A platinum electrode was illuminated with an intermittent Ar+ laser be
am in a flowing solution from the front side of the electrode. The cur
rent induced by this laser illumination was recorded as a function of
electrode potential with a lock-in amplifier and was directly observed
with an oscilloscope. Experimental results for the [Fe(CN)6]4-, [Fe(C
N)6]3-, Fe2+ and Fe3+ solutions indicated that the laser heating of th
e electrode promotes or depresses the electron transfer process, depen
ding on the standard entropy change of the electrode reaction, promote
s the mass transfer process and induces adsorption or desorption of an
ions. Further, the induced current was proportional to the concentrati
on and strongly depended on the chopping frequency and the flow rate.
This laser electrochemical (LEC) detection can be used as a new electr
ochemical detector in electroanalytical chemistry.