In this study, an
effective and simple direct printing
method was developed to create sensing devices on screen-printed carbon
electrodes (SPCEs) to detect multiple species simultaneously. Two
sensing materials, graphene oxide nanoribbons (GONRs) and poly(3,4-ethylenedioxythiophene):polystyrene
sulfonate (PEDOT:PSS), were printed on one SPCE for detection of multiple
biochemical substances. Printed layers of the GONRs and PEDOT:PSS
mixture (GONRs & PEDOT:PSS) on SPCE showed embedment of GONRs
in the PEDOT:PSS layer and diminished the electrochemical activity
of GONRs. In contrast, by printing the GONRs and PEDOT:PSS at separate
locations (GONRs + PEDOT:PSS) on the same SPCE, the electrochemical
activities of both GONRs and PEDOT:PSS can be preserved. Thus, without
synthesizing new materials, the modified electrode is able to simultaneously
detect ascorbic acid (AA), uric acid (UA), dopamine (DA), and nitrite
(NO2–), with high anodic oxidation currents
and well-separated voltammetric peaks, in differential pulse voltammetry
measurements. The detection limits for the four analytes are 41 nM
(AA), 30 nM (DA), 11 nM (UA), and 18 nM (NO2–), respectively. The electrode can either detect single species separately
or simultaneously determine specific concentrations of the four species
in aqueous mixtures, and this can be further extended for many other
electrochemical sensing applications.