Ti-doped α-Fe2O3 nanorods with controllable morphology by carbon layer coating for enhanced photoelectrochemical water oxidation

被引:21
|
作者
Yan, Dejian [1 ]
Liu, Jikai [1 ,2 ]
Shang, Zhichao [1 ]
Luo, He'an [1 ,2 ]
机构
[1] Xiangtan Univ, Sch Chem Engn, Xiangtan 411105, Peoples R China
[2] Xiangtan Univ, Natl & Local United Engn Res Ctr Chem Proc Simula, Xiangtan 411105, Peoples R China
基金
中国国家自然科学基金;
关键词
HETEROJUNCTION ARRAY; MESOPOROUS CARBON; ION BATTERIES; THIN-FILMS; HEMATITE; EFFICIENT; PHOTOANODES; ELECTRODES; CONVERSION; NANOFIBERS;
D O I
10.1039/c7dt00850c
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Ti-doped alpha-Fe2O3 nanorods (NRs) with carbon layer coating were fabricated for photoelectrochemical (PEC) water oxidation. The alpha-Fe2O3 NRs were grown on the surface of a Ti foil substrate by hydrothermal synthesis. Ti4+ was diffused from the Ti substrate and doped into the alpha-Fe2O3 NRs by sintering at 800 degrees C. The presence of Fe2+ in the alpha-Fe2O3 lattice was achieved by annealing the NRs in a lack of oxygen atmosphere, e.g. in argon. The co-existence of Ti4+ and Fe2+ results in significant enhancement of the PEC performance compared with the hematite NRs obtained by annealing in air, showing the absence of Fe2+. The carbon layer coating was conducted by the carbonization of glucose. Impressively, the coated carbon layer can not only facilitate the charge transfer of the photogenerated carriers but also effectively restrain the structural aggregation of the NRs upon high temperature sintering. The carbon layer coated NRs exhibited 1.2 times higher photocurrent density than the uncoated NRs due to the reduced charge recombination and well-distinct NR structures.
引用
收藏
页码:10558 / 10563
页数:6
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