RT info:eu-repo/semantics/article T1 Nanoscale Au-In alloy-oxide core-shell particles as electrocatalysts for efficient hydroquinone detection A1 Rodríguez Méndez, María Luz A1 Medina Plaza, Cristina A1 Sutter, Peter A1 Tong, Xiang A1 Sutter, Elli AB The presence of hydroquinone (HQ), a phenol ubiquitous in nature and widely used in industry, needs to be monitored because of its toxicity to the environment. Here we demonstrate efficient detection of HQ using simple, fast, and noninvasive electrochemical measurements on indium tin oxide (ITO) electrodes modified with nanoparticles comprising bimetallic Au–In cores and mixed Au–In oxide shells. Whereas bare ITO electrodes show very low activity for the detection of HQ, their modification with Au–In core–shell nanoparticles induces a pronounced shift of the oxidation peak to lower potentials, i.e., facilitated oxidation. The response of the different electrodes was correlated with the initial composition of the bimetallic nanoparticle cores, which in turn determined the amount of Au and In stabilized on the surface of the amorphous Au–In oxide shells available for the electrochemical reaction. While adding core–shell nanostructures with different compositions of the alloy core facilitates the electrocatalytic (reduction-) oxidation of HQ, the activity is highest for particles with AuIn cores (i.e., a Au:In ratio of 1). This optimal system is found to follow a single pathway, the two-electron oxidation of the quinone–hydroquinone couple, which gives rise to high oxidation peaks and is most effective in facilitating the electrode-to-analyte charge transfer and thus detection. The limits of detection (LOD) decreased when increasing the amount of Au exposed on the surface of the amorphous Au–In oxide shells. The LODs were in the range of 10–5–10–6 M and were lower than those obtained using bulk Au. YR 2015 FD 2015 LK http://uvadoc.uva.es/handle/10324/30594 UL http://uvadoc.uva.es/handle/10324/30594 LA eng NO The Journal of Physical Chemistry, C vol. 119 p. 25100-25107 DS UVaDOC RD 23-nov-2024