Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance work on Wednesday 27th March 2019 from 11:00 AM to 1:00 PM (GMT).

During this time our website performance may be temporarily affected. We apologise for any inconvenience this might cause and thank you for your patience.

Issue 26, 2012
Previous Article Next Article

Real time plasmonic spectroscopy of the interaction of Hg2+ with single noble metal nanoparticles

Author affiliations


In this work, we use dark-field optical microscopy (DFM) and hyper spectral imaging (HSI) to study the interactions of single Ag and Au nanoparticles (NPs) with Hg2+ in real time, at room temperature (25 °C). NPs were immobilized on glass substrates using 3-aminopropyltrimethoxysilane (APTMS) as the anchoring agent. Red, green and blue colors were assigned to the particles in hyper spectral images on the basis of their relative scattering intensities at 640, 550 and 460 nm, where the particles showed maxima in their scattering spectra. While Ag NPs showed all the colors, Au NPs were mostly red and rarely green in DFM images. The scattering spectra of Ag NPs were more blue shifted (with an average shift of 46 nm in the case of red particles) in a given time compared to Au NPs, after passing over Hg2+ solution and these shifts increased with time. Depending on the extent of blue shift, the colors of the particles got modified. Red particles appeared more reactive than green and blue, as revealed from the larger extent of shifts and their time dependence. The greater reactivity of red particles is attributed to their anisotropic nature possessing reactive tips, edges and more surface area due to their large size. The effect of quality of water on the scattering spectrum was checked by passing over deionized (DI) and tap waters separately, which showed that the effect is minimal compared to the presence of Hg2+, when data at a given time, flow rate and temperature were compared. Solution phase interactions of NPs with Hg2+ were also performed for comparison. These were characterized by UV-vis absorption spectroscopy, transmission electron microscopy (TEM) and energy dispersive analysis of X-rays (EDAX). Solution phase experiments showed citrate-induced aggregation of Ag NPs and partial reduction of Hg2+ to Hg0 upon exposure to Hg2+. Immobilized particles cannot aggregate and they show only reduction.

Graphical abstract: Real time plasmonic spectroscopy of the interaction of Hg2+ with single noble metal nanoparticles

Back to tab navigation

Supplementary files

Publication details

The article was received on 07 Jul 2012, accepted on 24 Aug 2012 and first published on 28 Aug 2012

Article type: Paper
DOI: 10.1039/C2RA21384B
Citation: RSC Adv., 2012,2, 10048-10056

  •   Request permissions

    Real time plasmonic spectroscopy of the interaction of Hg2+ with single noble metal nanoparticles

    M. S. Bootharaju, K. Chaudhari and T. Pradeep, RSC Adv., 2012, 2, 10048
    DOI: 10.1039/C2RA21384B

Search articles by author