论文标题
X射线吸收峰值移位的电子起源
Electronic origin of x-ray absorption peak shifts
论文作者
论文摘要
编码在瞬态X射线吸收(XAS)和磁循环(MCD)响应功能中,有大量超快脱氧化的微观过程信息。采用艺术状态的第一原理动态模拟我们表明,可以通过激光诱导的频段占用变化来解释,实验观察到了Ni中L3 XAS峰的能量转移,并且可以解释二分性MCD响应的相应移位。令人惊讶的是,我们预测,对于施加到CO的相同的超短泵脉冲将发生相反的效果:MCD峰的能量向上移动会大大转移,伴随着很小的变化XAS峰位置,这一事实与我们相关的$ D $ band band填充的事实使得coge的$ d $ band填充允许更大的能量范围上方的fermi能量上方的能量,从而激发了电荷。我们还仔细阐明了这种影响对泵脉冲参数的依赖性。这些发现(i)在瞬态XAS和MCD光谱中建立了电子起源,用于早期峰值变化,(ii)说明了从基础动力学系统的瞬态响应函数中提取的丰富信息。
Encoded in the transient x-ray absorption (XAS) and magnetic circular (MCD) response functions resides a wealth of information of the microscopic processes of ultrafast demagnetisation. Employing state of the art first principles dynamical simulations we show that the experimentally observed energy shift of the L3 XAS peak in Ni, and the absence of a corresponding shift in the dichroic MCD response, can be explained in terms of laser induced changes in band occupation. Strikingly, we predict that for the same ultrashort pump pulse applied to Co the opposite effect will occur: a substantial shift upwards in energy of the MCD peaks will be accompanied by very small change in the position of XAS peaks, a fact we relate to the reduced $d$-band filling of Co that allows a greater energetic range above the Fermi energy into which charge can be excited. We also carefully elucidate the dependence of this effect on pump pulse parameters. These findings (i) establish a electronic origin for early time peak shifts in transient XAS and MCD spectroscopy and (ii) illustrate the rich information that may be extracted from transient response functions of the underlying dynamical system.