4.5 Article

Electroreduction of Aryldiazonium Ion at the Polar and Non-Polar Faces of ZnO: Characterisation of the Grafted Films and Their Influence on Near-Surface Band Bending

期刊

CHEMPHYSCHEM
卷 22, 期 13, 页码 1344-1351

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cphc.202100240

关键词

chemisorption; cyclic voltammetry; nitrophenyl; XPS; valence band spectra

资金

  1. MacDiarmid Institute for Advanced Materials and Nanotechnology
  2. University of Canterbury

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ZnO is a strong candidate for transparent electronic devices due to its wide band gap and earth-abundance, but its practical use is limited by surface metallicity. Modification of ZnO single crystal surfaces with aryl films and NP films can decrease the downward surface band bending, with evidence of Zn-O-C bonding provided by XPS measurements.
ZnO is a strong candidate for transparent electronic devices due to its wide band gap and earth-abundance, yet its practical use is limited by its surface metallicity arising from a surface electron accumulation layer (SEAL). The SEAL forms by hydroxylation of the surface under normal atmospheric conditions, and is present at all crystal faces of ZnO, although with differing hydroxyl structures. Multilayer aryl films grafted from aryldiazonium salts have previously been shown to decrease the downward bending at O-polar ZnO thin films, with Zn-O-C bonds anchoring the aryl films to the substrate. Herein we show that the Zn-polar (0001), O-polar (0001? ), and non-polar m-plane (101? 0) faces of ZnO single crystals, can also be successfully electrografted with nitrophenyl (NP) films. In all cases, X-ray photoelectron spectroscopy (XPS) measurements reveal that the downward surface band bending decreases after modification. XPS provides strong evidence for Zn-O-C bonding at each face. Electrochemical reduction of NP films on O-polar ZnO single crystals converts the film to a mainly aminophenyl layer, although with negligible further change in band bending. This contrasts with the large upward shifts in band bending caused by X-ray induced reduction.

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