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PdAgHx金属氢化物正电子湮没研究

左翼 郑永男 周冬梅 杜恩鹏 袁大庆 段晓 朱升云

左翼, 郑永男, 周冬梅, 杜恩鹏, 袁大庆, 段晓, 朱升云. PdAgHx金属氢化物正电子湮没研究[J]. 原子核物理评论, 2005, 22(1): 115-117. doi: 10.11804/NuclPhysRev.22.01.115
引用本文: 左翼, 郑永男, 周冬梅, 杜恩鹏, 袁大庆, 段晓, 朱升云. PdAgHx金属氢化物正电子湮没研究[J]. 原子核物理评论, 2005, 22(1): 115-117. doi: 10.11804/NuclPhysRev.22.01.115
ZUO Yi, ZHENG Yong-nan, ZHOU Dong-mei, DU En-peng, YUAN Da-qing, DUAN Xiao, ZHU Sheng-yun. Investigation of Metal Hydride PdAgHx by Positron Annihilation[J]. Nuclear Physics Review, 2005, 22(1): 115-117. doi: 10.11804/NuclPhysRev.22.01.115
Citation: ZUO Yi, ZHENG Yong-nan, ZHOU Dong-mei, DU En-peng, YUAN Da-qing, DUAN Xiao, ZHU Sheng-yun. Investigation of Metal Hydride PdAgHx by Positron Annihilation[J]. Nuclear Physics Review, 2005, 22(1): 115-117. doi: 10.11804/NuclPhysRev.22.01.115

PdAgHx金属氢化物正电子湮没研究

doi: 10.11804/NuclPhysRev.22.01.115

Investigation of Metal Hydride PdAgHx by Positron Annihilation

  • 摘要: 在77—295 K温区和氢浓度0—0.35范围采用正电子湮没寿命测量方法研究了Pd0.75Ag0.25Hx氢化物合金. 充氢后正电子湮没寿命谱可以用两个寿命成分表征. 短寿命成分τ1不随温度和氢浓度变化, 是自由正电子湮没寿命; 长寿命成分τ2及其相对强度I2不随温度变化, 但随氢浓度的增加分别增大和减小, τ2是氢气泡捕获的正电子湮没寿命, τ2增大和I2减小说明随氢浓度增大氢聚集成的气泡的尺度增大, 而浓度减小. 实验结果表明, 氢脆的微观机理是氢气泡致脆. The metal hydride PdAgHx with a hydrogen concentration x ranging from 0 to 0.35 has been investigated by positron annihilation lifetime method in the temperature region between 77 K and 295 K. The measured lifetime spectra in metal hydride PdAgHx are characterized by two lifetimes τ1 and τ2. The short lifetime τ1 is independent of both hydrogen concentration and temperature, which is ascribed to the annihilation lifetime of free positrons. The long lifetime τ2 and its intensity I2 do not change with temperature, while τ2 increases and I2 decreases with increasing of hydrogen concentration. τ2 is attributed to the lifetime of positrons trapped at the hydrogen bubble. The increase of τ2 indicates the growth of the hydrogen bubble, and the decrease of I2 shows the reduction of the hydrogen bubble concentration. The experimental result shows a microscopic mechanism that the hydrogen bubble produced causes hydrogen embrittlement.
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出版历程
  • 收稿日期:  1900-01-01
  • 修回日期:  1900-01-01
  • 刊出日期:  2005-03-20

PdAgHx金属氢化物正电子湮没研究

doi: 10.11804/NuclPhysRev.22.01.115

摘要: 在77—295 K温区和氢浓度0—0.35范围采用正电子湮没寿命测量方法研究了Pd0.75Ag0.25Hx氢化物合金. 充氢后正电子湮没寿命谱可以用两个寿命成分表征. 短寿命成分τ1不随温度和氢浓度变化, 是自由正电子湮没寿命; 长寿命成分τ2及其相对强度I2不随温度变化, 但随氢浓度的增加分别增大和减小, τ2是氢气泡捕获的正电子湮没寿命, τ2增大和I2减小说明随氢浓度增大氢聚集成的气泡的尺度增大, 而浓度减小. 实验结果表明, 氢脆的微观机理是氢气泡致脆. The metal hydride PdAgHx with a hydrogen concentration x ranging from 0 to 0.35 has been investigated by positron annihilation lifetime method in the temperature region between 77 K and 295 K. The measured lifetime spectra in metal hydride PdAgHx are characterized by two lifetimes τ1 and τ2. The short lifetime τ1 is independent of both hydrogen concentration and temperature, which is ascribed to the annihilation lifetime of free positrons. The long lifetime τ2 and its intensity I2 do not change with temperature, while τ2 increases and I2 decreases with increasing of hydrogen concentration. τ2 is attributed to the lifetime of positrons trapped at the hydrogen bubble. The increase of τ2 indicates the growth of the hydrogen bubble, and the decrease of I2 shows the reduction of the hydrogen bubble concentration. The experimental result shows a microscopic mechanism that the hydrogen bubble produced causes hydrogen embrittlement.

English Abstract

左翼, 郑永男, 周冬梅, 杜恩鹏, 袁大庆, 段晓, 朱升云. PdAgHx金属氢化物正电子湮没研究[J]. 原子核物理评论, 2005, 22(1): 115-117. doi: 10.11804/NuclPhysRev.22.01.115
引用本文: 左翼, 郑永男, 周冬梅, 杜恩鹏, 袁大庆, 段晓, 朱升云. PdAgHx金属氢化物正电子湮没研究[J]. 原子核物理评论, 2005, 22(1): 115-117. doi: 10.11804/NuclPhysRev.22.01.115
ZUO Yi, ZHENG Yong-nan, ZHOU Dong-mei, DU En-peng, YUAN Da-qing, DUAN Xiao, ZHU Sheng-yun. Investigation of Metal Hydride PdAgHx by Positron Annihilation[J]. Nuclear Physics Review, 2005, 22(1): 115-117. doi: 10.11804/NuclPhysRev.22.01.115
Citation: ZUO Yi, ZHENG Yong-nan, ZHOU Dong-mei, DU En-peng, YUAN Da-qing, DUAN Xiao, ZHU Sheng-yun. Investigation of Metal Hydride PdAgHx by Positron Annihilation[J]. Nuclear Physics Review, 2005, 22(1): 115-117. doi: 10.11804/NuclPhysRev.22.01.115

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