Novel nano-crystalline Er₂O₃ hydrogen isotopes permeation barriers

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• 作者：Qun Li^a ; Jie Wang^a ; Qing-yun Xiang^a ; Kai Yan^a ; Tao Tang^b ; Yong-Chu Rao^b ; Jiang-Li Cao^a ; ^{perov@sina.com" class="auth_mail" title="E-mail the corresponding author}
• 关键词：Nano-crystalline ; Er2O3 coatings ; Thermonuclear fusion ; Deuterium permeation ; D-PRFD-prf
• 刊名：Journal of the European Ceramic Society
• 出版年：2017
• 出版时间：January 2017
• 年：2017
• 卷：37
• 期：1
• 页码：249-254
• 全文大小：2064 K

文摘

Hydrogen Isotopes permeation barriers (HIPB) are used to reduce hydrogen isotopes permeation and leakage in the fields such as thermonuclear fusion energy, hydrogen energy, petroleum industry and vacuum solar receiver. In this study, nano-crystalline Er₂O₃ HIPB with about 5–10 nm grain size were made by sol-gel method. Their performances, including deuterium-permeation reduction factor (D-PRF), micro-structure, mechanical property and electrical property were reported. The D-PRF of 0.2 μm nano-crystalline Er₂O₃ HIPB reached 300 at 700 °C and did not deteriorate after 128 h deuterium permeation. The bonding strength and the nano-hardness steadily remained about 13 N and 10 GPa after 128 h deuterium permeation at 700 °C, respectively. The morphology and micro-structures of the nano-crystalline Er₂O₃ HIPB showed no measurable changes after 128 h deuterium permeation, which ensured the stable D-PRF and mechanical properties. However, the electrical resistivity of the nano-crystalline Er₂O₃ HIPB decreased after deuterium permeation at 700 °C. The electrical resistivity decreased from 9 × 10⁹ Ω cm by over three orders of magnitude and then tended to be stable, which might be attributed to oxygen loss or deuterium invasion.