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Differential ionization cross-section calculations for hydrogenic targets with Z <= 4 using a propagating exterior complex scaling method

机译:Z <= 4的氢靶标的微分电离截面计算,采用传播的外部复标度方法

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摘要

A propagating exterior complex scaling method, with iterative coupling, has been adapted for the electron impact of charged hydrogenic targets. Using this fully ab initio method for solving the Schrodinger equation, which has no uncontrolled approximations, we present highly accurate total, single-differential, double-differential, and triple-differential cross-section calculations for the electron-impact ionization of hydrogenic targets with nuclear charge Zless than or equal to4 (H, He+, Li2+, Be3+). For a fixed scaled energy, the total and differential cross sections begin to converge with respect to increasing Z when scaled by Z(4) and Z(6), respectively, and converge more rapidly with increasing incident-electron energy. The angular distributions of the differential cross sections change systematically with increasing nuclear charge for energies above the peak total ionization cross section, but for some lower-energy kinematics the triple-differential cross section for charged targets is significantly different from that of atomic hydrogen.
机译:具有迭代耦合的传播性外部复杂缩放方法已适应于带电氢靶的电子撞击。使用这种完全从头算的方法来求解没有不受控制的近似值的Schrodinger方程,我们提出了高度精确的总,单微分,双微分和三微分截面计算,用于氢靶的电子碰撞电离。核电荷Z小于或等于4(H,He +,Li2 +,Be3 +)。对于固定比例的能量,当分别用Z(4)和Z(6)进行比例缩放时,总截面和微分横截面开始随Z的增加而收敛,并随着入射电子能量的增加而更快地收敛。对于高于峰值总电离截面的能量,微分截面的角分布会随着核电荷的增加而系统地变化,但对于某些低能运动学,带电靶的三微分截面与原子氢的截面明显不同。

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