Effect of pH on stability and plasmonic properties of cysteine-functionalized silver nanoparticle dispersion

Citrate-stabilized spherical silver nanoparticles (Ag NPs) with d = 8.25 ± 1.25 nm diameter were prepared and functionalized with l-cysteine (Cys) in aqueous dispersion. The nanosilver–cysteine interactions have been investigated by Raman and 1H NMR spectroscopy. The effect of pH on stability of biofunctionalized Ag NPs was investigated. The cysteine-capped nanosilver dispersions remain stable at higher pH (pH > 7), while the degree of aggregation increased as the pH decreased. Below pH ∼7, the characteristic surface plasmon band of bare silver nanoparticles was back-shifted from λ measured bare Ag NP = 391   nm to λ measured 1 = 387 – 391   nm , while the presence of a new band at λ measured 2 = 550 – 600   nm was also observed depending on pH. Finite element method (FEM) was applied to numerically compute the absorption spectra of aqueous dispersions containing bare and cysteine-functionalized Ag NPs at different pH. Both the dynamic light scattering (DLS) measurements, Zeta potential values and the transmission electron microscopic (TEM) images confirmed our supposition. Namely, electrostatic interaction arose between the deprotonated carboxylate (COO−) and protonated amino groups (NH3+) of the amino acid resulting in cross-linking network of the Ag NPs between pH ∼3 and 7. If the pH is measurable lower than ∼3, parallel with the protonation of citrate and l-cysteine molecules the connection of the particles via l-cysteine is partly decomposed resulting in decrease of second plasmon band intensity.