Photoactivity of Transparent Nanocrystalline Fe2O3 Electrodes Prepared via Anodic Electrodeposition

被引:143
作者
Spray, Ryan L. [1 ]
Choi, Kyoung-Shin [1 ]
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
关键词
ELECTROCHEMICAL DEPOSITION ROUTE; ALPHA-FE2O3; THIN-FILMS; IRON-OXIDE FILMS; FERRIC-OXIDE; PHOTOELECTROCHEMICAL PROPERTIES; WATER; OXIDATION; PHOTOANODES;
D O I
10.1021/cm803099k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Highly transparent nanocrystalline alpha-Fe2O3 films were prepared via anodic electrodeposition using a slightly acidic aqueous medium (pH 4.1). The deposition mechanism involved oxidation of Fe2+ ions to Fe3+ ions followed by precipitation of Fe3+ ions as amorphous gamma-FeOOH films. The as-deposited films were then converted to transparent nanocrystalline alpha-Fe2O3 films by annealing at 520 degrees C in air. The as-deposited and annealed films were characterized by Raman and UV-vis spectroscopy, X-ray diffraction, and scanning electron microscopy. The photoactivity of the as-deposited and annealed films was studied by measuring short-circuit photocurrents in a 60:40 solution of propylene carbonate:acetonitrile containing 0.5 M tetrabutylammonium iodide and 0.04 M iodine. Both Films show n-type behavior generating anodic photocurrent. alpha-Fe2O3 films with various thicknesses were prepared to study the effect of film thickness on photon absorption and photocurrent. The short-circuit photocurrent of alpha-Fe2O3 films increased gradually as the film thickness increased to 400-500 nm because of the corresponding increase in photon absorption and surface area of the films, However, when the film thickness exceeded 400-500 nm, aggregation of Fe2O3 particles at the film/substrate interface became severe. This increased recombination losses near the collector electrode, and with no significant gain in photon absorption, led to ail overall decrease in photocurrent. alpha-Fe2O3 Films were also prepared by annealing FeOOH films produced via anodic deposition in a neutral medium (pH 7.5). The film prepared from the neutral medium was two times thicker and possessed a surface roughness factor two times higher than the film prepared from the acidic medium when the two films contained the same amount of alpha-Fe2O3. Comparing photocurrent of these films allowed for better understanding the effect of electrode structures (i.e., surface area, film thickness) on photocurrent generation in alpha-Fe2O3 electrodes with poor charge transport properties.
引用
收藏
页码:3701 / 3709
页数:9
相关论文
共 44 条
[1]   Metal oxide photoanodes for solar hydrogen production [J].
Alexander, Bruce D. ;
Kulesza, Pawel J. ;
Rutkowska, Iwona ;
Solarska, Renata ;
Augustynski, Jan .
JOURNAL OF MATERIALS CHEMISTRY, 2008, 18 (20) :2298-2303
[2]   Photoelectrochemistry of tin-doped iron oxide electrodes [J].
Aroutiounian, V. M. ;
Arakelyan, V. M. ;
Shahnazaryan, G. E. ;
Hovhannisyan, H. R. ;
Wang, Heli ;
Turner, John A. .
SOLAR ENERGY, 2007, 81 (11) :1369-1376
[3]   Investigation of ceramic Fe2O3⟨Ta⟩ photoelectrodes for solar energy photoelectrochemical converters [J].
Aroutiounian, VM ;
Arakelyan, VM ;
Shahnazaryan, GE ;
Stepanyan, GM ;
Turner, JA ;
Khaselev, O .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2002, 27 (01) :33-38
[4]   1. Molecular mechanism of surface recognition. Azo dyes degradation on Fe, Ti, and Al oxides through metal sulfonate complexes [J].
Bandara, J ;
Mielczarski, JA ;
Kiwi, J .
LANGMUIR, 1999, 15 (22) :7670-7679
[5]   Photoelectrochemical studies of oriented nanorod thin films of hematite [J].
Beermann, N ;
Vayssieres, L ;
Lindquist, SE ;
Hagfeldt, A .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2000, 147 (07) :2456-2461
[6]  
BJORKSTEN U, 1994, CHEM MATER, V6, P858
[7]  
Cornell R. M, 2003, IRON OXIDES
[8]   ELECTROCHEMISTRY AND PHOTOELECTROCHEMISTRY OF IRON(III) OXIDE [J].
DAREEDWARDS, MP ;
GOODENOUGH, JB ;
HAMNETT, A ;
TREVELLICK, PR .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1983, 79 :2027-2041
[9]  
deFaria DLA, 1997, J RAMAN SPECTROSC, V28, P873, DOI 10.1002/(SICI)1097-4555(199711)28:11<873::AID-JRS177>3.0.CO
[10]  
2-B