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首页> 外文期刊>Nuclear Instruments & Methods in Physics Research >Stopping powers of LiF thin filrns deposited onto self-supporting Al foils for swift protons
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Stopping powers of LiF thin filrns deposited onto self-supporting Al foils for swift protons

机译:沉积在自支撑铝箔上的LiF薄膜的阻挡力,用于快速质子

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摘要

The energy losses of ~(0.273-3.334) MeV protons in LiF thin films deposited by vacuum evaporation onto self-supporting Al foils have been measured using the transmission method. The thicknesses of selected and used LiF/Al target samples were accurately determined via systematic energy loss measurements for alpha particles from a very thin mixed ~(241)Am/~(239)Pu/~(233)U radioactive source. The samples were investigated in detail for their stoichiometry and their impurity contents by backscattering Rutherford spec-trometry and nuclear reaction analysis. Then, LiF stopping powers have been determined with overall relative uncertainty of less than 2.7% arising mainly from errors in the determination of target sample thicknesses. These S(E) data are reported and discussed in comparison to previous experimental data sets from the literature and to values calculated by the Sigmund-Schinner binary collision stopping theory both for molecular LiF, and for the LiF compound assuming Bragg-Kleeman's additivity rule. Our S(£) data show to be in excellent agreement with the latter theory for molecular LiF over the whole proton energy range explored, which supports the use of modified electronic hydrogen wave functions for evaluating atomic shell corrections in the case of low-Z_2 target materials. In contrast, they exhibit a slightly increasing deviation from theoretical values derived for the LiF compound with assuming stopping force additivity as the proton energy decreases from E ≈ 400 keV towards lower proton velocities. This deviation in excess relative to experimental data, amounting only up to (at most) ~2.5%, can be ascribed to strong effects of 2s-state valence electrons of Li atoms within the LiF compound. Besides, the comparison to values calculated by the SRIM-2008 computer code indicates that this program satisfactorily accounts for our S(E) data above E≈1.30 MeV but underestimates them with substantially increasing deviations (up to ~11%) towards lower proton velocities where the Bragg-Kleeman additivity rule therefore appears to be inapplicable.
机译:使用透射法测量了真空蒸发沉积在自支撑铝箔上的LiF薄膜中〜(0.273-3.334)MeV质子的能量损失。通过对来自非常薄的〜(241)Am /〜(239)Pu /〜(233)U放射源的α粒子的系统能量损失测量,可以准确地确定所选和使用的LiF / Al目标样品的厚度。通过反向散射卢瑟福光谱和核反应分析详细研究了样品的化学计量和杂质含量。然后,已确定LiF停止能力,其总体相对不确定度小于2.7%,这主要是由于目标样品厚度的确定误差所致。报告和讨论了这些S(E)数据,并将其与文献中的先前实验数据集进行比较,并与Sigmund-Schinner二元碰撞停止理论针对分子LiF以及假设Bragg-Kleeman加性规则的LiF化合物计算得出的值进行了比较。我们的S(£)数据表明与后者在整个质子能谱范围内对分子LiF的理论非常吻合,该理论支持在低Z_2目标的情况下使用改进的电子氢波函数评估原子壳层校正材料。相反,假设质子能量从E≈400 keV朝较低的质子速度降低,则在假定停止力加和的情况下,它们与LiF化合物的理论值略有增加。相对于实验数据而言,这种过量的偏差最多(最多)〜2.5%,可以归因于LiF化合物中Li原子的2s态价电子的强大影响。此外,与由SRIM-2008计算机代码计算出的值的比较表明,该程序令人满意地说明了我们在E≈1.30MeV以上的S(E)数据,但是低质子速度的偏差大大增加(高达〜11%),低估了它们。因此Bragg-Kleeman可加性规则似乎不适用。

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