Published December 2015 | Version v1
Journal article

The influence of nitrogen co-deposition in mixed layers on deuterium retention and thermal desorption

  • 1. Jožef Stefan Institute, Jamova Cesta 39, 1000 Ljubljana (Slovenia)
  • 2. National Institute for Laser, Radiation and Plasma Physics, Atomistilor 409, 077125 Magurele (Romania)

Description

The influence of nitrogen co-deposition in ITER relevant mixed layers on retention and release dynamics of deuterium was studied in situ by Nuclear Reaction Analysis (NRA) and thermodesorption spectroscopy. W:Al and W:Be mixed layers deposited by thermionic vacuum arc (TVA) method were used in order to verify the possibility of Al being used as proxy material for Be in experiments regarding D uptake. Samples were exposed to neutral deuterium atom beam with fluence of 3.24 × 1019 D/cm2 (flux 4.5 × 1014 D/cm2s) at 390 K and NRA with 3He ions was used for depth profile analysis of deuterium content after the exposure. For the investigation of deuterium release dynamics the samples were linearly heated to around 1000 K and during this process NRA spectra at single energy were collected every minute. Complementary to NRA a quadrupole mass spectrometer was used, following masses 2, 3 and 4 in the background vacuum. The numeric simulation of deuterium thermal desorption was performed and desorption energies of desorption sites were calculated. Same experiments were performed with mixed material samples produced by TVA in the presence of nitrogen atmosphere. Nitrogen co-deposition in the mixed layers was found to have an important influence on deuterium retention. The concentration of deuterium in the sample increased by a factor of 4.8 in the presence of nitrogen in the W:Al and by a factor of 1.8 in the W:Be layer compared to the nitrogen-free sample.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jnucmat.2015.09.044

Additional details

Identifiers

DOI
10.1016/j.jnucmat.2015.09.044;
PII
S0022-3115(15)30233-6;

Publishing Information

Journal Title
Journal of Nuclear Materials
Journal Volume
467
Journal Issue
Part 1
Journal Page Range
p. 472-479
ISSN
0022-3115
CODEN
JNUMAM

Optional Information

Copyright
Copyright (c) 2015 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.