Coupling of Phthalocyanines with Plasmonic Gold Nanoparticles by Click Chemistry for an Enhanced Singlet Oxygen Based Photoelectrochemical Sensing

Author:

Khan Shahid U.123,Matshitse Refilwe4,Borah Rituraj23,Nemakal Manjunatha4,Moiseeva Ekaterina O.56,Dubinina Tatiana V.6,Nyokong Tebello4,Verbruggen Sammy W.23,De Wael Karolien13

Affiliation:

1. A-Sense Lab University of Antwerp Groenenborgerlaan 171 2020 Antwerp Belgium

2. Sustainable Energy Air & Water Technology (DuEL) Department of Bioscience Engineering University of Antwerp Groenenborgerlaan 171 2020 Antwerp Belgium

3. NANOlab Center of Excellence University of Antwerp Groenenborgerlaan 171 2020 Antwerp Belgium

4. Institute for Nanotechnology Innovation Rhodes University Makhanda South Africa

5. Skolkovo Institute of Science and Technology 3 Nobelya Str. Moscow 121205 Russia

6. Department of Chemistry Lomonosov Moscow State University 119991 Moscow Russian Federation

Abstract

AbstractCoupling photosensitizers (PSs) with plasmonic nanoparticles increases the photocatalytic activity of PSs as the localized surface plasmon resonance (LSPR) of plasmonic nanoparticles leads to extreme concentration of light in their vicinity known as the near‐field enhancement effect. To realize this in a colloidal phase, efficient conjugation of the PS molecules with the plasmonic nanoparticle surface is critical. In this work, we demonstrate the coupling of phthalocyanine (Pc) molecules with gold nanoparticles (AuNPs) in the colloidal phase via click chemistry. This conjugated Pc‐AuNPs colloidal system is shown to enhance the photocatalytic singlet oxygen (1O2) production over non‐conjugated Pcs and hence improve the photoelectrochemical detection of phenols. The plasmonic enhancement of the 1O2 generation by Pcs was clearly elucidated by complementary experimental and computational classical electromagnetic models. The dependence of plasmonic enhancement on the spectral position of the excitation laser wavelength and the absorbance of the Pc molecules with respect to the wavelength specific near‐field enhancement is clearly demonstrated. A high 8 times enhancement is obtained with green laser (532 nm) at the LSPR due to the maximum near‐field enhancement at the resonance wavelength.

Funder

Universiteit Antwerpen

Publisher

Wiley

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