posted on 2013-04-25, 00:00authored byAhamed Irshad, Nookala Munichandraiah
Photoassisted
electrolysis of water is considered as an effective
way of storing solar energy in the form of hydrogen fuel. This overall
reaction involves the oxidation of water to oxygen at the anode and
the reduction of protons to hydrogen at the cathode. Cobalt–phosphate-based
catalyst (Co–Pi) is a potentially useful material for oxygen
evolution reaction. In the present study, electrochemical deposition
of Co–Pi catalyst is carried out on Au-coated quartz crystal
from 0.1 M phosphate buffer (pH 7) containing 0.5 mM Co2+ ion, along with the simultaneous measurement of mass changes at
the electrode surface. Cyclic voltammograms and mass variations are
recorded during the course of deposition. A current peak is observed
at 0.92 V vs Ag/AgCl, 3 M KCl corresponding to oxidation of Co2+ ion. The mass of the electrode starts increasing at this
potential, suggesting the deposition of a Co(III)-based insoluble
product on the electrode surface. The stability of the catalyst is
also studied at several potentials in both buffered and nonbuffered
electrolyte by monitoring the real-time mass variations.