4.8 Article

Ultrathin Amorphous Titania on Nanowires: Optimization of Conformal Growth and Elucidation of Atomic-Scale Motifs

Journal

NANO LETTERS
Volume 19, Issue 6, Pages 3457-3463

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.8b04888

Keywords

Amorphous titania; zinc oxide; photocatalysis; XANES; density functional theory

Funding

  1. Natinal Energy Research Scientific Computing Center (NERSC), a U.S. Department of Energy Office of Science User Facility [DE-AC02-05CH11231]
  2. LDRD Project at BNL [16-039]
  3. Office of Naval Research through the Naval Research Laboratory's Basic Research Program
  4. Brookhaven National Laboratory (BNL) [DE-SC0012704]

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Due to its chemical stability, titania (TiO2) thin films increasingly have significant impact when applied as passivation layers. However, optimization of growth conditions, key to achieving essential film quality and effectiveness, is challenging in the few-nanometers thickness regime. Furthermore, the atomic-scale structure of the nominally amorphous titania coating layers, particularly when applied to nanostructured supports, is difficult to probe. In this Letter, the quality of titania layers grown on ZnO nanowires is optimized using specific strategies for processing of the nanowire cores prior to titania coating. The best approach, low-pressure O-2 plasma treatment, results in significantly more-uniform titania films and a conformal coating. Characterization using X-ray absorption near edge structure (XANES) reveals the titania layer to be highly amorphous, with features in the Ti spectra significantly different from those observed for bulk TiO2 polymorphs. Analysis based on first-principles calculations suggests that the titania shell contains a substantial fraction of under-coordinated Ti4+ ions. The best match to the experimental XANES spectrum is achieved with a glassy TiO2 model that contains , similar to 50% of under-coordinated Ti4+ ions, in contrast to bulk crystalline TiO2 that only contains 6-coordinated Ti4+ ions in octahedral sites.

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