3 years ago

Role of AuxPt1–x Clusters in the Enhancement of the Electrochemical Activity of ZnO Nanorod Electrodes

Role of AuxPt1–x Clusters in the Enhancement of the Electrochemical Activity of ZnO Nanorod Electrodes
Didier Grandjean, Ting-Wei Liao, Vincenzina Strano, Anupam Yadav, Salvatore Cosentino, Salvo Mirabella, Yosi Shacham-Diamand, Peter Lievens, Kuo-juei Hu, Giorgia Fiaschi, Nofar Mintz Hemed
This study quantitatively elucidates the role of metal clusters in the electrochemical activation of metal-oxide nanostructured electrodes. Through the deposition of nearly monodisperse AuxPt1–x (x = 0, 0.5, 1) clusters, smaller than 3 nm, on the ZnO nanorod (NR) electrode surface, a controlled enhancement of charge transfer and activation of electrocatalytic processes was achieved. The interfacial electrical states of the hybrid electrodes were probed by electrochemical impedance spectroscopy (EIS). Analysis of the charge-transfer resistance and interface capacitance, estimated by modeling EIS curves in different bias regimes, indicated the presence of a large amount of active donor states (∼1020 cm–3) at the surface of the ZnO NRs. Decoration of the ZnO NRs with AuxPt1–x clusters strongly increased the charge-transfer process at the cluster–ZnO/electrolyte interface. This induced a more effective depletion of the electron charge available in the donor states of the ZnO NRs, leading to the formation of a positively charged layer at the interface between ZnO and the clusters. These two effects, intrinsically linked with the alignment between the electronic states of the AuxPt1–x clusters and ZnO, strongly enhance the interface reactivity of the ZnO NR electrodes toward the redox reaction of potassium ferricyanide. This is particularly relevant for understanding and improving the performance of electrochemical biosensors.

Publisher URL: http://dx.doi.org/10.1021/acs.jpcc.7b00480

DOI: 10.1021/acs.jpcc.7b00480

You might also like
Discover & Discuss Important Research

Keeping up-to-date with research can feel impossible, with papers being published faster than you'll ever be able to read them. That's where Researcher comes in: we're simplifying discovery and making important discussions happen. With over 19,000 sources, including peer-reviewed journals, preprints, blogs, universities, podcasts and Live events across 10 research areas, you'll never miss what's important to you. It's like social media, but better. Oh, and we should mention - it's free.

  • Download from Google Play
  • Download from App Store
  • Download from AppInChina

Researcher displays publicly available abstracts and doesn’t host any full article content. If the content is open access, we will direct clicks from the abstracts to the publisher website and display the PDF copy on our platform. Clicks to view the full text will be directed to the publisher website, where only users with subscriptions or access through their institution are able to view the full article.