Compositions and chemical states on the co-deposition layer of lithiated tungsten of plasma-facing components of EAST
Creators
- 1. Key Laboratory of Materials Modification by Laser, Ion and Electron Beams, Chinese Ministry of Education, School of Physics and Optical Electronic Technology, Dalian University of Technology, Dalian, 116024 (China)
- 2. Institute of Plasma Physics, Chinese Academy of Sciences, PO. Box 1126, Hefei, 230031 (China)
Description
Highlights: • The chemical compositions and states of the Li-W co-deposition layer on W were determined by a post-mortem analysis of X-ray photoelectron spectroscopy (XPS) after an analysis of laser-induced breakdown spectroscopy (LIBS) approach. • The analysis of XPS shew the observable Li2CO3 XPS peaks due to a series of reaction after exposure of air on the lithiated W surface. The Li2CO3 XPS peaks at 289 eV and 531.6 eV were obviously changed with the Li distribution. • In addition, high proportional W oxides were formed on the surface of Li-W co-deposition layer of lithiated W. Elemental W peaks at the laser ablation spots were more obvious than them at the Li-W co-deposition layer surface without laser ablation. - Abstract: Lithiation is beneficial to enhance plasma performance in EAST by reducing hydrogen and impurities recycling via lithium (Li) wall conditioning. High-Z materials like tungsten (W) have been selected as up–divertor in EAST tokamak. However, the nature of the chemical compositions and states on Li-W co-deposition layer is still unclear. In this paper, pure W plasma-facing component experiments with Li deposition layer were carried out by a cascaded-arc linear plasma generator. An in-situ laser-induced breakdown spectroscopy (LIBS) system with spatial resolution about 1 mm and depth resolution about 200 nm was developed to real time monitor the composition and distribution on Li-W co-deposition layer. The chemical states of the co-deposition layer and laser ablation spots were determined by a post-mortem analysis of X-ray photoelectron spectroscopy (XPS). Both LIBS and XPS results shew that higher concentration of Li could be observed at the region closed to the Li source. The XPS spectra indicated that Li2CO3 peaks intensities at 289 eV and 531.6 eV were obviously changed with the Li distribution. In addition, high proportional W oxides were formed on the surface of Li-W co-deposition layer in the lithiated W sample. Elemental W signals corresponding to the laser ablation spots were much more obvious than them in the area of Li-W co-deposition layer surface without laser ablation. This work could improve the understanding of the Li-wall conditioning for tungsten divertor in EAST tokamak.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.nme.2017.02.002Additional details
Identifiers
- DOI
- 10.1016/j.nme.2017.02.002;
- PII
- S2352179116301466;
Publishing Information
- Journal Title
- Nuclear Materials and Energy
- Journal Volume
- 12
- Journal Page Range
- p. 1209-1213
- ISSN
- 2352-1791
Conference
- Title
- 22. International Conference on Plasma-Surface Interactions in Controlled Fusion Devices
- Acronym
- PSI-22
- Dates
- 30 May - 3 Jun 2016
- Place
- Rome (Italy)
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 50079958
- Subject category
- S70: PLASMA PHYSICS AND FUSION TECHNOLOGY;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- ABLATION; BREAKDOWN; CHEMICAL COMPOSITION; CHEMICAL STATE; DISTRIBUTION; FIRST WALL; HT-7U TOKAMAK; LASERS; LAYERS; LITHIUM CARBONATES; OXIDES; PEAKS; SPATIAL RESOLUTION; TUNGSTEN; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- ALKALI METAL COMPOUNDS; CARBON COMPOUNDS; CARBONATES; CHALCOGENIDES; CLOSED PLASMA DEVICES; ELECTRON SPECTROSCOPY; ELEMENTS; LITHIUM COMPOUNDS; METALS; OXYGEN COMPOUNDS; PHOTOELECTRON SPECTROSCOPY; REFRACTORY METALS; RESOLUTION; SPECTROSCOPY; THERMONUCLEAR DEVICES; THERMONUCLEAR REACTOR WALLS; TOKAMAK DEVICES; TRANSITION ELEMENTS
Optional Information
- Notes
- © 2017 Published by Elsevier Ltd.