Photoelectrochemical decomposition of bio-related compounds at a nanoporous semiconductor film photoanode and their photocurrent-photovoltage characteristics

被引:26
作者
Kaneko, Masao [1 ]
Suzuki, Shinji [2 ]
Ueno, Hirohito [1 ,2 ]
Nemoto, Junichi [1 ]
Fujii, Yuki [2 ]
机构
[1] Inst Biophotochemon Co Ltd, Mito, Ibaraki 3108512, Japan
[2] Ibaraki Univ, Fac Sci, Mito, Ibaraki 3108512, Japan
基金
日本科学技术振兴机构;
关键词
TiO(2) mesoporous film photoanode; Amino acids; Photoelectrochemical decomposition; Photocurrent-photovoltage characteristics; Quantum efficiency; TIO2; BIOMASS; CELL; PHOTOOXIDATION; EFFICIENCY; NITROGEN; WASTES;
D O I
10.1016/j.electacta.2010.01.046
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Photoelectrochemical decomposition of bio-related compounds such as amino acids was investigated with a biophotochemical cell comprising a mesoporous TiO(2) thin film photoanode and an O(2)-reducing cathode. It was concluded that a kind of Schottky junction formed at the surface of the TiO(2) (called as liquid junction) induced the photodecomposition followed by generation of photocurrent/photovoltage. Complete photodecomposition was investigated by the CO(2) formation yield. The photocurrent-photovoltage (J-V) characteristics of amino acids and other typical bio-related compounds were investigated, and the short circuit photocurrent (J(sc)), open circuit photovoltage (V(oc)), and Fill factor (ff) were exhibited. Effect of pH on the photodecomposition of phenylalanine and cysteine were studied; for cysteine alkaline conditions gave a high efficiency, which was interpreted by the high electron-donating ability of the dissociated -S(-) group. The incident light-to-current conversion efficiency (IPCE) of cysteine was 25% at 350 nm. It was for the first time shown that organic acids gave high internal quantum efficiency (eta ') over 8 (=800%) in the photodecomposition: for oxalic acid it was 9.3 (=930%) and for butyric acid 8.2. The alternating current impedance spectroscopy of glycine showed that the cell performance is determined by the chemical reactions at TiO(2) or Pt electrodes. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3068 / 3074
页数:7
相关论文
共 19 条
[1]   Photooxidation Products of Ethanol During Photoelectrochemical Operation Using a Nanocrystalline Titania Anode and a Two Compartment Chemically Biased Cell [J].
Antoniadou, Maria ;
Kondarides, Dimitris I. ;
Lianos, Panagiotis .
CATALYSIS LETTERS, 2009, 129 (3-4) :344-349
[2]   Photoelectrochemical oxidation of organic substances over nanocrystalline titania: Optimization of the photoelectrochemical cell [J].
Antoniadou, Maria ;
Lianos, Panagiotis .
CATALYSIS TODAY, 2009, 144 (1-2) :166-171
[3]   ELECTROCHEMICAL PHOTOLYSIS OF WATER AT A SEMICONDUCTOR ELECTRODE [J].
FUJISHIMA, A ;
HONDA, K .
NATURE, 1972, 238 (5358) :37-+
[4]  
Fujishima A., 1999, TIO2 PHOTOCATALYSIS
[5]   ELECTROCHEMISTRY OF ZNO MONOCRYSTAL SPECTRAL SENSITIVITY [J].
GERISCHER, H ;
TRIBUTSCH, H .
BERICHTE DER BUNSEN-GESELLSCHAFT FUR PHYSIKALISCHE CHEMIE, 1968, 72 (03) :437-+
[6]  
Gerischer H., 1960, SURFACE CHEM METALS, P177
[7]   LIGHT-INDUCED REDOX REACTIONS IN NANOCRYSTALLINE SYSTEMS [J].
HAGFELDT, A ;
GRATZEL, M .
CHEMICAL REVIEWS, 1995, 95 (01) :49-68
[8]   Photoelectrochemical reaction of biomass and bio-related compounds with nanoporous TiO2 film photoanode and O2-reducing cathode [J].
Kaneko, M ;
Nemoto, J ;
Ueno, H ;
Gokan, N ;
Ohnuki, K ;
Horikawa, M ;
Saito, R ;
Shibata, T .
ELECTROCHEMISTRY COMMUNICATIONS, 2006, 8 (02) :336-340
[9]   Artificial photochemical nitrogen cycle to produce nitrogen and hydrogen from ammonia by platinized TiO2 and its application to a photofuel cell [J].
Kaneko, M ;
Gokan, N ;
Katakura, N ;
Takei, Y ;
Hoshino, M .
CHEMICAL COMMUNICATIONS, 2005, (12) :1625-1627
[10]  
KANEKO M, 2009, J NEMOTO CATAL LETT, V131, P184