Comparative Study of Tungsten Monocarbide and Platinum as Counter Electrodes in Polysulfide-Based Photoelectrochemical Solar Cells

被引:28
作者
Esposito, Daniel V. [1 ,2 ,3 ]
Dobson, Kevin D. [3 ]
McCandless, Brian E. [3 ]
Birkmire, Robert W. [3 ]
Chen, Jingguang G. [1 ,2 ]
机构
[1] Univ Delaware, Dept Chem Engn, Newark, DE 19716 USA
[2] Univ Delaware, Ctr Catalyt Sci & Technol, Newark, DE 19716 USA
[3] Univ Delaware, Inst Energy Convers, Newark, DE 19716 USA
关键词
cadmium compounds; catalysts; electrochemical electrodes; electrochemistry; electrolytes; II-VI semiconductors; photoelectrochemical cells; platinum; semiconductor thin films; solar cells; tungsten compounds; voltammetry (chemical analysis); wide band gap semiconductors; X-ray photoelectron spectra; ENERGY-CONVERSION; SURFACE SCIENCE; HYDROGEN-PRODUCTION; MOLYBDENUM CARBIDE; CHEMICAL-REACTIONS; SULFUR ADSORPTION; POTENTIAL STEP; MODIFIED WC; FUEL-CELLS; ELECTROCATALYSTS;
D O I
10.1149/1.3148304
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The stability and the electrocatalytic activity of polycrystalline tungsten monocarbide (WC) and platinum (Pt) electrodes in a concentrated polysulfide electrolyte were examined in an electrochemical half-cell and an integrated photoelectrochemical cell (PEC) device. Cyclic voltammetry and linear sweep voltammetry measurements found WC electrodes to be approximately twice as active as Pt electrodes toward polysulfide reduction. Electrochemical and X-ray photoelectron spectroscopy (XPS) measurements indicated that WC was stable in a polysulfide electrolyte, with no appreciable W sulfide formation. In contrast, XPS showed significant levels of sulfide species on the Pt surface, which might explain the differences in the electrochemical behavior of the two electrode materials. The performance of integrated PEC devices comprised of thin-film CdSe photoanodes and WC or Pt counter electrodes in a polysulfide electrolyte was consistent with that predicted from electrochemical half-cell measurements.
引用
收藏
页码:B962 / B969
页数:8
相关论文
共 58 条
[1]   ELECTROCHEMISTRY OF SULPHUR .1. OVERPOTENTIAL IN THE DISCHARGE OF THE SULPHIDE ION [J].
ALLEN, PL ;
HICKLING, A .
TRANSACTIONS OF THE FARADAY SOCIETY, 1957, 53 (12) :1626-1635
[2]   On-line mass spectrometry of the electro-oxidation of methanol in acidic media on tungsten carbide [J].
Angelucci, Camilo A. ;
Deiner, L. Jay ;
Nart, Francisco C. .
JOURNAL OF SOLID STATE ELECTROCHEMISTRY, 2008, 12 (12) :1599-1603
[3]  
[Anonymous], CHEM TRANSITION META
[4]   Competitive effects of S-containing catalyst poisons on the UPD of H in relation to H-2 evolution kinetics and OPD of H at Pt [J].
Barber, JH ;
Conway, BE .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1996, 92 (20) :3709-3717
[5]   MODIFICATIONS OF THE ATOMIC-STRUCTURE OF PLATINUM AGGREGATES INDUCED BY H2S, SO2, AND ELEMENTAL SULFUR ADSORPTION [J].
BERGERET, G ;
GALLEZOT, P .
JOURNAL OF CATALYSIS, 1984, 87 (01) :86-92
[6]   TUNGSTEN CARBIDE ELECTRODES FOR FUEL CELLS WITH ACID ELECTROLYTE [J].
BINDER, H ;
KOHLING, A ;
KUHN, W ;
LINDNER, W ;
SANDSTEDE, G .
NATURE, 1969, 224 (5226) :1299-+
[7]  
BOEHM H, 1968, WISS BER AEG TELEFUN, V41, P46
[8]   ADSORPTION AND ANODIC OXIDATION OF HYDROGEN ON TUNGSTEN CARBIDE [J].
BOHM, H .
ELECTROCHIMICA ACTA, 1970, 15 (07) :1273-&
[9]   Electrochemical oxidation of WC in acidic sulphate solution [J].
Bozzini, B ;
De Gaudenzi, GP ;
Fanigliulo, A ;
Mele, C .
CORROSION SCIENCE, 2004, 46 (02) :453-469
[10]   Tetralin hydrogenation catalyzed by Mo2C/Al2O3 and WC/Al2O3 in the presence of H2S [J].
Da Costa, P ;
Lemberton, JL ;
Potvin, C ;
Manoli, JM ;
Perot, G ;
Breysse, M ;
Djega-Mariadassou, G .
CATALYSIS TODAY, 2001, 65 (2-4) :195-200