Abstract
AbstractGold–copper nanostructures are promising in solar-driven processes because of their optical, photocatalytic and photoelectrochemical properties, especially those which result from the synergy between the two metals. Increasing interest in their internal structure, such as the composition or distribution of the Au and Cu as well as the size and shape of the nanoparticles, have developed to define their physicochemical properties.In this work, we present the influence of thermal treatment in temperature ranges from 100 to 600 °C on the formation process of bimetallic AuCu structures and their properties. AuCu materials were placed on nanostructured titanium foil substrates that were fabricated using electrochemical anodisation and chemical etching. Thin layers of AuCu mixture, as well as Au and Cu, were sputtered on the obtained Ti nanodimples. The materials were then annealed in a rapid thermal annealing furnace in an air atmosphere. Thermal treatment strongly affected the morphology and optical properties of the fabricated materials. AuCu NPs formed at 400 °C in titanium dimples. The material exhibits absorption of visible light in the range from c.a. 400 to 700 nm. The characterisation of the chemical nature of the samples was determined using X-ray photoelectron spectroscopy. In addition, X-ray diffraction and Raman spectroscopy defined composition and crystallinity. Based on photoelectrochemical studies carried out with the use of linear voltammetry in 0.1 M NaOH, it is possible to distinguish two types of interactions of light with the materials such as photogenerated charge accumulation and electron–hole pair separation. A 10AuCu electrode annealed at 300 °C achieved the highest current registered under illumination at − 0.17 V vs. Ag/AgCl/0.1 M KCl. The value was 11 times higher than for a non-annealed structure.
Publisher
Springer Science and Business Media LLC
Subject
Electrical and Electronic Engineering,Condensed Matter Physics,Atomic and Molecular Physics, and Optics,Electronic, Optical and Magnetic Materials
Cited by
1 articles.
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