Su Zhengxiong, Wang Sheng, Lu Chenyang, Peng Qing
Department of Nuclear Science and Technology, Xi'an Jiaotong University, No. 28, Xianning West Road, Xi'an 710049, Shaanxi, China.
Physics Department, King Fahd University of Petroleum & Minerals, Dhahran 31261, Saudi Arabia.
Materials (Basel). 2020 Jan 10;13(2):322. doi: 10.3390/ma13020322.
Hydrogen plays a significant role in the microstructure evolution and macroscopic deformation of materials, causing swelling and surface blistering to reduce service life. In the present work, the atomistic mechanisms of hydrogen bubble nucleation in vanadium were studied by first-principles calculations. The interstitial hydrogen atoms cannot form significant bound states with other hydrogen atoms in bulk vanadium, which explains the absence of hydrogen self-clustering from the experiments. To find the possible origin of hydrogen bubble in vanadium, we explored the minimum sizes of a vacancy cluster in vanadium for the formation of hydrogen molecule. We show that a freestanding hydrogen molecule can form and remain relatively stable in the center of a 54-hydrogen atom saturated 27-vacancy cluster.
氢在材料的微观结构演变和宏观变形中起着重要作用,会导致材料肿胀和表面起泡,从而缩短使用寿命。在本工作中,通过第一性原理计算研究了钒中氢气泡成核的原子机制。间隙氢原子在块状钒中不能与其他氢原子形成显著的束缚态,这解释了实验中未出现氢自聚集的现象。为了找到钒中氢气泡可能的起源,我们探索了钒中形成氢分子所需的空位团簇的最小尺寸。我们发现,一个独立的氢分子可以在由54个氢原子饱和的27个空位团簇中心形成并保持相对稳定。