with tungsten and carbon (W, C) by sequentially annealing W-precursor-coated TiO2 nanowires in flame and carbon monoxide gas. The unique advantages of flame annealing are that the high temperature (>1,000 degrees C) and fast heating rate of flame enable rapid diffusion of W into TiO2 without damaging the nanowire morphology and crystallinity. This is the first experimental demonstration that codoped TiO2:(W, C) nanowires outperform monodoped TiO2:W and TiO2:C and double the saturation photocurrent of undoped TiO2 for photoelectrochemical water splitting. Such significant performance enhancement originates from a greatly improved electrical conductivity and activity for oxygen-evolution reaction due to the synergistic effects of codoping.
引用
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页数:8
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