Tuesday, April 1, 2008 - 3:30 PM

A Novel Low-Cost Photoelectrochemical Cell for Solar Hydrogen Generation

Mano Misra, University of Nevada, Reno

Hydrogen generation through water splitting using only the sun light is considered one of the best sources of alternate energy for various applications. The main limiting factor in realizing the commercial success of solar water splitting using semiconductor electrodes is the stability of the photo active materials. Among the available semiconductor materials, TiO2 is the most stable material against photo corrosion. However, its photo conversion efficiency is limited by the wide band gap.

 

In this presentation, we report construction of a novel photo electrochemical cell for generation of hydrogen using solar light. The photo anode is produced by synthesis of ordered nanotubular arrays of TiO2 by a single step electrochemical anodization process in fluoride containing organic solutions (typically ethylene glycol). Subsequent annealing of the nanotubular arrays in hydrogen environment yields optimum volume fraction of anatase plus rutile phases and incorporation of carbon in the TiO2 lattice. The diffusion of carbon into the TiO2 lattice introduces defect states in the band gap and also modifies the band gap to 2.1 eV.  The nanotubular TiO2 photo anodes formed by the anodization process show more superior charge transport properties and structural integrity than the anodes made by spray pyrolysis of nano-particles. Further, construction of very large area (active on both sides) electrode materials with uniform electronic and mechanical properties is easily achievable using the proposed electrochemical anodization process. Conventionally, a Pt sheet is used as cathode for solar water splitting. In this new cell, the Pt sheet electrode is replaced with a TiO2 nanotubular template loaded with 3-6 nm size Pt nano-particles (0.4 mg/cm2). Nickel nano-particles loaded TiO2 cathode also is developed. These new cathode materials have larger surface areas than the conventional electrodes, and these are much cheaper.

 

Photo electrochemical studies are carried out on these carbon modified double sided nanotubular TiO2 photo anodes and Pt or Ni nano-particles loaded TiO2 nanotubular cathodes. The surface area of the electrode is 8 cm2. Photo current is recorded as a function of both applied external bias potential and light wavelength using a simulated solar light source with band pass filters. Photo current is observed at wavelengths less than 600 nm. The maximum observed photo current density using the entire solar light is 3.3 mA/cm2 at 0.2 V Ag/AgCl. The maximum photo conversion efficiency using only the UV portion of the solar spectra is 13.3%. When considering only the visible portion of the solar light at 520 ± 46 nm, the maximum photo conversion efficiency is 8.5 %. Further studies are being carried out to improve the overall solar to hydrogen efficiency of the system in the entire solar spectra.