English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

The changes in the structure and elemental composition of Au and Co-W thin layers after thermal treatment of 200 h at 200-300 oC and 50 h at 450 oC were systematically studied using the X-ray microanalysis of scanning electron microscope XL-30 ESEN Philips. The phase stability was evaluated by X-ray diffraction (XRD). The electrodeposited Co-W layer (W 46.0-53.0 wt. % depending on the electrodeposition regime) is amorphous and maintains its amorphous state after heating at 200 oC for 200 h and subsequent heating (+) at 300 oC for 150 h. Co-W amorphous layers prevent interdiffusion of Au and Cu atoms and formation of intermetallics AuCu in the systems of layers Au chemically reduced; Au electrodeposited /Co-W/Cu sputtered / glass-ceramics. The chemically reduced 0.4  m Au layers maintain their structure and phase in the systems of layers upon heating at 200 oC for 200 h and subsequent heating (+) at 300 oC for 50 h. The Au layer maintains its Au content 85-86 wt. % upon heating at 450 oC for 50 h, the cobalt content of the layer up to 8.6 wt. % and content of oxygen bonded to Au of 8.6 wt. %. The electrodeposited Au layers (0.8 - 1.0  m) maintain their structure at heating at 200 oC and 300 oC for 200 h. After additional heating at 450 oC for 30-50 h gold content in the layer decreases from 98.4 wt. % to 85.0 wt. %, cobalt content increases to 7.6 wt. % and oxygen to 7.2 wt. %. Functional properties of the above multilayer systems deteriorate by mutual diffusion of metal atoms and formation of brittle intermetallics. The latter may give rise to the formation of monolithic films, cause the deterioration of mutual adhesion of the layers and complete reactions of the upper conducting Sn, Au layers with the base metal Ni, Cu, Ti, Sn (15, 16). This diffusion can worsen the properties of very thin (0.5-1.0  m) metal layers electrodeposited on a Cu layer (1-2  m) sputtered on glass-ceramics (15).

the open surface science journal

Stability of Structure, Phase and Elemental Composition of Chemically Deposited and Electrodeposited Gold Layers in Multilayer Systems Auchemically reduced; electrodeposited /Co-W/Cusputtered / Glass-Ceramics~!2009-07-13~!2010-01-28~!2010-03-18~!