Graphene-supported Pd/Pt nano-catalysts for enhanced colorimetric detection of dopamine and NADH using paper-based
Ruri Agung Wahyuono1,2, Jovin Jovin1, Ignacius Gilbert Chano1
1Department of Engineering Physics, Institut Teknologi Sepuluh Nopember, Surabaya 60111, Indonesia.
Background And Purpose:
Dopamine and nicotinamide adenine dinucleotide (NADH) are key biomarkers associated with neurological and metabolic disorders. Developing rapid, low-cost, and portable detection platforms of these biomarkers is essential for a point-of-care diagnostic kit. In this work, we report a colorimetric sensing approach using paper-based microfluidic devices (μPADs) modified with graphene-supported palladium (G/Pd) and platinum (G/Pt) nanocatalysts to enhance detection performance.
Experimental Approach:
Monolayer G/Pd and G/Pt nanocomposites were synthesized via a hydrothermal method with precursor concentrations ranging from 0.1 to 10 mM. The catalytic behaviour and metal-graphene interactions were further investigated using spin-polarized density functional theory (DFT) calculation (PHASE/0). Microfluidic paper-based analytical devices (μPADs) were laser-printed on commercial filter paper and folded into 3D origami structures. Colorimetric responses were quantified using red, green, blue (RGB) and hue, saturation, value (HSV) analysis, where time-dependent Euclidean distance in RGB colour space was used to assess the reaction kinetics.
Key Results:
DFT results indicate that Pd and Pt clusters preferentially adopt a top-site configuration on graphene, facilitating interfacial charge redistribution and enhancing catalytic activity experimentally. Catalyst-modified μPADs significantly improve reaction kinetics, reducing detection time by up to 3.7× for dopamine and 2.5× for NADH compared to unmodified devices. G/Pt (10 mM) exhibits the best overall performance, achieving limits of detection of 0.16 μM for dopamine and 0.195 μM for NADH with good linearity (R 2 = 0.91). G/Pd displays competitive sensitivity, particularly at lower precursor concentration.
Conclusion:
The findings highlight that optimizing catalyst morphology and interfacial electronic structure is more critical than minimizing activation energy for achieving high-performance colorimetric sensing. The resulting platform shows potential as a cost-effective and portable tool for the detection of clinically relevant biomarkers in point-of-care settings.
