Li + diffusivity in 5 mol% MgO-doped LiNbO 3 crystal and Li-poor vapor transport equilibration effect on its surface composition

Li + diffusivity in 5 mol% MgO-doped LiNbO 3 crystal and Li-poor vapor transport equilibration effect on its surface composition
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DOI:
10.1016/j.jallcom.2012.01.127
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发表时间:
2012-07
影响因子:
6.2
通讯作者:
Zhen Wang;P. Hua;Shuai Zhang;D. Yu;E. Pun;De‐Long Zhang
Zhen Wang;P. Hua;Shuai Zhang;D. Yu;E. Pun;De‐Long Zhang
中科院分区:
材料科学2区
文献类型:
--
作者:
Zhen Wang;P. Hua;Shuai Zhang;D. Yu;E. Pun;De‐Long Zhang

文献摘要

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Diffusivity of Li+in 5mol% (in growth melt) MgO-doped LiNbO3crystal has been studied as a function of Li2O-content ranging from 43.4 to 44.4mol% under different temperatures. First, diffusion-limited Li2O-content depth profiles were produced by carrying out Li-poor vapour transport equilibration (VTE) treatments on two 0.5-mm-thick MgO-doped LiNbO3plates at 1100 and 1130°C for 40h. Second, the profiles were obtained by alternatively doing the optical polish to one crystal surface and the Li2O-content characterization on the polished surface through the measurement of birefringence. Third, Boltzmann–Matano method was applied to the profile to derive the Li+diffusivity as a function of Li2O-content. The results show that the diffusivity decreases with the reduced Li2O-content by at least two orders of magnitude as the Li2O-content reduces by 1mol% from the as-grown state. In the Li2O-content range studied, the diffusivity at 1130°C is at least two times larger than that at 1100°C. In addition, we also studied the time dependence of the Li-poor-VTE-induced reduction of Li2O-content on surface of the same MgO-doped crystal. The results show that the surface Li2O-content reduction induced has a square-root dependence on the VTE duration. Based upon this dependence, the mathematical solution to the Li+diffusion equation, an integral of error function complement, is obtained and verified by the experimental result. It is concluded that the MgO doping has less effect on both the Li+diffusivity and the dependence of surface Li2O-content reduction on the VTE duration.