A systematic study was performed to determine the mechanism of the nitric o
xide (NO) reduction on polycrystalline platinum. Both the reduction of NO i
n the presence of NO in the solution and the reduction of adsorbed NO in a
clean electrolyte have been investigated. The adsorbate reduction takes pla
ce through a combined proton-electron transfer in equilibrium followed by a
rate-determining chemical step. NH3 is the only product in the absence of
NO in solution. The reduction in the presence of NO in the solution at pote
ntials between 0.4 and 0.8 V versus RHE yields N2O as the only product. The
mechanism of this reaction is not of the Langmuir-Hinshelwood type, but ra
ther involves the combination of a surface-bonded NO molecule with an NO mo
lecule from the solution and a simultaneous electron transfer. A protonatio
n has to take place prior to this step. In alkaline solutions a chemical st
ep appears to be partially rate determining. The continuous reduction of NO
at potentials lower than 0.4 V yields mainly NH3. The mechanism of this re
action is the same as for the adsorbate reduction. (C) 2001 Elsevier Scienc
e Ltd. All rights reserved.