Localized surface plasmon resonance
(LSPR) sensors are used in
a broad range of detection applications across the chemical, biological,
environmental, and medical disciplines. These types of sensors traditionally
use the plasmon resonance wavelength of a nanoparticle array to detect
changes in refractive index at the sensor surface and, therefore,
require expensive spectroscopic instrumentation for readout. However,
simple, portable, and low-cost LSPR sensors can be achieved by transitioning
to colorimetric measurements, in which refractive index changes are
quantified using the R, G, and B pixel intensities from digital nanoparticle
images. In this study, we use R, G, and B pixel intensities to quantify
color coordinates in the HSV, CIE L*a*b*, and rgb chromaticity color
spaces. We show that for sensors comprising 115 nm diameter nanoparticles,
hue (H) is the most sensitive color parameter, with a change per refractive
index unit (Δhue/ΔRIU) of 0.71 and a figure of merit of
183 RIU–1. Furthermore, we compared hue figures
of merit (FOM) for nanoparticles in four different diameters (34.1,
59.8, 81.5, and 115 nm) and showed that hue sensitivity peaks at a
diameter of 81.5 nm, with a FOM of 222 RIU–1. In
contrast, the spectroscopic sensitivity, quantified in units of Δnm/ΔRIU,
increased continually with nanoparticle size. Therefore, the design
requirements for colorimetric plasmonic sensors differ from those
for spectroscopic plasmonic sensors. This difference in size dependence
was explored further using Mie calculations to simulate nanoparticle
extinction spectra. Our results revealed that, while λmax responds linearly to refractive index changes, hue responds in a
sigmoidal fashion. As a result, the nanoparticle size used in colorimetric
sensors relying on hue measurement should be carefully selected to
achieve a linear sensor response. We provide general design rules
for optimizing hue-based colorimetric sensors and demonstrate that
our sensor can be used with a smartphone to detect antibody–antigen
interactions.
