ITC technique to monitor interactions between dislocations and aliovalent cations in alkali halides

R. Capelletti, A. Gainotti, M. Suszyńska
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引用次数: 1

Abstract

The features of C-peak appearing in the ITC spectra (300–370 K) of alkali halides doped with divalent cations are unusual. Its position and amplitude Hc are functions of thermal treatment, plastic deformation, impurity concentration, sample thickness and nature of contacts. Hc is strongly reduced by plastic deformation, according to the square root of the screw dislocation density; it is partially recovered by sample annealing in the 290–350 K range. Most of the results, obtained in a wide class of systems (such as LiF:Be, KC1 and NaCl:Eu, Pb, Ni), can be explained in terms of interfacial polarization induced by Cottrell atmosphere surrounding dislocations. The role of air gaps between sample and electrodes is also considered.
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监测碱卤化物中位错与价阳离子相互作用的ITC技术
掺杂二价阳离子的碱卤化物在300 ~ 370 K的ITC光谱中出现的c峰特征是不寻常的。其位置和振幅Hc是热处理、塑性变形、杂质浓度、试样厚度和接触性质的函数。根据螺位错密度的平方根,Hc被塑性变形强烈降低;样品在290 ~ 350 K范围内退火后部分恢复。在广泛的体系(如LiF:Be, KC1和NaCl:Eu, Pb, Ni)中获得的大多数结果都可以用Cottrell气氛周围位错引起的界面极化来解释。还考虑了样品和电极之间气隙的作用。
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