Photo-renewable engineered sensor based on silica, silver nanoparticles and titania

Electrode surface passivation and fouling are important challenges in electroanalysis when using modified electrodes in complex matrices, especially in the biomedical and environmental fields [1-2]. In order to overcome such problems, the production of highly engineered ad hoc designed devices could provide really effective sensors [2]. In particular, a reliable and reusable sensor, that could be cleaned by a simple irradiation with UV or solar light, could be perfect for this purpose. In this context, a three-layered transparent electrode, in which silver nanoparticles are embedded between a bottom silica and a top titania layer is developed [3-4]. Such structure confers to the device multifunctional properties which can be conveniently used in the detection and quantification of some neurotransmitters: dopamine, norepinephrine and serotonin. The sensor is thoroughly investigated by structural, morphological and electrochemical characterizations in order to understand the role of each component with the aim to improve the robustness and efficiency of the electroanalytical system. In particular, the size distribution of silver nanoparticles, the device architecture and surface homogeneity are inspected by electron microscopy. As confirmed by X-ray diffraction the overlayer is made of anatase (the active polymorph of titanium dioxide), capable of photodegrading model contaminants. Furthermore, electrochemical techniques (cyclic voltammetry and electrochemical impedance spectroscopy) revealed that a highly ordered distribution of silver nanoparticles constitutes the active analytical core of the device, allowing easier electron transfer and better quantification of the analytes. The system presents good sensing performances, reaching low detection limits even in the presence of typical interferents such as ascorbic and uric acids. Moreover, the titania photoactive top layer allows the complete recovery of the device performance in terms of sensitivity after a fast and simple UV-A cleaning step, affordable with different UV sources. In particular, three lamps (different in terms of power and wavelength) were tested, reaching the total removal of the contaminants in 10-15 minutes [5]. This “self-cleaning” property, combined with a remarkable resistance against aging and ease of use, allows to employ the sensor also for detection in real matrixes, such as liquor and serum. ACKNOWLEDGEMENTS The Authors would like to thank MIUR (Ministero dell’Istruzione, dell’Università e della Ricerca) for the fundings in the framework of the PRIN 2012 Project (20128ZZS2H) REFERENCES [1] C.M.A. Brett, Pure Appl. Chem. 73, 2001, pp 1969–1977. [2] C.M. Welch, R.G. Compton, Anal. Bioanal. Chem. 384, 2006, pp 601–619. [3] G. Maino, D. Meroni, V. Pifferi, L. Falciola, G. Soliveri, G. Cappelletti, S. Ardizzone, J. Nanoparticle Res. 15, 2013, pp 2087. [4] G. Soliveri, V. Pifferi, G. Panzarasa, S. Ardizzone, G. Cappelletti, D. Meroni, K. Sparnacci, L. Falciola, Analyst 140, 2015, 1486-1494. [5] V. Pifferi, G. Soliveri, G. Panzarasa, S. Ardizzone, G. Cappelletti, D. Meroni, L. Falciola, RSC Advances, 5, 2015, 71210-71214.