Electrodes with the functionality of amino acids can be easily prepared by
taking advantage of strong sulfur-gold interactions and immersing gold elec
trodes into cysteine solutions. Such electrodes exhibit excellent sensitivi
ty and selectivity toward copper(II) determination, because the bidentate c
helation of amino acids toward copper(II) is effective and far superior tha
n that toward any other metal ions. In this study, we demonstrate that at a
preconcentration time of 5 min the cysteine-modified electrode has a dynam
ic range of 2 orders of magnitude (from 5.0 to 0.050 mu g/L) and the detect
ion limit is as low as 25 ng/L (0.39 nM). This method is applied to the det
ermination of copper(II) in two reference materials, SLEW-2 (river water, 1
.62 mu g/L) and CASS-3 (seawater, 0.517 mu g/L). The results agree satisfac
torily with the certified values.